Proximal
endothelial cell of umbilical vein(Human) | 16901 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:10697477-10697653 | Common:3; Rare:82; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:10729966-10730128 | Common:3; Rare:36 | ||||
| chr17:11997414-11997588 | Rare:64 | ||||
| chr17:13017098-13017262 | Rare:42 | ||||
| chr17:13017377-13017478 | Common:1; Rare:24 | ||||
| chr17:13017609-13017837 | Common:1; Rare:100; Clinvar (benign):3 | ||||
| chr17:13017937-13018302 | Common:6; Rare:118; Clinvar (benign):2 | ||||
| chr17:14069395-14069593 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:15260701-15261027 | Common:2; Rare:108; Clinvar (benign):5 | ||||
| chr17:15503246-15503504 | Common:4; Rare:63 | ||||
| chr17:15699528-15699823 | Common:4; Rare:85 | ||||
| chr17:15999461-15999907 | Common:4; Rare:220; Clinvar:6; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr17:15999984-16000253 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:16000324-16000653 | Common:2; Rare:75 | ||||
| chr17:16024828-16025028 | Common:3; Rare:35 |
- 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