chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4144204903144204904AG67GENIChomozygous56964165
4144205496144205497AG49GENIChomozygous56964166
4144205764144205765AG53GENIChomozygous56964167
4144205800144205801AC55GENICpossibly homozygous56964168
4144205923144205924CT56GENIChomozygous56964169
4144206050144206051A-41GENICpossibly homozygous56964170
4144207343144207344GA36GENICpossibly homozygous56964171
4144207346144207348AG--29GENICpossibly homozygous56964172
4144207362144207363TC46GENICheterozygous56964173
4144207787144207788GT76GENICpossibly homozygous56964174
4144208447144208448TC29GENIChomozygous56964175
4144208597144208598GA42GENIChomozygous56964176
4144209288144209289GT53GENIChomozygous56964177
4144209938144209941GAG---50GENIChomozygous56964178
4144209965144209966TA52GENICpossibly homozygous56964179
4144210725144210726AG40GENIChomozygous56964180
4144210979144210980TC83GENIChomozygous56964181
4144211341144211342AATG60GENIChomozygous56964182
4144211676144211677AC47GENIChomozygous56964183
4144212107144212108CT52GENIChomozygous56964184
4144211244144211245GA68GENIChomozygous57342573