chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
791759579175959TT65GENIChomozygous137934627
791762359176236TC51GENIChomozygous137999763
791768889176890TT52GENIChomozygous137934628
791773649177376TGGGTGGATGGG32GENIChomozygous137934629
791797319179732CG55GENIChomozygous137999767
791768579176858CG59GENIChomozygous137999764
791770469177047AG60GENIChomozygous137999765
791783359178336CT48GENIChomozygous137999766
791797979179798G44GENIChomozygous137934630
791810889181089CT67GENIChomozygous137999768
791811419181141TG59GENICpossibly homozygous137934631
791820909182091TC63GENIChomozygous137999769
791824869182487TG51GENIChomozygous137999770
791824879182488TA49GENIChomozygous137999771
791825909182590TCTTAT55GENIChomozygous137934632
791830549183055CT51GENIChomozygous137999772
791832759183276TC52GENIChomozygous137999773
791856659185666AT60GENIChomozygous137999774
791857819185782AG44GENIChomozygous137999775
791862349186235GA47GENIChomozygous137999776
791870709187071AG62GENIChomozygous137999777
791871589187159CT52GENIChomozygous137999778
791883399188340TG58GENIChomozygous137999780
791886159188616AT57GENIChomozygous137999781
791892199189220GA37GENIChomozygous137999782
791893059189306T44GENIChomozygous137934633
791905599190560AG52GENIChomozygous137999783
791909459190946TC54GENIChomozygous137999784
791912679191268TA26GENIChomozygous137999785
791921299192129C20GENIChomozygous137934634
791925959192596TC49GENIChomozygous137999788
791934249193425AG49GENIChomozygous137999789
791939289193929TC46GENIChomozygous137999790
791835619183562GA7GENIChomozygous140893474
791835659183566GA6GENIChomozygous140893475
791835819183582AG3GENIChomozygous140893476
791835719183572G5GENIChomozygous140891648