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 |
|---|---|---|---|---|---|---|---|---|
| chr5 | 170103374 | 170103378 | YY1 | TRANSFAC | yes | 70759396 | ||
| chr5 | 170103395 | 170103410 | HNF1A | JASPAR | yes | 70759397 | ||
| chr5 | 170103396 | 170103409 | HNF1B | JASPAR | yes | 70759398 | ||
| chr5 | 170103396 | 170103410 | ONECUT1 | JASPAR | yes | 70759399 | ||
| chr5 | 170103396 | 170103410 | ONECUT2 | JASPAR | yes | 70759400 | ||
| chr5 | 170103396 | 170103410 | ONECUT3 | JASPAR | yes | 70759401 | ||
| chr5 | 170103408 | 170103425 | PAX1 | JASPAR | yes | 70759402 | ||
| chr5 | 170103408 | 170103425 | PAX9 | JASPAR | yes | 70759403 | ||
| chr5 | 170103420 | 170103423 | MYB | TRANSFAC | yes | 70759404 |
| chrom | Position | dbSNP ID | Reference Allele | Alternative Allele | is SNP in TFBS | id | More |
|---|---|---|---|---|---|---|---|
| chr5 | 170103424 | rs75444782 | C | A,T |
|
8692247 |
| Chrom | Start | End | Strand | Gene Name | Ensembl ID | TSS | TSI of Normal tissues | TSI of Cancer tissues | Distance between enhancer and TSS | id | More |
|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5 | 170190354 | 170241051 | + | GABRP | ENSG00000094755.12 | 170190354 | 0.98 | 0.98 | 5971 | 13072 |
| Chrom | Start | End | Strand | miRNA Name | miRBase ID | TSS | Score | TSI of Normal tissues | TSI of Cancer tissues | id | More |
|---|