| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166627566-166627708 | Rare:50 | ||||
| chr6:166999028-166999415 | Common:1; Rare:132 | ||||
| chr6:167826799-167827154 | Common:2; Rare:204 | ||||
| chr6:169701963-169702149 | Common:1; Rare:81 | ||||
| chr6:169724502-169724868 | Rare:107 | ||||
| chr6:169725503-169725577 | Rare:24 | ||||
| chr6:169751446-169751835 | Common:3; Rare:149; Clinvar (benign):5 | ||||
| chr6:170306464-170306820 | Common:2; Rare:111 | ||||
| chr6:170553132-170553423 | Common:3; Rare:111 | ||||
| chr6:170554150-170554420 | Common:1; Rare:80 | ||||
| chr6:170584439-170584782 | Common:2; Rare:115 | ||||
| chr7:712421-712725 | Common:2; Rare:55 | ||||
| chr7:727236-727304 | Rare:21; Clinvar:1 | ||||
| chr7:727604-727765 | Rare:22 | ||||
| chr7:768451-768654 | Common:2; Rare:67 |