| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76353612-76353677 | Rare:27 | ||||
| chr17:76353839-76353994 | Rare:58 | ||||
| chr17:76585759-76585975 | Common:5; Rare:65 | ||||
| chr17:76725833-76726085 | Common:1; Rare:68 | ||||
| chr17:76726453-76726886 | Common:5; Rare:165 | ||||
| chr17:76737251-76737710 | Common:5; Rare:189 | ||||
| chr17:76737870-76738121 | Common:4; Rare:72 | ||||
| chr17:77280602-77280615 | Rare:1 | ||||
| chr17:77319435-77319663 | Common:3; Rare:59; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:77320077-77320323 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:77450496-77450785 | Rare:57 | ||||
| chr17:78130655-78130810 | Rare:29 | ||||
| chr17:78168493-78168702 | Common:3; Rare:55 | ||||
| chr17:78187018-78187370 | Common:3; Rare:119 | ||||
| chr17:78782213-78782572 | Common:9; Rare:120 |