Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:91880633-91880807 | Common:1; Rare:51 | ||||
| chr7:91940181-91940440 | Rare:49 | ||||
| chr7:91940685-91940978 | Common:5; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:92134377-92134636 | Common:1; Rare:78 | ||||
| chr7:92134779-92134944 | Common:2; Rare:54 | ||||
| chr7:92178921-92179083 | Rare:36 | ||||
| chr7:92245470-92245696 | Rare:59; Clinvar (benign):1 | ||||
| chr7:92245855-92246274 | Common:6; Rare:108; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92447263-92447520 | Common:3; Rare:80 | ||||
| chr7:92528370-92528814 | Common:3; Rare:136; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92589982-92590157 | Common:1; Rare:65 | ||||
| chr7:92590336-92590534 | Rare:62 | ||||
| chr7:92833780-92834270 | Common:1; Rare:103 | ||||
| chr7:92835264-92835424 | Common:1; Rare:39 | ||||
| chr7:92836519-92836677 | Rare:43 |
- 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