chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10107039855107039856GT23GENICpossibly homozygous116714131
10107053293107053294GC25GENIChomozygous116714133
10107053457107053458CT5GENIChomozygous116714135
10107053458107053459TC5GENIChomozygous116714137
10107099373107099374AC2GENIChomozygous117232492
10107112225107112226CT31GENICheterozygous116714143
10107116001107116002TA11GENIChomozygous116714145