chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79973216699732167CT42GENIChomozygous115785938
79981096399810964AT27GENICheterozygous122829795
79981097399810974TC28GENICheterozygous122829796
79981210699812107TG23GENIChomozygous128560357
79982788899827889A71GENIChomozygous128499405
79980798599807986CG9GENICheterozygous130358540
79980804599808046GT8GENICheterozygous130358541
79980888099808881GA10GENICheterozygous130358542
79980892899808929AC10GENICheterozygous130358543
79980806399808064T10GENICheterozygous128499403
79982788099827880T71GENIChomozygous128499404
79984391299843912TTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGCAAGCA10GENIChomozygous128499406
79984762899847629TA70GENIChomozygous115785950
79984763299847633TC69GENIChomozygous115785952
79984763699847637TC69GENIChomozygous115785954
79984764199847642CA72GENIChomozygous115785956
79984766499847665TC68GENIChomozygous115785958
79984766899847669CG68GENIChomozygous116062689
79984766999847670CT67GENIChomozygous116062691
79984767199847672TC68GENIChomozygous118282293
79984767399847674CT67GENIChomozygous118282294
79984767899847679CT64GENIChomozygous115785960
79984767999847680CG64GENIChomozygous115785962