chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
136883223368832234TA43GENIChomozygous936125894
136883299368832994GA31GENIChomozygous936125895
136883386368833864TA40GENIChomozygous936125896
136883451768834518GC19GENIChomozygous936125897
136883481168834812AG15GENIChomozygous936125898
136883486768834868AG15GENIChomozygous936125899
136883547868835479GC40GENIChomozygous936125900
136883564068835641GC32GENIChomozygous936125901
136883652168836522CG16GENIChomozygous936125902
136883722168837222TC31GENIChomozygous936125903
136883812668838127CA12GENIChomozygous936125904
136883813468838135GA13GENIChomozygous936125905
136883842068838421TC21GENIChomozygous936125906
136883875168838752GA18GENIChomozygous936125907
136883926968839270GC26GENIChomozygous936125908
136883949268839493CT33GENIChomozygous936125909
136884290968842910GA26GENIChomozygous936125910
136884345268843453CT12GENIChomozygous936125911
136884375168843752TA11GENIChomozygous936125912
136884425368844254GA28GENIChomozygous936125913
136884470368844704TC41GENIChomozygous936125914
136884527668845277AT27GENIChomozygous936125915
136884593368845934AG34GENIChomozygous936125916
136884654968846550GA32GENIChomozygous936125917
136884667168846672GA16GENIChomozygous936125918
136884683568846836CT25GENIChomozygous936125919
136884815168848152GA21GENIChomozygous936125920
136884916268849163AC26GENICpossibly homozygous936125921
136884936368849364CT30GENIChomozygous936125922
136884988168849882GA33GENIChomozygous936125923
136885083968850840TC23GENIChomozygous936125924
136885136768851368GT27GENIChomozygous936125925
136885154368851544GA44GENIChomozygous936125926
136885168968851690AG31GENIChomozygous936125927
136885266668852667TA19GENIChomozygous936125928
136885352068853521AG25GENIChomozygous936125929
136885644668856447GA20GENIChomozygous936125930
136885649468856495TC20GENIChomozygous936125931
136885681268856813AG20GENIChomozygous936125932
136885927868859279AG23GENIChomozygous936125933
136885941568859416AG15GENIChomozygous936125934