Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4767118-4767406 | Common:2; Rare:91 | ||||
| chr16:4802139-4802438 | Common:1; Rare:159; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:4802621-4802806 | Rare:60; Clinvar:5 | ||||
| chr16:4802870-4803140 | Common:4; Rare:133; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:4847234-4847525 | Common:3; Rare:139 | ||||
| chr16:4937135-4937406 | Common:5; Rare:91 | ||||
| chr16:4957755-4957857 | Common:2; Rare:28 | ||||
| chr16:5033851-5034010 | Rare:68 | ||||
| chr16:5071765-5071912 | Rare:85; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:5072107-5072306 | Common:1; Rare:46 | ||||
| chr16:5097682-5097943 | Common:4; Rare:107 | ||||
| chr16:8572770-8573300 | Common:5; Rare:142 | ||||
| chr16:8621575-8621752 | Common:1; Rare:66 | ||||
| chr16:8674363-8674661 | Common:2; Rare:105; Clinvar:2 | ||||
| chr16:8797606-8797888 | Common:1; Rare:112; Clinvar:2; Clinvar (benign):2; 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