chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109215150109215162ACACACACACAC------------7GENIChomozygous739580005
6109215292109215293AG16GENIChomozygous621950858
6109215591109215592GGT30GENIChomozygous739580008
6109215956109215957CT28GENIChomozygous621950859
6109216387109216389GT--25GENIChomozygous739580009
6109217437109217438GA18GENIChomozygous621950860
6109217869109217870CCTT7GENIChomozygous739580011
6109218078109218079TG14GENIChomozygous621950861
6109218533109218534TC27GENIChomozygous621950862
6109219613109219614T-6GENIChomozygous739580014
6109219644109219645CG2GENIChomozygous621950863
6109220143109220144AAGTTGTTGTTGTTGTTGTT22GENIChomozygous739580015
6109220171109220172AG31GENIChomozygous621950864
6109220957109220958T-20GENIChomozygous739580018
6109220959109220971TATACATGTTAT------------22GENIChomozygous739580019
6109221202109221203AATTTTT16GENICpossibly homozygous739580021
6109221479109221480AG22GENIChomozygous621950865
6109222374109222375TTTCCAGCCC20GENIChomozygous739580022
6109222377109222378TTTGTTTTATTTAATAACCCA7GENIChomozygous739580023
6109224345109224346CCTT2GENICheterozygous739580024
6109224345109224346CCTTT2GENICheterozygous739580025
6109224503109224504CT9GENIChomozygous621950866
6109225632109225633TC30GENIChomozygous621950867
6109225969109225970GC18GENIChomozygous621950868
6109226303109226304G-17GENIChomozygous739580026
6109226595109226596GA24GENIChomozygous621950869
6109226868109226869CCT16GENIChomozygous739580028
6109227028109227029AAGTGTGT5GENIChomozygous739580029
6109227068109227069AT5GENIChomozygous621950870
6109227093109227094CCAG5GENICheterozygous739580030
6109227291109227292CCTGTTT14GENIChomozygous739580032
6109227301109227302CCTGTTTGTTTGTT15GENIChomozygous739580035
6109227384109227385TC20GENICpossibly homozygous621950871
6109227502109227503GA21GENIChomozygous621950872
6109227690109227691AT11GENIChomozygous621950873
6109227989109227990AG26GENIChomozygous621950874