| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47941334-47941600 | Rare:54; Clinvar:1 | ||||
| chr17:48048038-48048400 | Common:1; Rare:98 | ||||
| chr17:49210527-49210712 | Rare:30 | ||||
| chr17:49414833-49415120 | Common:1; Rare:68 | ||||
| chr17:49646468-49646829 | Common:2; Rare:64 | ||||
| chr17:49788557-49788745 | Common:1; Rare:61 | ||||
| chr17:50187218-50187550 | Common:2; Rare:62; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:50189051-50189316 | Rare:63; Clinvar:2 | ||||
| chr17:50191107-50191133 | Rare:5 | ||||
| chr17:50192155-50192414 | Common:1; Rare:56 | ||||
| chr17:50192443-50192717 | Common:1; Rare:72; Clinvar:4; Clinvar (benign):8 | ||||
| chr17:50192779-50193055 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr17:50194282-50194475 | Rare:54; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:50194551-50194865 | Common:2; Rare:94; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
| chr17:50194885-50195351 | Common:1; Rare:120; Clinvar:1; Clinvar (benign):5 |