chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X6537672765376728GA27GENICpossibly homozygous783298611
X6538633765386338GA77GENICheterozygous783298612
X6538634665386347CT70GENICheterozygous783298613
X6538635265386353GA78GENICheterozygous783298614
X6538641965386420TA82GENICheterozygous783298615
X6538648365386484AT36GENICheterozygous783298616
X6538799865387999TG19GENIChomozygous783298617
X6538800965388010TG18GENIChomozygous783298618
X6538803465388035CA10GENIChomozygous783298619
X6539077965390780GT132GENICheterozygous783298620
X6539081265390813AG171GENICheterozygous783298621
X6539083665390837AT234GENICheterozygous783298622
X6539395665393957GA47GENIChomozygous783298623
X6539426865394269TA44GENICpossibly homozygous783298624
X6539496265394963GA100GENICheterozygous783298625
X6539503865395039AG94GENICheterozygous783298626
X6539544665395447AG97GENICheterozygous783298627
X6539551265395513CG92GENICheterozygous783298628
X6539555965395560TA115GENICheterozygous783298629