chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142830430142830431G-16GENIChomozygous60876664
1142831432142831433GA12GENIChomozygous62162308
1142831560142831561TC9GENIChomozygous60876666
1142831748142831749AG31GENIChomozygous60876667
1142833294142833295AG13GENIChomozygous60876677
1142835950142835951CT14GENIChomozygous62021037
1142837169142837171AG--15GENIChomozygous62021038
1142837655142837656CT18GENICpossibly homozygous62021039
1142837929142837930AT17GENIChomozygous60876699
1142837997142837998AAG6GENIChomozygous60876701
1142838062142838063AAT6GENIChomozygous60876705
1142838076142838077TC11GENIChomozygous60876706
1142838128142838129CCT16GENICpossibly homozygous62021040
1142841122142841123TA22GENIChomozygous60876720
1142842423142842433TTTTCTTTTC----------8GENIChomozygous62312996
1142844793142844794AATCTC5GENIChomozygous62312997