Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219177819-219177954 | Common:4; Rare:28 | ||||
| chr2:219178095-219178320 | Common:6; Rare:114 | ||||
| chr2:219206648-219206923 | Rare:97 | ||||
| chr2:219207018-219207234 | Common:3; Rare:68 | ||||
| chr2:219218304-219218704 | Common:1; Rare:205; Clinvar (pathogenic):1 | ||||
| chr2:219218925-219219180 | Common:2; Rare:82 | ||||
| chr2:219229513-219229943 | Common:2; Rare:127 | ||||
| chr2:219245364-219245569 | Common:1; Rare:61 | ||||
| chr2:219253875-219254064 | Common:2; Rare:60 | ||||
| chr2:219277746-219277959 | Common:1; Rare:40 | ||||
| chr2:219279190-219279430 | Common:2; Rare:75 | ||||
| chr2:219279660-219280220 | Common:1; Rare:139; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:219298710-219299070 | Common:4; Rare:93 | ||||
| chr2:219387357-219387485 | Rare:22 | ||||
| chr2:219433890-219434400 | Common:1; Rare:100 |
- 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