chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
193783036037830361AG34GENIChomozygous801091150
193783077337830774CT42GENIChomozygous801091151
193783240737832408TC27GENIChomozygous801091152
193783367037833671AT21GENIChomozygous801091153
193783393937833940TC25GENIChomozygous801091154
193783479037834791TC25GENIChomozygous801091155
193783609237836093TC21GENIChomozygous801091156
193783647437836475AG27GENICpossibly homozygous801091157
193783716037837161AG48GENIChomozygous801091158
193783776637837767GC29GENIChomozygous801091159
193783807737838078TC21GENIChomozygous801091160
193783807937838080AG19GENIChomozygous801091161
193783892337838924TC27GENIChomozygous801091162
193783960137839602CT29GENIChomozygous801091163
193783961037839611AG28GENIChomozygous801091164
193784035237840353AC27GENICpossibly homozygous801091165
193784056037840561TC32GENIChomozygous801091166
193784212237842123GT19GENICpossibly homozygous801091167
193784307837843079GA25GENIChomozygous801091168
193784455537844556AG32GENIChomozygous801091169