| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:170306521-170306810 | Common:1; Rare:97 | ||||
| chr6:170403471-170403871 | Common:3; Rare:150 | ||||
| chr6:170553196-170553354 | Common:2; Rare:74 | ||||
| chr6:170554142-170554446 | Common:2; Rare:90 | ||||
| chr6:170584579-170584806 | Common:1; Rare:71 | ||||
| chr7:192410-192583 | Common:1; Rare:36 | ||||
| chr7:193369-193807 | Rare:175; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:518951-519458 | Common:1; Rare:200 | ||||
| chr7:726564-726723 | Common:2; Rare:64 | ||||
| chr7:727019-727317 | Rare:127; Clinvar:12; Clinvar (benign):8 | ||||
| chr7:816355-816667 | Common:2; Rare:104 | ||||
| chr7:842599-843403 | Common:10; Rare:287; Clinvar:2 | ||||
| chr7:876206-876632 | Common:8; Rare:190 | ||||
| chr7:876740-876970 | Common:1; Rare:84 | ||||
| chr7:901487-901887 | Common:1; Rare:193 |