chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41925830219258304CC17GENICpossibly homozygous128012149
41925835219258352T18GENIChomozygous128012150
41928672919286729A27GENIChomozygous128012169
41929036719290368AG28GENIChomozygous112535763
41929040319290404AG20GENIChomozygous112535769
41931457819314579T47GENICpossibly homozygous128012194
41932076419320764T10GENIChomozygous128012197
41932076719320767T8GENIChomozygous128012198
41932077219320772A11GENIChomozygous128012199
41932078519320786G13GENIChomozygous128012200
41932088619320887T4GENIChomozygous128012201
41932089619320951TCCTCCTCCTCCTCTCTCCTCTCCTCCTCCTTCCTCTCCCTCACTCTTCTCCTCA3GENICheterozygous132463411
41936789719367898TG39GENIChomozygous112998954
41936789819367899GT39GENIChomozygous119273992
41936800419368004TG28GENICpossibly homozygous128012219
41937565619375657A39GENIChomozygous128012228
41937568219375683G41GENIChomozygous128012229
41937959919379601TG9GENICheterozygous132395877
41941234819412349AC27GENICheterozygous128119925
41941235319412354AC28GENICheterozygous128119926
41941235819412359AC28GENICheterozygous131847930