chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186061976660619767TG27GENIChomozygous995480896
186061977660619777TC20GENIChomozygous995480897
186061977860619779TC20GENIChomozygous995480898
186061978060619781TC18GENIChomozygous995480899
186061978260619783TC19GENIChomozygous995480900
186062046560620466TC38GENIChomozygous995480901
186062060360620604TC23GENICpossibly homozygous995480902
186062123660621237CT13GENICpossibly homozygous995480903
186062123860621239CT13GENICpossibly homozygous995480904
186062124060621241CT13GENICpossibly homozygous995480905
186062134660621347GA30GENIChomozygous995480906
186062424960624250GA49GENICpossibly homozygous995480907
186062429760624298TA47GENICpossibly homozygous995480908
186062429860624299AT48GENICpossibly homozygous995480909
186062580060625801TC11GENIChomozygous995480910
186062624260626243AT22GENICpossibly homozygous995480911
186062663260626633TC28GENIChomozygous995480912
186062687160626872CT25GENIChomozygous995480913
186062748460627485TC29GENIChomozygous995480914
186062880060628801AG19GENIChomozygous995480915
186063125160631252CT30GENICpossibly homozygous995480916
186063150960631510GA27GENIChomozygous995480917