| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42980390-42980566 | Common:1; Rare:51 | ||||
| chr17:42980727-42980943 | Common:1; Rare:53 | ||||
| chr17:43125338-43125723 | Rare:95; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170292-43170730 | Common:3; Rare:86 | ||||
| chr17:43170986-43171267 | Common:1; Rare:95 | ||||
| chr17:43211758-43211887 | Common:1; Rare:28 | ||||
| chr17:43483663-43484079 | Rare:121 | ||||
| chr17:43778845-43779094 | Common:1; Rare:65 | ||||
| chr17:44005404-44005711 | Rare:67 | ||||
| chr17:44070612-44070947 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44091395-44091685 | Rare:80 | ||||
| chr17:44123599-44123840 | Common:3; Rare:68 | ||||
| chr17:44186620-44187026 | Common:1; Rare:143 | ||||
| chr17:44187161-44187425 | Common:1; Rare:62 | ||||
| chr17:44198737-44198851 | Rare:38 |