chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55015013150150132AC27GENIChomozygous114200580
55015026550150266GA21GENIChomozygous113791786
55015035150150352CT17GENIChomozygous114200581
55015062350150624TA31GENIChomozygous113791787
55015073550150736AC19GENIChomozygous114500882
55015094050150941TC30GENIChomozygous114200582
55015096350150964GT30GENIChomozygous114200583
55015551250155513CA17GENIChomozygous114500884
55015650750156508CT30GENIChomozygous114200588
55015677350156774CT18GENIChomozygous113791795
55016565850165659TC28GENIChomozygous114200592
55016836650168367GC32GENIChomozygous114200594
55016874650168747CT31GENIChomozygous114500888
55016878850168789CG22GENIChomozygous114500890
55016907750169078TC20GENIChomozygous114500892
55017435850174359AG21GENIChomozygous114500900
55017578250175783CT38GENIChomozygous114500902
55017706650177067AC24GENIChomozygous113791823
55017790750177908AG26GENIChomozygous114200617
55017797850177979TG22GENIChomozygous114500904
55017943350179434TC26GENIChomozygous113791825
55017973450179735AG36GENIChomozygous114200620