| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139359690-139359974 | Common:2; Rare:114 | ||||
| chr7:139483643-139483864 | Common:3; Rare:72 | ||||
| chr7:140696607-140696731 | Rare:41 | ||||
| chr7:140924690-140925030 | Common:3; Rare:115; Clinvar:2; Clinvar (benign):5 | ||||
| chr7:141014618-141014744 | Rare:21 | ||||
| chr7:141014915-141015120 | Rare:46 | ||||
| chr7:141551200-141551437 | Common:3; Rare:59; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738192-141738524 | Rare:113 | ||||
| chr7:142855000-142855138 | Common:2; Rare:43 | ||||
| chr7:143380931-143381307 | Common:1; Rare:113 | ||||
| chr7:143407612-143407814 | Common:1; Rare:39 | ||||
| chr7:143408814-143408978 | Rare:37 | ||||
| chr7:143902121-143902292 | Common:5; Rare:55 | ||||
| chr7:144195559-144195789 | |||||
| chr7:144355224-144355472 | Rare:2 |