chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124248772942487730TC29GENIChomozygous50209169
124248825642488257AG12GENIChomozygous50804595
124248841242488421TTTTTTTAA---------6GENICheterozygous50209173
124248860642488607CT31GENIChomozygous50563866
124248890942488910AT30GENIChomozygous50563868
124248903642489037CT27GENIChomozygous50563870
124248991442489915CT30GENIChomozygous50563872
124249025242490253G-21GENIChomozygous50592216
124249053842490539AG29GENIChomozygous50209176
124249065742490658CT14GENIChomozygous50209180
124249087642490877AC20GENIChomozygous50563880
124249139342491394CT8GENIChomozygous50209181
124249059842490603CACGC-----7GENICpossibly homozygous50885553