chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8106876908106876909AG49GENIChomozygous138409235
8106877378106877378G30GENIChomozygous138263087
8106877501106877502TC43GENIChomozygous138409236
8106877998106877998T47GENIChomozygous138263088
8106878435106878436C47GENIChomozygous138263089
8106878903106878904AG45GENIChomozygous138409237
8106879257106879258TC43GENIChomozygous138409238
8106879427106879428AT35GENIChomozygous138409239
8106880006106880007TA40GENIChomozygous138409240
8106880809106880810GC50GENIChomozygous138409241
8106877385106877386TA34GENIChomozygous154538721
8106877385106877386TG34GENICheterozygous154538722
8106882125106882126CT37GENIChomozygous138409242
8106882163106882164TC42GENIChomozygous138409243
8106882749106882750TA17GENICheterozygous154538725
8106882855106882856TC34GENIChomozygous138409244
8106883052106883052T29GENICpossibly homozygous138263090
8106883600106883601AG23GENIChomozygous138409245
8106883847106883848AG39GENIChomozygous138409246
8106884197106884198AG52GENIChomozygous138409247
8106884239106884240AG47GENIChomozygous138409248
8106885330106885330TGGGCGTCT33GENIChomozygous138263091
8106885535106885536TC41GENIChomozygous138409249
8106885546106885547GA40GENIChomozygous138409250
8106882749106882750T17GENICheterozygous403248240
8106887324106887325G40GENIChomozygous138263092
8106887326106887331AAGAG40GENIChomozygous138263093
8106887573106887574AT34GENIChomozygous138409251
8106887708106887709A40GENICheterozygous140896605
8106887708106887709AT40GENICpossibly homozygous154538728
8106887861106887862G33GENIChomozygous138263094
8106887865106887866CT33GENIChomozygous138409252
8106887952106887953TC30GENIChomozygous138409253
8106889012106889013AG42GENIChomozygous138409254
8106889085106889085AG49GENIChomozygous138263095