chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5165436892165436898AGAAAA12GENICpossibly homozygous128268837
5165436905165436910AGACA13GENICheterozygous128268838
5165436911165436917ACACAG14GENICheterozygous128268839
5165436922165436923CG15GENICheterozygous119054786
5165436924165436924TAAGAG16GENICheterozygous128268840
5165436927165436934TCCTGGA16GENICheterozygous128268841
5165436938165436948GAACAGTTGT18GENICheterozygous128268842
5165440971165440971T10GENIChomozygous128268843
5165440976165440977A11GENIChomozygous128268844
5165440988165440989C11GENIChomozygous128268845
5165441014165441015T11GENIChomozygous128268846
5165441037165441037T14GENIChomozygous128268847
5165441100165441100GC16GENIChomozygous128268848
5165441121165441122C13GENIChomozygous128268849
5165441135165441136T14GENIChomozygous128268850
5165441142165441143A14GENIChomozygous128268851
5165441160165441161GC17GENIChomozygous114081800
5165441165165441166AC17GENIChomozygous114081801
5165441168165441169AC16GENIChomozygous114081802