Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1462713-1463113 | Common:9; Rare:135 | ||||
| chr17:1463284-1463586 | Common:1; Rare:67 | ||||
| chr17:1485081-1485499 | Common:5; Rare:194 | ||||
| chr17:1486931-1487064 | Rare:28 | ||||
| chr17:1516651-1516970 | Common:1; Rare:114 | ||||
| chr17:1562733-1562984 | Common:3; Rare:89 | ||||
| chr17:1628389-1628544 | Rare:48 | ||||
| chr17:1628809-1629030 | Rare:79 | ||||
| chr17:1648852-1649270 | Common:4; Rare:154 | ||||
| chr17:1649497-1649604 | Common:1; Rare:41 | ||||
| chr17:1684798-1685082 | Common:2; Rare:94; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1710346-1710505 | Rare:43 | ||||
| chr17:1716183-1716754 | Common:5; Rare:176 | ||||
| chr17:1717020-1717347 | Common:1; Rare:68 | ||||
| chr17:1730924-1731324 | Common:1; Rare:184; Clinvar (pathogenic):2 |
- Legend for epigenomic status:
- : Enriched for H3K27ac and DNaseI signal
- : Enriched for H3K4me3 and DNaseI signal
- : Enriched for CTCF binding signal
- Legend for core promoter element:
- : Found Initiator
- : Found DPR
- : Enriched TATA box