chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5154781114154781115CG44GENIChomozygous114062619
5154781501154781502CT40GENIChomozygous114062621
5154781784154781785TA35GENIChomozygous114062623
5154782235154782236CT47GENIChomozygous114062625
5154782437154782438GA29GENIChomozygous114062627
5154782441154782442AC32GENIChomozygous114062629
5154782501154782502AG33GENIChomozygous114062631
5154782502154782503AC33GENIChomozygous114062633
5154783139154783140GC52GENIChomozygous114062635
5154783365154783366AC52GENIChomozygous114062637
5154783602154783603TC50GENIChomozygous114062639
5154783879154783959TCCACAGAGACCAAAGGTCAACTGCAGCAGCACACAGGAAGCCATATCCGATTTAAGGTGCCCCACCCCCCAAAGCTCCC47GENIChomozygous128260884
5154784154154784155GA48GENIChomozygous114062641
5154784267154784268TG57GENIChomozygous114062643
5154784480154784481GA36GENIChomozygous114062645
5154784899154784900GA39GENIChomozygous114062647
5154785028154785029GT39GENIChomozygous114062649
5154785091154785092CT48GENIChomozygous114062651
5154786273154786273TGGT34GENIChomozygous128260885
5154787043154787044CT49GENIChomozygous114062653
5154787174154787174TGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGCAAGCA19GENIChomozygous128260886
5154787188154787189TC23GENIChomozygous114062655
5154787224154787224AA25GENIChomozygous128260887
5154789553154789554CT33GENIChomozygous114062657
5154789557154789558TC33GENIChomozygous114062659
5154792850154792850AACC55GENIChomozygous128260888
5154795006154795007AG29GENIChomozygous114062669
5154796471154796472CT35GENIChomozygous114062671
5154797275154797276GT51GENIChomozygous114062673
5154797804154797805GA41GENIChomozygous114062675
5154799267154799268GA43GENIChomozygous114062677
5154799292154799293GA48GENIChomozygous114062679
5154799346154799348CT52GENIChomozygous128260889
5154799962154799963TA47GENIChomozygous114062681
5154799965154799972TGCGTCC47GENIChomozygous128260890
5154800016154800017TG36GENIChomozygous114062683