| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139340275-139340508 | Common:1; Rare:61 | ||||
| chr7:139341194-139341390 | Rare:51 | ||||
| chr7:139359682-139359980 | Common:3; Rare:120 | ||||
| chr7:139828924-139829312 | Common:1; Rare:83 | ||||
| chr7:140062537-140062648 | Rare:45 | ||||
| chr7:140176939-140177093 | Common:1; Rare:46 | ||||
| chr7:140479314-140479658 | Rare:105 | ||||
| chr7:141551335-141551428 | Rare:28; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738033-141738463 | Common:4; Rare:132 | ||||
| chr7:142854989-142855133 | Common:2; Rare:42 | ||||
| chr7:143263341-143263522 | Rare:56 | ||||
| chr7:143288047-143288452 | Common:2; Rare:137 | ||||
| chr7:143380894-143381362 | Common:1; Rare:143 | ||||
| chr7:148884187-148884478 | Common:1; Rare:135; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:149028449-149028557 | Common:2; Rare:41 |