chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186110885461108855TA35GENIChomozygous110370645
186110961461109615CT26GENIChomozygous110370647
186111078461110785AT10GENIChomozygous110815337
186111085461110855AT10GENIChomozygous110815339
186111485261114853GA23GENIChomozygous110815341
186111666061116661TC38GENIChomozygous110370655
186111810861118109AC24GENIChomozygous110370659
186111825761118258CT26GENIChomozygous110815343
186112201561122016AG38GENIChomozygous110815345
186112213861122139TC42GENIChomozygous110815347
186112326361123264AG28GENIChomozygous110815349
186112379261123793AG29GENIChomozygous110370663
186112427561124276CG24GENIChomozygous110370665
186112519161125192GA20GENIChomozygous110370669
186112812961128130TA33GENIChomozygous110815351
186113130961131310TG40GENIChomozygous110370675
186113141561131416CT25GENIChomozygous110815353
186113225161132252CG26GENIChomozygous110815355
186113225561132256CT25GENIChomozygous110370677
186113375161133752CT18GENIChomozygous110815357
186113393761133938AG21GENIChomozygous110370679
186113714661137147TC36GENIChomozygous110370685
186113864061138641AG39GENIChomozygous110370691
186113980961139810CA21GENIChomozygous110815359
186114163061141631TC32GENIChomozygous110370693
186114319061143191CG25GENIChomozygous110815361
186114356361143564GA20GENIChomozygous110815363
186115318961153190AT17GENIChomozygous110815365
186115415361154154AG28GENIChomozygous110815367
186115426461154265GA33GENIChomozygous110815369
186115519861155199TC20GENIChomozygous110815371
186115704361157044AT31GENIChomozygous110815373
186115733561157336GA15GENIChomozygous110815375
186115799461157995TC27GENIChomozygous110370707
186115938061159381AG29GENIChomozygous110370709
186115963761159638GA38GENIChomozygous110370711
186114238261142383CA15GENIChomozygous110481053
186114216461142165CT33GENIChomozygous110481051