chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1232544839232544840TC19GENIChomozygous61121146
1232544882232544883AG18GENIChomozygous61121148
1232544952232544953CT15GENIChomozygous61121150
1232546081232546082CT7GENICpossibly homozygous61121152
1232546229232546230GA7GENICheterozygous61121154
1232546305232546306GA11GENICpossibly homozygous61606207
1232547061232547062AG19GENIChomozygous61121156
1232547235232547236GC6GENICheterozygous61121158
1232547709232547710TC9GENICpossibly homozygous61121162
1232548299232548300TC19GENIChomozygous61121164
1232548432232548433AC18GENICheterozygous61121166
1232548787232548788AG12GENIChomozygous61121168
1232548895232548896GA8GENICpossibly homozygous61121170
1232549254232549255TC19GENICpossibly homozygous61121172
1232549969232549970AG12GENIChomozygous61121176
1232550964232550965CT5GENIChomozygous61121177
1232551056232551057CA15GENIChomozygous61606210
1232551166232551167AG18GENICpossibly homozygous61121179
1232551232232551233TG12GENIChomozygous61121181
1232551334232551335TA17GENIChomozygous61121183
1232551824232551825CT18GENIChomozygous61121185
1232551848232551849GA10GENICpossibly homozygous61121187
1232552646232552647TC12GENIChomozygous61121189
1232553039232553040TC13GENIChomozygous61121191
1232553124232553125CT12GENIChomozygous61121193
1232553190232553191GT7GENICpossibly homozygous61121195
1232553279232553280AG3GENIChomozygous61606212
1232553281232553282AG2GENIChomozygous61121197
1232553285232553286TA2GENIChomozygous62103515
1232553286232553287TC2GENIChomozygous62103516
1232553354232553355GA14GENIChomozygous61121201
1232553390232553391CG11GENIChomozygous61121203