| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:141074010-141074313 | Rare:75 | ||||
| chr7:141551318-141551434 | Rare:34; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141701987-141702295 | Common:2; Rare:83 | ||||
| chr7:141738228-141738489 | Rare:98 | ||||
| chr7:142854990-142855166 | Common:3; Rare:50 | ||||
| chr7:143263324-143263576 | Rare:80 | ||||
| chr7:143284773-143284981 | Rare:39 | ||||
| chr7:143288277-143288461 | Common:1; Rare:74 | ||||
| chr7:143380874-143381409 | Common:2; Rare:164 | ||||
| chr7:143407666-143407815 | Common:1; Rare:25 | ||||
| chr7:143882810-143882937 | Rare:32 | ||||
| chr7:143885368-143885468 | Common:1; Rare:35 | ||||
| chr7:144195565-144195893 | Rare:4 | ||||
| chr7:144355124-144355498 | Rare:4 | ||||
| chr7:144835976-144836109 | Common:1; Rare:39; Clinvar (benign):1 |