chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41925830219258304CC19GENIChomozygous128012149
41925835219258352T18GENIChomozygous128012150
41928672919286729A39GENIChomozygous128012169
41929036719290368AG26GENIChomozygous112535763
41929040319290404AG22GENIChomozygous112535769
41929281419292816AG2GENIChomozygous134126794
41929942319299424GA47GENIChomozygous119422463
41930228919302290CT54GENICpossibly homozygous119422465
41931457819314579T45GENIChomozygous128012194
41932076419320764T20GENIChomozygous128012197
41932076719320767T20GENIChomozygous128012198
41932077219320772A19GENIChomozygous128012199
41932078519320786G18GENIChomozygous128012200
41932088619320887T9GENIChomozygous128012201
41934189519341897AC43GENICheterozygous128012202
41932089619320951TCCTCCTCCTCCTCTCTCCTCTCCTCCTCCTTCCTCTCCCTCACTCTTCTCCTCA3GENICheterozygous132463411
41935816819358170CA14GENICheterozygous132294904
41936789719367898TG63GENIChomozygous112998954
41936800419368004TG32GENICpossibly homozygous128012219
41937565619375657A42GENIChomozygous128012228
41937568219375683G43GENIChomozygous128012229
41936789819367899GT61GENIChomozygous119273992