chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37968627579686276CA17GENICpossibly homozygous112132908
37968851479688515C18GENIChomozygous127900051
37968853779688540GCA14GENIChomozygous127900052
37968854579688546G14GENIChomozygous127900053
37968854979688550G14GENIChomozygous127900054
37968856679688567GA8GENIChomozygous127984524
37968857879688578T7GENIChomozygous127900055
37968859179688592G6GENIChomozygous127900056
37968863479688636CA8GENIChomozygous127900057
37968865479688655C9GENIChomozygous127900058
37968865779688658C10GENIChomozygous127900059
37968868379688684AT14GENIChomozygous120017852
37968868779688688GA15GENIChomozygous120017853
37968870179688705CTAA20GENIChomozygous127900060
37968870779688707T20GENIChomozygous127900061
37968871279688714AG20GENIChomozygous127900062
37968874179688742CT24GENIChomozygous111634512
37968874479688746TG23GENIChomozygous127900063
37968878679688789GCA30GENIChomozygous127900064
37968879579688795AC31GENIChomozygous127900065
37968881579688815A35GENIChomozygous127900066
37968882179688822C38GENIChomozygous127900067
37968886779688868C32GENIChomozygous127900068
37968888479688885A31GENIChomozygous127900069
37968888779688887G32GENIChomozygous127900070
37968888879688889CT32GENIChomozygous119650290
37968892879688929TA40GENIChomozygous111634513
37968894679688947T43GENIChomozygous127900071
37968895979688960A43GENIChomozygous127900072
37968909479689094C35GENIChomozygous127900073
37968910179689101T35GENIChomozygous127900074
37968914079689140T36GENIChomozygous127900075
37968915379689153T38GENIChomozygous127900076
37968917179689171T44GENIChomozygous127900077
37968927779689278C60GENIChomozygous127900078
37968935779689359AC54GENIChomozygous127900079
37968936079689361GT55GENIChomozygous120045400