Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:100722600-100723090 | Common:5; Rare:363 | ||||
| chr8:100924217-100925301 | Common:6; Rare:240; Clinvar (pathogenic):1 | ||||
| chr8:100948587-100949201 | Common:2; Rare:183; Clinvar (pathogenic):2 | ||||
| chr8:100950366-100950766 | Common:57; Rare:667 | ||||
| chr8:100950711-100951567 | Common:21; Rare:684 | ||||
| chr8:100951592-100952799 | Common:12; Rare:1167 | ||||
| chr8:100952845-100953290 | Common:18; Rare:412 | ||||
| chr8:100953279-100953841 | Common:8; Rare:341 | ||||
| chr8:101204660-101205470 | Common:5; Rare:438 | ||||
| chr8:101205528-101206030 | Common:27; Rare:876 | ||||
| chr8:101206076-101206476 | Common:1; Rare:135 | ||||
| chr8:101206615-101207015 | Common:3; Rare:75 | ||||
| chr8:102238442-102239946 | Common:68; Rare:1513; Clinvar:6; Clinvar (benign):27; Clinvar (pathogenic):7 | ||||
| chr8:102411927-102412510 | Common:6; Rare:364 | ||||
| chr8:102412582-102413108 | Common:21; Rare:620 |
- 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