| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109691104-109691335 | Common:3; Rare:56; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179590-110179727 | Rare:50 | ||||
| chr6:110179780-110180420 | Common:3; Rare:152 | ||||
| chr6:110815127-110815292 | Common:1; Rare:61 | ||||
| chr6:110815295-110815672 | Common:4; Rare:115 | ||||
| chr6:110815832-110816125 | Common:2; Rare:73 | ||||
| chr6:110874346-110874496 | Rare:34 | ||||
| chr6:110874522-110874785 | Common:5; Rare:95 | ||||
| chr6:110958537-110958809 | Common:6; Rare:104 | ||||
| chr6:110981905-110982120 | Common:3; Rare:107 | ||||
| chr6:111087328-111087514 | Common:2; Rare:56 | ||||
| chr6:111259093-111259383 | Common:3; Rare:89 | ||||
| chr6:111482862-111483115 | Rare:104 | ||||
| chr6:111483141-111483566 | Common:1; Rare:148 | ||||
| chr6:111483607-111483912 | Common:1; Rare:124 |