chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162486311324863114CCGT17GENICpossibly homozygous766480788
162486313224863133TA16GENIChomozygous665554982
162486320324863204TA19GENIChomozygous665554983
162486376124863762GA25GENIChomozygous665554984
162486389124863892GC20GENIChomozygous665554985
162486399024863991GGT18GENICpossibly homozygous766480789
162486527524865276A-23GENIChomozygous766480790
162486561624865617CT22GENIChomozygous665554986
162486565224865664TCTTTCTTTCTT------------12GENIChomozygous766480793
162486670024866701TC27GENIChomozygous665554987
162486680224866803CT21GENIChomozygous665554988
162486702724867028CCT19GENIChomozygous766480794
162486775724867758AG25GENIChomozygous665554989
162486855024868551CT29GENIChomozygous665554990
162486918724869188CT30GENIChomozygous665554991
162486920124869202GA28GENIChomozygous665554992
162486940724869408TA33GENIChomozygous665554993
162486964924869653TAAG----35GENIChomozygous766480795
162486971724869718GC24GENIChomozygous665554994
162486974824869749A-25GENIChomozygous766480796
162487027424870275CG19GENIChomozygous665554995
162487138124871382GGT10GENICpossibly homozygous766480797
162487154224871543TC1GENIChomozygous665554996
162487154424871545CG1GENIChomozygous665554997
162487169924871700CT10GENIChomozygous665554998
162487173724871738CA10GENIChomozygous665554999