| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43170885-43171546 | Common:1; Rare:187 | ||||
| chr17:43211465-43212016 | Common:3; Rare:107 | ||||
| chr17:43212571-43212906 | Common:1; Rare:52 | ||||
| chr17:43398876-43399016 | Common:1; Rare:44 | ||||
| chr17:43483560-43484130 | Rare:149 | ||||
| chr17:43484211-43484340 | Common:3; Rare:32 | ||||
| chr17:43545754-43545847 | Common:1; Rare:12 | ||||
| chr17:43546287-43546637 | Common:2; Rare:82 | ||||
| chr17:43778230-43778456 | Rare:42 | ||||
| chr17:43778884-43779099 | Common:1; Rare:57 | ||||
| chr17:44014870-44015129 | Common:2; Rare:83 | ||||
| chr17:44066245-44066403 | Rare:48 | ||||
| chr17:44066597-44066827 | Common:1; Rare:87 | ||||
| chr17:44070510-44070782 | Rare:66; Clinvar:2 | ||||
| chr17:44070790-44071022 | Common:3; Rare:83; Clinvar:3; Clinvar (benign):2 |