chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5149077622149077623AT40GENIChomozygous114154893
5149077677149077678GA34GENICpossibly homozygous114050437
5149078013149078014AG45GENIChomozygous114050439
5149078792149078793TC54GENIChomozygous114154895
5149079019149079020TG35GENICheterozygous114651402
5149079153149079154AT41GENIChomozygous114050441
5149080854149080855TA37GENIChomozygous114154896
5149081434149081435TG44GENIChomozygous114154899
5149081439149081440AC45GENIChomozygous114154901
5149082518149082519TG25GENICheterozygous114154902
5149082818149082819CT28GENIChomozygous114154903
5149082987149082988GA40GENIChomozygous114154905
5149083169149083170AG41GENICpossibly homozygous114154906
5149083195149083196AC35GENIChomozygous114050449
5149083225149083226GA29GENICpossibly homozygous114154907
5149083229149083230AG28GENICpossibly homozygous114050451
5149083332149083333TG33GENIChomozygous114154909
5149083886149083887CT50GENIChomozygous114154911
5149084467149084468CT35GENIChomozygous114050455
5149085549149085550TA81GENIChomozygous114050459
5149085705149085706TC39GENIChomozygous114050465