chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154748874247488743CT13GENIChomozygous112501521
154748917947489180AT13GENIChomozygous112501527
154748918047489181GA13GENIChomozygous112501529
154752094147520942GT5GENIChomozygous112808924
154752093647520937GT6GENIChomozygous112808920
154752093747520938AG5GENIChomozygous112808922
154752095047520951GT4GENIChomozygous112808928
154756645247566453GT21GENIChomozygous112501737
154756646647566467AT22GENIChomozygous112501739
154768015047680151GA22GENIChomozygous112501891
154768015147680152AT22GENIChomozygous112501893
154768019647680197CT25GENIChomozygous112501895
154768054847680549TA20GENIChomozygous112680118
154773662047736621GA23GENIChomozygous112501998
154773662147736622CG23GENIChomozygous112502000
154773717947737180AC14GENIChomozygous112502002
154775601347756014CT19GENIChomozygous112502038
154775601947756020GC17GENIChomozygous112502040
154775603547756036GT20GENIChomozygous112502042
154775604647756047GC21GENIChomozygous112680120
154775606847756069GC23GENIChomozygous112680122
154775607347756074GA23GENIChomozygous112680124
154775610547756106GA24GENIChomozygous112502044
154775610647756107GC24GENIChomozygous112502046
154775611247756113GT27GENIChomozygous112502048
154775614947756150GT26GENIChomozygous112502050
154775616447756165CT27GENIChomozygous112502052
154777685347776854GC14GENIChomozygous112680126
154778190447781905GT20GENIChomozygous112502086
154758878247588783GT16GENICheterozygous113000675