Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:34646504-34646733 | Common:1; Rare:73; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr9:34646902-34647057 | Rare:36; Clinvar (benign):1 | ||||
| chr9:34651973-34652221 | Rare:75 | ||||
| chr9:34664400-34664589 | Common:2; Rare:30 | ||||
| chr9:34665330-34665678 | Rare:105 | ||||
| chr9:34666034-34666196 | Common:2; Rare:37 | ||||
| chr9:34989312-34989752 | Common:2; Rare:112 | ||||
| chr9:34991710-34992030 | Common:1; Rare:71 | ||||
| chr9:34992352-34992752 | Common:6; Rare:121 | ||||
| chr9:35072536-35073010 | Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35079660-35079871 | Rare:38 | ||||
| chr9:35079904-35080197 | Common:5; Rare:79; Clinvar:3; Clinvar (benign):4 | ||||
| chr9:35096003-35096371 | Common:1; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:35096562-35096664 | Common:1; Rare:24 | ||||
| chr9:35103108-35103307 | Common:1; Rare:60 |
- 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