| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159044922-159045193 | Common:1; Rare:53 | ||||
| chr6:159693253-159693631 | Common:5; Rare:113 | ||||
| chr6:159726948-159727308 | Rare:132 | ||||
| chr6:159727341-159727703 | Common:5; Rare:148 | ||||
| chr6:159761862-159762036 | Common:4; Rare:85 | ||||
| chr6:159789617-159789958 | Common:3; Rare:112 | ||||
| chr6:159968943-159969151 | Common:1; Rare:81 | ||||
| chr6:166342544-166342675 | Common:3; Rare:51 | ||||
| chr6:166956236-166956313 | Rare:14; Clinvar:3 | ||||
| chr6:166956469-166956687 | Common:4; Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:169702053-169702347 | Common:5; Rare:117 | ||||
| chr6:169751541-169751646 | Rare:39; Clinvar (benign):2 | ||||
| chr6:170554157-170554369 | Common:1; Rare:58 | ||||
| chr7:1028305-1028526 | Common:1; Rare:78 | ||||
| chr7:1570018-1570088 | Common:1; Rare:24 |