Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50343176-50343402 | Common:2; Rare:96 | ||||
| chr22:50475005-50475245 | Common:5; Rare:75 | ||||
| chr22:50481450-50481579 | Rare:43 | ||||
| chr22:50508395-50508553 | Common:2; Rare:44 | ||||
| chr22:50525491-50525870 | Common:7; Rare:197; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:50526099-50526271 | Common:2; Rare:90; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
| chr22:50529978-50530203 | Common:1; Rare:58; Clinvar:2 | ||||
| chr22:50530275-50530486 | Common:1; Rare:78 | ||||
| chr22:50530953-50531092 | Rare:45 | ||||
| chr22:50531820-50531967 | Rare:47 | ||||
| chr22:50532148-50532263 | Rare:30 | ||||
| chr22:50562881-50563106 | Common:3; Rare:55 | ||||
| chr22:50582387-50582704 | Common:1; Rare:151; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr22:50582740-50583185 | Common:9; Rare:164; Clinvar:2; Clinvar (benign):5 | ||||
| chr22:50600350-50600820 | Common:1; Rare:121 |
- 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