chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162486311324863114CCGT19GENIChomozygous734495727
162486313224863133TA19GENIChomozygous611344112
162486320324863204TA14GENIChomozygous610413988
162486376124863762GA12GENIChomozygous611344113
162486389124863892GC15GENIChomozygous610413989
162486399024863991GGT11GENIChomozygous734495728
162486527524865276A-12GENIChomozygous734495729
162486561624865617CT17GENIChomozygous610413990
162486564424865664TCTTTCTTTCTTTCTTTCTT--------------------6GENIChomozygous734495731
162486670024866701TC41GENIChomozygous611344114
162486680224866803CT35GENIChomozygous611344115
162486702724867028CCT13GENIChomozygous734495733
162486775724867758AG32GENIChomozygous611344116
162486855024868551CT17GENIChomozygous610413991
162486918724869188CT28GENIChomozygous611344117
162486920124869202GA29GENIChomozygous611344118
162486940724869408TA20GENIChomozygous610413992
162486964924869653TAAG----22GENIChomozygous734495734
162486971724869718GC22GENIChomozygous611344119
162486974824869749A-20GENIChomozygous734495735
162487027424870275CG17GENIChomozygous611344120
162487135524871356CG7GENIChomozygous610413993
162487138124871382GGT2GENICheterozygous734495736
162487154224871543TC1GENIChomozygous611344121
162487154424871545CG1GENIChomozygous611344122
162487156524871566TA4GENIChomozygous611344123
162487169924871700CT7GENIChomozygous611344124
162487173724871738CA11GENIChomozygous611344125