| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44689685-44690058 | Common:1; Rare:113 | ||||
| chr17:44690091-44690484 | Rare:82 | ||||
| chr17:44708508-44708675 | Rare:36 | ||||
| chr17:44708677-44708913 | Common:4; Rare:73 | ||||
| chr17:44775629-44775773 | Rare:35 | ||||
| chr17:44829502-44829634 | Rare:31 | ||||
| chr17:44829658-44829733 | Common:1; Rare:20 | ||||
| chr17:44829749-44829851 | Common:1; Rare:18 | ||||
| chr17:44830147-44830298 | Common:1; Rare:74 | ||||
| chr17:44830637-44830728 | Rare:13 | ||||
| chr17:44898996-44899086 | Rare:26 | ||||
| chr17:44899344-44899747 | Common:2; Rare:121; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:44946930-44947248 | Common:2; Rare:55 | ||||
| chr17:44947265-44947319 | Rare:9 | ||||
| chr17:44947420-44947484 | Rare:15 |