| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42964422-42964528 | Rare:52 | ||||
| chr17:42998317-42998547 | Common:4; Rare:69 | ||||
| chr17:43022365-43022494 | Rare:34 | ||||
| chr17:43125313-43125654 | Rare:90; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:43170292-43170511 | Common:2; Rare:43 | ||||
| chr17:43171003-43171255 | Rare:84 | ||||
| chr17:43398856-43399002 | Common:1; Rare:44 | ||||
| chr17:43778899-43779125 | Common:1; Rare:62 | ||||
| chr17:44070627-44070947 | Common:3; Rare:112; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44141663-44141956 | Common:2; Rare:57 | ||||
| chr17:44186666-44187283 | Common:1; Rare:189 | ||||
| chr17:44221269-44221427 | Rare:47 | ||||
| chr17:44222103-44222306 | Rare:43 | ||||
| chr17:44324774-44324977 | Common:2; Rare:75 | ||||
| chr17:44345075-44345327 | Rare:54; Clinvar:5; Clinvar (benign):3 |