| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:45111676-45111799 | Common:1; Rare:46 | ||||
| chr7:45921270-45921411 | Rare:36 | ||||
| chr7:50450306-50450447 | Common:1; Rare:57 | ||||
| chr7:55572341-55572617 | Common:1; Rare:104 | ||||
| chr7:56051433-56051845 | Common:1; Rare:158; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56106363-56106671 | Common:8; Rare:117 | ||||
| chr7:64563032-64563250 | Common:3; Rare:59 | ||||
| chr7:66114740-66114910 | Common:1; Rare:75 | ||||
| chr7:66115179-66115360 | Rare:41 | ||||
| chr7:66682036-66682185 | Common:5; Rare:70 | ||||
| chr7:66996574-66996850 | Common:2; Rare:54 | ||||
| chr7:72828175-72828458 | Rare:74 | ||||
| chr7:73683418-73683622 | Common:3; Rare:81 | ||||
| chr7:74174027-74174441 | Common:1; Rare:176 | ||||
| chr7:74209829-74210037 | Rare:50 |