chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6112463253112463254T-37GENIChomozygous54644430
6112464289112464290TG55GENICheterozygous55332139
6112464993112464995AC--10GENICpossibly homozygous54948161
6112466894112466908ACACACACACACAC--------------9GENICpossibly homozygous54948162
6112466963112466964TG36GENIChomozygous54644436
6112467132112467133CG50GENIChomozygous54644438
6112471865112471866GA39GENICpossibly homozygous54948163
6112472182112472183CT51GENIChomozygous54948164
6112472989112473003AAAAAAAAAAAAAA--------------5GENIChomozygous54948165
6112474697112474698AG36GENIChomozygous54644446
6112475234112475235GGA17GENICpossibly homozygous54644448
6112477255112477258TCC---40GENIChomozygous54644454
6112477978112477979GA39GENICheterozygous54948166
6112479267112479268GA45GENIChomozygous54948167
6112479737112479738GT35GENIChomozygous54948168
6112479914112479918AAAT----47GENIChomozygous54948169
6112480211112480212GA36GENICheterozygous54644456
6112482603112482604TC47GENIChomozygous54948171
6112482780112482781AG13GENICheterozygous54948172
6112482834112482835T-2GENIChomozygous54644460
6112485176112485188CTCTCTCTCTCT------------9GENICheterozygous54948173
6112489821112489822T-25GENIChomozygous54644464
6112490069112490070GGTGTGTA39GENIChomozygous54644466
6112490075112490076GA44GENICheterozygous54644468
6112492092112492093TA67GENIChomozygous54644470
6112492323112492324TC59GENIChomozygous54644472
6112492639112492640GT47GENICheterozygous55332141
6112493017112493018TC39GENIChomozygous54644474
6112493374112493375T-26GENICheterozygous55097224
6112494228112494229CT43GENIChomozygous54948174
6112496329112496330GT44GENICpossibly homozygous54948175
6112496785112496786G-40GENIChomozygous54948176
6112496872112496873CT50GENIChomozygous54948177
6112497383112497384AG41GENIChomozygous54644484