chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71238275012382751GT29GENIChomozygous53790805
71238302412383025CT31GENIChomozygous53790806
71238318512383186A-25GENIChomozygous53790807
71238328312383285CT--29GENIChomozygous53790808
71238339412383395TTTC14GENIChomozygous53790809
71238392212383923GT39GENIChomozygous53790810
71238484612384858GAGAGAGAGAGG------------2GENICheterozygous53790811
71238545612385457AG6GENIChomozygous53790813
71238548012385481A-4GENIChomozygous54954890
71238548212385493GGTCGGGATCT-----------4GENIChomozygous54954892
71238561912385620AAGGGTCTGGGTCTGGGTCT10GENICheterozygous55057496
71238568712385688AG17GENIChomozygous53790824
71238594912385950CA32GENIChomozygous53790825
71238614612386147GA34GENIChomozygous53790826
71238663012386633GGG---33GENIChomozygous53790827
71238663412386635AAT31GENIChomozygous53790828
71238688012386881TC26GENIChomozygous53790829
71238726712387268TC24GENIChomozygous53790830
71238733212387333AG21GENIChomozygous53790831
71238742212387423GA26GENIChomozygous53790832
71238811512388116CT3GENIChomozygous53790833
71238811612388117TC3GENIChomozygous53790834
71238815512388156CT7GENIChomozygous54884981
71238561812385619CCGGGGTCGGGGTCTGGGTCGGG10GENICpossibly homozygous54884975
71238561912385620AATCAGGGTCTGGGTCTGGGTCT10GENICpossibly homozygous54884977
71238663512386636CG31GENIChomozygous54884979
71238815612388157TC8GENIChomozygous53790835
71238854912388550T-2GENIChomozygous54954894
71238855312388570CACCATCCTCCCATCTC-----------------5GENIChomozygous54954896
71238863112388632CT25GENIChomozygous53790839
71238897012388971GA22GENIChomozygous53790841
71239014812390156CACACACA--------8GENICheterozygous53790842
71239015012390156CACACA------8GENICpossibly homozygous54954898
71239079412390795CT27GENIChomozygous53790844