chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12925995929259960CA39GENICpossibly homozygous108066331
12928388329283884GA45GENIChomozygous108066332
12928388729283888GT45GENIChomozygous108066333
12928390629283906A44GENIChomozygous127368929
12935471829354720TA15GENIChomozygous127368933
12935475929354760G8GENIChomozygous127368934
12935480129354802T3GENIChomozygous127368935
12935482029354820T2GENIChomozygous127368936
12937378929373790C24GENIChomozygous127368937
12937379729373798A23GENIChomozygous127368938
12937380529373806C21GENIChomozygous127368939
12937381129373812C12GENIChomozygous127368940
12937381529373815T11GENIChomozygous127368941
12937381929373819G9GENIChomozygous127368942
12937383329373833C9GENIChomozygous127368943
12937384529373845G8GENIChomozygous130618481