Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128322388-128322643 | Common:1; Rare:78 | ||||
| chr9:128322704-128322935 | Common:3; Rare:104; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr9:128340089-128340261 | Common:4; Rare:69 | ||||
| chr9:128340485-128340593 | Common:1; Rare:40 | ||||
| chr9:128371128-128371477 | Common:1; Rare:124 | ||||
| chr9:128420331-128420475 | Common:1; Rare:33 | ||||
| chr9:128420550-128420910 | Common:3; Rare:101 | ||||
| chr9:128455794-128456220 | Common:2; Rare:130 | ||||
| chr9:128456812-128457011 | Common:1; Rare:51 | ||||
| chr9:128504500-128504792 | Common:2; Rare:117; Clinvar:5 | ||||
| chr9:128552380-128552609 | Rare:83; Clinvar:1 | ||||
| chr9:128635270-128635590 | Common:2; Rare:90 | ||||
| chr9:128635739-128635886 | Rare:38 | ||||
| chr9:128635990-128636370 | Common:7; Rare:113; Clinvar (benign):2 | ||||
| chr9:128656619-128657147 | Common:3; Rare:173; Clinvar (pathogenic):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