| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:22822766-22822954 | Common:3; Rare:69 | ||||
| chr7:23014062-23014418 | Common:7; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:23105661-23105819 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:23181840-23182146 | Common:2; Rare:126 | ||||
| chr7:23299111-23299425 | Common:4; Rare:145 | ||||
| chr7:23470366-23470580 | Common:1; Rare:63 | ||||
| chr7:23531943-23532141 | Common:2; Rare:79 | ||||
| chr7:23597242-23597416 | Rare:56 | ||||
| chr7:23680023-23680203 | Common:5; Rare:50 | ||||
| chr7:24719061-24719440 | Common:5; Rare:100; Clinvar:4; Clinvar (benign):7 | ||||
| chr7:24980108-24980377 | Common:6; Rare:110 | ||||
| chr7:25125230-25125643 | Rare:166; Clinvar:3 | ||||
| chr7:26200593-26201024 | Common:2; Rare:208 | ||||
| chr7:26201404-26201818 | Common:2; Rare:194 | ||||
| chr7:26291779-26292019 | Common:2; Rare:75 |