| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:106629425-106629682 | Common:5; Rare:68 | ||||
| chr6:107459485-107459645 | Common:1; Rare:46; Clinvar:1 | ||||
| chr6:107958069-107958393 | Common:2; Rare:98; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108260764-108261025 | Rare:116 | ||||
| chr6:108294806-108295085 | Common:1; Rare:74 | ||||
| chr6:108560730-108560960 | Rare:96 | ||||
| chr6:109009432-109009682 | Common:2; Rare:77 | ||||
| chr6:109094827-109095195 | Common:5; Rare:112 | ||||
| chr6:109095415-109095561 | Rare:30 | ||||
| chr6:109382209-109382241 | Rare:14 | ||||
| chr6:109382245-109382328 | Rare:36 | ||||
| chr6:109382332-109382597 | Common:5; Rare:106; Clinvar (benign):2 | ||||
| chr6:109691158-109691348 | Common:3; Rare:43; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179947-110180162 | Common:2; Rare:62 | ||||
| chr6:110415493-110415690 | Rare:48 |