| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:386209-386400 | Common:3; Rare:44 | ||||
| chr17:714777-714901 | Common:2; Rare:41 | ||||
| chr17:752146-752379 | Common:3; Rare:92 | ||||
| chr17:775554-775823 | Rare:83 | ||||
| chr17:997081-997158 | Common:1; Rare:34 | ||||
| chr17:1078942-1079062 | Rare:39 | ||||
| chr17:1109075-1109141 | Rare:21 | ||||
| chr17:1400046-1400408 | Common:3; Rare:150 | ||||
| chr17:1516588-1516978 | Common:2; Rare:137 | ||||
| chr17:1684780-1685038 | Common:2; Rare:87; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:1761892-1762121 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:1762693-1762839 | Common:3; Rare:40 | ||||
| chr17:1763189-1763304 | Rare:25 | ||||
| chr17:1829780-1830096 | Common:8; Rare:133 | ||||
| chr17:2303444-2303650 | Rare:77 |