chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
179027010390270104AT35GENIChomozygous809849578
179027124690271247CT46GENIChomozygous809849579
179027801790278018TG51GENIChomozygous809849580
179027943890279439GA44GENIChomozygous809849581
179027996690279967AT34GENIChomozygous809849582
179028073890280739AC4GENIChomozygous809849583
179028079890280799CT7GENIChomozygous809849584
179028080290280803CA8GENIChomozygous809849585
179028103790281038AG34GENIChomozygous809849586
179028104590281046TA29GENIChomozygous809849587
179028157290281573TC27GENIChomozygous809849588
179028874690288747CA43GENIChomozygous809849589
179028895690288957CA25GENIChomozygous809849590
179029652390296524GA55GENIChomozygous809849591
179030007390300074CT31GENIChomozygous809849592
179030019490300195AG31GENIChomozygous809849593
179030019590300196AG32GENIChomozygous809849594
179030107490301075AG71GENICheterozygous809849595
179030200390302004GA71GENICheterozygous809849596
179030211190302112AT238GENICheterozygous809849597
179030212090302121AT248GENICheterozygous809849598
179030212390302124TA249GENICheterozygous809849599
179030216790302168AT233GENICheterozygous809849600
179030221090302211CT190GENICheterozygous809849601
179030371590303716CT64GENICheterozygous809849602
179030373490303735TC72GENICheterozygous809849603
179030377290303773CT73GENICheterozygous809849604
179030547990305480TC45GENIChomozygous809849605
179030613790306138GA54GENIChomozygous809849606
179030711990307120CT51GENIChomozygous809849607
179030767790307678AT30GENIChomozygous809849608
179030978890309789TC58GENIChomozygous809849609
179031080990310810CT57GENIChomozygous809849610
179031367590313676AG37GENIChomozygous809849611