| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:12753984-12754189 | Common:1; Rare:77 | ||||
| chr8:13133181-13133565 | Common:14; Rare:116 | ||||
| chr8:13514648-13514803 | Common:1; Rare:38 | ||||
| chr8:13566760-13566920 | Common:6; Rare:61 | ||||
| chr8:17234837-17234882 | Rare:13 | ||||
| chr8:17246572-17247108 | Common:5; Rare:215 | ||||
| chr8:17413301-17413490 | Common:3; Rare:97 | ||||
| chr8:17496874-17497171 | Common:5; Rare:118 | ||||
| chr8:17634003-17634162 | Rare:62 | ||||
| chr8:17651944-17651951 | Rare:1 | ||||
| chr8:17692206-17692370 | Rare:45 | ||||
| chr8:17801080-17801344 | Common:7; Rare:99 | ||||
| chr8:17922599-17923018 | Common:5; Rare:165 | ||||
| chr8:17923215-17923362 | Rare:52 | ||||
| chr8:18084779-18084868 | Common:1; Rare:42; Clinvar (benign):1 |