chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13110007053110007054AG9GENIChomozygous114444234
13110009681110009682GA28GENIChomozygous114444242
13110015054110015055TC21GENIChomozygous114444244
13110015167110015168GA17GENIChomozygous114444246
13110015630110015631GA28GENIChomozygous114444248
13110015904110015905TC21GENIChomozygous114444250
13110017264110017265AG18GENIChomozygous114991564
13110017921110017922TC8GENIChomozygous114444254
13110018150110018151AG15GENIChomozygous114444256
13110019223110019224CT17GENIChomozygous114444258
13110019926110019927TA18GENIChomozygous114444260
13110020403110020404AG21GENIChomozygous114444262
13110023363110023364GA16GENIChomozygous114444266
13110023837110023838AG25GENIChomozygous114444268
13110024739110024740TC25GENIChomozygous114444270
13110024932110024933GA26GENIChomozygous114444272
13110025379110025380CA17GENIChomozygous114444276
13110026340110026341CT11GENIChomozygous114444278
13110026957110026958GA15GENIChomozygous114444280
13110027015110027016AG19GENIChomozygous114444282
13110028768110028769AG19GENIChomozygous114444286
13110028808110028809AG14GENIChomozygous114444288
13110029703110029704AT23GENIChomozygous114701794
13110030628110030629AG18GENIChomozygous114444298
13110030645110030646TC20GENIChomozygous114444300
13110030683110030684TC21GENIChomozygous114444302
13110030737110030738CT14GENIChomozygous114444304
13110031376110031377TC21GENIChomozygous114444308
13110032349110032350CT17GENIChomozygous114444310
13110032649110032650TC6GENIChomozygous126159654
13110017069110017070CA22GENICheterozygous126074745
13110018296110018297CT17GENIChomozygous126159650
13110022366110022367GA32GENIChomozygous126159651
13110028066110028067CT8GENIChomozygous126159652
13110028070110028071GA9GENIChomozygous126159653
13110032656110032657AG8GENIChomozygous114444312