chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134610888134610889GC21GENIChomozygous137628289
5134611275134611276CA22GENIChomozygous137628290
5134611526134611527GA25GENIChomozygous137628291
5134615160134615161TC24GENIChomozygous137628292
5134615622134615623AC21GENICpossibly homozygous137628293
5134615676134615677AG27GENIChomozygous137628294
5134615860134615861A14GENICheterozygous403159126
5134615860134615861AC14GENIChomozygous403159127
5134616525134616526GA28GENIChomozygous137628295
5134617537134617538T15GENICheterozygous403159128
5134617537134617538TA15GENICheterozygous403159129
5134617563134617564T21GENICheterozygous403159133
5134617503134617518TGTGTGTGTGTGTGC19GENICheterozygous145534287
5134617561134617562TA15GENICheterozygous403159130
5134617561134617562T15GENICheterozygous403159131
5134617563134617564TA21GENIChomozygous403159132
5134617879134617880CT18GENIChomozygous137628296
5134617959134617960CT15GENIChomozygous137628297
5134619788134619789TC24GENIChomozygous137628298
5134619958134619959TC21GENIChomozygous137628299
5134622747134622748AG21GENIChomozygous137628300