chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108396355108396371GTGTGTGTGTGTGTGT----------------4GENIChomozygous51596094
10108396766108396767TC20GENIChomozygous51596096
10108397090108397091GT20GENIChomozygous51596098
10108397389108397390GA14GENIChomozygous51953756
10108396469108396470AG29GENIChomozygous51953747
10108396843108396844GA23GENIChomozygous51953750
10108397341108397342TC17GENIChomozygous51953753
10108398923108398924CT20GENIChomozygous51953759
10108399390108399391AG27GENIChomozygous51953762
10108399592108399593CT19GENIChomozygous51596108
10108400014108400015CCTCT16GENIChomozygous51953766
10108400020108400021TC18GENICpossibly homozygous51953769
10108400065108400066CA19GENIChomozygous51953772
10108401441108401449GTGTGTGT--------7GENICpossibly homozygous51596114
10108401449108401450GA15GENICheterozygous51953775
10108401486108401487TC20GENICpossibly homozygous51596116
10108402283108402284AG25GENIChomozygous51596118
10108403425108403426GA19GENIChomozygous51953778
10108403550108403551TTAAC20GENIChomozygous51596120
10108403553108403554GGGGCTAC15GENIChomozygous51596122
10108405663108405664TTC22GENIChomozygous51596126
10108408887108408888TTC10GENICheterozygous51596134
10108408887108408888TC11GENIChomozygous51953781
10108409221108409222TTCA19GENICheterozygous51596138
10108409222108409223A-19GENICpossibly homozygous51953784
10108409485108409486AG19GENIChomozygous51596140
10108411962108411963AG19GENICheterozygous51953787
10108411969108411970CT13GENICheterozygous51953790
10108411969108411970CCAT12GENIChomozygous51953793
10108412067108412068CCT28GENIChomozygous51596149
10108412524108412525CT19GENIChomozygous51596151
10108412774108412775TC24GENIChomozygous51596153