| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42760974-42761254 | Rare:72 | ||||
| chr17:42798654-42798767 | Rare:36 | ||||
| chr17:42833284-42833607 | Common:1; Rare:106 | ||||
| chr17:42853085-42853326 | Common:1; Rare:45 | ||||
| chr17:42964428-42964537 | Rare:51 | ||||
| chr17:43011980-43012195 | Rare:51 | ||||
| chr17:43125466-43125654 | Rare:45; Clinvar (benign):1 | ||||
| chr17:43170292-43170718 | Common:3; Rare:82 | ||||
| chr17:43171000-43171278 | Common:1; Rare:95 | ||||
| chr17:43778853-43779041 | Rare:43 | ||||
| chr17:43907501-43907773 | Rare:78 | ||||
| chr17:44070612-44070947 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44111225-44111438 | Rare:60 | ||||
| chr17:44123579-44123840 | Common:3; Rare:75 | ||||
| chr17:44170661-44170714 | Rare:14 |