chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141297492712974928AG22GENIChomozygous956133168
141297572712975728TC35GENIChomozygous956133169
141297600712976008TC29GENIChomozygous956133170
141297603412976035AT24GENIChomozygous956133171
141297859112978592CT8GENIChomozygous956133172
141297897412978975AT25GENIChomozygous956133173
141297912512979126GT35GENIChomozygous956133174
141298061312980614GA26GENIChomozygous956133175
141298096712980968GA33GENIChomozygous956133176
141298248612982487TC23GENIChomozygous956133177
141298580612985807AG26GENIChomozygous956133178
141298595912985960TG25GENIChomozygous956133179
141298767512987676AG20GENIChomozygous956133180
141298792112987922AT21GENIChomozygous956133181
141298835612988357GC25GENIChomozygous956133182
141298846512988466TG12GENIChomozygous956133183
141298866412988665CA25GENIChomozygous956133184
141298876812988769GA31GENIChomozygous956133185
141298877612988777AT37GENIChomozygous956133186
141298885412988855TG41GENIChomozygous956133187
141298889712988898TG36GENIChomozygous956133188
141298932912989330GA24GENIChomozygous956133189
141298998812989989AT8GENIChomozygous956133190
141299016312990164TA19GENICpossibly homozygous956133191
141299411712994118TC21GENIChomozygous956133192
141299423612994237CG22GENIChomozygous956133193
141299473212994733TG30GENIChomozygous956133194
141299581612995817CG11GENIChomozygous956133195