chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14104808431104808432GA25GENIChomozygous613341800
14104808450104808451GT12GENIChomozygous615397620
14104808457104808458AT8GENIChomozygous615397621
14104808463104808464TC10GENIChomozygous615397622
14104808464104808465GC10GENIChomozygous615397623
14104808506104808507GT30GENIChomozygous613341801
14104809686104809687A-39GENIChomozygous736464455
14104810828104810829CT24GENIChomozygous613341802
14104810999104811000CT25GENIChomozygous613341803
14104811010104811011GT30GENIChomozygous613341804
14104811161104811162AAGT22GENICheterozygous736464458
14104811854104811862CCTTCAAA--------19GENIChomozygous736464460
14104811969104811970TTTA25GENICpossibly homozygous736464461
14104812136104812137GA34GENIChomozygous613341805
14104812395104812396AAC4GENICheterozygous736464462
14104813080104813097GGTGGCTAAAACTCTGT-----------------22GENIChomozygous736464463
14104813102104813103C-13GENIChomozygous736464464
14104813107104813108GGT14GENIChomozygous736464465
14104813114104813115TG16GENIChomozygous615397624
14104813115104813116GT17GENIChomozygous615397625
14104813125104813126TC23GENIChomozygous613341806
14104813178104813179TG20GENIChomozygous613341807
14104813411104813412GA26GENIChomozygous613341808
14104813852104813853CT26GENICpossibly homozygous613341809
14104814048104814049AC36GENIChomozygous613341810