chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109444614094446141AAAAAG11GENIChomozygous51747159
109444642494446425AG21GENIChomozygous51548898
109444711794447118TC14GENIChomozygous51548899
109444720894447209AG17GENIChomozygous51548900
109444851294448513AG11GENIChomozygous51747161
109444854894448549CA11GENICpossibly homozygous52511402
109444913294449133GA14GENIChomozygous51747165
109444918294449183AC16GENIChomozygous51747167
109444920394449204CA18GENIChomozygous51747169
109445005894450059GT23GENIChomozygous51747171
109445008794450088CT25GENIChomozygous51548904
109445046794450468CT20GENIChomozygous51747173
109445108194451082G-2GENIChomozygous51747177
109445108394451084C-1GENIChomozygous51747179
109445158794451588TG15GENIChomozygous51747190
109445163594451636TC16GENIChomozygous51548908