chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212232148212232149CA18GENIChomozygous937132768
1212232401212232402GT23GENIChomozygous937132769
1212234575212234576CT29GENIChomozygous937132770
1212234680212234681CT19GENIChomozygous937132771
1212234842212234843GA20GENIChomozygous937132772
1212235696212235697TC29GENIChomozygous937132773
1212235726212235727GA30GENIChomozygous937132774
1212236314212236315AG26GENIChomozygous937132775
1212237796212237797TA26GENIChomozygous937132776
1212238003212238004CT19GENIChomozygous937132777
1212238216212238217GA24GENIChomozygous937132778
1212240228212240229CT18GENIChomozygous937132779
1212240599212240600CT18GENIChomozygous937132780
1212245421212245422GC12GENIChomozygous937132781
1212246250212246251GA31GENIChomozygous937132782
1212246483212246484GA23GENIChomozygous937132783
1212246839212246840TC23GENIChomozygous937132784
1212246883212246884GT21GENIChomozygous937132785
1212246890212246891CT19GENIChomozygous937132786
1212246939212246940CG13GENIChomozygous937132787
1212247414212247415CT22GENIChomozygous937132788
1212248070212248071TC17GENIChomozygous937132789
1212248719212248720TC10GENIChomozygous937132790
1212249516212249517GA10GENIChomozygous937132791
1212249751212249752CT18GENIChomozygous937132792
1212254921212254922GC13GENIChomozygous937132793
1212255735212255736CA24GENIChomozygous937132794
1212256305212256306AG20GENIChomozygous937132795
1212259075212259076GA15GENIChomozygous937132796
1212260007212260008TC20GENIChomozygous937132797
1212265540212265541CA1GENIChomozygous937132798
1212265544212265545CA2GENIChomozygous937132799
1212267724212267725AG20GENIChomozygous937132800
1212268387212268388AG12GENIChomozygous937132801
1212269320212269321GA15GENIChomozygous937132802
1212272665212272666GT23GENIChomozygous937132803
1212274307212274308GT28GENIChomozygous937132804
1212276381212276382CT16GENIChomozygous937132805
1212278108212278109GA18GENIChomozygous937132806
1212278160212278161GA23GENIChomozygous937132807