| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33200654-33200987 | Common:3; Rare:94 | ||||
| chr6:33204521-33204679 | Common:2; Rare:64 | ||||
| chr6:33208443-33208522 | Rare:22 | ||||
| chr6:33271632-33272149 | Common:4; Rare:186 | ||||
| chr6:33288991-33289084 | Rare:32 | ||||
| chr6:33289166-33289730 | Common:4; Rare:135 | ||||
| chr6:33299408-33299497 | Common:1; Rare:15 | ||||
| chr6:33322893-33323257 | Common:5; Rare:114 | ||||
| chr6:33391687-33391901 | Common:1; Rare:50 | ||||
| chr6:33417255-33417511 | Rare:74 | ||||
| chr6:33417864-33418500 | Common:3; Rare:181 | ||||
| chr6:33420059-33420301 | Rare:52; Clinvar (benign):1 | ||||
| chr6:33454406-33454593 | Rare:54 | ||||
| chr6:33580180-33580351 | Common:2; Rare:49 | ||||
| chr6:33711549-33711891 | Common:3; Rare:126; Clinvar (benign):3 |