| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139777683-139778322 | Common:3; Rare:148 | ||||
| chr7:140351867-140352089 | Common:4; Rare:51 | ||||
| chr7:140479350-140479463 | Rare:30 | ||||
| chr7:140640804-140641088 | Rare:81 | ||||
| chr7:140924706-140924772 | Common:1; Rare:21; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:141551265-141551432 | Common:1; Rare:48; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738043-141738464 | Common:4; Rare:131 | ||||
| chr7:143263952-143264167 | Common:1; Rare:57 | ||||
| chr7:143288047-143288451 | Common:2; Rare:137 | ||||
| chr7:143380900-143381409 | Common:1; Rare:157 | ||||
| chr7:143382593-143382898 | Common:1; Rare:105 | ||||
| chr7:143882801-143882963 | Rare:40 | ||||
| chr7:148698798-148699010 | Common:2; Rare:70 | ||||
| chr7:149028322-149028568 | Common:2; Rare:94 | ||||
| chr7:149028597-149028891 | Common:4; Rare:107 |