| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:131327715-131327894 | Rare:63 | ||||
| chr7:134646566-134646898 | Common:6; Rare:107 | ||||
| chr7:135170627-135170831 | Common:2; Rare:81 | ||||
| chr7:135662406-135662541 | Common:2; Rare:61 | ||||
| chr7:139133707-139133816 | Rare:29 | ||||
| chr7:139359692-139359982 | Common:3; Rare:115 | ||||
| chr7:141014916-141015007 | Rare:24 | ||||
| chr7:141551322-141551423 | Rare:32; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738021-141738444 | Common:4; Rare:130 | ||||
| chr7:143380925-143381047 | Rare:31 | ||||
| chr7:148698826-148698979 | Common:1; Rare:49 | ||||
| chr7:149028586-149028974 | Common:5; Rare:134 | ||||
| chr7:149090682-149090865 | Rare:48 | ||||
| chr7:151028149-151028484 | Rare:116 | ||||
| chr7:151080785-151080947 | Rare:47 |