| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:142939401-142939582 | Common:2; Rare:48 | ||||
| chr7:142943284-142943516 | Common:1; Rare:66 | ||||
| chr7:142943524-142943727 | Rare:57 | ||||
| chr7:142957684-142957936 | Common:1; Rare:59; Clinvar (benign):1 | ||||
| chr7:143263404-143263651 | Rare:76 | ||||
| chr7:143288000-143288250 | Common:1; Rare:68 | ||||
| chr7:143288251-143288473 | Common:1; Rare:86 | ||||
| chr7:143380931-143381319 | Common:1; Rare:119 | ||||
| chr7:143395678-143395805 | Common:3; Rare:27 | ||||
| chr7:143408847-143408960 | Rare:29 | ||||
| chr7:143885329-143885485 | Common:1; Rare:54 | ||||
| chr7:143902089-143902248 | Common:6; Rare:59 | ||||
| chr7:144738892-144739120 | Common:1; Rare:51 | ||||
| chr7:144835969-144836110 | Common:1; Rare:42; Clinvar (benign):2 | ||||
| chr7:148697828-148698473 | Common:8; Rare:168 |