| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:117542462-117542769 | Common:1; Rare:79 | ||||
| chr10:117542886-117543041 | Common:3; Rare:15 | ||||
| chr10:117543382-117543511 | Rare:40 | ||||
| chr10:117543855-117543866 | Rare:3 | ||||
| chr10:118046408-118046736 | Common:1; Rare:82 | ||||
| chr10:118046802-118047081 | Common:3; Rare:84 | ||||
| chr10:118341790-118342067 | Rare:50 | ||||
| chr10:118342087-118342416 | Common:3; Rare:77 | ||||
| chr10:118754365-118754568 | Rare:81 | ||||
| chr10:118754914-118755515 | Common:2; Rare:190 | ||||
| chr10:119029265-119029763 | Common:1; Rare:174 | ||||
| chr10:119029935-119029996 | Rare:13 | ||||
| chr10:119030009-119030149 | Common:3; Rare:49; Clinvar (pathogenic):1 | ||||
| chr10:119030494-119030817 | Common:2; Rare:95 | ||||
| chr10:119080064-119080313 | Rare:72 |