chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2051087005108701AG19GENIChomozygous125177177
2051089725108973GA7GENIChomozygous125210374
2051093085109309CG34GENIChomozygous125177180
2051095645109565TC23GENIChomozygous125177181
2051096585109659TC23GENIChomozygous125177182
2051097035109704AC20GENIChomozygous125177183
2051097245109725AC5GENIChomozygous125177184
2051097485109749GA4GENICheterozygous125210375
2051097565109757TC3GENICheterozygous125177185
2051100835110084GA19GENIChomozygous125210376
2051101945110195TC28GENIChomozygous125177186
2051106935110694AT22GENIChomozygous125177187
2051108265110827AG4GENICheterozygous125210377
2051108335110834TA8GENIChomozygous125210378
2051110045111005AG26GENIChomozygous125177190
2051112605111261GA26GENIChomozygous125177192
2051114515111452GA29GENIChomozygous125177193
2051116885111689TA18GENIChomozygous125177194
2051118615111862GA24GENIChomozygous125210379
2051120835112084AG17GENIChomozygous125177195
2051124705112471TC7GENIChomozygous125177197
2051125065112507GA5GENIChomozygous125210380
2051126055112606TC11GENIChomozygous125177199
2051126355112636AG7GENIChomozygous125177200
2051132595113260CT14GENIChomozygous125177203
2051133475113348GA8GENIChomozygous125177204