chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104793144447931445TG38GENIChomozygous116878977
104793178547931786GA39GENIChomozygous116878979
104793367347933674GA18GENICpossibly homozygous118083145
104793562447935625AG22GENICpossibly homozygous117344587
104793600047936001GT40GENIChomozygous116588121
104793738147937382TC39GENIChomozygous116588123
104793770347937704CT31GENIChomozygous117195100
104793858047938581AG39GENIChomozygous116588129
104793899947939000CT10GENICpossibly homozygous117993712
104793910347939104CG25GENIChomozygous116588131
104793935847939359GT31GENIChomozygous116588133
104794020647940207TC30GENIChomozygous116588135
104794150247941503GA20GENICpossibly homozygous117218353
104794205047942051GA41GENIChomozygous116588137
104794478547944786TG24GENIChomozygous116588143
104794566247945663CT27GENICpossibly homozygous116588145
104794576947945770TC24GENIChomozygous116588147
104794803947948040AC19GENIChomozygous116588153
104794804947948050TC21GENICpossibly homozygous116588155
104794840547948406CT22GENIChomozygous116588157
104794924947949250AG28GENICpossibly homozygous116588159