chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75904731859047319AT11GENIChomozygous674888033
75905214059052142AC--2GENIChomozygous771045626
75905647159056472CCTTTTT9GENICheterozygous771045627
75906325159063252AG11GENIChomozygous674888034
75906325359063254AC11GENIChomozygous674888035
75906325759063258TA11GENIChomozygous674888036
75906325859063259GA11GENIChomozygous674888037
75906326859063269GT11GENIChomozygous674888038
75906327459063275GT10GENIChomozygous674888039
75906328159063282AT9GENIChomozygous674888040
75906329359063294G-8GENIChomozygous771045629
75906331059063311AT4GENIChomozygous674888041
75906331359063314A-4GENIChomozygous771045630
75906331659063317AT4GENIChomozygous674888042
75906331759063318AT4GENIChomozygous674888043
75906332059063321CT4GENIChomozygous674888044
75906332459063325G-4GENIChomozygous771045631
75906332659063327G-3GENIChomozygous771045632
75906333659063337A-3GENIChomozygous771045633
75906333859063339GT3GENIChomozygous674888045
75906334659063347GT1GENIChomozygous674888046
75906334959063350CCTTTTCACTT1GENIChomozygous771045634
75906335459063355GT1GENIChomozygous674888047
75906335859063362GGAA----1GENIChomozygous771045635
75906338159063382GT1GENIChomozygous674888048
75906338259063383AT1GENIChomozygous674888049
75906338359063384AT1GENIChomozygous674888050
75906338559063386GT1GENIChomozygous674888051
75906338759063388GT1GENIChomozygous674888052
75906339159063392GT3GENIChomozygous674888053
75906368559063686TTAC2GENICheterozygous771045636
75906368559063686TTACAC2GENICheterozygous771045637
75906998459069985AATATC23GENIChomozygous771045639