chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2844912728449127T10GENIChomozygous129730850
X2844922928449230AG35GENICheterozygous131245671
X2844923228449233GT33GENICheterozygous131245672
X2844924128449242AG34GENICpossibly homozygous120024623
X2844934428449345GT25GENIChomozygous120024624
X2844959728449598AT11GENIChomozygous125102807
X2844974228449743CT4GENIChomozygous125160712
X2845039428450395AG6GENIChomozygous125102808
X2845119428451195C3GENIChomozygous129730851
X2844931728449318AT28GENIChomozygous131973505
X2845083028450831TC18GENIChomozygous119912654
X2846814428468144ATCC20GENIChomozygous129730855
X2846861228468613GA22GENIChomozygous108476544
X2846975128469752GA10GENIChomozygous108248927
X2847233028472331A25GENIChomozygous129730861
X2847235128472352CG24GENIChomozygous108248939
X2846827928468280AC8GENICheterozygous119992124
X2846531328465314CT22GENIChomozygous108547231
X2846764628467647TG21GENIChomozygous108547233
X2846810728468108CA17GENIChomozygous108547235
X2847228528472286CG27GENIChomozygous108547237
X2847247328472474AT22GENIChomozygous108547239
X2846628528466286C10GENICheterozygous132370335
X2846832128468322TG8GENIChomozygous108441600