| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:16645839-16646196 | Common:3; Rare:119 | ||||
| chr7:17298444-17298659 | Common:3; Rare:54 | ||||
| chr7:17940398-17940595 | Common:2; Rare:94 | ||||
| chr7:18027844-18027861 | Common:1; Rare:3 | ||||
| chr7:20330768-20331163 | Common:2; Rare:102 | ||||
| chr7:20331733-20331846 | Common:1; Rare:39 | ||||
| chr7:21427870-21428254 | Common:4; Rare:150 | ||||
| chr7:22500136-22500296 | Common:2; Rare:55 | ||||
| chr7:23014045-23014308 | Common:2; Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:23105673-23105841 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181921-23182092 | Rare:74 | ||||
| chr7:23299177-23299524 | Common:2; Rare:169 | ||||
| chr7:23531958-23532098 | Common:1; Rare:55 | ||||
| chr7:23710095-23710321 | Common:5; Rare:106 | ||||
| chr7:24284127-24284275 | Rare:47 |