chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4168196974168196975A41GENICheterozygous128102456
4168204450168204451GA74GENIChomozygous112943432
4168209099168209099A35GENICheterozygous129905445
4168230035168230036TC56GENIChomozygous112943476
4168240034168240034GGAGGGAGGGAGGGAGGGAGGGAGGGAG9GENIChomozygous129905447
4168262086168262087AC39GENIChomozygous112943508
4168272952168272954AG36GENICheterozygous129905448
4168281428168281428C49GENIChomozygous128102483
4168284448168284449AT59GENICpossibly homozygous112943551
4168309774168309775AT7GENIChomozygous112943589
4168313769168313770TC33GENIChomozygous112943601
4168301555168301555CGCACGCG27GENICpossibly homozygous132060628
4168291957168291957A39GENIChomozygous128102487
4168292028168292028G34GENIChomozygous128102488
4168309863168309864G1GENIChomozygous132060629
4168314075168314076AG10GENIChomozygous128140570
4168317020168317021AT27GENICheterozygous130307406
4168317020168317020T27GENICheterozygous133395938
4168317023168317025TT28GENICpossibly homozygous128102501
4168323574168323575G19GENIChomozygous128102504
4168323578168323579T19GENIChomozygous128102505
4168323591168323592A18GENIChomozygous128102506
4168323595168323596A19GENIChomozygous128102507
4168323596168323597GT19GENIChomozygous119283012