chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108148924281489243TC26GENIChomozygous614041778
108148927381489274CA38GENIChomozygous614041779
108148994081489942AA--18GENIChomozygous736175126
108149263681492637CT23GENIChomozygous614041780
108149286481492865GA35GENIChomozygous614041781
108149407581494076TC34GENIChomozygous614041782
108149566181495662AG26GENIChomozygous614041783
108149598281495983TTGATC27GENICpossibly homozygous736175127
108149604181496055CACACACACACACA--------------16GENIChomozygous736175128
108149643181496432TC24GENIChomozygous614041784
108149643381496434CT25GENIChomozygous614041785