chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6145549279145549280TTTCAAATGTTATTCCCTTTC3GENICheterozygous55977628
6145555344145555345GGC12GENIChomozygous55869336
6145556646145556648AC--13GENICheterozygous55735151
6145577474145577489CAGAAGGTGTGCTGC---------------3GENIChomozygous56011408
6145589796145589800CTCC----15GENIChomozygous54764672
6145590628145590629AAT13GENIChomozygous54764673
6145591020145591021CCTTTT2GENIChomozygous55546927
6145591118145591120TT--13GENICpossibly homozygous54764676
6145598227145598228A-21GENIChomozygous54764691
6145627137145627138GGCCTTATGTGTGTCCACACTCTTCTCCTGCAGGTGGCCTTATGTGTGCCCACACTC25GENICheterozygous55735157
6145644844145644845AC29GENIChomozygous54764888
6145652328145652330TA--2GENICheterozygous56187072
6145652359145652360T-5GENIChomozygous54764915
6145652371145652372GA4GENIChomozygous54764916
6145652396145652397AC6GENIChomozygous54764917
6145660060145660062GT--16GENICheterozygous56075780