Proximal
endothelial cell of umbilical vein(Human) | 16901 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:73498730-73498910 | Rare:58 | ||||
| chr5:73565366-73565811 | Common:7; Rare:136 | ||||
| chr5:73625498-73625780 | Common:2; Rare:51 | ||||
| chr5:73625939-73626322 | Common:4; Rare:100 | ||||
| chr5:73794148-73794453 | Common:5; Rare:64; Clinvar (benign):1 | ||||
| chr5:73882856-73883168 | Common:1; Rare:58 | ||||
| chr5:74632252-74632471 | Rare:42 | ||||
| chr5:74640429-74640699 | Common:1; Rare:81 | ||||
| chr5:74640711-74640934 | Common:1; Rare:69 | ||||
| chr5:74685281-74685556 | Common:2; Rare:100; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr5:74693551-74693700 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:74715373-74715690 | Common:2; Rare:74; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr5:74718554-74718881 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr5:74720190-74720742 | Common:2; Rare:155; Clinvar:2; Clinvar (pathogenic):5 | ||||
| chr5:74742297-74742481 | Common:1; Rare:41 |
- 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