chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113772366937723670CG22GENIChomozygous51002531
113772384837723849CG28GENIChomozygous51002532
113772418237724184TG--24GENIChomozygous50931288
113772430337724304AATG22GENIChomozygous50931292
113772433737724338AG27GENIChomozygous50737212
113772434437724346TG--25GENIChomozygous50737213
113772442037724424TGTG----21GENIChomozygous51002533
113772453037724540TGTGTGTATA----------13GENIChomozygous50737216
113772455137724552GA13GENIChomozygous51002534
113772538237725383TC9GENIChomozygous51002535
113772584537725846AATT17GENIChomozygous51002536
113772586037725861TA18GENIChomozygous51160012
113772604037726041TC17GENIChomozygous51180432
113772626537726266AG17GENIChomozygous50737230
113772660637726607CT26GENIChomozygous51002537
113772670437726705CA21GENIChomozygous50737233
113772678437726786AA--26GENIChomozygous51002538
113772724337727244CT5GENIChomozygous51002541
113772816337728164TTCTC2GENIChomozygous51180436
113772825237728253AG19GENIChomozygous51002542
113772856837728569AG14GENIChomozygous50737252
113772858437728586AT--13GENIChomozygous50878017
113772979437729795TC14GENIChomozygous50737257
113773008737730088TC15GENIChomozygous50737261
113773012937730143CCTGTGTGGTTTCT--------------16GENIChomozygous51002543
113773033437730335CT26GENIChomozygous51002544
113773062837730629TTCCCCGGTCTGGAGACCCTTTCA21GENIChomozygous50737262
113773089537730896GA9GENIChomozygous51002545
113773098737730988GA18GENIChomozygous50737263
113773100137731002TC18GENIChomozygous50737264
113773131537731316GA26GENIChomozygous51002546
113773180037731801AG14GENIChomozygous51002547