chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101351474613514747GA63GENIChomozygous142217837
101351518813515189TC56GENIChomozygous142217838
101351543613515437C61GENIChomozygous142196752
101351545113515452AC65GENIChomozygous142217839
101351656413516564AAGA32GENIChomozygous142196754
101351715413517155CT69GENIChomozygous142217840
101351816413518165TA17GENICheterozygous142217841
101351816613518167TA15GENICheterozygous142217842
101351816813518169TA15GENICheterozygous142217843
101351822313518224AG32GENIChomozygous142217844
101351835413518355CT41GENIChomozygous142217845
101351899813518999CT63GENIChomozygous142217846
101351919213519193TC50GENIChomozygous142217847
101351942913519430AC70GENIChomozygous142217849
101352241913522420GA59GENIChomozygous142217850
101352262013522620CA56GENICpossibly homozygous142196757
101352304613523047AC60GENIChomozygous142217851
101352359913523600GA79GENIChomozygous142217852
101352465413524655GA74GENIChomozygous142217853
101352498913524990GA62GENIChomozygous142217854
101351856313518563TC15GENIChomozygous143429825
101351816413518165T17GENICheterozygous403631738
101352506913525070CT57GENIChomozygous142217855
101352507613525077TG52GENIChomozygous142217856
101352530513525306GA65GENIChomozygous142217857
101352645613526457GA77GENIChomozygous142217858
101352694913526950AG86GENIChomozygous142217859
101352973413529735CT67GENIChomozygous142217860