chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
58366073483660738TTTT----16GENIChomozygous55510818
58366083083660831CG20GENIChomozygous55510824
58366099283660993TC22GENIChomozygous55510826
58366100483661005TA24GENIChomozygous55510828
58366178983661790TTTC3GENICheterozygous55510832
58366178983661790TTTCTCTC3GENICheterozygous56430371
58366197983661980CA18GENIChomozygous55510834
58366311783663118AG35GENIChomozygous55510838
58366519683665197TC37GENIChomozygous55510840
58366576783665768TC36GENIChomozygous55510842
58366657683666577GA20GENIChomozygous55510844
58366674783666748GA20GENIChomozygous55510846
58366681583666816TA22GENIChomozygous55510848
58366727283667273CG18GENIChomozygous55510850
58366747483667475TTATA23GENIChomozygous55510852
58366789983667900CT35GENIChomozygous55510854
58366803583668036GA28GENIChomozygous55510856
58366810783668108GA33GENIChomozygous55510858
58366432783664331GTGT----6GENIChomozygous56220898
58366923483669238TCTC----26GENIChomozygous55510860
58366926983669270G-26GENIChomozygous55510862
58366970583669706TC30GENIChomozygous55510864
58366996583669966AG29GENIChomozygous55510868
58367076683670767AT20GENIChomozygous55510870
58367082183670822TC22GENIChomozygous55510872
58367117883671179GA32GENIChomozygous55510874
58367245583672456AC21GENIChomozygous55510876
58367268983672691TA--23GENIChomozygous55510878
58367298883672989AG26GENIChomozygous55510880
58367505083675053CCC---14GENIChomozygous56220899
58367539883675399GA34GENIChomozygous55510886
58367591383675931ATGCGTGTGTGTGTGTGT------------------11GENICheterozygous55510888
58367591383675925ATGCGTGTGTGT------------11GENICheterozygous55510890
58367618883676189T-20GENICpossibly homozygous55887664
58366987083669871A-23GENICpossibly homozygous56318915