chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5147852838147852839TC55GENIChomozygous114047564
5147853059147853060TC40GENIChomozygous114153179
5147853618147853619GT51GENIChomozygous114153180
5147854300147854301TA26GENIChomozygous114153181
5147857362147857363AG46GENIChomozygous114047568
5147857469147857470GA62GENICpossibly homozygous114153185
5147857821147857822TC52GENIChomozygous114047572
5147857840147857841TC57GENIChomozygous114047574
5147859177147859178TC57GENIChomozygous114047576
5147861018147861019TA99GENICheterozygous114153186
5147861053147861054AC112GENICheterozygous114153187
5147861056147861057GT111GENICheterozygous114153188
5147861076147861077TC98GENICheterozygous114153189
5147861077147861078TC100GENICheterozygous114153190
5147863981147863982GT28GENICpossibly homozygous114047578
5147863989147863990CT26GENICpossibly homozygous114153191
5147864032147864033TA30GENICpossibly homozygous114153192
5147864672147864673AG29GENICheterozygous114153193
5147864782147864783TC46GENIChomozygous114047586
5147864786147864787TC49GENIChomozygous114047588
5147864961147864962TC67GENIChomozygous114047590
5147865366147865367AG58GENIChomozygous114047594
5147866293147866294AG35GENIChomozygous114047598
5147866724147866725AC55GENICpossibly homozygous114047600
5147867335147867336AC6GENIChomozygous114047602