| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42761027-42761351 | Common:2; Rare:94 | ||||
| chr17:42773362-42773483 | Rare:37 | ||||
| chr17:42798661-42798767 | Rare:33 | ||||
| chr17:42833351-42833471 | Rare:47 | ||||
| chr17:42964408-42964557 | Common:1; Rare:66 | ||||
| chr17:42998372-42998828 | Common:4; Rare:118 | ||||
| chr17:43017840-43018043 | Rare:57 | ||||
| chr17:43025121-43025263 | Rare:32 | ||||
| chr17:43125351-43125669 | Rare:69; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170268-43170723 | Common:3; Rare:90 | ||||
| chr17:43171014-43171288 | Common:1; Rare:94 | ||||
| chr17:43211758-43211903 | Common:1; Rare:32 | ||||
| chr17:43530469-43530505 | Rare:7 | ||||
| chr17:43778841-43779100 | Common:1; Rare:67 | ||||
| chr17:44070612-44070954 | Common:3; Rare:121; Clinvar:4; Clinvar (benign):2 |