| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76072487-76072664 | Rare:54 | ||||
| chr17:76103696-76103882 | Common:6; Rare:64 | ||||
| chr17:76353605-76353675 | Rare:31 | ||||
| chr17:76383008-76383272 | Rare:47 | ||||
| chr17:76384284-76384659 | Common:3; Rare:100 | ||||
| chr17:76385208-76385404 | Rare:48 | ||||
| chr17:76476940-76477257 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:76501618-76501776 | Common:1; Rare:24 | ||||
| chr17:76725821-76726069 | Common:1; Rare:67 | ||||
| chr17:76726456-76726886 | Common:5; Rare:165 | ||||
| chr17:76737302-76737687 | Common:4; Rare:140 | ||||
| chr17:76737861-76738070 | Common:3; Rare:56 | ||||
| chr17:77127754-77127885 | Rare:23 | ||||
| chr17:77129956-77130110 | Rare:26 | ||||
| chr17:77140652-77141086 | Common:2; Rare:149 |