chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121967729919677300GC15GENIChomozygous139106050
121967732919677329CCC12GENIChomozygous139045835
121967734419677344T11GENIChomozygous139045836
121967748219677482AGG10GENIChomozygous139045837
121967788519677886CT25GENIChomozygous139106051
121967788819677889GA25GENIChomozygous139106052
121967858419678585AG19GENIChomozygous139106053
121967870619678707CT20GENICpossibly homozygous139106054
121967901019679011TC23GENIChomozygous139106055
121968014219680143AG16GENIChomozygous139106056
121968099319680994AG20GENIChomozygous139106057
121968245719682458AG31GENIChomozygous139106058
121968273019682731AC26GENIChomozygous139106059
121968292019682921GA28GENIChomozygous139106060
121968383119683832TA21GENIChomozygous139106061
121968467919684680C7GENICheterozygous403319837
121967747119677472GA12GENIChomozygous154743620
121968467919684680CA7GENICheterozygous403319836
121968466419684665C7GENICheterozygous403845986
121968466419684665CG7GENICheterozygous403845987
121968471319684714AG7GENICheterozygous403319838
121968471319684714A7GENICheterozygous403319839
121968473219684733CA7GENICheterozygous403319840
121968473219684733C7GENICheterozygous403319841
121968535219685353GA20GENIChomozygous139106064
121968538119685382GT18GENIChomozygous139106065
121968665219686653CT18GENIChomozygous139106066