Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:5950467-5950667 | Common:8; Rare:55 | ||||
chr20:13784884-13785080 | Common:2; Rare:87; Clinvar (benign):3 | ||||
chr20:16573321-16573540 | Common:1; Rare:59 | ||||
chr20:17968461-17968656 | Common:4; Rare:90 | ||||
chr20:17968784-17969122 | Common:3; Rare:120 | ||||
chr20:18288487-18288564 | Rare:21 | ||||
chr20:20017143-20017372 | Rare:69 | ||||
chr20:32207712-32207944 | Common:3; Rare:91 | ||||
chr20:33401511-33401582 | Rare:19 | ||||
chr20:34303281-34303305 | Common:1; Rare:11; Clinvar (benign):1 | ||||
chr20:34677090-34677291 | Rare:52 | ||||
chr20:34955736-34955868 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):2 | ||||
chr20:35147316-35147461 | Rare:43 | ||||
chr20:35284724-35285040 | Common:2; Rare:76 | ||||
chr20:35455040-35455201 | Common:1; Rare:53 |