| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139341197-139341380 | Rare:45 | ||||
| chr7:139359692-139359984 | Common:3; Rare:116 | ||||
| chr7:140398441-140398604 | Common:1; Rare:53 | ||||
| chr7:141014929-141015023 | Rare:24 | ||||
| chr7:141551342-141551428 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738033-141738474 | Common:4; Rare:134 | ||||
| chr7:142854990-142855133 | Common:2; Rare:42 | ||||
| chr7:143263394-143263511 | Rare:35 | ||||
| chr7:143288164-143288451 | Common:1; Rare:107 | ||||
| chr7:143380880-143381323 | Common:2; Rare:130 | ||||
| chr7:144835989-144836106 | Rare:35 | ||||
| chr7:148698379-148698978 | Common:6; Rare:202 | ||||
| chr7:149028402-149028615 | Common:4; Rare:85 | ||||
| chr7:149028617-149028967 | Common:3; Rare:116 | ||||
| chr7:149090662-149090908 | Rare:66 |