Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:64313696-64314096 | Common:8; Rare:270 | ||||
| chr7:64314243-64314664 | Common:4; Rare:134 | ||||
| chr7:64562574-64562974 | Common:4; Rare:111 | ||||
| chr7:64562976-64563376 | Common:14; Rare:295 | ||||
| chr7:64665829-64666261 | Common:14; Rare:203 | ||||
| chr7:64666450-64666820 | Common:3; Rare:81 | ||||
| chr7:64794148-64794994 | Common:28; Rare:545 | ||||
| chr7:64902878-64903334 | Common:12; Rare:390 | ||||
| chr7:65006066-65007050 | Common:18; Rare:585 | ||||
| chr7:65007056-65007456 | Common:4; Rare:82 | ||||
| chr7:65141050-65141570 | Common:10; Rare:50 | ||||
| chr7:65373551-65374336 | Common:3; Rare:323 | ||||
| chr7:65872784-65873872 | Common:27; Rare:802 | ||||
| chr7:65980757-65981385 | Common:1; Rare:187 | ||||
| chr7:65981996-65982594 | Common:17; Rare:534; Clinvar:17; Clinvar (benign):19; Clinvar (pathogenic):8 |
- 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