chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2174150356174150357GC54GENICpossibly homozygous141422284
2174154168174154169AT60GENIChomozygous141422285
2174157763174157764CT56GENIChomozygous141422286
2174161025174161026CA44GENIChomozygous136372766
2174156824174156825CT48GENIChomozygous136372765
2174154395174154396CT60GENIChomozygous136372764
2174158704174158706TG12GENICheterozygous141334179
2174161182174161183CA60GENIChomozygous136372767
2174162784174162785AG54GENIChomozygous136372769
2174162896174162897TG62GENIChomozygous136372770
2174163252174163253AC62GENIChomozygous136372771
2174164742174164743TA48GENIChomozygous136372775
2174170831174170832A40GENICpossibly homozygous135961088
2174173179174173180GC60GENIChomozygous141422287
2174175779174175780GC55GENIChomozygous141422288
2174175922174175922A52GENIChomozygous135961089
2174176903174176904GA58GENIChomozygous136372779