Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:46973555-46973757 | Rare:85 | ||||
chr16:47461027-47461374 | Common:2; Rare:135; Clinvar (benign):2 | ||||
chr16:50693490-50693621 | Rare:55 | ||||
chr16:50741933-50742195 | Common:2; Rare:94; Clinvar:1 | ||||
chr16:50742745-50742782 | Rare:6 | ||||
chr16:53054884-53055055 | Common:1; Rare:36 | ||||
chr16:53504393-53504521 | Common:1; Rare:17 | ||||
chr16:53703821-53704213 | Common:1; Rare:123; Clinvar:4; Clinvar (benign):2 | ||||
chr16:54286789-54286995 | Common:1; Rare:61 | ||||
chr16:55479424-55479630 | Rare:75; Clinvar:4 | ||||
chr16:56451306-56451605 | Common:1; Rare:98 | ||||
chr16:56608429-56608775 | Common:3; Rare:102 | ||||
chr16:56608918-56609083 | Rare:53 | ||||
chr16:56625658-56625845 | Rare:56 | ||||
chr16:56632190-56632752 | Common:2; Rare:171 |