chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2240626970240626971CG20GENIChomozygous110334626
2240629350240629351TC18GENIChomozygous110334630
2240629475240629476TC13GENIChomozygous110334632
2240629823240629824AG12GENIChomozygous110334634
2240630554240630555CA21GENIChomozygous110334636
2240631606240631607TC22GENIChomozygous110334638
2240631792240631793GT15GENIChomozygous111289883
2240631800240631801TG17GENIChomozygous110632342
2240632450240632451TA17GENIChomozygous110334640
2240633212240633213AT33GENIChomozygous110334642
2240633781240633782GA44GENIChomozygous110334644
2240634792240634793TG31GENIChomozygous110334646
2240636244240636245AG16GENIChomozygous110334648
2240636537240636538TG20GENIChomozygous110334650
2240636763240636764GA34GENIChomozygous110334652
2240638992240638993GA27GENIChomozygous110334654
2240639143240639144GA30GENIChomozygous110334656
2240639524240639525TC20GENIChomozygous110334658
2240642613240642614AT14GENIChomozygous120131639
2240642744240642745CT7GENIChomozygous110334660
2240642780240642781GT12GENIChomozygous110334662
2240643623240643624AG18GENIChomozygous110334664
2240645839240645840GA30GENIChomozygous110334666
2240646082240646083GA24GENIChomozygous110334668
2240646549240646550GA28GENIChomozygous110334670
2240647279240647280AG24GENIChomozygous110334672
2240647404240647405CT19GENIChomozygous110334674
2240647967240647968CT18GENIChomozygous110334676
2240650194240650195AG58GENIChomozygous110334678
2240651673240651674AG18GENIChomozygous110334682
2240652833240652834AC38GENIChomozygous110334684