Input Chromosomal region, for example: chr1:1000-10000 to view the enhancers around this region
| Chrom. | Start | End | TF Name | Source | Predicted site? | Tissue/Cell line | id | More |
|---|---|---|---|---|---|---|---|---|
| chr2 | 204668907 | 204668922 | RUNX2 | JASPAR | yes | 22195378 | ||
| chr2 | 204668907 | 204668922 | RUNX2 | JASPAR | yes | 80267053 | ||
| chr2 | 204668910 | 204668921 | RUNX1 | JASPAR | yes | 22195379 | ||
| chr2 | 204668910 | 204668921 | RUNX1 | JASPAR | yes | 80267054 | ||
| chr2 | 204668911 | 204668921 | RUNX3 | JASPAR | yes | 22195380 | ||
| chr2 | 204668911 | 204668921 | RUNX3 | JASPAR | yes | 80267055 | ||
| chr2 | 204668912 | 204668921 | RUNX2 | JASPAR | yes | 22195381 | ||
| chr2 | 204668912 | 204668921 | RUNX2 | JASPAR | yes | 80267056 | ||
| chr2 | 204668953 | 204668956 | MYB | TRANSFAC | yes | 22195382 | ||
| chr2 | 204668953 | 204668956 | MYB | TRANSFAC | yes | 80267057 | ||
| chr2 | 204668970 | 204668977 | SPIB | JASPAR | yes | 22195383 | ||
| chr2 | 204668970 | 204668977 | SPIB | JASPAR | yes | 80267058 | ||
| chr2 | 204668982 | 204668997 | STAT1 | JASPAR | yes | 22195384 | ||
| chr2 | 204668982 | 204668997 | STAT1 | JASPAR | yes | 80267059 | ||
| chr2 | 204668984 | 204668995 | STAT1 | JASPAR | yes | 22195385 | ||
| chr2 | 204668984 | 204668995 | STAT3 | JASPAR | yes | 22195386 | ||
| chr2 | 204668984 | 204668995 | STAT1 | JASPAR | yes | 80267060 | ||
| chr2 | 204668984 | 204668995 | STAT3 | JASPAR | yes | 80267061 | ||
| chr2 | 204669011 | 204669025 | EBF1 | JASPAR | yes | 22195387 | ||
| chr2 | 204669011 | 204669025 | EBF1 | JASPAR | yes | 80267062 | ||
| chr2 | 204669070 | 204669080 | MAX | JASPAR | yes | 22195388 | ||
| chr2 | 204669070 | 204669080 | MAX | JASPAR | yes | 80267063 | ||
| chr2 | 204669071 | 204669081 | CLOCK | JASPAR | yes | 22195389 | ||
| chr2 | 204669071 | 204669081 | MAX | JASPAR | yes | 22195390 | ||
| chr2 | 204669071 | 204669081 | CLOCK | JASPAR | yes | 80267064 | ||
| chr2 | 204669071 | 204669081 | MAX | JASPAR | yes | 80267065 | ||
| chr2 | 204669073 | 204669078 | MYC | TRANSFAC | yes | 22195391 | ||
| chr2 | 204669073 | 204669078 | USF1 | TRANSFAC | yes | 22195392 | ||
| chr2 | 204669073 | 204669078 | USF2 | TRANSFAC | yes | 22195393 | ||
| chr2 | 204669073 | 204669078 | MYC | TRANSFAC | yes | 80267066 | ||
| chr2 | 204669073 | 204669078 | USF1 | TRANSFAC | yes | 80267067 | ||
| chr2 | 204669073 | 204669078 | USF2 | TRANSFAC | yes | 80267068 | ||
| chr2 | 204669073 | 204669080 | USF1 | JASPAR | yes | 22195394 | ||
| chr2 | 204669073 | 204669080 | USF1 | JASPAR | yes | 80267069 | ||
| chr2 | 204669077 | 204669090 | ZBTB18 | JASPAR | yes | 22195395 | ||
| chr2 | 204669077 | 204669090 | ZBTB18 | JASPAR | yes | 80267070 | ||
| chr2 | 204669078 | 204669082 | LFA1 | TRANSFAC | yes | 22195396 | ||
| chr2 | 204669078 | 204669082 | LFA1 | TRANSFAC | yes | 80267071 | ||
| chr2 | 204669095 | 204669107 | TEAD1 | JASPAR | yes | 22195397 | ||
| chr2 | 204669095 | 204669107 | TEAD1 | JASPAR | yes | 80267072 | ||
| chr2 | 204669096 | 204669102 | PEA3 | TRANSFAC | yes | 22195398 | ||
| chr2 | 204669096 | 204669102 | PEA3 | TRANSFAC | yes | 80267073 | ||
| chr2 | 204669097 | 204669107 | TEAD1 | JASPAR | yes | 22195399 | ||
| chr2 | 204669097 | 204669107 | TEAD4 | JASPAR | yes | 22195400 | ||
