chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134610888134610889GC43GENIChomozygous137628289
5134611275134611276CA43GENICpossibly homozygous137628290
5134611526134611527GA43GENIChomozygous137628291
5134615160134615161TC30GENIChomozygous137628292
5134615622134615623AC51GENIChomozygous137628293
5134615676134615677AG42GENIChomozygous137628294
5134616525134616526GA38GENIChomozygous137628295
5134617503134617518TGTGTGTGTGTGTGC20GENICheterozygous145534287
5134617879134617880CT31GENIChomozygous137628296
5134617959134617960CT30GENIChomozygous137628297
5134619788134619789TC52GENIChomozygous137628298
5134619958134619959TC44GENIChomozygous137628299
5134622747134622748AG60GENIChomozygous137628300