| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139109704-139109808 | Common:1; Rare:26 | ||||
| chr7:139133666-139133798 | Rare:30 | ||||
| chr7:139341197-139341380 | Rare:45 | ||||
| chr7:139359648-139359988 | Common:3; Rare:140 | ||||
| chr7:140696602-140696747 | Common:1; Rare:50 | ||||
| chr7:141014617-141014744 | Rare:22 | ||||
| chr7:141014929-141015120 | Rare:43 | ||||
| chr7:141551342-141551428 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738021-141738551 | Common:4; Rare:152 | ||||
| chr7:142854990-142855133 | Common:2; Rare:42 | ||||
| chr7:143288050-143288457 | Common:2; Rare:138 | ||||
| chr7:143380886-143381293 | Common:2; Rare:121 | ||||
| chr7:143902122-143902276 | Common:5; Rare:52 | ||||
| chr7:148698573-148698932 | Common:3; Rare:130 | ||||
| chr7:149028326-149028399 | Rare:23 |