chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1103187001103187002GA39INTERGENIChomozygous74265154
1103187287103187288GT26INTERGENIChomozygous74265157
1103187971103187972AT11INTERGENIChomozygous74265166
1103188147103188148GA25INTERGENIChomozygous74265168
1103188293103188294GA24INTERGENIChomozygous74265171
1103188494103188495TC25INTERGENIChomozygous74265174
1103188508103188509CA22INTERGENIChomozygous74265177
1103188542103188543TC14INTERGENIChomozygous74265180
1103188550103188551AG13INTERGENICpossibly homozygous74265183
1103188636103188637AG15INTERGENIChomozygous74265186
1103188706103188707TC29INTERGENIChomozygous74265189
1103188710103188711GA27INTERGENIChomozygous74265192
1103188908103188909TC11INTERGENIChomozygous74265195
1103188944103188945TG13INTERGENIChomozygous74265198
1103188977103188978GA22INTERGENIChomozygous74265201
1103189496103189497AC21INTERGENIChomozygous74265216
1103189251103189252AG7INTERGENIChomozygous74265210
1103189326103189327TC21INTERGENICpossibly homozygous74265213