| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68036213-68036365 | Common:1; Rare:36 | ||||
| chr17:68247437-68247519 | Common:2; Rare:17 | ||||
| chr17:68247627-68248168 | Common:7; Rare:191 | ||||
| chr17:68259084-68259266 | Rare:62 | ||||
| chr17:68291344-68291864 | Common:3; Rare:137 | ||||
| chr17:68291891-68292047 | Rare:54 | ||||
| chr17:68456753-68456947 | Common:1; Rare:39 | ||||
| chr17:68457418-68457977 | Common:13; Rare:183 | ||||
| chr17:68511583-68511766 | Common:4; Rare:47 | ||||
| chr17:68511801-68512186 | Common:1; Rare:92 | ||||
| chr17:68512201-68512511 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:68512575-68512940 | Rare:125 | ||||
| chr17:68513034-68513050 | Rare:4 | ||||
| chr17:68513155-68513386 | Common:2; Rare:63 | ||||
| chr17:68600594-68600641 | Common:1; Rare:17; Clinvar (benign):1; Clinvar (pathogenic):1 |