chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121738156417381565CT29GENICpossibly homozygous50880888
121738162117381622AG24GENIChomozygous50085125
121738185417381855CT12GENIChomozygous50880890
121738191217381913CCAAA9GENIChomozygous50748308
121738211817382119CCA17GENIChomozygous50880892
121738358317383584TC14GENIChomozygous50880894
121738374417383745CA20GENIChomozygous50880896
121738231217382313GT24GENIChomozygous50718512
121738327817383279A-20GENIChomozygous50718514
121738451417384515CA24GENIChomozygous50880898
121738508517385086GA29GENIChomozygous50880900
121738626917386270GA32GENIChomozygous50880902
121738640117386402G-16GENIChomozygous50880904
121738649217386493CT12GENIChomozygous50880906
121738651417386515GGA7GENIChomozygous50880908
121738652617386527CCAAA4GENIChomozygous50557345
121738704517387046TG33GENIChomozygous50880910
121738738517387386TG16GENICpossibly homozygous50718523