Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:46689483-46689714 | Common:2; Rare:91; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr16:46973550-46973768 | Rare:91 | ||||
chr16:47461007-47461362 | Common:2; Rare:139; Clinvar (benign):2 | ||||
chr16:52547401-52547421 | Rare:3 | ||||
chr16:53054884-53055048 | Common:1; Rare:36 | ||||
chr16:53703809-53704206 | Common:1; Rare:125; Clinvar:4; Clinvar (benign):2 | ||||
chr16:55479088-55479207 | Rare:33 | ||||
chr16:56191077-56191418 | Common:5; Rare:125 | ||||
chr16:56191581-56191694 | Rare:24 | ||||
chr16:56191708-56191831 | Rare:40 | ||||
chr16:56192108-56192284 | Common:1; Rare:35; Clinvar (benign):2 | ||||
chr16:56451289-56451605 | Common:1; Rare:103 | ||||
chr16:56519973-56520150 | Common:4; Rare:65; Clinvar:6; Clinvar (benign):5 | ||||
chr16:56608434-56608694 | Common:2; Rare:80 | ||||
chr16:56657859-56658020 | Common:2; Rare:48 |