| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42682338-42682641 | Common:1; Rare:64 | ||||
| chr17:42745006-42745107 | Common:2; Rare:41 | ||||
| chr17:42773384-42773527 | Rare:43 | ||||
| chr17:42798465-42798785 | Rare:110; Clinvar (pathogenic):1 | ||||
| chr17:42833340-42833672 | Common:2; Rare:104 | ||||
| chr17:42834513-42834877 | Rare:79 | ||||
| chr17:42964408-42964542 | Rare:63 | ||||
| chr17:42980390-42980591 | Common:1; Rare:68 | ||||
| chr17:42998308-42998651 | Common:4; Rare:92 | ||||
| chr17:43025084-43025325 | Rare:57 | ||||
| chr17:43125309-43125690 | Rare:99; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:43170185-43170534 | Common:2; Rare:79 | ||||
| chr17:43171000-43171306 | Common:1; Rare:104 | ||||
| chr17:43483933-43484094 | Rare:67 | ||||
| chr17:43491226-43491523 | Rare:56 |