chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1231809346231809348AC--12GENICpossibly homozygous748072595
1231811290231811294ATAC----14GENIChomozygous748072596
1231811797231811798TC28GENIChomozygous635390655
1231811824231811825TC26GENIChomozygous635390656
1231812453231812454AG28GENIChomozygous635390657
1231813110231813112TT--20GENICpossibly homozygous748072598
1231813111231813112T-20GENICheterozygous748072599
1231813549231813550GA29GENIChomozygous635390658
1231814810231814811GGA24GENICheterozygous748072601
1231815067231815071AAAG----8GENICheterozygous748072602
1231815176231815177TC26GENIChomozygous635390659
1231815334231815335AG31GENIChomozygous635390660
1231815342231815343GA31GENIChomozygous635390661
1231815550231815551GA45GENIChomozygous635390662
1231815839231815845ACACAC------12GENICheterozygous748072603
1231815843231815845AC--12GENICpossibly homozygous748072604
1231816099231816109TCTCTCTCTC----------9GENICpossibly homozygous748072607
1231817003231817004GGTGTGTGTGTGTGTGT10GENICheterozygous748072609
1231817007231817009CA--13GENICheterozygous748072610
1231817066231817067AATGTG19GENIChomozygous748072611
1231817462231817463TC26GENIChomozygous635390663
1231817774231817775CCA21GENICheterozygous748072613
1231817774231817775CCAA21GENICpossibly homozygous748072614
1231818284231818285AG46GENIChomozygous635390664
1231818599231818600TC32GENIChomozygous635390665
1231819317231819318GA52GENIChomozygous635390666