| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139359692-139360010 | Common:3; Rare:123 | ||||
| chr7:140177042-140177344 | Common:2; Rare:111 | ||||
| chr7:140924702-140925052 | Common:3; Rare:123; Clinvar:2; Clinvar (benign):5 | ||||
| chr7:141014910-141015006 | Rare:24 | ||||
| chr7:141551342-141551428 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738021-141738472 | Common:4; Rare:136 | ||||
| chr7:142854998-142855138 | Common:2; Rare:43 | ||||
| chr7:143288165-143288457 | Common:1; Rare:109 | ||||
| chr7:143380910-143381362 | Common:1; Rare:141 | ||||
| chr7:143381761-143382306 | Common:1; Rare:149 | ||||
| chr7:143882818-143882960 | Rare:36 | ||||
| chr7:144835993-144836106 | Rare:33 | ||||
| chr7:148698501-148699000 | Common:5; Rare:177 | ||||
| chr7:149090657-149090907 | Rare:70 | ||||
| chr7:149126220-149126438 | Common:6; Rare:73 |