| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:135662323-135662511 | Common:4; Rare:74 | ||||
| chr7:135977303-135977530 | Common:2; Rare:88 | ||||
| chr7:139109334-139109675 | Common:1; Rare:94 | ||||
| chr7:139109718-139109821 | Common:1; Rare:27 | ||||
| chr7:139133669-139133809 | Rare:33 | ||||
| chr7:139341188-139341385 | Rare:49 | ||||
| chr7:139359690-139360008 | Common:3; Rare:123 | ||||
| chr7:140696629-140696735 | Common:1; Rare:34 | ||||
| chr7:141551290-141551428 | Rare:43; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738033-141738464 | Common:4; Rare:132 | ||||
| chr7:144836022-144836106 | Rare:26 | ||||
| chr7:149028449-149028539 | Common:2; Rare:35 | ||||
| chr7:149028641-149028943 | Common:1; Rare:96 | ||||
| chr7:149090682-149090907 | Rare:57 | ||||
| chr7:149195305-149195501 | Rare:41 |