chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1657769185776919CT58GENIChomozygous139861010
1657798385779839TC51GENIChomozygous139861011
1657807355780736AG57GENIChomozygous139861012
1657820245782025CT32GENIChomozygous139861013
1657840755784076CT37GENIChomozygous139861014
1657861895786190TC70GENIChomozygous139861015
1657873315787332CT54GENIChomozygous139861016
1657881385788139GA34GENIChomozygous139861017
1657883855788386GA53GENIChomozygous139861018
1657886225788623AT36GENIChomozygous139861019
1657892335789234AC30GENICpossibly homozygous139861020
1657898175789818AG41GENIChomozygous139861021
1657899405789941AG39GENIChomozygous139861022
1657901705790171TC33GENIChomozygous139861023
1657907945790795TC40GENIChomozygous139861024
1657938575793858CT48GENIChomozygous139861025
1657953965795397TC53GENIChomozygous139861026
1657971545797155CT43GENIChomozygous139861027
1657976965797697TC33GENIChomozygous139861028
1657977385797739GA41GENIChomozygous139861029
1657825205782521G59GENIChomozygous139818695
1657842305784230CAGAG60GENIChomozygous139818696
1657891925789193A25GENICpossibly homozygous139818697
1657892115789211A29GENIChomozygous139818698
1657892225789223C34GENIChomozygous139818699
1657891045789105CA14GENICheterozygous147614644
1657979665797967GA40GENIChomozygous139861030
1657982615798262AG49GENIChomozygous139861031
1657986695798670CG31GENIChomozygous139861032
1657986885798689CG28GENIChomozygous139861033
1658000815800082CA52GENIChomozygous139861034
1658011595801160GA48GENICpossibly homozygous139861035
1658019705801971GA51GENIChomozygous139861036
1658036665803667TA28GENIChomozygous139861037
1658060205806021CT53GENIChomozygous139861038
1658063375806338AG40GENIChomozygous139861039
1658070345807035CA61GENIChomozygous139861040