chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
791759579175959TT61GENIChomozygous137934627
791762359176236TC58GENIChomozygous137999763
791768579176858CG36GENIChomozygous137999764
791768889176890TT40GENIChomozygous137934628
791770469177047AG48GENIChomozygous137999765
791773649177376TGGGTGGATGGG21GENIChomozygous137934629
791783359178336CT61GENIChomozygous137999766
791797319179732CG51GENIChomozygous137999767
791797979179798G52GENIChomozygous137934630
791810889181089CT59GENIChomozygous137999768
791811419181141TG58GENICpossibly homozygous137934631
791820909182091TC59GENIChomozygous137999769
791824869182487TG45GENIChomozygous137999770
791824879182488TA41GENIChomozygous137999771
791825909182590TCTTAT34GENIChomozygous137934632
791830549183055CT39GENIChomozygous137999772
791832759183276TC34GENIChomozygous137999773
791856659185666AT57GENIChomozygous137999774
791857819185782AG55GENIChomozygous137999775
791892199189220GA70GENIChomozygous137999782
791862349186235GA44GENIChomozygous137999776
791870709187071AG52GENIChomozygous137999777
791871589187159CT48GENIChomozygous137999778
791883399188340TG44GENIChomozygous137999780
791886159188616AT74GENIChomozygous137999781
791893059189306T66GENICpossibly homozygous137934633
791905599190560AG52GENIChomozygous137999783
791909459190946TC51GENIChomozygous137999784
791912679191268TA24GENICpossibly homozygous137999785
791921299192129C15GENIChomozygous137934634
791925959192596TC41GENIChomozygous137999788
791934249193425AG35GENIChomozygous137999789
791939289193929TC46GENIChomozygous137999790
791942689194269T24GENICheterozygous403199519
791942199194220GA27GENICheterozygous154425179
791942199194220G27GENICheterozygous403199518
791942689194269TC24GENIChomozygous154425180