chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1231808897231808898AG17GENIChomozygous61968472
1231809340231809342AC--3GENIChomozygous61117979
1231809932231809933CA25GENIChomozygous61968473
1231811797231811798TC13GENIChomozygous61117983
1231811824231811825TC14GENIChomozygous61117985
1231812025231812026TTA12GENICheterozygous61605863
1231812026231812027A-12GENICheterozygous61808612
1231812255231812256GT9GENIChomozygous61117987
1231812396231812397TA7GENICheterozygous61605867
1231812400231812401TA7GENICheterozygous61605868
1231812453231812454AG13GENIChomozygous61117998
1231814431231814432CT17GENIChomozygous61968474
1231814810231814811GGA19GENICheterozygous61118004
1231815176231815177TC29GENICpossibly homozygous61118006
1231815334231815335AG21GENIChomozygous61118008
1231815342231815343GA20GENIChomozygous61118010
1231816972231816973GGGT9GENICpossibly homozygous61118018
1231817003231817004GGT16GENICheterozygous61118020
1231817066231817067AATGTG21GENIChomozygous61118022
1231817562231817563TTTTG13GENIChomozygous61968475
1231817775231817776A-10GENIChomozygous61605873
1231818284231818285AG20GENIChomozygous61118030
1231818599231818600TC26GENIChomozygous61118032
1231819757231819758GT15GENIChomozygous61968476