| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63741769-63741930 | Common:2; Rare:59 | ||||
| chr17:63773474-63773835 | Common:2; Rare:118 | ||||
| chr17:63827057-63827492 | Common:5; Rare:125 | ||||
| chr17:64130010-64130368 | Common:6; Rare:92 | ||||
| chr17:64448784-64449163 | Common:2; Rare:45 | ||||
| chr17:64506513-64506778 | Common:3; Rare:92 | ||||
| chr17:64662305-64662453 | Common:1; Rare:75 | ||||
| chr17:64919459-64919599 | Common:5; Rare:21 | ||||
| chr17:65056582-65056947 | Common:4; Rare:149 | ||||
| chr17:67245165-67245288 | Rare:41 | ||||
| chr17:67366449-67366773 | Rare:105 | ||||
| chr17:67717669-67717956 | Common:2; Rare:94 | ||||
| chr17:68247813-68248189 | Common:6; Rare:158 | ||||
| chr17:68291249-68291531 | Common:1; Rare:77 | ||||
| chr17:68512302-68512548 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):3 |