| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:143395149-143395374 | Common:1; Rare:68 | ||||
| chr7:143408801-143408982 | Rare:40 | ||||
| chr7:144195577-144195852 | Rare:3 | ||||
| chr7:144355091-144355478 | Rare:4 | ||||
| chr7:144836041-144836088 | Rare:15 | ||||
| chr7:148698552-148698986 | Common:5; Rare:154 | ||||
| chr7:148884267-148884453 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:149028322-149028700 | Common:7; Rare:154 | ||||
| chr7:149090657-149090908 | Rare:70 | ||||
| chr7:149126212-149126438 | Common:6; Rare:75 | ||||
| chr7:149261900-149262317 | Common:3; Rare:130 | ||||
| chr7:149838860-149838944 | Rare:17 | ||||
| chr7:149873852-149874056 | Common:3; Rare:80 | ||||
| chr7:150323164-150323202 | Rare:12 | ||||
| chr7:150323447-150323558 | Rare:28 |