| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159000166-159000279 | Rare:27 | ||||
| chr6:159726948-159727178 | Rare:89 | ||||
| chr6:159789559-159790004 | Common:4; Rare:153 | ||||
| chr6:159790438-159790514 | Common:1; Rare:27 | ||||
| chr6:166342513-166342679 | Common:3; Rare:66 | ||||
| chr6:166956529-166956687 | Common:2; Rare:53; Clinvar:3 | ||||
| chr6:166999129-166999423 | Common:1; Rare:96 | ||||
| chr6:169702018-169702340 | Common:5; Rare:137 | ||||
| chr6:169751538-169751644 | Rare:38; Clinvar (benign):1 | ||||
| chr6:170306571-170306799 | Common:1; Rare:73 | ||||
| chr6:170554221-170554404 | Common:1; Rare:62 | ||||
| chr7:727240-727281 | Rare:14; Clinvar:1 | ||||
| chr7:945786-945992 | Rare:38 | ||||
| chr7:975495-975719 | Common:1; Rare:94 | ||||
| chr7:1028305-1028525 | Common:1; Rare:78 |