chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135138492051384921T-14GENICpossibly homozygous50036919
135138554451385545GGCA25GENICheterozygous49755916
135138554551385547CA--25GENICheterozygous50495125
135139141951391421GT--22GENICheterozygous50550989
135139248051392481CCA2GENIChomozygous49755944
135140165251401653TTGTATGACAAA26GENIChomozygous49755993
135140224451402246CA--6GENICheterozygous50617184
135140390151403902TTG11GENIChomozygous49756005
135140901451409015AT20GENIChomozygous49756025
135140912151409124GAA---3GENIChomozygous50580339
135141925851419259G-9GENICheterozygous49756064
135142152751421528AT28GENIChomozygous49756069
135142208651422087CCATAT1GENIChomozygous49947083
135142358751423588C-3GENICheterozygous49756078
135142580451425805GGAC13GENICheterozygous49756079
135142580551425807AC--13GENICheterozygous50580340
135142593351425935GA--14GENICheterozygous50517759
135142743551427436CCATCT8GENIChomozygous50617185
135144105751441058TTAC4GENICheterozygous50517760
135144918251449183AC1GENIChomozygous50580342
135145299951453000C-27GENIChomozygous49756154
135145300251453005ACG---26GENIChomozygous49756155
135145300751453011CCCG----26GENIChomozygous49756156
135145301351453014G-21GENIChomozygous49756157