| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49414845-49415140 | Common:2; Rare:72 | ||||
| chr17:49677961-49678308 | Rare:87 | ||||
| chr17:49788392-49788730 | Common:2; Rare:104 | ||||
| chr17:50129796-50130147 | Common:3; Rare:80 | ||||
| chr17:50186315-50186928 | Common:2; Rare:173; Clinvar:17; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:50188528-50189011 | Rare:125; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
| chr17:50192478-50192651 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:50195432-50195595 | Rare:35; Clinvar (benign):2 | ||||
| chr17:50200211-50200338 | Common:1; Rare:22 | ||||
| chr17:50345816-50346136 | Common:4; Rare:96 | ||||
| chr17:50372969-50373246 | Common:3; Rare:99 | ||||
| chr17:50508339-50508498 | Common:3; Rare:50 | ||||
| chr17:50707601-50707948 | Common:4; Rare:103 | ||||
| chr17:50719456-50719730 | Rare:112 | ||||
| chr17:50866351-50866805 | Common:3; Rare:121 |