| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159789599-159789977 | Common:3; Rare:129 | ||||
| chr6:166342502-166342638 | Common:2; Rare:53 | ||||
| chr6:166999081-166999397 | Common:1; Rare:107 | ||||
| chr6:169702047-169702384 | Common:5; Rare:132 | ||||
| chr6:169751590-169751677 | Common:1; Rare:42; Clinvar (benign):4 | ||||
| chr6:170554211-170554396 | Common:1; Rare:58 | ||||
| chr7:2242172-2242272 | Common:2; Rare:57 | ||||
| chr7:2354054-2354093 | Rare:21 | ||||
| chr7:5528004-5528590 | Common:1; Rare:159; Clinvar:3; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr7:6009062-6009326 | Common:3; Rare:103; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:6447922-6448057 | Common:1; Rare:48 | ||||
| chr7:6484077-6484267 | Common:1; Rare:96 | ||||
| chr7:19117407-19117954 | Common:3; Rare:168 | ||||
| chr7:23105698-23105830 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181794-23182107 | Common:2; Rare:120 |