chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103753530437535305GA77GENICheterozygous118035208
103753532037535321AC79GENICheterozygous118035209
103753659937536600GA33GENIChomozygous118080988
103753714237537143GA37GENICpossibly homozygous118080989
103753760837537609TA46GENIChomozygous118080990
103753803037538031GT40GENICpossibly homozygous118080991
103753861037538611TG58GENIChomozygous118080992
103753929637539297CT40GENIChomozygous118080993
103753974037539741TC27GENIChomozygous118080994
103754052337540524GA47GENIChomozygous118080995
103754453237544533TG33GENIChomozygous118080996
103754528837545289TG29GENICpossibly homozygous118080997
103754561337545614AT35GENIChomozygous118080998
103754591637545917TA47GENICpossibly homozygous118080999
103754592037545921TA48GENICpossibly homozygous118081000
103754592437545925TA45GENICpossibly homozygous118081001
103754629537546296TG50GENIChomozygous117989388
103754991437549915GC45GENIChomozygous118081002
103755006037550061GA56GENIChomozygous118081003
103755025537550256TC52GENIChomozygous117989389
103755055537550556CT63GENIChomozygous118081004
103755173437551735TC69GENIChomozygous118081005
103755329437553295CT40GENIChomozygous117989391
103755353837553539CT68GENIChomozygous117989392
103755426237554263GA14GENIChomozygous118081006
103755442137554422TC30GENIChomozygous118081007