| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44014835-44015176 | Common:2; Rare:101 | ||||
| chr17:44066227-44066433 | Rare:60 | ||||
| chr17:44066597-44066808 | Common:1; Rare:83 | ||||
| chr17:44070514-44071240 | Common:3; Rare:239; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr17:44071394-44071626 | Common:1; Rare:55 | ||||
| chr17:44086904-44087188 | Common:2; Rare:89 | ||||
| chr17:44111226-44111319 | Rare:26 | ||||
| chr17:44123530-44123911 | Common:3; Rare:112 | ||||
| chr17:44123968-44124274 | Common:1; Rare:70 | ||||
| chr17:44141781-44142095 | Common:1; Rare:79 | ||||
| chr17:44186470-44187061 | Common:3; Rare:177 | ||||
| chr17:44187143-44187314 | Common:1; Rare:45 | ||||
| chr17:44198401-44198578 | Common:2; Rare:41 | ||||
| chr17:44198960-44199107 | Rare:42 | ||||
| chr17:44199292-44199557 | Common:1; Rare:80 |