| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50476620-50476740 | Common:1; Rare:16 | ||||
| chr17:50656785-50657159 | Common:1; Rare:129 | ||||
| chr17:50660749-50661000 | Common:1; Rare:53 | ||||
| chr17:50909353-50909683 | Common:4; Rare:74 | ||||
| chr17:50919006-50919111 | Common:1; Rare:19 | ||||
| chr17:58324380-58324571 | Common:1; Rare:53 | ||||
| chr17:58332506-58332677 | Common:2; Rare:42 | ||||
| chr17:58518661-58518788 | Rare:25 | ||||
| chr17:58631832-58632150 | Common:3; Rare:137 | ||||
| chr17:58659293-58659558 | Common:3; Rare:90 | ||||
| chr17:59666517-59666872 | Rare:70 | ||||
| chr17:59673415-59673769 | Common:1; Rare:67; Clinvar (pathogenic):1 | ||||
| chr17:59679241-59679514 | Rare:52 | ||||
| chr17:59682479-59682793 | Rare:61 | ||||
| chr17:59690383-59690709 | Rare:46 |