| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:158819315-158819429 | Common:2; Rare:48 | ||||
| chr6:158999807-158999868 | Rare:26 | ||||
| chr6:159000146-159000282 | Common:1; Rare:35 | ||||
| chr6:159693235-159693593 | Common:5; Rare:101 | ||||
| chr6:159726918-159727173 | Common:1; Rare:99 | ||||
| chr6:159727333-159727692 | Common:5; Rare:145 | ||||
| chr6:159789538-159789998 | Common:4; Rare:153 | ||||
| chr6:159790244-159790617 | Common:10; Rare:142 | ||||
| chr6:159790730-159790895 | Rare:40 | ||||
| chr6:160991643-160991785 | Common:1; Rare:47 | ||||
| chr6:166342492-166342681 | Common:3; Rare:78 | ||||
| chr6:166999039-166999405 | Common:1; Rare:128 | ||||
| chr6:169701993-169702370 | Common:5; Rare:156 | ||||
| chr6:169751461-169751663 | Common:2; Rare:88; Clinvar (benign):3 | ||||
| chr6:170306559-170306820 | Common:2; Rare:83 |