| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:67245147-67245312 | Rare:51 | ||||
| chr17:67366449-67366709 | Rare:88 | ||||
| chr17:67717696-67717972 | Rare:94 | ||||
| chr17:67825324-67825523 | Common:2; Rare:60 | ||||
| chr17:68247792-68248126 | Common:6; Rare:147 | ||||
| chr17:68259070-68259200 | Rare:43 | ||||
| chr17:68291234-68291513 | Common:1; Rare:82 | ||||
| chr17:68511690-68512003 | Rare:87 | ||||
| chr17:68512292-68512543 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:69141803-69142041 | Common:2; Rare:50 | ||||
| chr17:69327010-69327327 | Common:4; Rare:102 | ||||
| chr17:69414627-69414754 | Rare:27 | ||||
| chr17:70169319-70169557 | Common:1; Rare:64 | ||||
| chr17:72120782-72121043 | Rare:68 | ||||
| chr17:73192817-73193099 | Common:15; Rare:118; Clinvar:3; Clinvar (benign):1 |