chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186061976660619767TG21GENIChomozygous962598992
186061977660619777TC15GENIChomozygous962598993
186061977860619779TC14GENIChomozygous962598994
186061978060619781TC15GENIChomozygous962598995
186061978260619783TC18GENIChomozygous962598996
186062046560620466TC26GENIChomozygous962598997
186062060360620604TC22GENIChomozygous962598998
186062123660621237CT19GENICheterozygous962598999
186062123860621239CT19GENIChomozygous962599000
186062124060621241CT19GENIChomozygous962599001
186062134660621347GA27GENIChomozygous962599002
186062424960624250GA28GENICpossibly homozygous962599003
186062429760624298TA29GENIChomozygous962599004
186062429860624299AT29GENIChomozygous962599005
186062580060625801TC17GENIChomozygous962599006
186062624260626243AT26GENIChomozygous962599007
186062663260626633TC15GENIChomozygous962599008
186062687160626872CT20GENIChomozygous962599009
186062748460627485TC19GENIChomozygous962599010
186062880060628801AG18GENIChomozygous962599011
186063125160631252CT35GENIChomozygous962599012
186063150960631510GA34GENIChomozygous962599013