| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:107459485-107459743 | Common:2; Rare:65; Clinvar:1 | ||||
| chr6:107958106-107958411 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:108074661-108074838 | Rare:57; Clinvar:1 | ||||
| chr6:108260907-108261286 | Common:2; Rare:154 | ||||
| chr6:108294636-108295093 | Common:1; Rare:111 | ||||
| chr6:108560726-108560978 | Rare:104 | ||||
| chr6:108848337-108848486 | Rare:54 | ||||
| chr6:108848642-108848761 | Rare:29 | ||||
| chr6:109009374-109009709 | Common:2; Rare:97 | ||||
| chr6:109094416-109094607 | Rare:46 | ||||
| chr6:109095222-109095557 | Common:1; Rare:66 | ||||
| chr6:109382239-109382328 | Rare:39 | ||||
| chr6:109382360-109382859 | Common:6; Rare:169; Clinvar (benign):1 | ||||
| chr6:109440520-109440849 | Common:1; Rare:120 | ||||
| chr6:109440934-109441023 | Rare:17 |