| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:138001751-138001827 | Rare:14 | ||||
| chr7:138002019-138002330 | Common:2; Rare:79 | ||||
| chr7:139109324-139109427 | Common:1; Rare:33 | ||||
| chr7:139109712-139109821 | Common:1; Rare:28 | ||||
| chr7:139231016-139231276 | Common:2; Rare:95 | ||||
| chr7:139341245-139341379 | Rare:30 | ||||
| chr7:139359690-139360008 | Common:3; Rare:123 | ||||
| chr7:140696366-140696743 | Common:2; Rare:90 | ||||
| chr7:141014910-141015030 | Rare:29 | ||||
| chr7:141551342-141551423 | Rare:23; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738021-141738464 | Common:4; Rare:134 | ||||
| chr7:142854990-142855138 | Common:2; Rare:44 | ||||
| chr7:143288282-143288451 | Common:1; Rare:69 | ||||
| chr7:143380910-143381082 | Rare:48 | ||||
| chr7:143382039-143382306 | Common:1; Rare:80 |