chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91017318710173188CT28GENIChomozygous117244150
91017481010174811TC23GENIChomozygous117244151
91017591710175918AG17GENIChomozygous117244155
91017692610176927TC17GENIChomozygous117244156
91018113110181132GA35GENIChomozygous117244157
91018178110181782TC28GENIChomozygous117244158
91018412610184127TC14GENIChomozygous117244160
91018544610185447CT30GENIChomozygous117244161
91018627710186278GA5GENIChomozygous117244162
91018811710188118AT29GENIChomozygous117244163
91018935010189351AG31GENICpossibly homozygous117244164
91019278710192788GA14GENIChomozygous117244166
91019368010193681CA27GENIChomozygous117244168
91019509210195093GT19GENIChomozygous117244169
91019534610195347AG15GENIChomozygous117244171
91019596810195969AT30GENIChomozygous117244172
91019603510196036CT31GENIChomozygous117244173
91019877710198778AT20GENIChomozygous117244177
91020083410200835AG13GENIChomozygous117244178
91020215110202152TA18GENIChomozygous117244179
91020302810203029TC34GENIChomozygous117244180