chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
78356571683565717AT14GENIChomozygous972922857
78356593483565935AG20GENIChomozygous972922858
78356603683566037TC21GENIChomozygous972922859
78356714483567145TC6GENIChomozygous972922860
78356820283568203CT21GENIChomozygous972922861
78356865483568655AT17GENIChomozygous972922862
78356865783568658TA16GENIChomozygous972922863
78356874483568745AG16GENIChomozygous972922864
78356909183569092GA24GENIChomozygous972922865
78356927283569273AG10GENIChomozygous972922866
78357093983570940CT13GENIChomozygous972922867
78357154283571543TG20GENIChomozygous972922868
78357207483572075CT20GENIChomozygous972922869
78357241383572414GC19GENIChomozygous972922870
78357313583573136CA19GENICpossibly homozygous972922871
78357557383575574TC8GENIChomozygous972922872
78357592183575922GA15GENIChomozygous972922873
78357616983576170TG10GENIChomozygous972922874
78357902083579021TC18GENIChomozygous972922875
78358005483580055AG12GENIChomozygous972922876
78358114783581148GA22GENIChomozygous972922877
78358150483581505GA41GENIChomozygous972922878
78358156183581562TG26GENIChomozygous972922879
78358222983582230GT24GENIChomozygous972922880