Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:17643877-17644214 | Common:1; Rare:99 | ||||
chr10:18651564-18651649 | Common:1; Rare:33 | ||||
chr10:24466386-24466533 | Rare:23 | ||||
chr10:27154315-27154474 | Rare:42 | ||||
chr10:27155203-27155414 | Common:6; Rare:90; Clinvar:2; Clinvar (benign):6 | ||||
chr10:27242102-27242221 | Common:1; Rare:44 | ||||
chr10:31319022-31319237 | Common:2; Rare:67 | ||||
chr10:31928777-31928926 | Common:2; Rare:57 | ||||
chr10:32958149-32958518 | Common:2; Rare:139 | ||||
chr10:35090562-35090688 | Rare:45 | ||||
chr10:35126718-35127007 | Common:3; Rare:89 | ||||
chr10:37857561-37857718 | Common:2; Rare:62 | ||||
chr10:42782667-42782823 | Rare:40 | ||||
chr10:43138307-43138514 | Common:3; Rare:80 | ||||
chr10:43409140-43409428 | Common:3; Rare:100 |