chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113171991631719917CT25GENIChomozygous786441189
113172086931720870AG31GENIChomozygous786441190
113172127731721278GA19GENICpossibly homozygous786441191
113172270531722706TA21GENIChomozygous786441192
113172301131723012CT21GENIChomozygous786441193
113172385431723855GA18GENIChomozygous786441194
113172416031724161CG20GENIChomozygous786441195
113172470331724704AC28GENIChomozygous786441196
113172824931728250CA21GENIChomozygous786441197
113173103631731037CT11GENIChomozygous786441198
113173257431732575CT21GENIChomozygous786441199
113173276931732770TC19GENIChomozygous786441200
113173279931732800AG25GENIChomozygous786441201
113173446031734461AG18GENIChomozygous786441202
113173630931736310GA23GENIChomozygous786441203
113173680031736801TC17GENIChomozygous786441204
113173794831737949AG18GENIChomozygous786441205
113173857731738578CT25GENIChomozygous786441206
113174003131740032TC20GENICpossibly homozygous786441207
113174057731740578GA25GENIChomozygous786441208
113174185231741853GA22GENIChomozygous786441209
113174263831742639TG32GENICheterozygous786441210
113174362231743623AT23GENIChomozygous786441211
113174391731743918GA24GENIChomozygous786441212
113174552431745525CT28GENIChomozygous786441213
113174664231746643CG15GENIChomozygous786441214
113174740931747410AT14GENIChomozygous786441215
113174928231749283AT12GENICpossibly homozygous786441216
113174963131749632GA29GENIChomozygous786441217
113174984131749842TC22GENIChomozygous786441218
113175017931750180GA20GENIChomozygous786441219
113175072231750723AG12GENIChomozygous786441220