| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1491615-1491816 | Common:1; Rare:62 | ||||
| chr17:1516578-1516978 | Common:2; Rare:143 | ||||
| chr17:1628812-1628933 | Rare:41 | ||||
| chr17:1645698-1645855 | Common:2; Rare:44 | ||||
| chr17:1648934-1649235 | Common:3; Rare:101 | ||||
| chr17:1673173-1673387 | Common:2; Rare:53; Clinvar:1 | ||||
| chr17:1684556-1684658 | Rare:35 | ||||
| chr17:1684773-1685010 | Common:1; Rare:82; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:1716172-1716550 | Common:3; Rare:123 | ||||
| chr17:1717092-1717287 | Common:1; Rare:44 | ||||
| chr17:1771350-1771824 | Common:1; Rare:114 | ||||
| chr17:1829786-1830051 | Common:8; Rare:112 | ||||
| chr17:2030012-2030215 | Common:1; Rare:87; Clinvar (pathogenic):1 | ||||
| chr17:2041271-2041497 | Common:2; Rare:72 | ||||
| chr17:2041596-2041691 | Common:1; Rare:41 |