chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79553218695532187GGGAGA12GENIChomozygous54989464
79553430095534301TTTC9GENICheterozygous54989466
79553445895534459AC24GENIChomozygous54029830
79553446895534469GT24GENIChomozygous54029831
79553449595534496GC26GENIChomozygous54029832
79553450395534504AC27GENIChomozygous54029833
79553451395534514AC26GENIChomozygous54029834
79553452095534521AC24GENIChomozygous54029835
79553455195534552AC19GENIChomozygous54029836
79553459495534595AATCCTCAGGCCATGGAGATG30GENIChomozygous54989468
79554481195544815TAGA----6GENIChomozygous54989474
79554881995548821GA--7GENICheterozygous54989476
79555993495559936TG--16GENICheterozygous54989478
79556169295561693C-8GENICpossibly homozygous54029947
79557142395571425AC--4GENICheterozygous54989482
79557695095576951CCT11GENICheterozygous55059218
79558098295580984CT--7GENICheterozygous54989484
79559022495590225T-5GENIChomozygous54030008
79560048495600485AAGTGTGT4GENICheterozygous54030042
79560842695608427GA4GENIChomozygous54030057
79560845495608455CT7GENIChomozygous54030059
79560845695608457GC7GENIChomozygous54030060
79560976695609767T-9GENICheterozygous54989488
79560480595604806A-15GENICheterozygous54487770
79561142095611421T-11GENICheterozygous55059219
79561699295616993TTAAAA1GENIChomozygous54989490
79562034795620348CCGT3GENICheterozygous54989494