| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48545106-48545237 | Rare:20 | ||||
| chr17:48553806-48554052 | Rare:27 | ||||
| chr17:48590203-48590440 | Common:1; Rare:52 | ||||
| chr17:48944758-48944935 | Common:2; Rare:62 | ||||
| chr17:48997388-48997527 | Rare:30 | ||||
| chr17:48998213-48998351 | Common:2; Rare:40 | ||||
| chr17:49677954-49678307 | Rare:87 | ||||
| chr17:49788567-49788730 | Common:1; Rare:50 | ||||
| chr17:50056032-50056121 | Common:1; Rare:31 | ||||
| chr17:50188533-50188798 | Rare:63; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
| chr17:50188903-50189277 | Rare:94; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:50192478-50192688 | Common:1; Rare:46; Clinvar:3; Clinvar (benign):5 | ||||
| chr17:50194349-50194831 | Common:3; Rare:136; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):5 | ||||
| chr17:50195048-50195288 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):4 | ||||
| chr17:50195923-50196202 | Common:2; Rare:74; Clinvar (benign):4; Clinvar (pathogenic):2 |