chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109444614094446141AAAAAG6GENIChomozygous51747159
109444642494446425AG20GENICheterozygous51548898
109444711794447118TC11GENIChomozygous51548899
109444720894447209AG9GENIChomozygous51548900
109444851294448513AG6GENICheterozygous51747161
109444913294449133GA27GENICpossibly homozygous51747165
109444918294449183AC17GENICpossibly homozygous51747167
109444920394449204CA15GENIChomozygous51747169
109445005894450059GT20GENIChomozygous51747171
109445008794450088CT25GENICpossibly homozygous51548904
109445046794450468CT18GENICpossibly homozygous51747173
109445158794451588TG14GENICpossibly homozygous51747190
109445163594451636TC29GENICpossibly homozygous51548908