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 |
|---|---|---|---|---|---|---|---|---|
| chr11 | 122888963 | 122888967 | ESR1 | TRANSFAC | yes | 114146951 | ||
| chr11 | 122888984 | 122888990 | NFE2 | TRANSFAC | yes | 114146952 | ||
| chr11 | 122889050 | 122889062 | ZBTB7A | JASPAR | yes | 114146953 | ||
| chr11 | 122889052 | 122889067 | NR2C2 | JASPAR | yes | 114146954 | ||
| chr11 | 122889062 | 122889077 | PRDM1 | JASPAR | yes | 114146955 | ||
| chr11 | 122889073 | 122889082 | NKX2-8 | JASPAR | yes | 114146956 | ||
| chr11 | 122889073 | 122889083 | NKX2-3 | JASPAR | yes | 114146957 | ||
| chr11 | 122889098 | 122889106 | GATA3 | JASPAR | yes | 114146958 | ||
| chr11 | 122889099 | 122889112 | ELF1 | JASPAR | yes | 114146959 | ||
| chr11 | 122889102 | 122889112 | GABPA | JASPAR | yes | 114146960 | ||
| chr11 | 122889103 | 122889108 | ETS2 | TRANSFAC | yes | 114146961 | ||
| chr11 | 122889133 | 122889138 | ETS2 | TRANSFAC | yes | 114146962 | ||
| chr11 | 122889143 | 122889156 | SCRT2 | JASPAR | yes | 114146963 | ||
| chr11 | 122889174 | 122889185 | FOSL1 | JASPAR | yes | 114146964 | ||
| chr11 | 122889175 | 122889186 | JUNB | JASPAR | yes | 114146965 | ||
| chr11 | 122889204 | 122889215 | NFE2L2 | JASPAR | yes | 114146966 | ||
| chr11 | 122889210 | 122889220 | MLX | JASPAR | yes | 114146967 | ||
| chr11 | 122889230 | 122889236 | YY1 | JASPAR | yes | 114146968 | ||
| chr11 | 122889240 | 122889260 | RREB1 | JASPAR | yes | 114146969 | ||
| chr11 | 122889245 | 122889257 | ZBTB7B | JASPAR | yes | 114146970 | ||
| chr11 | 122889245 | 122889257 | ZBTB7C | JASPAR | yes | 114146971 | ||
| chr11 | 122889246 | 122889258 | ZBTB7A | JASPAR | yes | 114146972 | ||
| chr11 | 122889262 | 122889272 | NFIA | JASPAR | yes | 114146973 | ||
| chr11 | 122889263 | 122889272 | NFIX | JASPAR | yes | 114146974 | ||
| chr11 | 122889264 | 122889270 | NFIC | JASPAR | yes | 114146975 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr11 | 122889006 | rs114172895 | G | A | no | 2327440 | |
| chr11 | 122889049 | rs146417696 | C | T | no | 2327441 | |
| chr11 | 122889128 | rs113015134 | C | T | no | 2327442 | |
| chr11 | 122889215 | rs368240731 | C | A,T |
|
2327443 | |
| chr11 | 122889271 | rs142217458 | C | A,G |
|
2327444 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11 | 122848278 | 122852428 | - | BSX | ENSG00000188909.4 | 122852428 | 1.0 | 1.0 | 11555 | 63547 | |
| chr11 | 122928197 | 122933938 | - | HSPA8 | ENSG00000109971.9 | 122933938 | 0.83 | 0.99 | 11556 | 55335 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|