chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73476719334767195TC32GENICheterozygous131870570
73476914734769148CT55GENIChomozygous115642519
73476757734767578CT61GENIChomozygous115642516
73476817234768173CA55GENIChomozygous115642517
73476909334769094CG53GENIChomozygous115642518
73476786734767867CACTGAACC64GENIChomozygous128452018
73476821134768212A60GENIChomozygous128452019
73476932334769324AT68GENIChomozygous115642520
73476993034769931CT41GENIChomozygous115642521
73477088634770887AG61GENIChomozygous115642522
73477103134771032GA53GENIChomozygous115642523
73477203434772035TC61GENIChomozygous115642525
73477314634773147AG57GENIChomozygous115642526
73477434534774346TC53GENIChomozygous115642527
73477485234774853CT48GENIChomozygous115642528
73477665034776651CT62GENIChomozygous115642529
73477704834777049TG41GENIChomozygous115642530
73477716334777164AC57GENIChomozygous115642531
73477768634777687TC60GENIChomozygous115642532
73478279634782797AG37GENICheterozygous115642533
73478508634785087CG52GENIChomozygous115642534
73478607434786075CT55GENIChomozygous115642535
73478664334786644C54GENIChomozygous128452020
73478668834786689G49GENIChomozygous128452021
73478675934786760CG23GENIChomozygous118252814
73478676234786763AC23GENIChomozygous118252816
73478676634786767A21GENIChomozygous128452022
73478676934786770T21GENIChomozygous128452023