| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:100881077-100881495 | Common:7; Rare:137 | ||||
| chr6:105137077-105137264 | Common:1; Rare:71 | ||||
| chr6:106086163-106086398 | Rare:64 | ||||
| chr6:106098643-106098970 | Common:2; Rare:76 | ||||
| chr6:106325551-106325871 | Common:1; Rare:104 | ||||
| chr6:106544647-106544890 | Common:2; Rare:71 | ||||
| chr6:106629462-106629661 | Common:3; Rare:47 | ||||
| chr6:107459495-107459691 | Common:1; Rare:51; Clinvar:1 | ||||
| chr6:107958106-107958416 | Common:1; Rare:95; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:108074647-108074866 | Common:1; Rare:77; Clinvar:1 | ||||
| chr6:108260758-108260862 | Rare:32 | ||||
| chr6:108260866-108261091 | Rare:104 | ||||
| chr6:108294806-108295079 | Common:1; Rare:74 | ||||
| chr6:108560713-108560984 | Rare:113 | ||||
| chr6:108656290-108656372 | Rare:11 |