Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:73879315-73880264 | Common:6; Rare:322 | ||||
| chr8:73971571-73971972 | Rare:185 | ||||
| chr8:73972040-73972682 | Common:14; Rare:1011 | ||||
| chr8:73972788-73973441 | Common:2; Rare:298 | ||||
| chr8:73975800-73976354 | Common:37; Rare:625; Clinvar:14; Clinvar (benign):13 | ||||
| chr8:73976280-73976540 | Common:1; Rare:88; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:73991116-73991516 | Common:6; Rare:196 | ||||
| chr8:74321460-74321770 | Common:3; Rare:94 | ||||
| chr8:74350070-74350560 | Common:4; Rare:243; Clinvar:2; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:76999840-77000563 | Common:47; Rare:1165; Clinvar:43; Clinvar (benign):4 | ||||
| chr8:77000530-77001130 | Common:10; Rare:340 | ||||
| chr8:78665830-78666220 | Common:5; Rare:424 | ||||
| chr8:78804500-78805260 | Common:1; Rare:190 | ||||
| chr8:79767500-79768500 | Common:8; Rare:826 | ||||
| chr8:80002559-80002959 | Common:1; Rare:73 |
- 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