| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89816607-89816769 | Common:2; Rare:81; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:89873469-89873789 | Common:2; Rare:148 | ||||
| chr16:89972470-89972860 | Common:3; Rare:143 | ||||
| chr16:90019376-90019686 | Common:6; Rare:93 | ||||
| chr16:90022552-90022716 | Common:1; Rare:66 | ||||
| chr17:714782-714976 | Common:3; Rare:63 | ||||
| chr17:732280-732705 | Common:2; Rare:146 | ||||
| chr17:752152-752310 | Common:2; Rare:66 | ||||
| chr17:752789-752850 | Rare:15 | ||||
| chr17:1492664-1492786 | Rare:26 | ||||
| chr17:1516582-1516986 | Common:2; Rare:144 | ||||
| chr17:1645730-1645858 | Common:2; Rare:25 | ||||
| chr17:1716186-1716477 | Common:1; Rare:89 | ||||
| chr17:1770216-1770523 | Common:3; Rare:75 | ||||
| chr17:1829746-1830106 | Common:9; Rare:148 |