chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109444614094446141AAAAAG5GENIChomozygous51747159
109444642494446425AG22GENICheterozygous51548898
109444711794447118TC21GENIChomozygous51548899
109444720894447209AG13GENICpossibly homozygous51548900
109444851294448513AG10GENICpossibly homozygous51747161
109444854894448549CA6GENICheterozygous52511402
109444913294449133GA25GENIChomozygous51747165
109444918294449183AC16GENICpossibly homozygous51747167
109444920394449204CA17GENIChomozygous51747169
109445005894450059GT18GENIChomozygous51747171
109445008794450088CT20GENIChomozygous51548904
109445046794450468CT23GENICpossibly homozygous51747173
109445158794451588TG19GENICpossibly homozygous51747190
109445163594451636TC20GENICpossibly homozygous51548908