chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2243578116243578117CT15GENICpossibly homozygous110348082
2243578117243578118AG15GENIChomozygous110348084
2243578241243578242AG16GENIChomozygous110348086
2243578365243578366AG14GENIChomozygous110348088
2243578698243578699TC13GENIChomozygous110348090
2243581211243581212TC6GENICheterozygous110348092
2243586314243586315GA34GENICheterozygous111187770
2243587068243587069AT65GENICheterozygous111291234
2243587206243587207TA40GENICheterozygous110633283
2243587209243587210AC39GENICheterozygous110348096
2243587371243587372CA37GENICheterozygous110348098
2243587451243587452CA47GENICheterozygous110348100
2243587733243587734AG26GENIChomozygous110348102
2243588896243588897AG33GENICheterozygous110348103
2243588904243588905GA31GENICheterozygous110348105
2243589148243589149GA16GENIChomozygous110348107
2243589273243589274AC16GENIChomozygous110348109
2243591982243591983CT20GENIChomozygous110348111
2243592629243592630CG24GENIChomozygous110348113
2243593340243593341GA22GENIChomozygous110348115
2243593358243593359TG26GENIChomozygous110348117
2243594317243594318TC33GENIChomozygous110348119
2243595511243595512GA23GENIChomozygous110348121
2243598435243598436CT17GENIChomozygous110348123
2243599330243599331GA23GENIChomozygous110348125