chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X13220121322013TC11GENIChomozygous125097974
X13233891323390TC15GENIChomozygous125097975
X13251051325106TC15GENIChomozygous108215902
X13308841330885CA5GENICheterozygous108437065
X13416201341621CT8GENIChomozygous108215910
X13418801341881AC7GENIChomozygous125097976
X13475551347556AG12GENIChomozygous108215912
X13592541359255AG8GENIChomozygous108215915
X13595731359574GC7GENIChomozygous108215917
X13642031364204AG15GENIChomozygous108215922
X13646871364688TA16GENIChomozygous108215925
X13672361367237GA11GENIChomozygous108215927
X13694001369401AC9GENIChomozygous108215930
X13699861369987TC11GENIChomozygous108215932
X13729121372913CT14GENIChomozygous108215934
X13749831374984GA11GENIChomozygous108215937
X13397271339728AG3GENICheterozygous125147488
X13681471368148TC3GENICheterozygous125147489