chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1232544839232544840TC8GENIChomozygous61121146
1232544882232544883AG15GENIChomozygous61121148
1232544952232544953CT14GENIChomozygous61121150
1232546081232546082CT25GENIChomozygous61121152
1232546229232546230GA28GENIChomozygous61121154
1232547061232547062AG10GENIChomozygous61121156
1232547235232547236GC6GENIChomozygous61121158
1232547242232547243T-4GENIChomozygous61121160
1232547709232547710TC13GENIChomozygous61121162
1232548299232548300TC20GENIChomozygous61121164
1232548432232548433AC8GENIChomozygous61121166
1232548787232548788AG21GENIChomozygous61121168
1232548895232548896GA14GENIChomozygous61121170
1232549254232549255TC21GENIChomozygous61121172
1232549907232549908GGAA11GENICpossibly homozygous61121174
1232549907232549908GGAAA11GENICheterozygous61322790
1232549969232549970AG15GENIChomozygous61121176
1232550964232550965CT13GENIChomozygous61121177
1232551166232551167AG17GENIChomozygous61121179
1232551232232551233TG19GENIChomozygous61121181
1232551334232551335TA15GENIChomozygous61121183
1232551824232551825CT13GENIChomozygous61121185
1232551848232551849GA22GENIChomozygous61121187
1232552646232552647TC15GENIChomozygous61121189
1232553039232553040TC25GENIChomozygous61121191
1232553124232553125CT25GENIChomozygous61121193
1232553190232553191GT21GENIChomozygous61121195
1232553281232553282AG20GENIChomozygous61121197
1232553314232553315GA18GENIChomozygous61121199
1232553354232553355GA17GENIChomozygous61121201
1232553390232553391CG15GENIChomozygous61121203