Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:82373139-82373338 | Common:1; Rare:78 | ||||
| chr4:82374125-82374475 | Common:2; Rare:121 | ||||
| chr4:82429404-82429689 | Common:1; Rare:158; Clinvar:12; Clinvar (benign):6 | ||||
| chr4:82429834-82429990 | Common:1; Rare:36 | ||||
| chr4:82430196-82430358 | Rare:44 | ||||
| chr4:82430391-82430696 | Common:3; Rare:108 | ||||
| chr4:82798758-82799062 | Common:6; Rare:106 | ||||
| chr4:82891103-82891428 | Common:2; Rare:124 | ||||
| chr4:82900339-82900836 | Common:1; Rare:144 | ||||
| chr4:82900874-82901291 | Common:2; Rare:146 | ||||
| chr4:83010736-83011115 | Rare:57 | ||||
| chr4:83012872-83013289 | Common:2; Rare:110 | ||||
| chr4:83034823-83035256 | Common:1; Rare:110 | ||||
| chr4:83284437-83284596 | Common:2; Rare:65; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:83284677-83284895 | Common:3; Rare:91; Clinvar (benign):7; Clinvar (pathogenic):1 |
- 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