chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38824071488240715AG31GENIChomozygous72688223
38824085888240859AT24GENIChomozygous72688227
38824102588241026GA31GENIChomozygous72688231
38824119988241200CT25GENIChomozygous72688234
38824458188244582CA21GENIChomozygous72688238
38824482488244825AG11GENIChomozygous72688241
38824496888244969CT19GENIChomozygous72688245
38824606088246061TC23GENIChomozygous72688247
38824647888246479TC15GENIChomozygous72688251
38824753988247540TC15GENIChomozygous72688255
38824973488249735TG15GENIChomozygous72688262
38825217888252179CA21GENIChomozygous72688266
38825244788252448AG15GENIChomozygous72688270
38825300388253004GA18GENIChomozygous72688274
38825882088258821GA24GENIChomozygous72688278
38825886188258862GA29GENICpossibly homozygous72688281
38825941788259418GA22GENIChomozygous72688285
38826038588260386AC9GENIChomozygous73048386
38826067888260679CT22GENIChomozygous73048387
38826119088261191CT23GENIChomozygous79684324
38826120088261201GC24GENIChomozygous72688289
38826158088261581TC11GENIChomozygous72688293
38826175288261753AT20GENIChomozygous72688296
38826223988262240CT18GENIChomozygous72688300
38826236488262365CT28GENIChomozygous72688304
38826253788262538TC26GENIChomozygous72688308
38826349088263491TG22GENIChomozygous72688310
38826416988264170AG36GENIChomozygous72688314
38826455688264557TG13GENICpossibly homozygous72688318
38826462088264621TC16GENIChomozygous72688323
38826481088264811CG42GENICheterozygous79723029
38826484988264850TC36GENICheterozygous72688338
38826613588266136GA32GENIChomozygous74039628
38826632488266325AC32GENIChomozygous72688342
38826658888266589GA27GENIChomozygous72688346
38826717988267180AG17GENIChomozygous72688350
38826847288268473CT29GENIChomozygous72688353
38826892288268923TG19GENIChomozygous72688357
38826939788269398CT12GENIChomozygous72688361
38826977788269778AT20GENIChomozygous72688365
38827018488270185TC25GENIChomozygous72688369
38827044188270442AG29GENIChomozygous72688372