chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56829939168299392C-1GENIChomozygous56159514
56830016668300167TG10GENICheterozygous55450275
56830030468300305GA5GENIChomozygous56159518
56830183368301834AG3GENIChomozygous55450290
56830227468302275TC11GENICpossibly homozygous55450299
56830369868303699TTA2GENICheterozygous55450309
56830609368306094CT9GENIChomozygous55450324
56830702968307030GC13GENIChomozygous55450330
56830783968307845GGAACT------8GENIChomozygous55450332
56830985668309857GA16GENICpossibly homozygous55450344
56831063868310639CT16GENIChomozygous56882714
56830645468306455CT25GENIChomozygous56882706
56830732068307321GA29GENICpossibly homozygous56882708
56831080268310803AC17GENICpossibly homozygous55450353
56831273468312735CCT5GENICheterozygous56882716
56831390968313910AG14GENICpossibly homozygous55450379
56831410968314110CT13GENIChomozygous56882718
56831607668316077CG2GENICheterozygous56882720
56831613468316214CAGACTGCCTCCAGGCCAGCATCTTCCTGAGTGTGGTAGGCAGACTGCCTCCAGGCCAGTATCTCTCTGAATGTGGTACC--------------------------------------------------------------------------------3GENICheterozygous56882722
56832016868320169A-1GENIChomozygous55450421
56832136168321362CT12GENICheterozygous56882724
56832144368321444CT23GENICpossibly homozygous56882726
56832338168323382G-12GENICpossibly homozygous55450440
56832788868327889TC17GENIChomozygous55450476
56832889368328898TTTGT-----1GENIChomozygous56882730
56833071668330717GT16GENIChomozygous56882732
56833241068332411GT25GENIChomozygous55450511
56833463868334639GA16GENIChomozygous56882734
56833609568336096CCCT9GENICheterozygous56882736
56833694168336942T-1GENIChomozygous56701986
56833736968337370G-2GENIChomozygous56668075
56833796768337968T-7GENIChomozygous55450556
56833905768339058GA20GENIChomozygous56882738