Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:30284322-30284668 | Common:6; Rare:132 | ||||
chr7:30504723-30505027 | Common:3; Rare:104 | ||||
chr7:30594709-30594967 | Common:4; Rare:121; Clinvar:6; Clinvar (benign):7 | ||||
chr7:30771319-30771472 | Common:1; Rare:49 | ||||
chr7:32490273-32490527 | Common:2; Rare:82 | ||||
chr7:32495272-32495602 | Common:1; Rare:84 | ||||
chr7:32495783-32496029 | Common:2; Rare:57 | ||||
chr7:33062632-33062905 | Common:3; Rare:115 | ||||
chr7:33109267-33109543 | Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
chr7:33129217-33129592 | Common:5; Rare:108 | ||||
chr7:33905352-33905539 | Common:2; Rare:30; Clinvar:1 | ||||
chr7:35694888-35695260 | Common:4; Rare:104 | ||||
chr7:35800552-35800713 | Rare:41 | ||||
chr7:35800721-35801264 | Common:2; Rare:207 | ||||
chr7:36367142-36367427 | Rare:95 |