chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1105206464105206466AG9INTERGENIChomozygous76081626
1105206707105206708TA19INTERGENIChomozygous76081627
1105207287105207288AG9INTERGENIChomozygous76081628
1105207835105207836TG8INTERGENIChomozygous74289289
1105207883105207884AG20INTERGENIChomozygous75106117
1105210385105210386TG24INTERGENIChomozygous76081629
1105211224105211224A4INTERGENIChomozygous76081630
1105212359105212359T21INTERGENICheterozygous76081631
1105212731105212732AG15INTERGENIChomozygous74289301
1105213107105213108AT20INTERGENIChomozygous75106125
1105214863105214864TA14INTERGENIChomozygous75106128
1105215176105215177GA18INTERGENIChomozygous76081632
1105215323105215324GA15INTERGENIChomozygous76081633
1105215725105215726TG17INTERGENIChomozygous74289304
1105215774105215775A7INTERGENICheterozygous76081634
1105216333105216334CA10INTERGENIChomozygous74289310
1105216335105216335C10INTERGENIChomozygous76081635
1105216873105216874GA17INTERGENIChomozygous76081636
1105216921105216922GT10INTERGENIChomozygous76081637
1105217349105217350T18INTERGENICheterozygous76081638
1105217622105217623CT20INTERGENIChomozygous76081639
1105217732105217733TC13INTERGENIChomozygous76081640
1105220058105220059AG11INTERGENIChomozygous74289316
1105220274105220275AG13INTERGENIChomozygous76081641
1105220536105220537GT13INTERGENIChomozygous76081642
1105220868105220869TC8INTERGENIChomozygous76081643
1105220872105220873CG12INTERGENIChomozygous76081644
1105220979105220980GC20INTERGENIChomozygous76081645
1105221230105221231CG15INTERGENIChomozygous74289319
1105221862105221863TC19INTERGENIChomozygous76081646
1105222620105222621AC14INTERGENIChomozygous76081647
1105223581105223582CG12INTERGENIChomozygous76081648
1105224017105224018AG5INTERGENIChomozygous76081649