| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63489062-63489452 | Common:2; Rare:99; Clinvar:1 | ||||
| chr17:63496060-63496504 | Common:1; Rare:122; Clinvar (benign):1 | ||||
| chr17:63550194-63550612 | Common:3; Rare:89 | ||||
| chr17:63700126-63700348 | Common:1; Rare:59 | ||||
| chr17:63741705-63741923 | Common:2; Rare:75 | ||||
| chr17:63773418-63773842 | Common:2; Rare:138 | ||||
| chr17:63827063-63827508 | Common:5; Rare:128 | ||||
| chr17:63827517-63827739 | Common:2; Rare:61 | ||||
| chr17:63831281-63831581 | Rare:87 | ||||
| chr17:64130023-64130354 | Common:5; Rare:86 | ||||
| chr17:64497019-64497077 | Common:1; Rare:24; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:64503973-64504260 | Common:2; Rare:95 | ||||
| chr17:64506075-64506804 | Common:8; Rare:308 | ||||
| chr17:64919463-64919692 | Common:5; Rare:53 | ||||
| chr17:65056525-65056907 | Common:4; Rare:152 |