| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43778917-43779041 | Rare:25 | ||||
| chr17:43833148-43833337 | Common:2; Rare:58 | ||||
| chr17:44070620-44070925 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44186699-44187021 | Rare:104 | ||||
| chr17:44324780-44324938 | Common:1; Rare:56 | ||||
| chr17:44899375-44899736 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:45061103-45061341 | Common:1; Rare:69 | ||||
| chr17:45148130-45148482 | Common:1; Rare:100 | ||||
| chr17:45148654-45148881 | Common:1; Rare:66 | ||||
| chr17:45161530-45161807 | Common:1; Rare:61 | ||||
| chr17:45487819-45488120 | Common:1; Rare:52 | ||||
| chr17:45490708-45490867 | Rare:55 | ||||
| chr17:47189250-47189588 | Rare:85 | ||||
| chr17:47323913-47323987 | Common:1; Rare:19 | ||||
| chr17:47591837-47592115 | Common:2; Rare:79 |