chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8106876908106876909AG34GENIChomozygous138409235
8106877385106877386TA14GENICheterozygous154538721
8106877385106877386TG14GENIChomozygous154538722
8106880212106880213TC37GENIChomozygous145673786
8106877998106877998T38GENIChomozygous138263088
8106878435106878436C44GENIChomozygous138263089
8106879257106879258TC63GENIChomozygous138409238
8106879427106879428AT44GENIChomozygous138409239
8106880006106880007TA50GENIChomozygous138409240
8106880174106880175AG39GENIChomozygous145673784
8106880192106880193AG37GENIChomozygous145673785
8106880213106880214GA38GENIChomozygous145673787
8106882749106882750TA35GENIChomozygous154538725
8106882869106882870AC55GENIChomozygous145673788
8106883600106883601AG37GENIChomozygous138409245
8106883847106883848AG43GENIChomozygous138409246
8106884197106884198AG41GENIChomozygous138409247
8106884239106884240AG45GENIChomozygous138409248
8106884284106884285CT50GENIChomozygous145673789
8106885330106885330TGGGCGTCT29GENIChomozygous138263091
8106885535106885536TC37GENIChomozygous138409249
8106885536106885537GA36GENIChomozygous145673790
8106885645106885646CA41GENICpossibly homozygous145673791
8106887573106887574AT31GENIChomozygous138409251
8106887708106887709A25GENICpossibly homozygous140896605
8106887708106887709AT25GENICheterozygous154538728
8106887795106887796TC42GENIChomozygous145673792
8106887865106887866CT31GENIChomozygous138409252
8106887952106887953TC31GENIChomozygous138409253
8106888430106888431GA25GENIChomozygous145673793
8106888506106888507GA29GENIChomozygous145673794
8106889012106889013AG28GENIChomozygous138409254
8106889085106889085AG34GENIChomozygous138263095
8106882754106882754A30GENIChomozygous145647974
8106882749106882750T35GENICheterozygous403248240