| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41739752-41740038 | Common:3; Rare:50 | ||||
| chr17:41756162-41756364 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:41757413-41757787 | Common:2; Rare:135; Clinvar:16; Clinvar (benign):23 | ||||
| chr17:41764713-41765085 | Rare:117; Clinvar:12; Clinvar (benign):9 | ||||
| chr17:41773093-41773482 | Common:1; Rare:77 | ||||
| chr17:41784079-41784354 | Common:1; Rare:64 | ||||
| chr17:41784417-41784500 | Rare:14 | ||||
| chr17:41868706-41869159 | Common:2; Rare:89 | ||||
| chr17:41877126-41877432 | Common:1; Rare:55 | ||||
| chr17:42266429-42266544 | Rare:13 | ||||
| chr17:42557353-42557408 | Common:2; Rare:11 | ||||
| chr17:43139819-43140114 | Common:1; Rare:71 | ||||
| chr17:43153588-43153642 | Common:1; Rare:5 | ||||
| chr17:44121118-44121405 | Common:2; Rare:58 | ||||
| chr17:44152375-44152425 | Rare:9 |