Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73293608-73293819 | Common:1; Rare:83 | ||||
| chr2:73385550-73386076 | Common:4; Rare:226; Clinvar:16; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73386183-73386348 | Common:1; Rare:61; Clinvar (benign):3 | ||||
| chr2:73737237-73737634 | Common:3; Rare:126 | ||||
| chr2:73780035-73780262 | Common:1; Rare:94 | ||||
| chr2:73783450-73783850 | Common:4; Rare:165 | ||||
| chr2:73828777-73829037 | Common:1; Rare:62 | ||||
| chr2:73926677-73926956 | Common:2; Rare:130; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74178845-74179091 | Common:3; Rare:79 | ||||
| chr2:74198326-74198635 | Common:1; Rare:104 | ||||
| chr2:74199099-74199335 | Rare:50 | ||||
| chr2:74391795-74392177 | Common:2; Rare:170 | ||||
| chr2:74421377-74421797 | Rare:113 | ||||
| chr2:74440523-74440698 | Rare:49 | ||||
| chr2:74440884-74441000 | Rare:16 |
- 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