Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:79009497-79009939 | Common:11; Rare:118; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:79024250-79024650 | Common:5; Rare:93 | ||||
| chr17:79074625-79074973 | Common:5; Rare:93 | ||||
| chr17:79777635-79777788 | Rare:31 | ||||
| chr17:79777874-79778264 | Common:1; Rare:167 | ||||
| chr17:79797002-79797439 | Common:1; Rare:152 | ||||
| chr17:79801291-79801477 | Common:1; Rare:33 | ||||
| chr17:79801530-79801950 | Rare:58 | ||||
| chr17:79839426-79839723 | Rare:76 | ||||
| chr17:79839885-79840019 | Common:1; Rare:38 | ||||
| chr17:80035819-80036060 | Common:1; Rare:77 | ||||
| chr17:80036498-80036694 | Common:2; Rare:54; Clinvar (benign):2 | ||||
| chr17:80101373-80101651 | Common:4; Rare:122; Clinvar (benign):4 | ||||
| chr17:80147139-80147470 | Common:7; Rare:120 | ||||
| chr17:80220273-80220459 | Common:1; Rare:76; Clinvar:1; Clinvar (pathogenic):2 |
- 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