| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:7566783-7567037 | Common:4; Rare:105 | ||||
| chr7:10940044-10940230 | Common:1; Rare:84; Clinvar (benign):3 | ||||
| chr7:10973643-10973921 | Common:1; Rare:122 | ||||
| chr7:13988874-13989006 | Common:1; Rare:26 | ||||
| chr7:16645635-16646208 | Common:3; Rare:197 | ||||
| chr7:17940412-17940589 | Common:2; Rare:88 | ||||
| chr7:19708981-19709204 | Common:4; Rare:85 | ||||
| chr7:20330732-20331061 | Common:2; Rare:91 | ||||
| chr7:20331718-20331784 | Common:1; Rare:20 | ||||
| chr7:21427819-21428194 | Common:3; Rare:136 | ||||
| chr7:21945831-21946215 | Common:3; Rare:123 | ||||
| chr7:22822749-22822969 | Common:3; Rare:84 | ||||
| chr7:23014054-23014373 | Common:5; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:23105631-23105841 | Common:4; Rare:109; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181912-23182088 | Rare:75 |