Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42017357-42017821 | Common:1; Rare:149 | ||||
| chr17:42019891-42020162 | Common:1; Rare:72 | ||||
| chr17:42028580-42028910 | Common:1; Rare:88 | ||||
| chr17:42107751-42107963 | Common:1; Rare:82 | ||||
| chr17:42154950-42155176 | Common:3; Rare:54 | ||||
| chr17:42194448-42194601 | Rare:29 | ||||
| chr17:42275849-42276141 | Common:2; Rare:51 | ||||
| chr17:42325009-42325409 | Common:1; Rare:73; Clinvar (benign):3 | ||||
| chr17:42388410-42388930 | Common:1; Rare:140; Clinvar:2 | ||||
| chr17:42423213-42423471 | Common:1; Rare:67; Clinvar:1 | ||||
| chr17:42458684-42458942 | Common:3; Rare:92 | ||||
| chr17:42520171-42520384 | Rare:45 | ||||
| chr17:42536101-42536273 | Common:2; Rare:56; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:42536470-42536786 | Common:2; Rare:83; Clinvar:4; Clinvar (pathogenic):4 | ||||
| chr17:42561971-42562231 | Common:1; Rare:80 |
- 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