chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1816978961697897AG43GENIChomozygous144190857
1816981371698137AGG48GENIChomozygous142627470
1816982231698224A38GENIChomozygous142627471
1816988191698820TG55GENIChomozygous142637675
1816990811699082TC51GENIChomozygous142637679
1816995851699585TGAGAAGAC64GENIChomozygous144185246
1816996451699646GT50GENIChomozygous142637686
1817002281700229CT43GENIChomozygous142637691
1817006101700611CT41GENIChomozygous142637692
1817010441701045GA29GENIChomozygous144190858
1817015921701593TA55GENIChomozygous144190859
1817025151702516TC44GENIChomozygous142637699
1817027671702768TC30GENIChomozygous142637701
1817027801702781GA33GENIChomozygous144190860
1817032071703208CT46GENIChomozygous144190861
1817033141703315GA35GENIChomozygous142637705
1817040931704094TG49GENICpossibly homozygous142637710
1817041671704168TC48GENIChomozygous142637711
1817050451705046G47GENIChomozygous142627475
1817056371705639GT32GENIChomozygous144185247
1817059211705922AG43GENIChomozygous142637722
1817065601706561GT64GENIChomozygous144190862
1817068061706807TC53GENIChomozygous144190863
1817068071706808CT54GENIChomozygous144190864
1817072361707237CG65GENIChomozygous142637724
1817056801705681T44GENICheterozygous403427041
1817056801705681TC44GENIChomozygous155071908