| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42760713-42760792 | Common:3; Rare:27 | ||||
| chr17:42761075-42761254 | Rare:50 | ||||
| chr17:42773369-42773478 | Rare:32 | ||||
| chr17:42798661-42798767 | Rare:33 | ||||
| chr17:42833351-42833501 | Rare:56 | ||||
| chr17:42964417-42964537 | Rare:56 | ||||
| chr17:43125338-43125662 | Rare:80; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170292-43170511 | Common:2; Rare:43 | ||||
| chr17:43171034-43171245 | Rare:63 | ||||
| chr17:43398878-43398993 | Common:1; Rare:32 | ||||
| chr17:43545882-43545993 | Common:1; Rare:16 | ||||
| chr17:43778918-43779057 | Rare:29 | ||||
| chr17:43833114-43833322 | Common:2; Rare:60 | ||||
| chr17:43907497-43907721 | Rare:66 | ||||
| chr17:44070612-44070922 | Common:3; Rare:105; Clinvar:4; Clinvar (benign):2 |