Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75270713-75270849 | Rare:35 | ||||
| chr17:75271167-75271393 | Common:3; Rare:39 | ||||
| chr17:75289365-75289733 | Common:3; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:75393784-75394064 | Common:1; Rare:64 | ||||
| chr17:75405609-75405923 | Common:2; Rare:103 | ||||
| chr17:75456392-75456690 | Common:2; Rare:95 | ||||
| chr17:75515600-75515777 | Rare:44 | ||||
| chr17:75516354-75516592 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:75524860-75525060 | Common:1; Rare:56 | ||||
| chr17:75525303-75525739 | Common:4; Rare:118 | ||||
| chr17:75557070-75557390 | Common:1; Rare:65 | ||||
| chr17:75633045-75633198 | Rare:35 | ||||
| chr17:75646060-75646530 | Common:5; Rare:94 | ||||
| chr17:75667125-75667420 | Common:4; Rare:102 | ||||
| chr17:75721330-75721546 | Common:3; Rare:68; Clinvar: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