| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32192843-32192977 | Rare:15 | ||||
| chr6:32838193-32838350 | Common:1; Rare:67; Clinvar (benign):2 | ||||
| chr6:32843971-32844119 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:32844530-32844890 | Common:3; Rare:122 | ||||
| chr6:32853662-32853815 | Common:1; Rare:140; Clinvar:4; Clinvar (benign):5 | ||||
| chr6:32853979-32854209 | Common:4; Rare:104 | ||||
| chr6:32968350-32968667 | Common:9; Rare:152 | ||||
| chr6:32968740-32969038 | Common:12; Rare:154 | ||||
| chr6:32969086-32969571 | Common:12; Rare:199 | ||||
| chr6:32970093-32970451 | Common:8; Rare:101 | ||||
| chr6:32970683-32971198 | Common:15; Rare:328 | ||||
| chr6:33199930-33200290 | Common:1; Rare:163 | ||||
| chr6:33200332-33200470 | Rare:76 | ||||
| chr6:33200637-33201034 | Common:6; Rare:196 | ||||
| chr6:33208411-33208522 | Common:1; Rare:29 |