chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148209411682094117AG60GENIChomozygous113603716
148209515982095161TT49GENIChomozygous131730680
148209531482095315G10GENICheterozygous131730681
148209564582095649TTTA29GENIChomozygous131730682
148210396982103970C41GENICpossibly homozygous131730683
148210141882101419TC51GENIChomozygous114098869
148210190582101906GA59GENIChomozygous114098870
148211051682110517TC58GENIChomozygous114098874
148210615382106154AG52GENIChomozygous114002613
148210990682109907CT51GENIChomozygous114002617
148210449682104497TA65GENIChomozygous114098871
148210569682105697GA60GENIChomozygous114098872
148210976882109769TG80GENICpossibly homozygous114098873
148210156382101564TA56GENIChomozygous113679759
148210659782106598A41GENICheterozygous131144926
148211265182112652TA75GENIChomozygous114098875
148211288282112883AG56GENIChomozygous114002621
148211342882113429CT82GENIChomozygous114098876
148211516082115161TC49GENIChomozygous114002625
148211540082115401TC60GENIChomozygous114002627
148211765782117658CT61GENIChomozygous114002629
148211776482117765TA55GENIChomozygous114098877