chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87151437671514377T36GENICheterozygous142025818
87151969971519700CT13GENIChomozygous138340152
87151970371519704CT13GENIChomozygous138340153
87151972071519721CT11GENIChomozygous138340154
87151972271519723CT12GENIChomozygous138340155
87151972971519730CT14GENIChomozygous138340156
87155558471555586GT29GENICheterozygous141118077
87156844671568447CG20GENICpossibly homozygous138340157
87158977971589780TC32GENIChomozygous138340158
87163005871630059TC22GENICpossibly homozygous144394967
87154590571545906GT49GENIChomozygous144394966