chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1220773114220773115AG29GENIChomozygous108543074
1220773326220773327TC23GENIChomozygous108543076
1220773700220773701TC32GENIChomozygous108543078
1220774041220774042CT16GENIChomozygous108543080
1220774083220774084AG27GENIChomozygous108543082
1220774364220774365TC24GENIChomozygous108543084
1220774419220774420GA28GENIChomozygous108543086
1220774528220774529CT26GENIChomozygous108543088
1220775501220775502CT21GENIChomozygous108543090
1220775678220775679TC21GENIChomozygous108543092
1220776071220776072GT21GENIChomozygous108543094
1220776234220776235AG20GENIChomozygous108543096
1220776379220776380CT29GENIChomozygous108543098
1220777756220777757GA20GENIChomozygous108543100
1220778184220778289AAGAACAACAGGTGTGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTTCCCAGCTCTGCAAAAAAAAAAAAAA10GENIChomozygous127485597
1220778599220778600CA19GENIChomozygous108543102
1220779004220779005CT15GENIChomozygous108543103
1220779105220779105GCAGTGAGCGCC20GENIChomozygous127485598
1220779176220779176TTTGT10GENIChomozygous127485599
1220779232220779232A12GENIChomozygous127485600
1220779412220779413CG18GENIChomozygous108543105
1220780373220780374AC21GENIChomozygous108543107
1220780398220780399CT23GENIChomozygous108543109
1220780664220780665CG22GENIChomozygous108543111
1220781248220781249AG14GENIChomozygous108543113
1220781828220781828A11GENIChomozygous127485601
1220781928220781929AG24GENIChomozygous108543115
1220781983220781984AG23GENIChomozygous108543117
1220782658220782659TG19GENIChomozygous108543123
1220783546220783547GA21GENIChomozygous108543124
1220783927220783928AG21GENIChomozygous108543126
1220786008220786009AG22GENIChomozygous108543128
1220786192220786193TC23GENIChomozygous108543130
1220786877220786878TC19GENIChomozygous108543132