Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:98807345-98808099 | Common:15; Rare:676; Clinvar:36; Clinvar (benign):11 | ||||
| chr9:98808470-98808820 | Rare:110 | ||||
| chr9:98848443-98848990 | Common:3; Rare:240; Clinvar:1 | ||||
| chr9:98943603-98944962 | Common:25; Rare:779 | ||||
| chr9:99103930-99104750 | Common:2; Rare:310 | ||||
| chr9:99104709-99105193 | Common:12; Rare:893; Clinvar (benign):6 | ||||
| chr9:99105420-99106290 | Common:6; Rare:302 | ||||
| chr9:99221290-99221659 | Rare:188; Clinvar:4; Clinvar (benign):6 | ||||
| chr9:99221717-99222439 | Common:26; Rare:1386; Clinvar:25; Clinvar (benign):30 | ||||
| chr9:99821568-99821968 | Rare:250 | ||||
| chr9:99906424-99906824 | Common:2; Rare:525 | ||||
| chr9:99906943-99907343 | Common:2; Rare:84 | ||||
| chr9:100098893-100099454 | Common:21; Rare:776; Clinvar:13; Clinvar (benign):1 | ||||
| chr9:100099430-100099830 | Rare:92 | ||||
| chr9:100352357-100353190 | Common:7; Rare:1016 |
- 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