chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1197988535197988536GA27GENIChomozygous108496608
1197988854197988855CT22GENIChomozygous109532337
1197988986197988987GA15GENIChomozygous108981870
1197989250197989251CT19GENICpossibly homozygous108981871
1197989512197989513AG18GENIChomozygous108496612
1197990710197990711GA26GENIChomozygous108981873
1197990829197990830TC18GENIChomozygous108496622
1197993461197993462CT6GENIChomozygous108981877
1197993994197993995GA19GENIChomozygous109532339
1197994408197994409GA28GENIChomozygous108981878
1197994496197994497CA19GENIChomozygous108981879
1197995048197995049AG23GENIChomozygous108496657
1197995744197995745GA13GENIChomozygous108981881
1197996925197996926CA26GENIChomozygous108496683
1197998769197998770AG23GENIChomozygous108981882
1197999056197999057CT13GENIChomozygous108981883
1197999689197999690GA15GENIChomozygous108496709