chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1153732834153732835CG21GENIChomozygous108946997
1153733082153733083TA19GENIChomozygous108314039
1153733575153733576AG29GENIChomozygous108946998
1153733878153733879GA31GENIChomozygous108946999
1153734789153734790AT14GENIChomozygous120515031
1153734788153734789GA14GENIChomozygous109150397
1153734996153734997GA14GENIChomozygous108947000
1153735449153735450TC22GENIChomozygous108947001
1153735543153735544TC16GENIChomozygous108314045
1153736357153736358AG37GENIChomozygous108314047
1153736727153736728CT21GENIChomozygous108314053
1153736730153736731GA22GENIChomozygous108947002
1153736810153736811AG26GENIChomozygous108314055
1153736898153736899TA20GENIChomozygous108947003
1153737290153737291CT33GENICpossibly homozygous108947004
1153737441153737442AG33GENIChomozygous108314059
1153737513153737514AG32GENIChomozygous108314061
1153737900153737901TC28GENIChomozygous108314065
1153737993153737994CG17GENIChomozygous108314067
1153738170153738171TG14GENIChomozygous108947005
1153738646153738647GA23GENIChomozygous120486830
1153738659153738660CT20GENIChomozygous108947006
1153740013153740014TA22GENIChomozygous108314073
1153740094153740095TC17GENIChomozygous108947007
1153740675153740676AG8GENIChomozygous108314079
1153741458153741459TC19GENIChomozygous108314081