Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94895628-94895843 | Common:2; Rare:59 | ||||
| chr8:94896069-94896469 | Common:5; Rare:156 | ||||
| chr8:94949291-94949599 | Common:3; Rare:83 | ||||
| chr8:95024851-95025112 | Common:2; Rare:103; Clinvar:1; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr8:95133540-95133970 | Common:4; Rare:137 | ||||
| chr8:95268613-95268898 | Common:10; Rare:82 | ||||
| chr8:95269160-95269337 | Common:6; Rare:76; Clinvar:1 | ||||
| chr8:95269340-95270114 | Common:13; Rare:285 | ||||
| chr8:96235493-96235774 | Common:2; Rare:133; Clinvar (benign):3 | ||||
| chr8:96261392-96261963 | Common:7; Rare:179 | ||||
| chr8:96645173-96645458 | Common:2; Rare:72 | ||||
| chr8:97643416-97643816 | Common:8; Rare:97 | ||||
| chr8:97644021-97644556 | Common:6; Rare:164 | ||||
| chr8:97644962-97645362 | Common:2; Rare:150 | ||||
| chr8:97775656-97776027 | Common:5; Rare:193; 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