| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89687361-89687519 | Rare:52 | ||||
| chr16:89701657-89701805 | Rare:57 | ||||
| chr16:89720865-89721049 | Common:1; Rare:59 | ||||
| chr16:89816617-89816769 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:89972455-89972658 | Common:1; Rare:74 | ||||
| chr16:90022552-90022713 | Rare:64 | ||||
| chr17:338999-339182 | Common:1; Rare:38 | ||||
| chr17:352506-352634 | Common:2; Rare:29 | ||||
| chr17:352768-352867 | Common:1; Rare:21 | ||||
| chr17:714769-714901 | Common:2; Rare:44 | ||||
| chr17:732319-732603 | Common:1; Rare:100 | ||||
| chr17:752152-752309 | Common:2; Rare:66 | ||||
| chr17:1456213-1456498 | Common:6; Rare:104 | ||||
| chr17:1516588-1516971 | Common:2; Rare:134 | ||||
| chr17:1645702-1645858 | Common:2; Rare:44 |