Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:133951922-133952076 | Common:3; Rare:32 | ||||
| chr6:133952559-133952712 | Common:1; Rare:23 | ||||
| chr6:133952716-133953246 | Common:3; Rare:121 | ||||
| chr6:134052638-134052784 | Common:1; Rare:23 | ||||
| chr6:134174803-134175128 | Common:1; Rare:164 | ||||
| chr6:135054774-135055045 | Common:6; Rare:83 | ||||
| chr6:135181138-135181276 | Rare:40 | ||||
| chr6:135497617-135498015 | Common:4; Rare:134; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136250257-136250598 | Common:2; Rare:97 | ||||
| chr6:136289309-136289456 | Rare:73 | ||||
| chr6:136289766-136290095 | Common:2; Rare:140 | ||||
| chr6:136550394-136550844 | Common:2; Rare:113 | ||||
| chr6:136792390-136792682 | Common:3; Rare:79 | ||||
| chr6:136822474-136822616 | Common:3; Rare:46; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:136822690-136823030 | Common:2; Rare:118; Clinvar:7; Clinvar (benign):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