| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42980473-42980571 | Common:1; Rare:38 | ||||
| chr17:42998073-42998529 | Common:5; Rare:112 | ||||
| chr17:43022319-43022484 | Rare:49 | ||||
| chr17:43025085-43025363 | Rare:70 | ||||
| chr17:43125333-43125654 | Rare:81; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:43170223-43170497 | Common:2; Rare:61 | ||||
| chr17:43170998-43171274 | Common:1; Rare:94 | ||||
| chr17:43211779-43211890 | Rare:23 | ||||
| chr17:43398878-43399027 | Common:1; Rare:50 | ||||
| chr17:43778922-43779041 | Rare:24 | ||||
| chr17:43833114-43833321 | Common:2; Rare:59 | ||||
| chr17:44070612-44070951 | Common:3; Rare:120; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44111225-44111453 | Rare:63 | ||||
| chr17:44123585-44123889 | Common:3; Rare:86 | ||||
| chr17:44141769-44141979 | Common:1; Rare:48 |