chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117562873175628732CT13GENIChomozygous118164571
117562888575628886TC24GENIChomozygous115904383
117564857075648571GC13GENIChomozygous115993665
117567499975675000CA14GENIChomozygous115993667
117571119875711199AC26GENIChomozygous116106130
117571121675711217TC23GENIChomozygous116106131
117590370175903702TG26GENIChomozygous115905570
117591160775911608TA11GENICpossibly homozygous116161805
117587266375872664GT25GENICheterozygous118199889
117597225675972257GT8GENIChomozygous116110653
117599496775994968AC6GENIChomozygous118195879
117602443276024433AG12GENIChomozygous115906016
117602460376024604CT22GENIChomozygous116110654
117602479076024791TG22GENIChomozygous115906022
117602479676024797TA22GENIChomozygous115906024
117602483276024833TG23GENIChomozygous115993671
117602486176024862GA12GENIChomozygous115906026
117603820076038201GA23GENIChomozygous118186826
117607191076071911CA15GENICpossibly homozygous115906375
117608347676083477AC23GENIChomozygous115906431
117613237676132377CG12GENIChomozygous116308718
117613245776132458TC3GENIChomozygous118164672
117615576476155765TC39GENICheterozygous115906663
117615578476155785TG36GENICheterozygous115906665
117615579376155794TC35GENICheterozygous115906667
117615589076155891TC43GENICheterozygous116323017
117615589376155894CT42GENICheterozygous116323019
117615594276155943GC29GENICheterozygous118164676