chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
78356571683565717AT14GENIChomozygous115728966
78356593483565935AG20GENIChomozygous116205622
78356603683566037TC21GENIChomozygous116205624
78356714483567145TC6GENIChomozygous116205626
78356820283568203CT21GENIChomozygous116205628
78356865483568655AT17GENIChomozygous115728967
78356865783568658TA16GENIChomozygous118280775
78356874483568745AG16GENIChomozygous115728968
78356909183569092GA24GENIChomozygous116205630
78356927283569273AG10GENIChomozygous116205632
78357093983570940CT13GENIChomozygous116205636
78357154283571543TG20GENIChomozygous116205638
78357207483572075CT20GENIChomozygous116205640
78357241383572414GC19GENIChomozygous116205642
78357313583573136CA19GENICpossibly homozygous116205644
78357557383575574TC8GENIChomozygous115728971
78357592183575922GA15GENIChomozygous116205646
78357616983576170TG10GENIChomozygous116205648
78357902083579021TC18GENIChomozygous116205654
78358005483580055AG12GENIChomozygous116205656
78358114783581148GA22GENIChomozygous115728974
78358150483581505GA41GENIChomozygous116205658
78358156183581562TG26GENIChomozygous116205660
78358222983582230GT24GENIChomozygous116205662