chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1696218309621831T-1GENIChomozygous47921634
1696294809629481GGA10GENIChomozygous47266420
1696294859629486T-12GENICpossibly homozygous47266422
1696494589649459GGT6GENICheterozygous47901636
1696558369655872AATATTTTTTTCTATATACTTTAACAACCATATGTA------------------------------------1GENIChomozygous47266617
1696558829655883CG5GENIChomozygous47266619
1696559429655943CG11GENIChomozygous47266620
1696588219658822A-10GENICpossibly homozygous47266651
1696588239658824CCA10GENICpossibly homozygous47266653
1696615959661596TA5GENIChomozygous47266711
1696616429661643CG6GENIChomozygous47266713
1696616579661658CG3GENIChomozygous47266715
1696616769661677CT1GENIChomozygous47266717
1696617419661742CG1GENIChomozygous47266739
1696617499661750TA3GENIChomozygous47266741
1696617619661762AG4GENIChomozygous47607571
1696617729661773CG4GENIChomozygous47784895
1696618069661807CG6GENICheterozygous47725694
1696618219661822TC4GENIChomozygous47725696
1696618339661834TG2GENIChomozygous47725698
1696618449661845AT1GENIChomozygous47725700
1696618779661878GT1GENIChomozygous47725708
1696626629662663C-1GENIChomozygous47901646
1696730109673011GGA14GENICpossibly homozygous47266783
1696730629673063AT6GENIChomozygous47266785
1696730659673066AT8GENIChomozygous47266787
1696836319683632CG24GENIChomozygous47266848