chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2185583884185583885CT13GENIChomozygous59907858
2185584416185584417TC24GENICpossibly homozygous59907859
2185584443185584444CT29GENICheterozygous59907860
2185584444185584445AG29GENICheterozygous59907861
2185585142185585143GA13GENICpossibly homozygous59907862
2185585558185585559A-9GENICpossibly homozygous59907863
2185585776185585780AAAG----3GENIChomozygous59907864
2185586736185586737TC13GENIChomozygous59287368
2185588812185588813CT16GENICpossibly homozygous59907866
2185589154185589155GA15GENICpossibly homozygous59907867
2185589344185589345CCAA6GENIChomozygous59287371
2185589358185589359AG5GENICheterozygous59287372
2185590976185590977TC7GENICpossibly homozygous59287379
2185594449185594450C-6GENICheterozygous59287388
2185598320185598321TA18GENICpossibly homozygous59287391
2185601875185601878ACA---3GENICheterozygous59907873
2185603713185603714CT20GENIChomozygous59907874
2185603868185603869AG10GENIChomozygous59907875
2185605048185605049AG9GENIChomozygous59907876
2185605821185605822TA9GENIChomozygous59907877
2185606227185606228CG18GENICpossibly homozygous59907878
2185607565185607566CG21GENIChomozygous59287404
2185608794185608795CT16GENIChomozygous59907879
2185610964185610965AG27GENICpossibly homozygous59287408
2185612679185612680TTGGTCTACTTAG1GENIChomozygous59287416
2185612810185612811GT9GENIChomozygous59287417
2185612811185612812GA9GENIChomozygous59907880
2185612950185612951GA22GENICpossibly homozygous59907881