chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
114003091440030915T-7GENICheterozygous51201317
114003182140031822CT49GENIChomozygous50743737
114003208240032098TATGTATGTATGTATG----------------17GENIChomozygous50743738
114003260740032608GA47GENIChomozygous50743739
114003336140033362AG44GENIChomozygous50743740
114003349440033495TTC32GENICpossibly homozygous50743741
114003421540034216CA42GENIChomozygous50743743
114003488340034884G-20GENIChomozygous50743744
114003605940036060AG12GENIChomozygous50743745
114003743840037439CCT28GENICheterozygous50743747
114003743840037439CCTT28GENICheterozygous50743748
114003795240037953CT30GENIChomozygous50743750
114004061740040618CT38GENIChomozygous50743751
114004082440040825CT33GENIChomozygous50743752
114003350040033501TC36GENICpossibly homozygous51181132