Proximal
endothelial cell of umbilical vein(Human) | 16901 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10960686-10961186 | Common:3; Rare:179; Clinvar (benign):2 | ||||
| chr19:11089295-11089564 | Rare:58; Clinvar:13; Clinvar (pathogenic):3 | ||||
| chr19:11170338-11170568 | Common:1; Rare:52 | ||||
| chr19:11197475-11197641 | Common:1; Rare:47 | ||||
| chr19:11217374-11217409 | Rare:10; Clinvar (pathogenic):1 | ||||
| chr19:11237765-11237823 | Rare:26 | ||||
| chr19:11237981-11238068 | Rare:26 | ||||
| chr19:11253101-11253209 | Rare:15 | ||||
| chr19:11262406-11262552 | Common:1; Rare:51 | ||||
| chr19:11344394-11344704 | Common:1; Rare:43 | ||||
| chr19:11374509-11374744 | Common:1; Rare:78 | ||||
| chr19:11374889-11375258 | Common:1; Rare:115 | ||||
| chr19:11435102-11435459 | Common:3; Rare:89; Clinvar (benign):1 | ||||
| chr19:11435589-11435757 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:11448201-11448628 | Common:3; Rare:137; Clinvar (benign):2; Clinvar (pathogenic):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