| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:100881063-100881528 | Common:7; Rare:152 | ||||
| chr6:105137151-105137299 | Rare:59 | ||||
| chr6:105179836-105180070 | Common:4; Rare:63 | ||||
| chr6:106086178-106086394 | Rare:60 | ||||
| chr6:106629432-106629689 | Common:5; Rare:66 | ||||
| chr6:107957261-107957422 | Rare:34 | ||||
| chr6:107957960-107958428 | Common:2; Rare:149; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108074650-108074936 | Common:1; Rare:101; Clinvar:1 | ||||
| chr6:108260763-108260865 | Rare:32 | ||||
| chr6:108260879-108261385 | Common:2; Rare:204 | ||||
| chr6:109009487-109009680 | Common:2; Rare:62 | ||||
| chr6:109094827-109095195 | Common:5; Rare:112 | ||||
| chr6:109095402-109095557 | Rare:34 | ||||
| chr6:109373123-109373190 | Rare:21 | ||||
| chr6:109382072-109382888 | Common:11; Rare:295; Clinvar (benign):2 |