chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186110885461108855TA4GENIChomozygous110370645
186110961461109615CT7GENIChomozygous110370647
186110984861109849AT11GENIChomozygous110370649
186111273361112734GA15GENICpossibly homozygous110370651
186111480161114802GA11GENIChomozygous110370653
186111666061116661TC7GENIChomozygous110370655
186111797261117973GA10GENIChomozygous110370657
186111810861118109AC7GENIChomozygous110370659
186112013261120133AG12GENIChomozygous110370661
186112379261123793AG8GENIChomozygous110370663
186112498561124986GA12GENIChomozygous110370667
186112519161125192GA9GENIChomozygous110370669
186112883761128838GA7GENIChomozygous110370671
186113080161130802TA10GENIChomozygous110370673
186113130961131310TG10GENIChomozygous110370675
186113225561132256CT8GENIChomozygous110370677
186113393761133938AG14GENIChomozygous110370679
186113396861133969AG11GENIChomozygous110370681
186113495961134960CG3GENIChomozygous110370683
186113714661137147TC9GENIChomozygous110370685
186113730361137304CT6GENIChomozygous110370687
186113787361137874AT11GENIChomozygous110370689
186113864061138641AG12GENIChomozygous110370691
186114163061141631TC16GENIChomozygous110370693
186114216461142165CT10GENIChomozygous110481051
186114238261142383CA6GENIChomozygous110481053
186114916161149162CT5GENIChomozygous110370695
186114991461149915GC11GENIChomozygous110370697
186115042761150428GT3GENIChomozygous110370699
186115274661152747GA8GENIChomozygous110370701
186115650161156502CT3GENIChomozygous110370705
186115799461157995TC10GENIChomozygous110370707
186115938061159381AG6GENIChomozygous110370709
186115963761159638GA6GENIChomozygous110370711
186116223961162240GT12GENIChomozygous110370713