chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135384512953845130TC19GENICpossibly homozygous776961735
135384691053846911GA36GENIChomozygous776961736
135384719153847192AG58GENIChomozygous776961737
135384720353847204GA54GENIChomozygous776961738
135384748453847485AG16GENIChomozygous776961739
135384748653847487AT10GENIChomozygous776961740
135384764953847650AG20GENICpossibly homozygous776961741
135384766153847662CG15GENICpossibly homozygous776961742
135384781953847820GC43GENICheterozygous776961743
135384796953847970GC55GENICheterozygous776961744
135384939353849394GA31GENIChomozygous776961745
135384961753849618AG50GENIChomozygous776961746
135384968053849681TC42GENIChomozygous776961747
135385007053850071GA29GENIChomozygous776961748
135385014953850150TC30GENIChomozygous776961749
135385036653850367AG21GENIChomozygous776961750
135385080653850807CA31GENIChomozygous776961751