Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:30534841-30535084 | Common:2; Rare:80 | ||||
chr16:30923242-30923599 | Common:1; Rare:87 | ||||
chr16:31190808-31191078 | Common:1; Rare:102; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr16:31202686-31202970 | Common:2; Rare:102 | ||||
chr16:31459324-31459517 | Common:1; Rare:79 | ||||
chr16:31471950-31472186 | Rare:54 | ||||
chr16:31508370-31508477 | Common:1; Rare:42 | ||||
chr16:46689111-46689320 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
chr16:46689504-46689740 | Common:2; Rare:104; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr16:46973632-46973815 | Rare:85 | ||||
chr16:47461032-47461377 | Common:2; Rare:134; Clinvar (benign):2 | ||||
chr16:48610178-48610340 | Common:2; Rare:66 | ||||
chr16:53703821-53704221 | Common:1; Rare:126; Clinvar:4; Clinvar (benign):2 | ||||
chr16:54286740-54287011 | Common:1; Rare:86 | ||||
chr16:56451182-56451756 | Common:4; Rare:193 |