chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41923347319233475GA35GENICheterozygous130648059
41925830219258304CC12GENICpossibly homozygous128012149
41925835219258352T12GENIChomozygous128012150
41928672919286729A32GENIChomozygous128012169
41929036719290368AG28GENIChomozygous112535763
41929040319290404AG21GENIChomozygous112535769
41932076419320764T20GENIChomozygous128012197
41932076719320767T20GENIChomozygous128012198
41932077219320772A19GENIChomozygous128012199
41932078519320786G18GENIChomozygous128012200
41932088619320887T8GENIChomozygous128012201
41934189519341897AC34GENICheterozygous128012202
41935309319353095TG20GENICheterozygous130648060
41936789719367898TG51GENIChomozygous112998954
41936789819367899GT51GENIChomozygous119273992
41936800419368004TG30GENICpossibly homozygous128012219
41937565619375657A28GENIChomozygous128012228
41937568219375683G39GENIChomozygous128012229