| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:70217038-70217125 | Rare:28; Clinvar:5 | ||||
| chr6:71293422-71293582 | Rare:29 | ||||
| chr6:71301284-71301533 | Common:2; Rare:54 | ||||
| chr6:71420807-71421018 | Common:1; Rare:70 | ||||
| chr6:73517649-73518267 | Common:2; Rare:163 | ||||
| chr6:75128303-75128618 | Common:3; Rare:72; Clinvar (benign):1 | ||||
| chr6:78947622-78948021 | Common:2; Rare:75 | ||||
| chr6:78959599-78959657 | Rare:9 | ||||
| chr6:78963163-78963373 | Rare:50 | ||||
| chr6:78966768-78966985 | Common:1; Rare:40 | ||||
| chr6:78970788-78971127 | Common:2; Rare:88; Clinvar (pathogenic):1 | ||||
| chr6:79017474-79017693 | Rare:48; Clinvar:1 | ||||
| chr6:79043840-79044078 | Rare:52 | ||||
| chr6:79060486-79060835 | Rare:81 | ||||
| chr6:79233666-79233730 | Common:2; Rare:18 |