| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4206338-4206634 | Common:1; Rare:77 | ||||
| chr17:4483592-4483864 | Rare:49 | ||||
| chr17:4881032-4881178 | Rare:37 | ||||
| chr17:4981804-4981879 | Rare:19 | ||||
| chr17:4999944-5000276 | Common:4; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:5434882-5435140 | Common:2; Rare:60 | ||||
| chr17:7556676-7556879 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:7556925-7557195 | Rare:76 | ||||
| chr17:7559875-7560091 | Rare:63 | ||||
| chr17:7834130-7834251 | Rare:44 | ||||
| chr17:7835525-7835786 | Common:4; Rare:79 | ||||
| chr17:7836331-7836479 | Common:1; Rare:43 | ||||
| chr17:7841922-7841954 | Rare:13 | ||||
| chr17:7842571-7842762 | Rare:39 | ||||
| chr17:7849909-7850166 | Rare:58 |