chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15749228857492289TC38GENICpossibly homozygous108111642
15749277957492780TG30GENIChomozygous108111643
15749562957495630AG30GENIChomozygous108111644
15749694657496947CT9GENIChomozygous108723952
15749840657498407TG21GENIChomozygous108111646
15749919157499192AG19GENIChomozygous108111647
15749931857499319AG26GENIChomozygous108111648
15749974357499744GA21GENIChomozygous108111649
15750027357500274CT20GENIChomozygous108111650
15750028157500282GA20GENICpossibly homozygous108111651
15750036857500369AG27GENIChomozygous108111652
15750046857500469AG25GENIChomozygous108111653
15750094257500943TC21GENIChomozygous108111654
15750106157501062CT23GENIChomozygous108111655
15750182957501830TC26GENIChomozygous108111656
15750229657502297AG29GENIChomozygous108111657
15750325057503251GA26GENIChomozygous108111658
15750584457505845CT41GENIChomozygous108111659
15750690057506901GA31GENIChomozygous108111660
15750693457506935GA29GENIChomozygous108111661
15750719857507199GA31GENIChomozygous108111662
15750729257507293AC28GENIChomozygous108857455
15750795357507954AG24GENIChomozygous108111663
15750855757508558CT32GENIChomozygous108111664
15750890457508905GA26GENIChomozygous108111665
15750929157509292GA41GENIChomozygous108111666