chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121738109517381096CT25GENIChomozygous50925329
121738162117381622AG19GENIChomozygous50085125
121738174617381747CCA29GENIChomozygous50823250
121738201417382015AG19GENIChomozygous50925332
121738211817382119CCA16GENIChomozygous50880892
121738261717382618AG24GENIChomozygous50823252
121738531717385318AG18GENIChomozygous50823256
121738541117385412GA19GENIChomozygous50925335
121738555317385554CT24GENIChomozygous50925338
121738579617385797GA25GENIChomozygous50925341
121738231217382313GT14GENIChomozygous50718512
121738327817383279A-14GENIChomozygous50718514
121738191217381913CCA10GENICheterozygous50367374
121738640117386402G-19GENIChomozygous50880904
121738649217386493CT16GENICpossibly homozygous50880906
121738738517387386TG14GENIChomozygous50718523
121738741517387416TC18GENIChomozygous50718525
121738765017387651CG28GENIChomozygous50925344
121738191217381913CCAA10GENICheterozygous50535178
121738652617386527CCAAA7GENIChomozygous50557345