chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117255687117255688TC10GENIChomozygous52829587
8117255982117255983TC32GENIChomozygous52829588
8117256146117256148TC--29GENIChomozygous52829589
8117256438117256439GC31GENIChomozygous52829590
8117256714117256715T-39GENIChomozygous52829592
8117256717117256719TT--40GENIChomozygous52829594
8117256819117256820GA20GENIChomozygous52829595
8117256878117256879A-24GENIChomozygous52829596
8117257551117257552GGGGT1GENIChomozygous52829599
8117257640117257641A-21GENIChomozygous53523827
8117257645117257646AG21GENIChomozygous53523829
8117258176117258177AAAAACAGGGCTGGAGTGGTGGCTCAGTGGTTAAGAGCACTGACTGCTCTCCCAGAGGTCCTGAGTT4GENIChomozygous53411533
8117258274117258275AG18GENIChomozygous52829603
8117258417117258418CT28GENIChomozygous53051997
8117258431117258432AG30GENIChomozygous53051999
8117258517117258533TTTTTTTTTTTTTTTT----------------28GENIChomozygous53052001
8117260482117260483TC25GENIChomozygous52829605
8117266619117266620T-19GENICpossibly homozygous53222801
8117256721117256722TG40GENIChomozygous53368066
8117257002117257003GA40GENIChomozygous53222797
8117257051117257052GA35GENIChomozygous53222798
8117260291117260292CT29GENIChomozygous53222800
8117267943117267945TT--14GENICheterozygous53454680
8117267944117267945T-14GENICheterozygous53454682
8117268778117268779CCGT8GENICheterozygous53523831