chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228235223228235224CT8GENIChomozygous61106850
1228235542228235543TG6GENICheterozygous61106851
1228235599228235600CT6GENIChomozygous61603431
1228236119228236120CA4GENIChomozygous61106852
1228236430228236431GGA10GENICheterozygous61603432
1228236972228236973GA5GENIChomozygous61603434
1228237551228237552CA5GENIChomozygous61106856
1228240584228240585CA4GENIChomozygous61603435
1228242140228242141AG18GENICpossibly homozygous61603438
1228243111228243112GA15GENICpossibly homozygous61603439
1228243790228243791TC7GENIChomozygous61106866
1228243797228243798TC7GENIChomozygous61106867
1228244009228244010CA7GENIChomozygous61603442
1228244111228244112GA7GENIChomozygous61106868
1228244222228244223CA8GENICpossibly homozygous61106869
1228244486228244487GA6GENICheterozygous61603443
1228244491228244492A-5GENIChomozygous61603444
1228245165228245166GA13GENIChomozygous61106871
1228245521228245522GT12GENIChomozygous61106873
1228245701228245702AG8GENIChomozygous61603445
1228245900228245901GA12GENICpossibly homozygous61603446
1228246120228246121TA11GENICpossibly homozygous61106874
1228246677228246678CT5GENIChomozygous61603448
1228246680228246681CA6GENIChomozygous61603449
1228248552228248553CT7GENICpossibly homozygous61603450
1228248622228248623GT9GENICpossibly homozygous61603451
1228248681228248682TC11GENICheterozygous61106878
1228250431228250432G-9GENIChomozygous61603453
1228251364228251371TGGGATC-------1GENIChomozygous61603454
1228251821228251822TTAA1GENIChomozygous61321792
1228252043228252044TC16GENICpossibly homozygous61106885
1228252683228252685AA--1GENIChomozygous61106888
1228253180228253181TC4GENIChomozygous61106889
1228254209228254210CG20GENICpossibly homozygous62485919