| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76501372-76501579 | Rare:70; Clinvar (benign):3 | ||||
| chr17:76643574-76643961 | Common:2; Rare:87 | ||||
| chr17:76726458-76726874 | Common:5; Rare:155 | ||||
| chr17:76737241-76737537 | Common:4; Rare:145 | ||||
| chr17:76737861-76738043 | Common:3; Rare:50 | ||||
| chr17:77288181-77288280 | Common:1; Rare:23 | ||||
| chr17:78128621-78128855 | Common:7; Rare:61 | ||||
| chr17:78130503-78130806 | Common:2; Rare:61 | ||||
| chr17:78168456-78168626 | Rare:49 | ||||
| chr17:78187045-78187418 | Common:3; Rare:130 | ||||
| chr17:78736638-78736977 | Common:1; Rare:79 | ||||
| chr17:78782203-78782577 | Common:9; Rare:122 | ||||
| chr17:78840736-78841114 | Common:2; Rare:144 | ||||
| chr17:79009680-79009924 | Common:9; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:79023875-79024211 | Common:1; Rare:70 |