chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
499369579936958CT6GENICheterozygous879698981
499370719937072AG8GENIChomozygous879698982
499370759937076TC9GENIChomozygous879698983
499372749937275GA11GENIChomozygous879698984
499372869937287CT8GENIChomozygous879698985
499372989937299GA10GENIChomozygous879698986
499373219937322GA18GENIChomozygous879698987
499373999937400GA11GENIChomozygous879698988
499374609937461CA28GENIChomozygous879698989
499375489937549CT21GENIChomozygous879698990
499376549937655TG25GENIChomozygous879698991
499377019937702GA23GENIChomozygous879698992
499377219937722GA9GENIChomozygous879698993
499377349937735AC9GENIChomozygous879698994
499377469937747AG11GENIChomozygous879698995
499379589937959GT22GENIChomozygous879698996
499380479938048CG16GENIChomozygous879698997
499381759938176AG16GENIChomozygous879698998
499382179938218TA20GENIChomozygous879698999
499382519938252TA12GENIChomozygous879699000
499384169938417CG8GENIChomozygous879699001
499384349938435GT9GENIChomozygous879699002
499384509938451TC11GENIChomozygous879699003
499384829938483GT20GENIChomozygous879699004
499388009938801GT15GENIChomozygous879699005
499388499938850CT10GENIChomozygous879699006