| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:128862964-128863357 | Common:2; Rare:96 | ||||
| chr7:129054878-129055226 | Common:2; Rare:66 | ||||
| chr7:129611625-129611814 | Common:1; Rare:59 | ||||
| chr7:131109875-131110085 | Common:1; Rare:37 | ||||
| chr7:131327686-131327897 | Rare:66 | ||||
| chr7:135148022-135148151 | Rare:33 | ||||
| chr7:135170685-135170841 | Common:2; Rare:61 | ||||
| chr7:135193379-135193584 | Common:1; Rare:52 | ||||
| chr7:139036003-139036188 | Rare:52 | ||||
| chr7:140176946-140177242 | Common:2; Rare:98 | ||||
| chr7:141014926-141015030 | Rare:26 | ||||
| chr7:141738043-141738474 | Common:4; Rare:133 | ||||
| chr7:143288047-143288351 | Common:1; Rare:90 | ||||
| chr7:143380955-143381356 | Common:1; Rare:127 | ||||
| chr7:148884219-148884492 | Common:1; Rare:126; Clinvar:1; Clinvar (benign):1 |