Proximal
endothelial cell of umbilical vein(Human) | 16901 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:65006608-65006856 | Common:2; Rare:74 | ||||
| chr7:65373667-65373946 | Rare:87 | ||||
| chr7:65872944-65873392 | Common:5; Rare:153 | ||||
| chr7:65967888-65968045 | Common:1; Rare:36; Clinvar (pathogenic):1 | ||||
| chr7:65975287-65975317 | |||||
| chr7:65982132-65982390 | Common:3; Rare:75; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:66075598-66075974 | Rare:97; Clinvar (benign):1 | ||||
| chr7:66114750-66114965 | Common:1; Rare:96 | ||||
| chr7:66115179-66115381 | Rare:48 | ||||
| chr7:66205144-66205366 | Rare:45 | ||||
| chr7:66628636-66629110 | Common:3; Rare:171; Clinvar:8; Clinvar (benign):5 | ||||
| chr7:66682028-66682210 | Common:6; Rare:85 | ||||
| chr7:66921063-66921482 | Common:1; Rare:124 | ||||
| chr7:66995289-66995444 | Common:1; Rare:64; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr7:66996541-66996932 | Common:3; Rare:94 |
- 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