chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264095442264095443AG56GENIChomozygous108783032
1264095886264095887AG51GENIChomozygous108783033
1264097432264097433TC24GENIChomozygous108783034
1264097633264097634AC70GENIChomozygous108635089
1264097682264097683GA79GENIChomozygous108783035
1264098597264098598CT30GENIChomozygous108783036
1264098630264098631AG31GENIChomozygous108783037
1264098735264098736CT52GENICheterozygous108783038
1264099882264099883CT40GENIChomozygous108783039
1264099931264099932CT53GENIChomozygous108783040
1264100059264100060TA42GENIChomozygous108783041
1264100188264100189AG50GENIChomozygous108783042
1264100432264100433GA66GENIChomozygous108635095
1264100637264100638TC54GENIChomozygous108783043
1264101191264101192TC43GENIChomozygous108783044
1264101219264101220CT27GENICpossibly homozygous108783045
1264102022264102023CT53GENIChomozygous108783049
1264101725264101726TA45GENIChomozygous108783046
1264101841264101842AG51GENIChomozygous108783047
1264102013264102014GA58GENIChomozygous108783048
1264102091264102092GA61GENICpossibly homozygous108783050
1264102112264102113TC57GENIChomozygous108783051
1264102373264102374GA71GENIChomozygous108783052
1264102418264102419TC68GENIChomozygous108783053
1264102632264102633CT54GENICpossibly homozygous108783054
1264102715264102716TG29GENIChomozygous109545537
1264103104264103105GA27GENIChomozygous108783055
1264103285264103286AG55GENIChomozygous108783056
1264103682264103683CT43GENIChomozygous108783057
1264104414264104415GA40GENIChomozygous108783058