chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
136883457768834578GA45GENIChomozygous809092272
136883481168834812AG57GENIChomozygous809092273
136883776968837770AT30GENICpossibly homozygous809092274
136883842068838421TC50GENICpossibly homozygous809092275
136883977268839773GT37GENICpossibly homozygous809092276
136884333568843336GA16GENIChomozygous809092277
136884527668845277AT37GENIChomozygous809092278
136884536968845370CT35GENIChomozygous809092279
136884649868846499GC42GENIChomozygous809092280
136884667168846672GA35GENIChomozygous809092281
136884683568846836CT45GENIChomozygous809092282
136885024968850250AT32GENIChomozygous809092283
136885036868850369TA33GENIChomozygous809092284
136885083968850840TC67GENIChomozygous809092285
136885168968851690AG66GENIChomozygous809092286
136885255868852559AC33GENIChomozygous809092287
136885300468853005TC60GENIChomozygous809092288
136885318368853184CT57GENIChomozygous809092289
136885352068853521AG33GENIChomozygous809092290
136885416168854162GA41GENIChomozygous809092291
136885515068855151CT43GENIChomozygous809092292
136885528768855288CT38GENICpossibly homozygous809092293
136885646368856464AG25GENIChomozygous809092294
136885664968856650TC37GENIChomozygous809092295
136885681268856813AG53GENIChomozygous809092296
136885927868859279AG51GENIChomozygous809092297
136885936868859369AG38GENICpossibly homozygous809092298
136885941568859416AG39GENIChomozygous809092299