Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66075555-66075980 | Rare:221; Clinvar (benign):2 | ||||
| chr7:66075915-66076315 | Common:1; Rare:96; Clinvar (benign):1 | ||||
| chr7:66114084-66114484 | Common:2; Rare:137 | ||||
| chr7:66114718-66114929 | Common:7; Rare:377 | ||||
| chr7:66115095-66115495 | Common:6; Rare:306 | ||||
| chr7:66204505-66205440 | Common:1; Rare:346 | ||||
| chr7:66628329-66628492 | Common:1; Rare:29 | ||||
| chr7:66628550-66629105 | Common:15; Rare:794; Clinvar:28; Clinvar (benign):9 | ||||
| chr7:66681592-66682261 | Common:33; Rare:690 | ||||
| chr7:66740404-66740800 | Common:14; Rare:445 | ||||
| chr7:66741090-66741275 | Common:2; Rare:88 | ||||
| chr7:66920151-66921428 | Common:12; Rare:767 | ||||
| chr7:66921580-66922674 | Common:5; Rare:312 | ||||
| chr7:66995035-66995435 | Common:2; Rare:127; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr7:66995462-66995890 | Common:4; Rare:282 |
- 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