| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166382819-166383324 | Common:5; Rare:165; Clinvar (benign):1 | ||||
| chr6:166627901-166628142 | Rare:56 | ||||
| chr6:166956535-166956724 | Common:4; Rare:70; Clinvar:3 | ||||
| chr6:166999028-166999418 | Common:1; Rare:132 | ||||
| chr6:167966598-167966809 | Common:3; Rare:41 | ||||
| chr6:169702021-169702193 | Common:3; Rare:88 | ||||
| chr6:169751478-169751663 | Common:1; Rare:81; Clinvar (benign):3 | ||||
| chr6:170306559-170306812 | Common:1; Rare:83 | ||||
| chr6:170553196-170553354 | Common:2; Rare:74 | ||||
| chr6:170554150-170554440 | Common:1; Rare:87 | ||||
| chr7:727241-727303 | Rare:19; Clinvar:1 | ||||
| chr7:975510-975674 | Common:1; Rare:67 | ||||
| chr7:1028284-1028526 | Common:1; Rare:90 | ||||
| chr7:1044461-1044639 | Common:3; Rare:79 | ||||
| chr7:1055297-1055393 | Rare:45 |