Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136409714-136410480 | Rare:309 | ||||
| chr9:136410448-136410780 | Common:41; Rare:809; Clinvar (pathogenic):1 | ||||
| chr9:136410791-136411453 | Common:8; Rare:314 | ||||
| chr9:136439296-136440151 | Common:5; Rare:498; Clinvar:8; Clinvar (benign):4 | ||||
| chr9:136482980-136483563 | Common:18; Rare:539 | ||||
| chr9:136483632-136484032 | Rare:283 | ||||
| chr9:136545817-136546243 | Common:7; Rare:715 | ||||
| chr9:136546282-136546452 | Common:2; Rare:38 | ||||
| chr9:136662360-136662600 | Common:1; Rare:53 | ||||
| chr9:136662650-136663535 | Common:9; Rare:471 | ||||
| chr9:136665401-136665895 | Common:13; Rare:604 | ||||
| chr9:136686925-136687325 | Common:3; Rare:253; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:136687320-136687742 | Common:12; Rare:589; Clinvar:32; Clinvar (benign):6 | ||||
| chr9:136687862-136688262 | Common:2; Rare:98 | ||||
| chr9:136712110-136712620 | Common:4; Rare:488 |
- 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