chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172328969172328970AG16GENIChomozygous55842135
5172329205172329206TC22GENIChomozygous55842136
5172329346172329347AG13GENIChomozygous56195859
5172329883172329884GA23GENIChomozygous55842139
5172330034172330035AAGC12GENIChomozygous55842140
5172330158172330159GA24GENIChomozygous56195860
5172331228172331229TC27GENIChomozygous55842141
5172331443172331444AT21GENIChomozygous55842142
5172331664172331666GT--22GENIChomozygous55842144
5172331824172331826TG--21GENIChomozygous55842145
5172332813172332814GA23GENIChomozygous55842146
5172333426172333427AG17GENIChomozygous55842147
5172333457172333458CT24GENIChomozygous55842148
5172333704172333705CT12GENIChomozygous55842149
5172333872172333876TGAG----6GENIChomozygous55842150
5172333880172333881TTC7GENIChomozygous55842151
5172333881172333882GA7GENIChomozygous56465970
5172333884172333888TGTG----7GENIChomozygous55842152
5172333892172333897TGTAT-----7GENIChomozygous55842153
5172333902172333903AG5GENIChomozygous55842154
5172333916172333917GGTATGATGTCATA3GENIChomozygous56465971
5172333958172333959AATATATATATATATGTGTGTGTGTGTGTG3GENIChomozygous56465972
5172334093172334223TAAAAACACGTTGTTAGGGTTGGGGATTTAGCTCAGTGGTAGAGTGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGGGAAAAAAAAAAAAAAAAGAACAAAAAAAAAAAAAAAGAA----------------------------------------------------------------------------------------------------------------------------------18GENIChomozygous56365641
5172334245172334246GA9GENIChomozygous55842157
5172335178172335179GGAC19GENICheterozygous55842161
5172335459172335461CA--23GENIChomozygous56091656
5172335539172335540GGCACACACA12GENICheterozygous55842164
5172335539172335540GGCACACACACA12GENICpossibly homozygous56195861
5172335908172335909TC16GENIChomozygous55842166
5172336411172336412AG13GENIChomozygous55842168