chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73477464434774645GGA34GENICheterozygous54191076
73478835134788352T-21GENICheterozygous54191090
73479040434790405AC34GENICheterozygous54191092
73479430034794301CT24GENICheterozygous54191096
73478796434787965CCAG29GENIChomozygous53870014
73478936634789367CA9GENICheterozygous53870015
73479313234793133CCGCCGG17GENIChomozygous53870016
73479360234793603AATTT24GENIChomozygous53870017
73478815134788152AC23GENIChomozygous54727340
73479255134792552CG38GENICpossibly homozygous54727342
73479554334795545TT--20GENIChomozygous54727344
73479833634798337C-21GENIChomozygous53870019
73480357234803573TC29GENICpossibly homozygous54727346
73480358834803595GCGCGTG-------19GENIChomozygous54191100
73480358934803590CT18GENICpossibly homozygous54727348
73480359134803592CT17GENICpossibly homozygous54727350
73480359434803595GGT19GENIChomozygous54191101
73480361234803616GTGT----10GENICpossibly homozygous53870020
73480475434804756GT--8GENICpossibly homozygous54354453
73480673434806735GGGT27GENICpossibly homozygous54646284
73480733934807340GGT10GENIChomozygous54727352
73480822534808226CG19GENIChomozygous53870022
73480823934808240TG21GENIChomozygous53870023
73480827934808280CCA15GENIChomozygous53870026
73480829034808291AAC17GENIChomozygous53870027
73480829634808297T-16GENIChomozygous53870028
73480831934808320G-20GENIChomozygous53870029
73481468234814683CA33GENIChomozygous54191103
73481481634814817CA32GENIChomozygous53870030
73481493934814940AC23GENIChomozygous53870033
73481507534815076TC35GENIChomozygous54727354
73481614734816148AG36GENIChomozygous53870035
73481615534816156AG32GENIChomozygous53870036
73481632234816326GAGA----28GENIChomozygous53870038
73481731934817320CCAACT25GENIChomozygous53870039