chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108928342989283430AT5GENIChomozygous51536970
108928444889284449GA17GENIChomozygous51536972
108928477889284779GA19GENIChomozygous51536973
108928548389285484CT20GENIChomozygous51536974
108928555989285560GA25GENIChomozygous51536975
108928637089286371AC10GENIChomozygous51536976
108928725289287253TC24GENICpossibly homozygous51536978
108928777589287776AT3GENIChomozygous51536979
108928782389287824AG5GENICheterozygous51536980
108928849489288495TG14GENIChomozygous51536981
108928859689288597TA6GENIChomozygous51536982
108928860189288602T-4GENIChomozygous51536983
108928965189289652GGTCTC8GENICheterozygous52072722
108929045389290454AG19GENICpossibly homozygous51536985
108929046889290469AG18GENICpossibly homozygous51536986
108929108789291088AG15GENICpossibly homozygous51536987
108929108989291090GA14GENICpossibly homozygous51536988
108929136989291370TC15GENICpossibly homozygous51536989