| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:127343527-127343645 | Common:1; Rare:34 | ||||
| chr6:128520569-128520787 | Common:1; Rare:83 | ||||
| chr6:129490616-129490726 | Common:1; Rare:19 | ||||
| chr6:129710147-129710322 | Rare:45 | ||||
| chr6:131135394-131135758 | Common:4; Rare:142 | ||||
| chr6:131951368-131951470 | Rare:29 | ||||
| chr6:132814255-132814781 | Common:7; Rare:220 | ||||
| chr6:133240697-133240880 | Rare:38 | ||||
| chr6:133240950-133241435 | Common:5; Rare:148 | ||||
| chr6:133953018-133953278 | Common:2; Rare:81 | ||||
| chr6:134174852-134175122 | Common:1; Rare:121 | ||||
| chr6:134175646-134175820 | Rare:57 | ||||
| chr6:134177843-134178188 | Common:1; Rare:47 | ||||
| chr6:135054769-135054984 | Common:6; Rare:65 | ||||
| chr6:135497578-135497813 | Common:4; Rare:85; Clinvar:2; Clinvar (benign):2 |