Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:46184423-46184736 | Common:4; Rare:28 | ||||
chr21:46286266-46286366 | Common:2; Rare:37 | ||||
chr21:46323863-46324202 | Common:2; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
chr22:17159207-17159350 | Common:4; Rare:68 | ||||
chr22:17628703-17628933 | Common:1; Rare:82 | ||||
chr22:17638684-17638811 | Rare:43 | ||||
chr22:18077829-18078006 | Common:3; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
chr22:19432269-19432581 | Common:3; Rare:128 | ||||
chr22:19479148-19479471 | Common:4; Rare:110 | ||||
chr22:19854811-19854939 | Rare:47 | ||||
chr22:20117183-20117606 | Common:3; Rare:135 | ||||
chr22:20319998-20320158 | Common:1; Rare:53 | ||||
chr22:20495787-20495982 | Common:2; Rare:72 | ||||
chr22:20982196-20982347 | Common:2; Rare:34; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr22:21002068-21002181 | Common:3; Rare:40 |