| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:143882765-143882995 | Rare:60 | ||||
| chr7:143885232-143885454 | Common:1; Rare:71 | ||||
| chr7:143902090-143902292 | Common:7; Rare:67 | ||||
| chr7:144835979-144836114 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr7:146115778-146115873 | Rare:18 | ||||
| chr7:146116520-146116687 | Common:1; Rare:30; Clinvar:3 | ||||
| chr7:148698328-148698340 | Rare:2 | ||||
| chr7:148698588-148698978 | Common:2; Rare:137 | ||||
| chr7:149028388-149028779 | Common:7; Rare:151 | ||||
| chr7:149090662-149090907 | Rare:66 | ||||
| chr7:149126234-149126438 | Common:6; Rare:68 | ||||
| chr7:149195397-149195629 | Rare:58 | ||||
| chr7:149873804-149874131 | Common:3; Rare:122 | ||||
| chr7:150323164-150323479 | Common:8; Rare:84 | ||||
| chr7:150341595-150341903 | Common:1; Rare:44 |