chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134608245134608246TC75GENIChomozygous143961776
5134617561134617562T21GENICheterozygous403159131
5134615860134615861A22GENICheterozygous403159126
5134615860134615861AC22GENIChomozygous403159127
5134617537134617538T13GENICheterozygous403159128
5134617537134617538TA13GENICheterozygous403159129
5134617561134617562TA21GENICpossibly homozygous403159130
5134617563134617564TA22GENICpossibly homozygous403159132
5134617563134617564T22GENICheterozygous403159133
5134619788134619789TC53GENIChomozygous137628298
5134619958134619959TC54GENIChomozygous137628299
5134622747134622748AG64GENIChomozygous137628300
5134611699134611699A49GENIChomozygous143944349
5134616298134616298TTT25GENIChomozygous143944350