| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:64975545-64975722 | Common:1; Rare:61 | ||||
| chr17:65100698-65100918 | Rare:67 | ||||
| chr17:68101481-68101566 | Common:3; Rare:44 | ||||
| chr17:68539959-68539971 | Rare:3 | ||||
| chr17:68555625-68555837 | Rare:59; Clinvar (pathogenic):1 | ||||
| chr17:68874337-68874495 | Common:1; Rare:28 | ||||
| chr17:72518989-72519067 | Rare:15 | ||||
| chr17:72571671-72572012 | Common:1; Rare:55 | ||||
| chr17:74436449-74436750 | Rare:48 | ||||
| chr17:74768292-74768566 | Common:1; Rare:87 | ||||
| chr17:75148527-75148852 | Rare:66 | ||||
| chr17:75242896-75243117 | Rare:78 | ||||
| chr17:75246495-75246520 | Rare:7 | ||||
| chr17:75565934-75566119 | Rare:32 | ||||
| chr17:75570165-75570463 | Common:3; Rare:101 |