chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174345544143455442GA22GENIChomozygous111053098
174345634843456349AG18GENIChomozygous111053100
174345715543457156TC51GENIChomozygous111053102
174345950943459510GA34GENICpossibly homozygous111053104
174346148343461484AG27GENIChomozygous111053106
174346167643461677GA34GENIChomozygous111053108
174346298243462983CT31GENIChomozygous111053110
174346309643463097AT38GENIChomozygous111053112
174346331243463313AG32GENIChomozygous111053114
174346391043463911AG56GENIChomozygous111053116
174346422143464222CT59GENIChomozygous111053118
174346422943464230AG56GENIChomozygous111053120
174346483543464836CG26GENIChomozygous111053122
174346498543464986TA14GENIChomozygous111053124
174346536943465370CA26GENIChomozygous111053126
174346575643465757TC27GENIChomozygous111053128
174346734043467341GA21GENIChomozygous111053130
174346810343468104GA24GENIChomozygous111053132
174346845443468455AG31GENIChomozygous111053134
174346914343469144GA57GENIChomozygous111053136
174346980543469806CT37GENIChomozygous111053138
174347022243470223AT29GENIChomozygous111053140
174347025043470251AG28GENIChomozygous111053142
174347081843470819AG61GENIChomozygous111053144
174347111143471112GA34GENIChomozygous111053146
174347116143471162CT31GENIChomozygous111053148
174347210043472101TC29GENIChomozygous111053150