chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3166578127166578128GC19GENICheterozygous58048760
3166578128166578129CT19GENICheterozygous57769810
3166578252166578253TC27GENIChomozygous57769811
3166579646166579647GA36GENIChomozygous57769812
3166579765166579766TA40GENIChomozygous57769813
3166580688166580689CCT15GENIChomozygous57769814
3166580692166580693T-14GENIChomozygous57769815
3166580708166580709GGC15GENIChomozygous57769816
3166580720166580721GGT18GENIChomozygous57769817
3166580729166580730TTC19GENIChomozygous57769818
3166580744166580745T-23GENIChomozygous57769819
3166581073166581074CT33GENIChomozygous57769820
3166581512166581513CCT22GENIChomozygous57769821
3166582612166582613TC22GENIChomozygous57769822
3166583092166583093CT7GENIChomozygous57769823
3166583161166583162CCTT5GENIChomozygous57769824
3166583848166583849GA13GENIChomozygous57769825
3166584009166584010AT18GENIChomozygous57769826
3166584042166584043CT15GENIChomozygous57769827
3166584648166584649AG45GENIChomozygous57769828
3166586660166586661CG24GENIChomozygous57769829
3166586681166586682C-19GENIChomozygous57769830