| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:6447952-6448049 | Rare:31 | ||||
| chr7:7182335-7182729 | Common:5; Rare:142 | ||||
| chr7:7566761-7567037 | Common:5; Rare:115 | ||||
| chr7:10973605-10973941 | Common:1; Rare:144 | ||||
| chr7:12211170-12211390 | Common:3; Rare:100 | ||||
| chr7:12687435-12687643 | Common:5; Rare:66 | ||||
| chr7:16645655-16646237 | Common:5; Rare:206 | ||||
| chr7:17940416-17940618 | Common:2; Rare:101 | ||||
| chr7:18495617-18495771 | Rare:34 | ||||
| chr7:20217382-20217577 | Common:1; Rare:45 | ||||
| chr7:21945869-21946196 | Common:3; Rare:92 | ||||
| chr7:22822766-22822954 | Common:3; Rare:69 | ||||
| chr7:23105666-23105841 | Common:4; Rare:92; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181853-23182107 | Common:2; Rare:103 | ||||
| chr7:23470294-23470407 | Rare:34 |