chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123898273238982733GC20GENIChomozygous115324530
123898396038983961TC22GENIChomozygous115324532
123898400438984005AG27GENIChomozygous115324534
123898453238984533GA34GENIChomozygous115324541
123898474338984744AG27GENIChomozygous115324543
123898488838984889CT23GENIChomozygous115324545
123898500738985008CA20GENIChomozygous115324547
123898502238985023CG20GENIChomozygous115324549
123898505238985053AG21GENIChomozygous115324551
123898512038985121AG27GENIChomozygous115324553
123898512438985125TC27GENIChomozygous115324555
123898566738985668TC17GENIChomozygous115324557
123898616538986166AG8GENIChomozygous115324559
123898645238986453AG32GENIChomozygous115324561
123898660238986603TG42GENIChomozygous115324563
123898799538987996AC31GENIChomozygous115324567
123898827938988280TA27GENIChomozygous115324569
123898836838988369AT32GENIChomozygous115324571
123898870438988705GA35GENIChomozygous115324573
123898884538988846TC28GENIChomozygous115324575
123898896538988966AG22GENIChomozygous115324577
123898898938988990AG24GENICpossibly homozygous115324579
123898923938989240TG20GENIChomozygous115324581
123898929138989292GA11GENIChomozygous115324583
123898930938989310CT14GENIChomozygous115324585
123898931138989312CT13GENIChomozygous115324587
123899062738990628CT23GENIChomozygous115383133
123899080538990806GT30GENIChomozygous115324589
123899118638991187TC31GENIChomozygous115324591
123899119238991193CT27GENIChomozygous115324593
123899137538991376AG30GENIChomozygous115324595
123899156138991562TG24GENIChomozygous115324597
123899174438991745AG29GENIChomozygous115324599
123899179038991791CA27GENIChomozygous115324601
123899187638991877CT29GENIChomozygous115324603
123899189038991891GA29GENIChomozygous115324605
123899263038992631GA30GENIChomozygous115324609
123899266938992670GT32GENIChomozygous115324611
123899350138993502TC30GENIChomozygous115324613
123899435538994356AG25GENIChomozygous115324615
123899515738995158GA10GENIChomozygous115324617