chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1105206707105206708TA12INTERGENIChomozygous76081627
1105207287105207288AG5INTERGENIChomozygous76081628
1105207835105207836TG14INTERGENIChomozygous74289289
1105210385105210386TG12INTERGENIChomozygous76081629
1105208297105208298TC7INTERGENIChomozygous76365627
1105207883105207884AG6INTERGENIChomozygous75106117
1105212731105212732AG7INTERGENIChomozygous74289301
1105213107105213108AT7INTERGENIChomozygous75106125
1105214863105214864TA16INTERGENIChomozygous75106128
1105215176105215177GA14INTERGENIChomozygous76081632
1105215323105215324GA10INTERGENIChomozygous76081633
1105215725105215726TG7INTERGENIChomozygous74289304
1105215950105215951CT15INTERGENIChomozygous74289307
1105216333105216334CA21INTERGENIChomozygous74289310
1105216873105216874GA7INTERGENIChomozygous76081636
1105216921105216922GT6INTERGENIChomozygous76081637
1105217622105217623CT12INTERGENIChomozygous76081639
1105217732105217733TC13INTERGENIChomozygous76081640
1105220058105220059AG2INTERGENIChomozygous74289316
1105220274105220275AG6INTERGENIChomozygous76081641
1105220536105220537GT12INTERGENIChomozygous76081642
1105220868105220869TC14INTERGENIChomozygous76081643
1105220872105220873CG12INTERGENIChomozygous76081644
1105220979105220980GC7INTERGENIChomozygous76081645
1105221230105221231CG5INTERGENIChomozygous74289319
1105221862105221863TC8INTERGENIChomozygous76081646
1105222620105222621AC11INTERGENIChomozygous76081647
1105223581105223582CG15INTERGENIChomozygous76081648
1105214328105214329TC14INTERGENICpossibly homozygous76685367
1105214554105214555CT15INTERGENIChomozygous76685368