| chr2 | 204669097 | 204669107 | TEAD1 | JASPAR | yes | 80267074 | ||
| chr2 | 204669097 | 204669107 | TEAD4 | JASPAR | yes | 80267075 | ||
| chr2 | 204669098 | 204669106 | TEAD3 | JASPAR | yes | 22195401 | ||
| chr2 | 204669098 | 204669106 | TEAD3 | JASPAR | yes | 80267076 | ||
| chr2 | 204669121 | 204669136 | PRDM1 | JASPAR | yes | 22195402 | ||
| chr2 | 204669121 | 204669136 | PRDM1 | JASPAR | yes | 80267077 | ||
| chr2 | 204669135 | 204669139 | H1TF2 | TRANSFAC | yes | 22195403 | ||
| chr2 | 204669135 | 204669139 | NFE | TRANSFAC | yes | 22195404 | ||
| chr2 | 204669135 | 204669139 | SRF | TRANSFAC | yes | 22195405 | ||
| chr2 | 204669135 | 204669139 | H1TF2 | TRANSFAC | yes | 80267078 | ||
| chr2 | 204669135 | 204669139 | NFE | TRANSFAC | yes | 80267079 | ||
| chr2 | 204669135 | 204669139 | SRF | TRANSFAC | yes | 80267080 | ||
| chr2 | 204669147 | 204669163 | RFX2 | JASPAR | yes | 22195406 | ||
| chr2 | 204669147 | 204669163 | RFX3 | JASPAR | yes | 22195407 | ||
| chr2 | 204669147 | 204669163 | RFX4 | JASPAR | yes | 22195408 | ||
| chr2 | 204669147 | 204669163 | RFX5 | JASPAR | yes | 22195409 | ||
| chr2 | 204669147 | 204669163 | RFX2 | JASPAR | yes | 80267081 | ||
| chr2 | 204669147 | 204669163 | RFX3 | JASPAR | yes | 80267082 | ||
| chr2 | 204669147 | 204669163 | RFX4 | JASPAR | yes | 80267083 | ||
| chr2 | 204669147 | 204669163 | RFX5 | JASPAR | yes | 80267084 | ||
| chr2 | 204669148 | 204669167 | RFX2 | JASPAR | yes | 22195410 | ||
| chr2 | 204669148 | 204669167 | RFX2 | JASPAR | yes | 80267085 | ||
| chr2 | 204669150 | 204669165 | RFX5 | JASPAR | yes | 22195411 | ||
| chr2 | 204669150 | 204669165 | RFX5 | JASPAR | yes | 80267086 | ||
| chr2 | 204669170 | 204669180 | HOXB13 | JASPAR | yes | 22195412 | ||
| chr2 | 204669170 | 204669180 | HOXB13 | JASPAR | yes | 80267087 | ||
| chr2 | 204669171 | 204669181 | HOXA13 | JASPAR | yes | 22195413 | ||
| chr2 | 204669171 | 204669181 | HOXA13 | JASPAR | yes | 80267088 | ||
| chr2 | 204669177 | 204669183 | HiNF-A | TRANSFAC | yes | 22195414 | ||
| chr2 | 204669177 | 204669183 | HiNF-A | TRANSFAC | yes | 80267089 | ||
| chr2 | 204669193 | 204669201 | MEIS2 | JASPAR | yes | 22195415 | ||
| chr2 | 204669193 | 204669201 | MEIS2 | JASPAR | yes | 80267090 | ||
| chr2 | 204669194 | 204669198 | NFE | TRANSFAC | yes | 22195416 | ||
| chr2 | 204669194 | 204669198 | NFE | TRANSFAC | yes | 80267091 | ||
| chr2 | 204669194 | 204669201 | MEIS1 | JASPAR | yes | 22195417 | ||
| chr2 | 204669194 | 204669201 | MEIS1 | JASPAR | yes | 80267092 | ||
| chr2 | 204669206 | 204669212 | TBP | TRANSFAC | yes | 22195418 | ||
| chr2 | 204669206 | 204669212 | TBP | TRANSFAC | yes | 80267093 | ||
| chr2 | 204669215 | 204669228 | SCRT2 | JASPAR | yes | 22195419 | ||
| chr2 | 204669215 | 204669228 | SCRT2 | JASPAR | yes | 80267094 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr2 | 204669019 | rs140300385 | G | A |
|
6303297 | |
| chr2 | 204669118 | rs114598919 | C | T | no | 6303298 | |
| chr2 | 204669208 | rs542692523 | A | T |
|
6303299 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2 | 204571198 | 204603635 | + | CD28 | ENSG00000178562.13 | 204571198 | 0.95 | 0.97 | 3072 | 2285 | |
| chr2 | 204732509 | 204738683 | + | CTLA4 | ENSG00000163599.10 | 204732509 | 0.89 | 0.99 | 3073 | 36709 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|