chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5154518241154518242AG59GENICheterozygous780359101
5154518254154518255CA53GENICheterozygous780359102
5154519443154519444AT51GENIChomozygous780359103
5154519709154519710CT57GENICpossibly homozygous780359104
5154524077154524078AG43GENIChomozygous780359105
5154524903154524904GC48GENICpossibly homozygous780359106
5154525514154525515CA48GENICpossibly homozygous780359107
5154527506154527507CT47GENIChomozygous780359108
5154527837154527838TC39GENIChomozygous780359109
5154528038154528039GT46GENICpossibly homozygous780359110
5154528250154528251TC77GENIChomozygous780359111
5154529162154529163CT45GENIChomozygous780359112
5154533476154533477TA43GENIChomozygous780359113
5154534013154534014GC55GENIChomozygous780359114
5154534294154534295CT68GENICpossibly homozygous780359115
5154534512154534513TG39GENIChomozygous780359116
5154534832154534833GC42GENICpossibly homozygous780359117
5154534908154534909CT45GENIChomozygous780359118
5154535499154535500AG48GENIChomozygous780359119
5154537361154537362CT34GENIChomozygous780359120
5154537989154537990GA48GENIChomozygous780359121
5154538190154538191AG54GENIChomozygous780359122
5154538999154539000AG49GENICpossibly homozygous780359123
5154539933154539934AG31GENIChomozygous780359124
5154540004154540005GA34GENIChomozygous780359125
5154540113154540114TG46GENIChomozygous780359126