chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176894297176894298TC20GENIChomozygous111842798
3176894767176894768GA15GENIChomozygous112219191
3176895749176895750TC20GENIChomozygous111842800
3176899012176899013AT18GENIChomozygous111842802
3176899261176899262A15GENIChomozygous127965493
3176899279176899280TC11GENIChomozygous111842804
3176900565176900566TC18GENIChomozygous111842808
3176900747176900748TA15GENIChomozygous111842810
3176901898176901899GT24GENIChomozygous111842812
3176903375176903376TC12GENIChomozygous112219192
3176906550176906551TC12GENIChomozygous111842818
3176907528176907529GA12GENIChomozygous112219193
3176908164176908165CT19GENIChomozygous112219194
3176910351176910352AC17GENIChomozygous112219195
3176915321176915322TA11GENIChomozygous111842826
3176915337176915338TA12GENIChomozygous111842828
3176919094176919095TC16GENIChomozygous111842836
3176919446176919447AG11GENIChomozygous111842838
3176929689176929690TG16GENIChomozygous112219196
3176935980176935981CG16GENIChomozygous111842850
3176938370176938370ATAT10GENIChomozygous127965498
3176904375176904375G11GENIChomozygous130916984
3176911242176911243G18GENIChomozygous130916985
3176932709176932709TT20GENIChomozygous130916988
3176938398176938398ATAC10GENIChomozygous130916989
3176925576176925584CAGGCAGG16GENIChomozygous131630244
3176938448176938452ACAT8GENIChomozygous130916990
3176938519176938520CT8GENIChomozygous111842856
3176938529176938530CT7GENIChomozygous111842859
3176938700176938702AC16GENIChomozygous130916991
3176938763176938764CT15GENIChomozygous111842863
3176939772176939772T19GENICpossibly homozygous127965501
3176942048176942049CT14GENIChomozygous111842865
3176946860176946861TC13GENIChomozygous111842873
3176947686176947687AG26GENIChomozygous111842875
3176948510176948514CAGA12GENIChomozygous130916992
3176951651176951652AG16GENIChomozygous111842883
3176952287176952288TC13GENIChomozygous111842887
3176957763176957764AT14GENIChomozygous111842920
3176938497176938498TC8GENIChomozygous112373542