chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7113187352113187353AG32GENIChomozygous145636143
7113188056113188056C11GENIChomozygous145610469
7113190184113190185CA51GENICpossibly homozygous145636144
7113188716113188716AT45GENIChomozygous141922785
7113191077113191078CG55GENIChomozygous145636145
7113191264113191265GA32GENIChomozygous145636146
7113191449113191450CT43GENIChomozygous145636147
7113191932113191933AG50GENIChomozygous142008789
7113192043113192044GA56GENIChomozygous145636148
7113192476113192477TG37GENIChomozygous142008791
7113192627113192628CT39GENIChomozygous145636149
7113194919113194920TA45GENIChomozygous142008794
7113195680113195681CT41GENICpossibly homozygous142008797
7113195814113195815AG59GENIChomozygous142008799
7113195847113195848AG62GENIChomozygous142008800
7113205052113205060GAGAGAGG10GENIChomozygous145610470
7113205132113205132G11GENIChomozygous145610471
7113205156113205160AGAG9GENIChomozygous145610472
7113206924113206925T37GENIChomozygous141922789
7113208880113208902GACCCTGGAGTGCCATCCTCCG46GENIChomozygous145610473
7113205059113205060GA10GENICheterozygous154494201
7113205059113205060G10GENIChomozygous403222694