chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
995794729579473CT39GENIChomozygous574324238
995820299582030CCA8GENICheterozygous714701817
995854589585459TTC16GENICpossibly homozygous714701819
995881049588105CT36GENIChomozygous574324239
995884589588459AC32GENIChomozygous574324240
995891849589185G-24GENIChomozygous714701820
995942079594208GGT15GENIChomozygous714701821
996008339600834C-30GENIChomozygous714701822
996036099603610TC36GENIChomozygous574324241
996076249607625GGA19GENICpossibly homozygous714701824
996135579613558TTC24GENIChomozygous714701825
996149809614982TT--16GENICpossibly homozygous714701827
996150059615006CT17GENIChomozygous574324242
996153869615387AT49GENIChomozygous574324243
996173039617304A-23GENIChomozygous714701829
996195799619580CCCA42GENIChomozygous714701830
996195829619583G-42GENIChomozygous714701831
996195849619585TTCA43GENIChomozygous714701832
996195859619586GC43GENIChomozygous574324244
996205209620521AG29GENIChomozygous574324245
996251939625194TG16GENIChomozygous574324246
996252029625203CCT11GENICpossibly homozygous714701833
996252389625243TTTTT-----3GENIChomozygous714701834
996268099626810AC15GENIChomozygous574324247
996269829626989GCCCCGG-------17GENICpossibly homozygous714701837
996270239627024AAGTCTCG23GENICpossibly homozygous714701838
996307999630800TTCACACACA18GENIChomozygous714701841
996327209632721AG32GENIChomozygous574324248
996340709634071C-21GENICpossibly homozygous714701843
996340729634085CACACACACACAC-------------21GENICpossibly homozygous714701844
996372449637245CA27GENIChomozygous574324249