| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139341238-139341380 | Rare:33 | ||||
| chr7:139359692-139360008 | Common:3; Rare:122 | ||||
| chr7:140177030-140177355 | Common:2; Rare:120 | ||||
| chr7:140696534-140696747 | Common:1; Rare:68 | ||||
| chr7:141551342-141551434 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738033-141738464 | Common:4; Rare:132 | ||||
| chr7:142854994-142855166 | Common:3; Rare:49 | ||||
| chr7:143288071-143288451 | Common:2; Rare:128 | ||||
| chr7:143380886-143381395 | Common:2; Rare:158 | ||||
| chr7:143382054-143382274 | Common:1; Rare:62 | ||||
| chr7:143902072-143902292 | Common:7; Rare:69 | ||||
| chr7:144355399-144355460 | |||||
| chr7:144835985-144836095 | Rare:34 | ||||
| chr7:148698475-148698992 | Common:5; Rare:179 | ||||
| chr7:149028595-149028938 | Common:5; Rare:116 |