chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186110885461108855TA22GENIChomozygous110370645
186110961461109615CT24GENIChomozygous110370647
186110984861109849AT15GENIChomozygous110370649
186111273361112734GA35GENIChomozygous110370651
186111480161114802GA26GENIChomozygous110370653
186111666061116661TC30GENIChomozygous110370655
186111797261117973GA24GENIChomozygous110370657
186111810861118109AC13GENIChomozygous110370659
186112013261120133AG26GENIChomozygous110370661
186112379261123793AG27GENIChomozygous110370663
186112427561124276CG23GENIChomozygous110370665
186112498561124986GA22GENIChomozygous110370667
186112519161125192GA28GENIChomozygous110370669
186112883761128838GA5GENIChomozygous110370671
186113080161130802TA19GENIChomozygous110370673
186113130961131310TG28GENIChomozygous110370675
186113225561132256CT38GENIChomozygous110370677
186113393761133938AG6GENIChomozygous110370679
186113396861133969AG10GENIChomozygous110370681
186113495961134960CG24GENIChomozygous110370683
186113714661137147TC39GENIChomozygous110370685
186113730361137304CT9GENIChomozygous110370687
186113787361137874AT37GENIChomozygous110370689
186113864061138641AG31GENIChomozygous110370691
186114163061141631TC19GENIChomozygous110370693
186114216461142165CT20GENIChomozygous110481051
186114916161149162CT11GENIChomozygous110370695
186114991461149915GC23GENIChomozygous110370697
186115274661152747GA11GENIChomozygous110370701
186115624461156245CT16GENIChomozygous110657289
186115650161156502CT32GENIChomozygous110370705
186115799461157995TC13GENIChomozygous110370707
186115938061159381AG9GENIChomozygous110370709
186115963761159638GA29GENIChomozygous110370711
186116223961162240GT11GENIChomozygous110370713