Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:34961479-34961575 | Common:1; Rare:43 | ||||
chr17:34980474-34980597 | Common:4; Rare:38 | ||||
chr17:35063625-35063827 | Rare:40 | ||||
chr17:35242943-35243100 | Rare:49 | ||||
chr17:35578545-35578707 | Common:1; Rare:43; Clinvar (benign):1 | ||||
chr17:35587183-35587519 | Rare:90 | ||||
chr17:35809294-35809575 | Rare:119 | ||||
chr17:36001415-36001468 | Common:1; Rare:17 | ||||
chr17:36001478-36001607 | Common:1; Rare:33 | ||||
chr17:36534772-36535042 | Common:3; Rare:113 | ||||
chr17:36544796-36544991 | Common:3; Rare:62 | ||||
chr17:36601483-36601622 | Rare:44 | ||||
chr17:37406745-37406924 | Rare:74 | ||||
chr17:37489740-37489928 | Common:1; Rare:71 | ||||
chr17:37609362-37609668 | Common:1; Rare:126 |