| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:140479169-140479430 | Common:2; Rare:91 | ||||
| chr7:140479471-140479639 | Rare:56 | ||||
| chr7:140696582-140696747 | Common:1; Rare:56 | ||||
| chr7:141014604-141014744 | Rare:22 | ||||
| chr7:141014888-141015126 | Rare:58 | ||||
| chr7:141551342-141551434 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141737907-141738227 | Common:5; Rare:66 | ||||
| chr7:141738228-141738639 | Common:1; Rare:128 | ||||
| chr7:142854998-142855133 | Common:2; Rare:41 | ||||
| chr7:143263386-143263532 | Rare:45 | ||||
| chr7:143288282-143288442 | Common:1; Rare:67 | ||||
| chr7:143902109-143902276 | Common:5; Rare:55 | ||||
| chr7:144835974-144836122 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr7:148698384-148699000 | Common:7; Rare:210 | ||||
| chr7:148884180-148884499 | Common:2; Rare:155; Clinvar:3; Clinvar (benign):1 |