| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47649399-47650045 | Common:2; Rare:224 | ||||
| chr17:47650134-47650441 | Rare:108 | ||||
| chr17:47650505-47650801 | Common:3; Rare:109 | ||||
| chr17:47694434-47694599 | Common:5; Rare:46 | ||||
| chr17:47831448-47831759 | Rare:97 | ||||
| chr17:47895717-47896127 | Common:3; Rare:113 | ||||
| chr17:47896331-47896568 | Common:1; Rare:54 | ||||
| chr17:47941345-47941732 | Rare:104; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47980588-47981073 | Rare:101 | ||||
| chr17:48048039-48048397 | Common:1; Rare:97 | ||||
| chr17:48048577-48048857 | Common:4; Rare:54 | ||||
| chr17:48544468-48544729 | Common:1; Rare:115 | ||||
| chr17:48892341-48892659 | Common:10; Rare:97 | ||||
| chr17:48908241-48908500 | Common:2; Rare:67 | ||||
| chr17:48944681-48944884 | Common:1; Rare:68 |