chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124175381341753814GT7GENICpossibly homozygous50572079
124175381641753817GA5GENICheterozygous50325836
124175382341753824AAG4GENIChomozygous50207683
124175382541753826CT4GENIChomozygous50544100
124175384041753841CCA4GENIChomozygous50207684
124175384141753842CA3GENIChomozygous50544101
124175384441753845CA3GENIChomozygous50207685
124175384741753848TA5GENIChomozygous50207686
124175385241753853GGCTATAA5GENIChomozygous50572081
124175386741753868TTG10GENIChomozygous50207688
124175386941753870GA10GENIChomozygous50544103
124175388041753881GA14GENIChomozygous50207689
124175388541753886GC15GENIChomozygous50207690
124175389641753897GA20GENIChomozygous50207691
124175390041753901G-22GENIChomozygous50544104
124175390241753903GGT22GENIChomozygous50544105
124175390341753904GC22GENIChomozygous50544106
124175392641753927GC28GENIChomozygous50207694
124175393841753939GC29GENIChomozygous50207695
124175394341753944GA30GENIChomozygous50207696
124175395041753951GA29GENIChomozygous50207697
124175396241753963GGT25GENIChomozygous50207698
124175396341753964GA25GENIChomozygous50544107
124175396641753967G-24GENIChomozygous50207699
124175397341753974CA25GENIChomozygous50207700
124175412641754127CCAAAAAAAACAAAACAAAACAAAACAAAACAAAAAAAAAAAAAAAAAAAA10GENICheterozygous50544108
124175476741754768TTTACA6GENICheterozygous50207705
124175634441756352GGCTCGTT--------9GENIChomozygous50325844
124175635141756352TTAA9GENIChomozygous50544110
124175676441756765GGATTTATTT1GENIChomozygous50696069
124175866841758669GA42GENIChomozygous50804340