Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:2242177-2242268 | Common:2; Rare:52 | ||||
chr7:6009029-6009330 | Common:3; Rare:129; Clinvar:3; Clinvar (benign):14 | ||||
chr7:6483993-6484256 | Common:2; Rare:124 | ||||
chr7:16645829-16646140 | Common:2; Rare:100 | ||||
chr7:23105636-23105825 | Common:4; Rare:96; Clinvar:2; Clinvar (benign):3 | ||||
chr7:26201528-26201800 | Common:2; Rare:145 | ||||
chr7:26864583-26864835 | Common:3; Rare:80 | ||||
chr7:27096027-27096184 | Rare:43 | ||||
chr7:30594732-30594959 | Common:3; Rare:108; Clinvar:5; Clinvar (benign):6 | ||||
chr7:32495272-32495569 | Rare:73 | ||||
chr7:35800945-35801252 | Common:2; Rare:130 | ||||
chr7:36661137-36661296 | Common:2; Rare:21 | ||||
chr7:38178074-38178393 | Common:3; Rare:96 | ||||
chr7:39566312-39566450 | Common:1; Rare:67 | ||||
chr7:39623538-39623747 | Rare:74 |