Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:64665947-64666261 | Common:5; Rare:73 | ||||
| chr7:64794236-64794505 | Common:4; Rare:80 | ||||
| chr7:64903097-64903318 | Common:2; Rare:65 | ||||
| chr7:65006627-65006878 | Common:3; Rare:76 | ||||
| chr7:65373666-65373946 | Rare:87 | ||||
| chr7:65872892-65873172 | Common:3; Rare:91 | ||||
| chr7:65980902-65981014 | Rare:21 | ||||
| chr7:65982163-65982370 | Common:3; Rare:67; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:66075663-66075969 | Rare:72; Clinvar (benign):1 | ||||
| chr7:66114727-66114921 | Common:2; Rare:83 | ||||
| chr7:66115179-66115322 | Rare:34 | ||||
| chr7:66205171-66205361 | Rare:36 | ||||
| chr7:66628250-66628530 | Common:1; Rare:48 | ||||
| chr7:66628626-66628903 | Common:2; Rare:90; Clinvar:2 | ||||
| chr7:66628977-66629141 | Common:1; Rare:56; Clinvar:5; Clinvar (benign):6 |
- 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