chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1816978961697897AG26GENIChomozygous144190857
1816981371698137AGG23GENIChomozygous142627470
1816982231698224A23GENIChomozygous142627471
1816988191698820TG15GENIChomozygous142637675
1816990811699082TC22GENIChomozygous142637679
1816995851699585TGAGAAGAC23GENIChomozygous144185246
1816996451699646GT25GENIChomozygous142637686
1817002281700229CT16GENIChomozygous142637691
1817006101700611CT15GENIChomozygous142637692
1817010441701045GA18GENIChomozygous144190858
1817015921701593TA29GENIChomozygous144190859
1817025151702516TC25GENIChomozygous142637699
1817027671702768TC28GENIChomozygous142637701
1817027801702781GA27GENIChomozygous144190860
1817032071703208CT26GENIChomozygous144190861
1817033141703315GA18GENIChomozygous142637705
1817040931704094TG28GENIChomozygous142637710
1817041671704168TC28GENIChomozygous142637711
1817050451705046G17GENICpossibly homozygous142627475
1817056371705639GT16GENIChomozygous144185247
1817056801705681TC24GENIChomozygous155071908
1817059211705922AG17GENIChomozygous142637722
1817065601706561GT16GENIChomozygous144190862
1817068061706807TC20GENIChomozygous144190863
1817068071706808CT20GENIChomozygous144190864
1817072361707237CG15GENIChomozygous142637724
1817056801705681T24GENICheterozygous403427041