chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139060579290605793TC26GENIChomozygous114574693
139060629290606293AG25GENIChomozygous114574695
139060641490606415TC12GENIChomozygous114574697
139060685190606852AC10GENIChomozygous118528910
139060729490607295TC11GENIChomozygous114693403
139060816590608166AC18GENIChomozygous114574699
139060900290609003GA24GENIChomozygous114574701
139060935990609360TG15GENIChomozygous114574703
139061125090611251AG19GENIChomozygous114574705
139061195890611959CT19GENIChomozygous114574707
139061236090612361TC18GENIChomozygous126070681
139061244590612446CG3GENICheterozygous114693405
139061401690614017TA21GENIChomozygous114574709
139061513990615140AT29GENIChomozygous114574713
139061630790616308GA29GENIChomozygous114574717
139061653090616531TC12GENIChomozygous114574719
139061890690618907CG5GENIChomozygous114574721
139061954790619548TC27GENIChomozygous114574723
139062094890620949AG11GENIChomozygous114574725
139062290990622910GA27GENIChomozygous114574727
139062296090622961GA18GENIChomozygous114574729
139062439290624393CT6GENIChomozygous114574733
139062813990628140AC14GENIChomozygous126070682
139063057990630580CT21GENIChomozygous114574735
139063083890630839AG17GENIChomozygous114574737
139063181690631817AG26GENIChomozygous114574739
139063196090631961CT9GENIChomozygous118528913
139063274190632742TA19GENIChomozygous126070684
139063547190635472TG13GENIChomozygous114574741
139063600690636007TA9GENIChomozygous126104348
139063657190636572AC20GENIChomozygous114574743
139063872390638724TA19GENIChomozygous114574753
139063903090639031GT15GENIChomozygous114574755
139063985090639851TC11GENIChomozygous114574757
139064090690640907CT22GENIChomozygous114574759
139064119290641193CT19GENIChomozygous114574761