chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
58366083083660831CG12GENIChomozygous55510824
58366099283660993TC9GENICheterozygous55510826
58366100483661005TA3GENICheterozygous55510828
58366197983661980CA14GENIChomozygous55510834
58366265683662657AT5GENIChomozygous55510836
58366311783663118AG26GENICpossibly homozygous55510838
58366519683665197TC21GENIChomozygous55510840
58366576783665768TC27GENIChomozygous55510842
58366657683666577GA11GENIChomozygous55510844
58366674783666748GA15GENIChomozygous55510846
58366681583666816TA13GENIChomozygous55510848
58366727283667273CG15GENIChomozygous55510850
58366789983667900CT32GENICpossibly homozygous55510854
58366803583668036GA29GENIChomozygous55510856
58366810783668108GA31GENICpossibly homozygous55510858
58366923483669238TCTC----10GENIChomozygous55510860
58366926983669270G-24GENICpossibly homozygous55510862
58366970583669706TC21GENIChomozygous55510864
58366986983669871AA--9GENICpossibly homozygous55510866
58366996583669966AG19GENICpossibly homozygous55510868
58367076683670767AT21GENICpossibly homozygous55510870
58367082183670822TC20GENIChomozygous55510872
58367117883671179GA22GENIChomozygous55510874
58367245583672456AC25GENICpossibly homozygous55510876
58367268983672691TA--20GENIChomozygous55510878
58367298883672989AG28GENICpossibly homozygous55510880
58367505183675053CC--4GENICheterozygous55510882
58367505283675053C-4GENICheterozygous55510884
58367539883675399GA16GENICpossibly homozygous55510886
58367618883676189T-1GENIChomozygous55887664