| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:89081048-89081350 | Common:2; Rare:119 | ||||
| chr6:89117937-89118080 | Common:1; Rare:59 | ||||
| chr6:89638713-89638829 | Common:3; Rare:43 | ||||
| chr6:89829620-89829909 | Rare:68 | ||||
| chr6:93419538-93419824 | Common:1; Rare:77 | ||||
| chr6:95577408-95577543 | Common:3; Rare:36 | ||||
| chr6:99425259-99425483 | Common:2; Rare:65 | ||||
| chr6:100881272-100881495 | Common:5; Rare:93 | ||||
| chr6:106086213-106086386 | Rare:43 | ||||
| chr6:106325657-106325892 | Common:1; Rare:80 | ||||
| chr6:106629448-106629617 | Common:1; Rare:36 | ||||
| chr6:108165859-108166095 | Rare:46 | ||||
| chr6:109094452-109094571 | Rare:25 | ||||
| chr6:109455742-109455942 | Common:1; Rare:55 | ||||
| chr6:109691158-109691315 | Common:1; Rare:38; Clinvar:4; Clinvar (benign):1 |