chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73476757734767578CT62GENIChomozygous115642516
73476786734767867CACTGAACC69GENIChomozygous128452018
73476817234768173CA60GENIChomozygous115642517
73476821134768212A59GENIChomozygous128452019
73476909334769094CG43GENIChomozygous115642518
73476914734769148CT43GENIChomozygous115642519
73476932334769324AT53GENIChomozygous115642520
73476993034769931CT59GENIChomozygous115642521
73477088634770887AG48GENIChomozygous115642522
73477103134771032GA54GENIChomozygous115642523
73477203434772035TC61GENIChomozygous115642525
73477314634773147AG55GENIChomozygous115642526
73477434534774346TC57GENICpossibly homozygous115642527
73477485234774853CT53GENIChomozygous115642528
73477665034776651CT62GENIChomozygous115642529
73477704834777049TG59GENICpossibly homozygous115642530
73477716334777164AC47GENICpossibly homozygous115642531
73477768634777687TC43GENIChomozygous115642532
73478279634782797AG29GENICpossibly homozygous115642533
73478508634785087CG56GENIChomozygous115642534
73478664334786644C38GENIChomozygous128452020
73478668834786689G38GENIChomozygous128452021
73478676634786767A25GENIChomozygous128452022
73478676934786770T24GENIChomozygous128452023
73478607434786075CT57GENIChomozygous115642535
73478675934786760CG26GENIChomozygous118252814
73478676234786763AC25GENIChomozygous118252816