chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123987301339873014GA10GENIChomozygous50947270
123987341639873419TGT---12GENIChomozygous50947274
123987438939874390AG13GENIChomozygous50201969
123987458839874589CT15GENIChomozygous50201971
123987477739874778AG8GENIChomozygous50380989
123987499239874993GA25GENIChomozygous50201973
123987503739875039GT--17GENIChomozygous50201975
123987535039875351GGTC31GENIChomozygous50201989
123987539739875398AG26GENIChomozygous50201993
123987551239875514TA--28GENIChomozygous50201997
123987580939875810CT28GENIChomozygous50201999
123987634639876347GT15GENIChomozygous50947277
123987647439876475TTG14GENIChomozygous50947280
123987776539877766G-15GENICpossibly homozygous50512107
123987784539877846CT25GENIChomozygous50947283
123987827539878276A-12GENIChomozygous50202013
123987841339878414TTAC10GENIChomozygous50202015
123987776439877766GG--15GENICheterozygous50571474
123987533139875332GGGTGTGTGTGT25GENICheterozygous50655135
123987825339878254CCAAAAAAAAA14GENIChomozygous50558948
123987921239879213GA16GENIChomozygous50202021
123987949539879496AG31GENIChomozygous50202023
123988018739880213ACACACACACACACACACACACACAC--------------------------5GENIChomozygous50947286
123988071039880711C-15GENIChomozygous50202027
123988148139881482CG26GENIChomozygous50202030
123987860839878611AAA---5GENICheterozygous50543396