| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:169702655-169703080 | Common:4; Rare:249 | ||||
| chr6:169723932-169724119 | Common:3; Rare:100 | ||||
| chr6:169724434-169724760 | Rare:143 | ||||
| chr6:169725189-169725501 | Common:2; Rare:115 | ||||
| chr6:169751483-169751755 | Common:3; Rare:203; Clinvar (benign):10 | ||||
| chr6:170306579-170306833 | Common:6; Rare:138 | ||||
| chr6:170553193-170553371 | Common:5; Rare:151 | ||||
| chr6:170554109-170554445 | Common:3; Rare:175 | ||||
| chr6:170584586-170584820 | Common:2; Rare:139 | ||||
| chr7:192330-192760 | Common:4; Rare:164 | ||||
| chr7:519150-519340 | Rare:84 | ||||
| chr7:519842-519984 | Common:8; Rare:43 | ||||
| chr7:726564-726759 | Common:3; Rare:144; Clinvar (benign):2 | ||||
| chr7:727209-727385 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:727588-727706 | Rare:20 |