| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:64020489-64020798 | Common:2; Rare:59 | ||||
| chr17:64130004-64130360 | Common:6; Rare:91 | ||||
| chr17:64390500-64390957 | Common:1; Rare:78 | ||||
| chr17:64413771-64413814 | Rare:7 | ||||
| chr17:64497033-64497136 | Common:1; Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:64506075-64506399 | Common:3; Rare:159 | ||||
| chr17:64506512-64506804 | Common:3; Rare:111 | ||||
| chr17:65055798-65055828 | Rare:3 | ||||
| chr17:65056589-65056907 | Common:4; Rare:126 | ||||
| chr17:67245147-67245288 | Rare:45 | ||||
| chr17:67717690-67717972 | Rare:97 | ||||
| chr17:68247866-68248142 | Common:6; Rare:115 | ||||
| chr17:68291261-68291523 | Common:1; Rare:73 | ||||
| chr17:68511686-68512081 | Rare:108 | ||||
| chr17:68512383-68512822 | Rare:158; Clinvar:2; Clinvar (benign):3 |