chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121967729919677300GC14GENIChomozygous139106050
121967732919677329CCC9GENIChomozygous139045835
121967734419677344T7GENIChomozygous139045836
121967748219677482AGG15GENICpossibly homozygous139045837
121967788519677886CT22GENIChomozygous139106051
121967788819677889GA21GENIChomozygous139106052
121967858419678585AG26GENIChomozygous139106053
121967870619678707CT19GENIChomozygous139106054
121967901019679011TC21GENIChomozygous139106055
121968014219680143AG20GENIChomozygous139106056
121968099319680994AG28GENIChomozygous139106057
121968245719682458AG27GENIChomozygous139106058
121968273019682731AC20GENIChomozygous139106059
121968292019682921GA31GENIChomozygous139106060
121968383119683832TA27GENIChomozygous139106061
121968535219685353GA17GENIChomozygous139106064
121967747119677472GA17GENICpossibly homozygous154743620
121968538119685382GT18GENIChomozygous139106065
121968665219686653CT24GENIChomozygous139106066