chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8106876908106876909AG30GENIChomozygous138409235
8106877378106877378G11GENIChomozygous138263087
8106877501106877502TC17GENIChomozygous138409236
8106877998106877998T15GENIChomozygous138263088
8106878435106878436C17GENIChomozygous138263089
8106878903106878904AG16GENIChomozygous138409237
8106879257106879258TC18GENIChomozygous138409238
8106879427106879428AT21GENIChomozygous138409239
8106880006106880007TA26GENIChomozygous138409240
8106880809106880810GC16GENIChomozygous138409241
8106882125106882126CT16GENIChomozygous138409242
8106882163106882164TC18GENIChomozygous138409243
8106882855106882856TC22GENIChomozygous138409244
8106883052106883052T19GENIChomozygous138263090
8106883600106883601AG16GENIChomozygous138409245
8106883847106883848AG22GENIChomozygous138409246
8106884197106884198AG23GENIChomozygous138409247
8106884239106884240AG22GENIChomozygous138409248
8106885330106885330TGGGCGTCT14GENIChomozygous138263091
8106885535106885536TC22GENIChomozygous138409249
8106885546106885547GA26GENIChomozygous138409250
8106887324106887325G14GENIChomozygous138263092
8106887326106887331AAGAG14GENIChomozygous138263093
8106887573106887574AT17GENIChomozygous138409251
8106887708106887709AT11GENIChomozygous154538728
8106877385106877386TA11GENIChomozygous154538721
8106877385106877386TG11GENICheterozygous154538722
8106882749106882750TA10GENICheterozygous154538725
8106887708106887709A11GENICheterozygous140896605
8106882749106882750T10GENIChomozygous403248240
8106887861106887862G17GENIChomozygous138263094
8106887865106887866CT17GENIChomozygous138409252
8106887952106887953TC9GENIChomozygous138409253
8106889012106889013AG14GENIChomozygous138409254
8106889085106889085AG18GENIChomozygous138263095