| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:104957050-104957153 | Rare:16 | ||||
| chr6:106325617-106325859 | Common:1; Rare:84 | ||||
| chr6:106629462-106629588 | Common:1; Rare:25 | ||||
| chr6:106975304-106975491 | Common:1; Rare:58 | ||||
| chr6:107459537-107459743 | Common:2; Rare:50 | ||||
| chr6:107958174-107958408 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:108260927-108261302 | Common:2; Rare:149 | ||||
| chr6:108294813-108295070 | Common:1; Rare:68 | ||||
| chr6:108848317-108848447 | Rare:42 | ||||
| chr6:109382075-109382225 | Common:4; Rare:59 | ||||
| chr6:109440552-109440847 | Common:1; Rare:109 | ||||
| chr6:109455634-109455865 | Common:4; Rare:65 | ||||
| chr6:109691165-109691348 | Common:3; Rare:41; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179962-110180163 | Common:2; Rare:60 | ||||
| chr6:110815867-110816124 | Common:2; Rare:59 |