Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:36190608-36191028 | Common:8; Rare:687 | ||||
| chr9:36257680-36258180 | Common:10; Rare:159 | ||||
| chr9:36258321-36258984 | Common:14; Rare:454; Clinvar:5; Clinvar (benign):7 | ||||
| chr9:36276885-36277285 | Common:3; Rare:182; Clinvar:15; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:36400010-36401443 | Common:42; Rare:1480 | ||||
| chr9:36486808-36487208 | Rare:169 | ||||
| chr9:36487353-36488060 | Common:7; Rare:887 | ||||
| chr9:36572638-36573087 | Common:5; Rare:483 | ||||
| chr9:36573133-36574297 | Common:5; Rare:236 | ||||
| chr9:37119911-37120640 | Common:13; Rare:968 | ||||
| chr9:37120825-37121492 | Common:3; Rare:151 | ||||
| chr9:37421960-37422410 | Common:2; Rare:79 | ||||
| chr9:37422464-37423050 | Common:20; Rare:724; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:37464543-37465213 | Common:11; Rare:330 | ||||
| chr9:37465140-37466150 | Common:32; Rare:1277 |
- 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