chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1461751986175199TG14GENIChomozygous959094994
1461753876175388AG13GENIChomozygous959094995
1461753886175389GA14GENIChomozygous959094996
1461767686176769AT15GENIChomozygous959094997
1461771496177150TC21GENIChomozygous959094998
1461774006177401GC33GENIChomozygous959094999
1461774566177457TC33GENIChomozygous959095000
1461776266177627AG28GENIChomozygous959095001
1461778266177827AG27GENIChomozygous959095002
1461811396181140GA13GENIChomozygous959095003
1462166006216601CT16GENIChomozygous959095004
1462189296218930CT28GENIChomozygous959095005
1462189636218964CG35GENIChomozygous959095006
1462193116219312CT16GENIChomozygous959095007
1462194456219446GA27GENICpossibly homozygous959095008
1462196006219601GA38GENIChomozygous959095009
1462202146220215CG16GENIChomozygous959095010
1462202236220224CT15GENIChomozygous959095011
1462204066220407GA15GENIChomozygous959095012
1462205506220551TA11GENIChomozygous959095013
1462205646220565GT12GENIChomozygous959095014
1462207146220715AG15GENIChomozygous959095015
1462207476220748TC10GENIChomozygous959095016
1462209816220982AG16GENIChomozygous959095017
1462212306221231TC5GENIChomozygous959095018