chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109215156109215160ACAC----3GENIChomozygous694083459
6109216387109216389GT--20GENIChomozygous694083461
6109216449109216450AC17GENIChomozygous532490070
6109216711109216712CG13GENIChomozygous532490071
6109217708109217709GA13GENIChomozygous532490072
6109217869109217870CCT7GENICheterozygous694083462
6109217869109217870CCTT7GENICheterozygous694083463
6109218078109218079TG16GENIChomozygous532490073
6109218132109218133GA13GENIChomozygous532490074
6109218533109218534TC7GENIChomozygous529627474
6109218971109218972CG9GENIChomozygous532490075
6109219610109219611T-2GENIChomozygous694083464
6109219644109219645CG3GENIChomozygous532490076
6109219945109219946GA21GENIChomozygous532490077
6109220171109220172AG13GENIChomozygous529627475
6109221479109221480AG17GENIChomozygous529627476
6109224251109224252CT23GENIChomozygous532490078
6109224345109224346CCTTT9GENICheterozygous694083465
6109224345109224346CCTT9GENICpossibly homozygous694083466
6109224503109224504CT29GENICpossibly homozygous529627477
6109225632109225633TC24GENIChomozygous529627478
6109225969109225970GC18GENIChomozygous529627479
6109226303109226304G-11GENIChomozygous694083467
6109226869109226870T-16GENIChomozygous694083469
6109227067109227069GA--3GENIChomozygous694083470
6109227093109227094CCAG1GENIChomozygous694083471
6109227125109227126TG6GENICheterozygous532490079
6109227134109227135GA5GENICheterozygous532490080
6109227301109227302C-18GENICheterozygous694083472
6109227301109227302CCTGTT13GENIChomozygous694083473
6109227384109227385TC18GENIChomozygous529627480
6109227512109227513TA13GENIChomozygous532490081
6109228010109228011GA20GENIChomozygous532490082