chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8106876908106876909AG51GENIChomozygous138409235
8106877378106877378G33GENIChomozygous138263087
8106877501106877502TC37GENIChomozygous138409236
8106877998106877998T55GENIChomozygous138263088
8106878435106878436C48GENIChomozygous138263089
8106878903106878904AG48GENIChomozygous138409237
8106879257106879258TC58GENIChomozygous138409238
8106879427106879428AT49GENIChomozygous138409239
8106880006106880007TA57GENIChomozygous138409240
8106880809106880810GC63GENIChomozygous138409241
8106877385106877386TA36GENIChomozygous154538721
8106877385106877386TG36GENICheterozygous154538722
8106882125106882126CT53GENIChomozygous138409242
8106882163106882164TC61GENIChomozygous138409243
8106882749106882750TA27GENICheterozygous154538725
8106882855106882856TC54GENIChomozygous138409244
8106883052106883052T33GENICpossibly homozygous138263090
8106883600106883601AG61GENIChomozygous138409245
8106883847106883848AG56GENIChomozygous138409246
8106884197106884198AG38GENIChomozygous138409247
8106884239106884240AG37GENIChomozygous138409248
8106885330106885330TGGGCGTCT35GENIChomozygous138263091
8106885535106885536TC43GENIChomozygous138409249
8106885546106885547GA46GENIChomozygous138409250
8106882748106882750AT27GENICheterozygous147268161
8106882749106882750T27GENICpossibly homozygous403248240
8106887573106887574AT37GENIChomozygous138409251
8106887708106887709AT42GENICpossibly homozygous154538728
8106887865106887866CT34GENIChomozygous138409252
8106887952106887953TC28GENIChomozygous138409253
8106887708106887709A42GENICheterozygous140896605
8106887324106887325G39GENIChomozygous138263092
8106887326106887331AAGAG39GENIChomozygous138263093
8106887861106887862G36GENIChomozygous138263094
8106889012106889013AG38GENIChomozygous138409254
8106889085106889085AG37GENIChomozygous138263095