chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101351474613514747GA32GENIChomozygous142217837
101351518813515189TC26GENIChomozygous142217838
101351543613515437C25GENIChomozygous142196752
101351545113515452AC28GENIChomozygous142217839
101351656413516564AAGA19GENIChomozygous142196754
101351715413517155CT28GENIChomozygous142217840
101351816613518167TA8GENICheterozygous142217842
101351816813518169TA8GENICheterozygous142217843
101351822313518224AG13GENIChomozygous142217844
101351835413518355CT14GENIChomozygous142217845
101351855413518558TTTT11GENICheterozygous142196755
101351856313518563TC11GENICpossibly homozygous143429825
101351899813518999CT23GENIChomozygous142217846
101351919213519193TC12GENIChomozygous142217847
101351942913519430AC26GENIChomozygous142217849
101352241913522420GA23GENIChomozygous142217850
101352262013522620CA25GENIChomozygous142196757
101352304613523047AC18GENIChomozygous142217851
101352359913523600GA18GENIChomozygous142217852
101352465413524655GA23GENIChomozygous142217853
101352498913524990GA30GENIChomozygous142217854
101352506913525070CT28GENIChomozygous142217855
101352507613525077TG26GENIChomozygous142217856
101352530513525306GA26GENIChomozygous142217857
101352645613526457GA27GENIChomozygous142217858
101352694913526950AG23GENIChomozygous142217859
101352973413529735CT20GENIChomozygous142217860