Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15699442-15699804 | Common:5; Rare:99 | ||||
| chr17:15944560-15944810 | Common:3; Rare:70 | ||||
| chr17:15944896-15945134 | Common:1; Rare:55 | ||||
| chr17:15945160-15945334 | Common:3; Rare:46 | ||||
| chr17:15999556-15999859 | Common:3; Rare:153; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:16215454-16215715 | Common:2; Rare:123 | ||||
| chr17:16217086-16217301 | Rare:69; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr17:16353283-16353752 | Common:1; Rare:148 | ||||
| chr17:16380654-16380779 | Common:2; Rare:25 | ||||
| chr17:16381001-16381424 | Common:4; Rare:179 | ||||
| chr17:16419244-16419359 | Rare:32 | ||||
| chr17:16491920-16492580 | Common:5; Rare:171 | ||||
| chr17:16653583-16653994 | Common:2; Rare:115 | ||||
| chr17:17042210-17042523 | Common:19; Rare:117 | ||||
| chr17:17237119-17237761 | Common:8; Rare:187; Clinvar:1; Clinvar (benign):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