| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:140696582-140696741 | Common:1; Rare:52 | ||||
| chr7:141014929-141015111 | Rare:40 | ||||
| chr7:141551342-141551423 | Rare:23; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738033-141738464 | Common:4; Rare:132 | ||||
| chr7:143902129-143902292 | Common:5; Rare:53 | ||||
| chr7:144355185-144355472 | Rare:2 | ||||
| chr7:148884206-148884478 | Common:1; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:149028595-149028938 | Common:5; Rare:116 | ||||
| chr7:149090706-149090870 | Rare:44 | ||||
| chr7:150323138-150323369 | Common:6; Rare:66 | ||||
| chr7:150323520-150323673 | Rare:50 | ||||
| chr7:150368488-150368859 | Common:1; Rare:101 | ||||
| chr7:151028250-151028471 | Rare:79 | ||||
| chr7:151080793-151080979 | Rare:62 | ||||
| chr7:152676128-152676316 | Common:2; Rare:80 |