Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:69165322-69165722 | Common:1; Rare:148 | ||||
| chrX:70133164-70133564 | Common:6; Rare:162 | ||||
| chrX:70133608-70134009 | Common:5; Rare:187 | ||||
| chrX:70176937-70177337 | Common:2; Rare:111 | ||||
| chrX:70289842-70290288 | Rare:355 | ||||
| chrX:70454800-70455240 | Common:2; Rare:208 | ||||
| chrX:70908620-70908890 | Rare:79 | ||||
| chrX:71067622-71068323 | Common:3; Rare:280 | ||||
| chrX:71068270-71068760 | Common:14; Rare:508 | ||||
| chrX:71095666-71096663 | Common:3; Rare:419 | ||||
| chrX:71104160-71104560 | Common:7; Rare:122 | ||||
| chrX:71106437-71106837 | Common:2; Rare:71 | ||||
| chrX:71110513-71110913 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chrX:71110955-71111355 | Common:2; Rare:146; Clinvar:1 | ||||
| chrX:71111419-71111819 | Rare:134; Clinvar:12; Clinvar (benign):1 |
- 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