| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:1087925-1088145 | Common:1; Rare:49 | ||||
| chr7:1504332-1504610 | Common:4; Rare:126 | ||||
| chr7:1537318-1537511 | Rare:65 | ||||
| chr7:1538039-1538305 | Common:1; Rare:86 | ||||
| chr7:1570007-1570146 | Common:1; Rare:45 | ||||
| chr7:2242177-2242268 | Common:2; Rare:52 | ||||
| chr7:2354047-2354111 | Rare:34 | ||||
| chr7:2403304-2403625 | Common:1; Rare:126 | ||||
| chr7:2555485-2555838 | Common:5; Rare:96 | ||||
| chr7:4775478-4775691 | Common:6; Rare:101; Clinvar:1 | ||||
| chr7:4882207-4882315 | Common:1; Rare:23 | ||||
| chr7:5045591-5045898 | Common:3; Rare:126 | ||||
| chr7:5423765-5424058 | Common:3; Rare:75 | ||||
| chr7:5513746-5513865 | Common:1; Rare:54 | ||||
| chr7:6009029-6009355 | Common:4; Rare:137; Clinvar:3; Clinvar (benign):15 |