chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2039742723974273TC32GENIChomozygous971381362
2039744553974456CT32GENIChomozygous971381363
2039745843974585AG32GENIChomozygous971381364
2039745903974591TC31GENIChomozygous971381365
2039746533974654AG36GENIChomozygous971381366
2039747803974781TC37GENIChomozygous971381367
2039748953974896CG36GENIChomozygous971381368
2039756243975625GA41GENIChomozygous971381369
2039756873975688CG43GENIChomozygous971381370
2039758073975808GA21GENIChomozygous971381371
2039758403975841AG24GENIChomozygous971381372
2039760623976063GA35GENICpossibly homozygous971381373
2039761793976180AG29GENIChomozygous971381374
2039766203976621GT31GENIChomozygous971381375
2039766623976663CT37GENIChomozygous971381376
2039766903976691GA32GENIChomozygous971381377
2039767503976751TA30GENIChomozygous971381378
2039767513976752TC30GENIChomozygous971381379
2039767833976784AC30GENIChomozygous971381380
2039768843976885GA24GENIChomozygous971381381
2039769823976983CA41GENIChomozygous971381382
2039769983976999AG42GENIChomozygous971381383
2039770483977049GA44GENIChomozygous971381384
2039771633977164CT34GENIChomozygous971381385
2039779063977907CT37GENIChomozygous971381386
2039783653978366GA18GENIChomozygous971381387
2039784063978407GT24GENIChomozygous971381388
2039786093978610CT28GENIChomozygous971381389