| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139341245-139341379 | Rare:30 | ||||
| chr7:139359692-139359992 | Common:3; Rare:118 | ||||
| chr7:141014624-141014758 | Rare:24 | ||||
| chr7:141014925-141015046 | Rare:28 | ||||
| chr7:141551330-141551428 | Rare:30; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738040-141738504 | Common:4; Rare:136 | ||||
| chr7:143288282-143288442 | Common:1; Rare:67 | ||||
| chr7:143382039-143382260 | Common:1; Rare:61 | ||||
| chr7:143882817-143882963 | Rare:38 | ||||
| chr7:144836026-144836176 | Common:1; Rare:56 | ||||
| chr7:148698540-148699010 | Common:5; Rare:163 | ||||
| chr7:149090691-149090870 | Rare:48 | ||||
| chr7:149126278-149126438 | Common:5; Rare:51 | ||||
| chr7:149714682-149714996 | Common:3; Rare:99 | ||||
| chr7:149873893-149874055 | Common:2; Rare:68 |