| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:169751590-169751648 | Rare:27; Clinvar (benign):2 | ||||
| chr6:170306556-170306796 | Common:1; Rare:79 | ||||
| chr6:170554318-170554403 | Rare:28 | ||||
| chr6:170584579-170584773 | Common:1; Rare:64 | ||||
| chr7:519166-519294 | Rare:34 | ||||
| chr7:975525-975653 | Common:1; Rare:48 | ||||
| chr7:1504317-1504433 | Common:1; Rare:59 | ||||
| chr7:2242173-2242255 | Common:2; Rare:49 | ||||
| chr7:2354047-2354098 | Rare:29 | ||||
| chr7:2354778-2354935 | Common:1; Rare:78 | ||||
| chr7:2403288-2403645 | Common:1; Rare:139 | ||||
| chr7:4775398-4775691 | Common:7; Rare:139; Clinvar:1 | ||||
| chr7:5423800-5424058 | Common:3; Rare:63 | ||||
| chr7:6009021-6009355 | Common:4; Rare:144; Clinvar:8; Clinvar (benign):15 | ||||
| chr7:6272618-6272759 | Common:1; Rare:53 |