| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42761065-42761264 | Rare:54 | ||||
| chr17:42773375-42773478 | Rare:32 | ||||
| chr17:42798668-42798767 | Rare:31 | ||||
| chr17:42833391-42833471 | Rare:37 | ||||
| chr17:42964430-42964528 | Rare:49 | ||||
| chr17:42998332-42998478 | Common:3; Rare:48 | ||||
| chr17:43125344-43125617 | Rare:57; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43171016-43171245 | Rare:73 | ||||
| chr17:44186691-44187002 | Rare:104 | ||||
| chr17:44187171-44187230 | Rare:16 | ||||
| chr17:44268099-44268411 | Rare:63; Clinvar:3 | ||||
| chr17:44324780-44324966 | Common:2; Rare:65 | ||||
| chr17:44352243-44352392 | Rare:47; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:44503377-44503713 | Rare:132 | ||||
| chr17:44846280-44846343 | Rare:7 |