| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1515540-1516000 | Common:6; Rare:121 | ||||
| chr17:1516659-1516955 | Common:1; Rare:107 | ||||
| chr17:1562743-1562955 | Common:3; Rare:77 | ||||
| chr17:1628267-1628565 | Common:1; Rare:91 | ||||
| chr17:1628805-1629074 | Rare:90 | ||||
| chr17:1648954-1649236 | Common:3; Rare:98 | ||||
| chr17:1684799-1685091 | Common:3; Rare:96; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1710397-1710561 | Rare:45 | ||||
| chr17:1716500-1716650 | Common:3; Rare:52 | ||||
| chr17:1717028-1717365 | Common:1; Rare:67 | ||||
| chr17:1724420-1724850 | Common:4; Rare:130 | ||||
| chr17:1742540-1743100 | Common:4; Rare:144 | ||||
| chr17:1769935-1770335 | Common:5; Rare:169; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:1829778-1830088 | Common:8; Rare:132 | ||||
| chr17:2030664-2030812 | Rare:30 |