chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X120624951120624952GC9GENIChomozygous108811466
X120625906120625907GT12GENIChomozygous108421287
X120626025120626026AC10GENIChomozygous108421290
X120627353120627354CG13GENIChomozygous108421294
X120631584120631585AG13GENIChomozygous108811468
X120632615120632616AG19GENIChomozygous108421314
X120634237120634238CA10GENIChomozygous108421320
X120637018120637019GC12GENIChomozygous108421330
X120637500120637501CT14GENIChomozygous108811470
X120638623120638624TC12GENIChomozygous108421338
X120639577120639578CG14GENIChomozygous108811472
X120640164120640165CA13GENIChomozygous108811474
X120641965120641966CT18GENIChomozygous108811476
X120641993120641994CT19GENIChomozygous108818622
X120643596120643597GA4GENIChomozygous108811478
X120643946120643947AG11GENIChomozygous108811480
X120644114120644115TG18GENIChomozygous108818623
X120646064120646065GA12GENIChomozygous108811482
X120647289120647290AG14GENIChomozygous108811484
X120647545120647546TG7GENIChomozygous108811486
X120647666120647667GA19GENIChomozygous108811488