Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42541485-42541671 | Common:2; Rare:50 | ||||
| chr8:42541682-42541937 | Common:1; Rare:83; Clinvar (benign):1 | ||||
| chr8:42842748-42842866 | Common:1; Rare:30 | ||||
| chr8:42842964-42843121 | Rare:52; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:42843252-42843540 | Common:3; Rare:80; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:42896390-42896556 | Common:2; Rare:88 | ||||
| chr8:42896827-42897011 | Rare:56 | ||||
| chr8:42897270-42897430 | Common:2; Rare:84 | ||||
| chr8:43055969-43056342 | Common:2; Rare:100 | ||||
| chr8:43093421-43093566 | Common:3; Rare:32; Clinvar (benign):1 | ||||
| chr8:43139926-43140513 | Common:2; Rare:195; Clinvar:5 | ||||
| chr8:43140618-43140785 | Common:3; Rare:63 | ||||
| chr8:47260714-47260990 | Common:3; Rare:123 | ||||
| chr8:47960101-47960306 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:47960642-47960996 | Common:2; Rare:137; Clinvar:13; Clinvar (benign):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