| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:140063067-140063109 | Rare:8 | ||||
| chr7:140177033-140177350 | Common:2; Rare:116 | ||||
| chr7:140398424-140398597 | Common:1; Rare:56 | ||||
| chr7:140478912-140479153 | Common:5; Rare:78 | ||||
| chr7:140479179-140479256 | Rare:25 | ||||
| chr7:140479350-140479594 | Rare:77 | ||||
| chr7:140696597-140696756 | Common:1; Rare:57 | ||||
| chr7:140924732-140925098 | Common:2; Rare:137; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:141014624-141014726 | Rare:18 | ||||
| chr7:141014893-141015031 | Rare:36 | ||||
| chr7:141551265-141551446 | Common:1; Rare:52; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738214-141738624 | Common:1; Rare:130 | ||||
| chr7:141841475-141841583 | Rare:21 | ||||
| chr7:141907675-141907825 | Common:4; Rare:26 | ||||
| chr7:142854990-142855138 | Common:2; Rare:44 |