| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49210539-49210718 | Rare:26 | ||||
| chr17:49230696-49230885 | Common:3; Rare:52 | ||||
| chr17:49414833-49415120 | Common:1; Rare:68 | ||||
| chr17:49707877-49707985 | Rare:56 | ||||
| chr17:49708100-49708369 | Common:1; Rare:88 | ||||
| chr17:49788557-49788782 | Common:1; Rare:76 | ||||
| chr17:50186315-50186685 | Common:2; Rare:95; Clinvar:10; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:50188946-50189172 | Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:50189223-50189479 | Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:50345897-50346136 | Common:4; Rare:82 | ||||
| chr17:50373151-50373277 | Common:3; Rare:54 | ||||
| chr17:50426106-50426268 | Common:1; Rare:40 | ||||
| chr17:50707615-50707950 | Common:4; Rare:100 | ||||
| chr17:50719472-50719792 | Rare:110 | ||||
| chr17:50866319-50866774 | Common:4; Rare:131 |