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 |
|---|---|---|---|---|---|---|---|---|
| chr19 | 19410083 | 19410102 | CTCF | JASPAR | yes | 70824663 | ||
| chr19 | 19410094 | 19410106 | PROX1 | JASPAR | yes | 70824664 | ||
| chr19 | 19410096 | 19410101 | SP1 | TRANSFAC | yes | 70824665 | ||
| chr19 | 19410112 | 19410117 | TFAP2A | TRANSFAC | yes | 70824666 | ||
| chr19 | 19410112 | 19410118 | MZF1 | JASPAR | yes | 70824667 | ||
| chr19 | 19410118 | 19410129 | NRL | JASPAR | yes | 70824668 | ||
| chr19 | 19410133 | 19410136 | MYB | TRANSFAC | yes | 70824669 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19 | 19312225 | 19314233 | - | NR2C2AP | ENSG00000184162.10 | 19314233 | 0.56 | 1.0 | 17278 | 4155 | |
| chr19 | 19322782 | 19363042 | + | NCAN | ENSG00000130287.9 | 19322782 | 0.78 | 1.0 | 17279 | 12704 | |
| chr19 | 19366450 | 19373605 | - | HAPLN4 | ENSG00000187664.8 | 19373605 | 0.96 | 0.95 | 17280 | 63527 | |
| chr19 | 19375173 | 19384200 | - | TM6SF2 | ENSG00000213996.8 | 19384200 | 0.98 | 0.92 | 17281 | 74122 | |
| chr19 | 19386827 | 19431653 | - | SUGP1 | ENSG00000105705.11 | 19431653 | 0.66 | 1.0 | 17282 | 78497 | |
| chr19 | 19431490 | 19469563 | + | MAU2 | ENSG00000129933.16 | 19431490 | 0.66 | 1.0 | 17283 | 78660 | |
| chr19 | 19496635 | 19619740 | + | GATAD2A | ENSG00000167491.13 | 19496635 | 0.69 | 1.0 | 17284 | 13515 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|