chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1197987317197987318CT8GENICheterozygous108981868
1197988535197988536GA15GENIChomozygous108496608
1197988986197988987GA29GENIChomozygous108981870
1197989250197989251CT18GENIChomozygous108981871
1197989512197989513AG29GENIChomozygous108496612
1197989719197989720CA18GENIChomozygous108981872
1197990710197990711GA18GENIChomozygous108981873
1197990829197990830TC22GENIChomozygous108496622
1197991028197991029AG15GENIChomozygous108981874
1197991835197991836GA20GENIChomozygous108981875
1197993146197993147TC4GENIChomozygous108496645
1197993461197993462CT17GENIChomozygous108981877
1197994408197994409GA25GENIChomozygous108981878
1197994496197994497CA8GENIChomozygous108981879
1197995048197995049AG19GENIChomozygous108496657
1197995308197995309GA16GENIChomozygous108981880
1197995744197995745GA16GENIChomozygous108981881
1197996925197996926CA9GENIChomozygous108496683
1197998769197998770AG23GENIChomozygous108981882
1197999056197999057CT18GENIChomozygous108981883
1197999689197999690GA14GENIChomozygous108496709
1197998791197998792CG6GENIChomozygous125468133
1197998790197998791GT6GENIChomozygous125468132