chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135526698255266983GT42INTERGENICpossibly homozygous809060621
135526700255267003GA38INTERGENICpossibly homozygous809060622
135526745555267456TG41INTERGENICheterozygous809060623
135526797155267972AC7INTERGENIChomozygous809060624
135526950355269504AG90INTERGENICheterozygous809060625
135526950555269506AG85INTERGENICheterozygous809060626
135527051855270519CG30INTERGENIChomozygous809060627
135527055855270559TA43INTERGENIChomozygous809060628
135527059155270592CT43INTERGENIChomozygous809060629
135527074455270745GT45INTERGENIChomozygous809060630
135527093955270940TC56INTERGENIChomozygous809060631
135527108355271084GT49INTERGENIChomozygous809060632
135527108955271090GA49INTERGENIChomozygous809060633
135527110555271106GC41INTERGENIChomozygous809060634
135527141355271414TC46INTERGENIChomozygous809060635
135527143255271433AG52INTERGENIChomozygous809060636
135527170555271706GT43INTERGENIChomozygous809060637
135527182555271826CT48INTERGENICpossibly homozygous809060638
135527186055271861CG50INTERGENIChomozygous809060639
135527198355271984TA41INTERGENIChomozygous809060640
135527210355272104AG46INTERGENIChomozygous809060641
135527216155272162AG47INTERGENICpossibly homozygous809060642
135527265155272652AG50INTERGENIChomozygous809060643
135527265555272656AC50INTERGENICpossibly homozygous809060644
135527285655272857AG34INTERGENIChomozygous809060645
135527304555273046AG20INTERGENIChomozygous809060646
135527329955273300CT43INTERGENIChomozygous809060647
135527372555273726AC60GENIChomozygous809060648
135527631055276311GA80GENIChomozygous809060649
135528086855280869GA16GENIChomozygous809060650
135528155455281555GA55GENIChomozygous809060651
135528363155283632TC51GENIChomozygous809060652
135528406455284065CT44GENIChomozygous809060653
135528576055285761GT50GENIChomozygous809060654