chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109216387109216389GT--21GENICpossibly homozygous727137322
6109216449109216450AC20GENICpossibly homozygous598311442
6109216711109216712CG9GENIChomozygous598311443
6109217708109217709GA15GENIChomozygous598311444
6109218132109218133GA5GENIChomozygous598311445
6109218533109218534TC10GENIChomozygous596421227
6109218971109218972CG19GENIChomozygous598311446
6109219644109219645CG3GENIChomozygous598311447
6109219668109219669TC4GENIChomozygous598311448
6109219684109219685GGTCGTTTGGTCAGTTTC1GENIChomozygous727137323
6109219945109219946GA28GENIChomozygous598311449
6109220171109220172AG14GENICpossibly homozygous596421228
6109221203109221204T-1GENIChomozygous727137324
6109221479109221480AG17GENIChomozygous596421229
6109222377109222378TTTGTTTTATTTAATAACCCA3GENICheterozygous727137327
6109225632109225633TC20GENIChomozygous596421230
6109225969109225970GC12GENICheterozygous596421231
6109226303109226304G-27GENIChomozygous727137328
6109226869109226870T-7GENIChomozygous727137329
6109227301109227302CCTGTT1GENIChomozygous727137331
6109227384109227385TC17GENICpossibly homozygous596421232
6109227512109227513TA16GENIChomozygous598311450
6109228010109228011GA19GENICpossibly homozygous598311451