| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63827051-63827500 | Common:5; Rare:132 | ||||
| chr17:64129998-64130360 | Common:6; Rare:93 | ||||
| chr17:64390561-64390957 | Common:1; Rare:72 | ||||
| chr17:64505935-64506227 | Common:6; Rare:145 | ||||
| chr17:64506244-64506801 | Common:8; Rare:216 | ||||
| chr17:64919463-64919579 | Common:5; Rare:16 | ||||
| chr17:65056553-65056907 | Common:4; Rare:140 | ||||
| chr17:65137269-65137469 | Rare:66 | ||||
| chr17:67366481-67366710 | Rare:78 | ||||
| chr17:67717754-67717820 | Rare:14 | ||||
| chr17:67717823-67717977 | Rare:65 | ||||
| chr17:68247928-68248142 | Common:5; Rare:89 | ||||
| chr17:68259160-68259204 | Rare:20 | ||||
| chr17:68291241-68291513 | Common:1; Rare:78 | ||||
| chr17:68512312-68512495 | Rare:61; Clinvar (benign):1 |