chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109106249991062500CG25GENIChomozygous529749858
109106390791063908GGGGTGGT14GENIChomozygous694426314
109106412191064122G-19GENICheterozygous694426315
109106417391064174TC17GENIChomozygous532402437
109106430591064306CA27GENIChomozygous532402438
109106473491064735AG28GENIChomozygous529749859
109106510391065104CT40GENIChomozygous532402439
109106592991065930C-22GENIChomozygous694426316
109106671791066718GA42GENIChomozygous529749860
109106689591066896CT30GENIChomozygous532402440
109106722191067223TG--15GENIChomozygous694426317
109106778791067788TC27GENIChomozygous532402441
109106818591068186AAT11GENICpossibly homozygous694426318
109106864791068648CT9GENIChomozygous532402442
109106890491068905CT17GENIChomozygous529749861
109106950991069510GA12GENIChomozygous529749862
109106955291069553TC12GENIChomozygous529749863
109106973291069733AG24GENICpossibly homozygous529749864
109106982491069825G-26GENIChomozygous694426319
109107004291070043GA17GENIChomozygous529749865
109107010691070107CCG12GENIChomozygous694426320
109107012991070131GA--8GENICpossibly homozygous694426321
109107033491070335CG26GENIChomozygous529749866
109107072991070731TG--32GENIChomozygous694426323
109107137491071375AG18GENIChomozygous529749867
109107167291071673TTA13GENIChomozygous694426324
109107222191072222AAT18GENICpossibly homozygous694426325
109107268491072685A-2GENIChomozygous694426328
109107286591072866CA18GENIChomozygous529749868