chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79553218695532187GGGA19GENICpossibly homozygous54029828
79553218695532187GA30GENICheterozygous54574014
79553445895534459AC36GENIChomozygous54029830
79553446895534469GT31GENIChomozygous54029831
79553449595534496GC23GENIChomozygous54029832
79553450395534504AC22GENIChomozygous54029833
79553451395534514AC22GENIChomozygous54029834
79553452095534521AC21GENIChomozygous54029835
79553455195534552AC17GENIChomozygous54029836
79553459995534600TTG5GENIChomozygous54029839
79553460495534605C-5GENIChomozygous54029840
79553460995534610CCATG6GENIChomozygous54029841
79555433395554334TG36GENICheterozygous54574016
79556169295561693C-11GENIChomozygous54029947
79556909995569101GG--4GENICheterozygous54029974
79556910095569101G-4GENICheterozygous54029975
79559022495590225T-8GENIChomozygous54030008
79559024195590242TC15GENICheterozygous54574018
79559024595590246TC14GENICheterozygous54574020
79559128595591286T-13GENICheterozygous54030010
79559869295598693TTTG7GENICheterozygous54030041
79560837995608381GG--18GENICheterozygous54030052
79560838795608388GT23GENIChomozygous54030053
79560840795608408GT20GENICpossibly homozygous54030054
79560841995608420AT20GENIChomozygous54030056
79560842695608427GA18GENIChomozygous54030057
79560843195608432GT15GENIChomozygous54030058
79560480595604806A-8GENICheterozygous54487770
79560845495608455CT14GENICpossibly homozygous54030059
79560845695608457GC14GENIChomozygous54030060
79561042095610424GTGT----18GENICheterozygous54030065
79561042295610424GT--18GENICheterozygous54030066