chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125133780851337809GC39GENIChomozygous50244415
125133829251338293AG33GENIChomozygous50244417
125133842351338424AT36GENIChomozygous50244419
125133898251338983GGGCGC7GENICheterozygous50547232
125133905951339061CA--6GENIChomozygous50547233
125133907351339074GC20GENIChomozygous50244427
125133942351339424CT32GENIChomozygous50244429
125133990451339905AT17GENIChomozygous50244431
125133991251339913TA17GENIChomozygous50244433
125134015251340153TC25GENIChomozygous50244435
125134026151340262AG23GENIChomozygous50244437
125134029051340291TC27GENIChomozygous50244439
125134030951340310GA25GENIChomozygous50244441
125134035151340352AG27GENIChomozygous50244443
125134087951340880TC9GENICpossibly homozygous50423290
125134088151340882TC21GENIChomozygous50423291
125134261251342613A-25GENIChomozygous50244453
125134261651342617A-25GENIChomozygous50244455
125134262351342624G-26GENIChomozygous50244457
125134288151342882GA33GENIChomozygous50244459
125134288751342888GA34GENIChomozygous50244461