Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144078272-144078770 | Common:7; Rare:682 | ||||
| chr8:144078960-144079360 | Common:5; Rare:217 | ||||
| chr8:144079314-144079714 | Common:1; Rare:165 | ||||
| chr8:144082290-144082901 | Common:17; Rare:777 | ||||
| chr8:144082864-144083400 | Common:4; Rare:288 | ||||
| chr8:144094809-144095209 | Common:12; Rare:433; Clinvar (benign):5 | ||||
| chr8:144095355-144095755 | Rare:136 | ||||
| chr8:144095946-144096733 | Common:5; Rare:575; Clinvar:3; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr8:144099123-144100095 | Common:5; Rare:434; Clinvar (benign):1 | ||||
| chr8:144100351-144100751 | Common:4; Rare:123 | ||||
| chr8:144103569-144103918 | Common:10; Rare:451; Clinvar (benign):1 | ||||
| chr8:144104070-144104590 | Common:23; Rare:1005 | ||||
| chr8:144104738-144105775 | Common:11; Rare:589; Clinvar (benign):1 | ||||
| chr8:144105745-144106929 | Common:4; Rare:450 | ||||
| chr8:144137300-144137440 | Rare:34 |
- 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