chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2243710509243710510GT25GENIChomozygous110914171
2243710516243710517AG23GENIChomozygous110914172
2243710694243710695AG28GENIChomozygous110914173
2243710776243710777AG18GENIChomozygous110914174
2243710777243710778AT18GENICpossibly homozygous110914175
2243711341243711342CT25GENIChomozygous110845855
2243712030243712031AG26GENIChomozygous110914176
2243712317243712318TC19GENIChomozygous110914177
2243712368243712369CA30GENICheterozygous110914178
2243712426243712427GA49GENICheterozygous110914179
2243712605243712606CT44GENICheterozygous110914180
2243712735243712736CT39GENICheterozygous110914181
2243712107243712108AG19GENIChomozygous110349479
2243712122243712123TG16GENIChomozygous110349481
2243715698243715699TC13GENICheterozygous110914182
2243716072243716073CG20GENIChomozygous110349491
2243716515243716516TC19GENIChomozygous110349493
2243716717243716718AT25GENIChomozygous110914183
2243716843243716844GA19GENIChomozygous110914184
2243718293243718294GA18GENIChomozygous110845863
2243716855243716856GA17GENIChomozygous110914185
2243717347243717348AG25GENIChomozygous110845862
2243717885243717886TG18GENIChomozygous110349495
2243718338243718339CT17GENIChomozygous110845864
2243719576243719577GA25GENIChomozygous110914186