chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1432052183205219GA13GENIChomozygous976929007
1432052253205226GT13GENIChomozygous976929008
1432056643205665CT26GENIChomozygous976929009
1432063373206338CA28GENIChomozygous976929010
1432081793208180CT23GENIChomozygous976929011
1432134853213486TG26GENIChomozygous976929012
1432150703215071AG31GENIChomozygous976929013
1432153673215368TC13GENIChomozygous976929014
1432160573216058GA6GENIChomozygous976929015
1432161473216148TA11GENIChomozygous976929016
1432169313216932GT27GENIChomozygous976929017
1432184303218431AG22GENIChomozygous976929018
1432208893220890GA22GENIChomozygous976929019
1432209233220924TC29GENIChomozygous976929020
1432213363221337CT33GENIChomozygous976929021
1432226683222669CT13GENIChomozygous976929022
1432228023222803GT26GENICpossibly homozygous976929023
1432239873223988CT24GENICpossibly homozygous976929024
1432254713225472CT27GENIChomozygous976929025
1432266743226675AG12GENIChomozygous976929026
1432293013229302TC26GENIChomozygous976929027
1432314983231499TC24GENIChomozygous976929028
1432321093232110AC33GENIChomozygous976929029
1432428213242822AC26GENIChomozygous976929030
1432441983244199TC10GENICheterozygous976929031
1432451503245151CT29GENIChomozygous976929032
1432455153245516GA26GENIChomozygous976929033
1432455893245590AG31GENIChomozygous976929034
1432456843245685GA40GENIChomozygous976929035
1432465683246569TC22GENIChomozygous976929036
1432469093246910AG25GENIChomozygous976929037
1432470153247016TC19GENIChomozygous976929038