| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3068912-3069062 | Common:1; Rare:66 | ||||
| chr6:3118290-3118357 | Rare:27 | ||||
| chr6:3118563-3118797 | Common:3; Rare:79 | ||||
| chr6:3157457-3157674 | Common:6; Rare:80 | ||||
| chr6:3227546-3227954 | Rare:102 | ||||
| chr6:3231732-3231840 | Rare:18 | ||||
| chr6:4021175-4021467 | Rare:123 | ||||
| chr6:4772884-4773205 | Common:4; Rare:74 | ||||
| chr6:5003649-5003832 | Common:5; Rare:56 | ||||
| chr6:5003994-5004110 | Common:2; Rare:56 | ||||
| chr6:5260654-5261060 | Common:6; Rare:148; Clinvar (benign):4 | ||||
| chr6:5261222-5261637 | Common:12; Rare:110 | ||||
| chr6:6320659-6320835 | Rare:55 | ||||
| chr6:7108369-7108436 | Rare:14 | ||||
| chr6:7313083-7313353 | Common:5; Rare:102 |