Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:19776407-19776596 | Common:2; Rare:54 | ||||
chr19:27793376-27793479 | Common:1; Rare:28 | ||||
chr19:27793667-27794035 | Rare:95 | ||||
chr19:36142655-36142963 | Rare:82 | ||||
chr19:36797303-36797534 | Rare:48 | ||||
chr19:37304365-37304452 | Common:1; Rare:51 | ||||
chr19:46411149-46411397 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):1 | ||||
chr19:46860835-46861111 | Common:3; Rare:89 | ||||
chr19:48966400-48966688 | Rare:95; Clinvar:1 | ||||
chr19:49491525-49491736 | Common:1; Rare:70 | ||||
chr19:49635654-49635848 | Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
chr19:55546159-55546374 | Rare:36 | ||||
chr2:17649264-17649565 | Common:1; Rare:67 | ||||
chr2:20447729-20447884 | Rare:42 | ||||
chr2:20448381-20448657 | Common:1; Rare:73 |