| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:140351864-140352091 | Common:4; Rare:51 | ||||
| chr7:140696472-140696741 | Common:1; Rare:72 | ||||
| chr7:140696791-140697038 | Common:1; Rare:65 | ||||
| chr7:140697066-140697329 | Rare:89 | ||||
| chr7:141551273-141551439 | Common:1; Rare:47; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738015-141738464 | Common:4; Rare:136 | ||||
| chr7:143263411-143263583 | Rare:54 | ||||
| chr7:143263952-143264154 | Common:1; Rare:54 | ||||
| chr7:143288075-143288455 | Common:2; Rare:126 | ||||
| chr7:143380615-143380823 | Common:1; Rare:48 | ||||
| chr7:143380842-143381790 | Common:2; Rare:303 | ||||
| chr7:143387749-143387798 | Rare:12 | ||||
| chr7:143388031-143388657 | Common:3; Rare:165 | ||||
| chr7:143885280-143885473 | Common:1; Rare:61 | ||||
| chr7:148698602-148699001 | Common:2; Rare:139 |