Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127897260-127897733 | Common:6; Rare:347 | ||||
| chr9:127898301-127899059 | Common:5; Rare:164 | ||||
| chr9:127899403-127899876 | Common:12; Rare:493 | ||||
| chr9:127914834-127915251 | Rare:162 | ||||
| chr9:127916920-127917355 | Common:4; Rare:421 | ||||
| chr9:127927113-127927851 | Common:5; Rare:477 | ||||
| chr9:127930747-127931147 | Common:4; Rare:105 | ||||
| chr9:127937033-127937552 | Common:7; Rare:159; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:127937698-127938199 | Common:15; Rare:528; Clinvar:32; Clinvar (benign):19 | ||||
| chr9:127938140-127938693 | Common:5; Rare:222; Clinvar:7; Clinvar (benign):4 | ||||
| chr9:127938615-127939015 | Common:7; Rare:64 | ||||
| chr9:127980390-127980790 | Common:5; Rare:219 | ||||
| chr9:127980936-127981372 | Common:13; Rare:558 | ||||
| chr9:128065858-128066673 | Common:10; Rare:368 | ||||
| chr9:128066882-128067605 | Common:16; Rare:395 |
- 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