chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99851529098515291TC35GENIChomozygous799577956
99851555498515555AG37GENIChomozygous799577957
99851563598515636TC30GENIChomozygous799577958
99851593698515937TC34GENIChomozygous799577959
99851596098515961TC35GENIChomozygous799577960
99851818998518190GA34GENIChomozygous799577961
99851854298518543AC34GENIChomozygous799577962
99851915298519153AG35GENIChomozygous799577963
99851974198519742CT32GENIChomozygous799577964
99851983498519835TC26GENIChomozygous799577965
99852311498523115AT20GENIChomozygous799577966
99852480998524810TC43GENIChomozygous799577967
99852518698525187GA32GENIChomozygous799577968
99852724198527242GC24GENIChomozygous799577969
99852731698527317AC24GENIChomozygous799577970
99852795598527956CT27GENIChomozygous799577971
99852795798527958CT26GENIChomozygous799577972
99852795898527959AG26GENIChomozygous799577973
99852900398529004GA30GENIChomozygous799577974
99852947898529479GA27GENIChomozygous799577975
99853040698530407GA21GENIChomozygous799577976
99853122498531225CA18GENIChomozygous799577977
99853145698531457AG35GENIChomozygous799577978
99853147998531480GA34GENIChomozygous799577979
99853210398532104CT25GENIChomozygous799577980
99853317598533176AG29GENICpossibly homozygous799577981
99853336598533366TA17GENIChomozygous799577982
99853439798534398GA27GENIChomozygous799577983
99853595998535960GA39GENIChomozygous799577984