Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95005136-95005250 | Rare:40 | ||||
| chr9:95048229-95048635 | Common:3; Rare:198 | ||||
| chr9:95048840-95049267 | Common:6; Rare:237 | ||||
| chr9:95316246-95316646 | Common:3; Rare:80 | ||||
| chr9:95316810-95317216 | Common:10; Rare:368 | ||||
| chr9:95317130-95317473 | Common:22; Rare:356 | ||||
| chr9:95317489-95317900 | Common:8; Rare:386; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr9:95505707-95507029 | Common:23; Rare:1688; Clinvar:47; Clinvar (benign):45; Clinvar (pathogenic):2 | ||||
| chr9:95507094-95507244 | Common:2; Rare:53 | ||||
| chr9:95507204-95508220 | Common:37; Rare:1609; Clinvar:9; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr9:95508443-95508843 | Common:2; Rare:111 | ||||
| chr9:95516140-95516791 | Common:3; Rare:262; Clinvar (benign):3 | ||||
| chr9:95516750-95517260 | Common:9; Rare:238; Clinvar (pathogenic):1 | ||||
| chr9:95875308-95875870 | Common:7; Rare:865 | ||||
| chr9:95875790-95876498 | Common:43; Rare:641; Clinvar (benign):5; Clinvar (pathogenic):5 |
- 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