chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1232544839232544840TC34GENIChomozygous61121146
1232544882232544883AG25GENIChomozygous61121148
1232544952232544953CT21GENIChomozygous61121150
1232545776232545777AG23GENIChomozygous61606206
1232546081232546082CT36GENIChomozygous61121152
1232546229232546230GA26GENIChomozygous61121154
1232546305232546306GA31GENIChomozygous61606207
1232547061232547062AG22GENIChomozygous61121156
1232547235232547236GC20GENIChomozygous61121158
1232547241232547243TT--19GENIChomozygous61322789
1232547709232547710TC18GENIChomozygous61121162
1232548299232548300TC22GENIChomozygous61121164
1232548432232548433AC24GENIChomozygous61121166
1232548787232548788AG16GENIChomozygous61121168
1232548895232548896GA22GENIChomozygous61121170
1232549254232549255TC25GENIChomozygous61121172
1232549820232549821GGA12GENIChomozygous61606208
1232549907232549908GGAA15GENICheterozygous61121174
1232549907232549908GGAAA15GENICpossibly homozygous61322790
1232549969232549970AG19GENIChomozygous61121176
1232550320232550321GA27GENIChomozygous61606209
1232550964232550965CT15GENIChomozygous61121177
1232551056232551057CA20GENIChomozygous61606210
1232551166232551167AG20GENIChomozygous61121179
1232551232232551233TG32GENIChomozygous61121181
1232551334232551335TA26GENIChomozygous61121183
1232551824232551825CT27GENIChomozygous61121185
1232551848232551849GA29GENIChomozygous61121187
1232552646232552647TC16GENIChomozygous61121189
1232553039232553040TC36GENIChomozygous61121191
1232553097232553098TC23GENIChomozygous61606211
1232553124232553125CT22GENIChomozygous61121193
1232553190232553191GT25GENIChomozygous61121195
1232553279232553280AG18GENIChomozygous61606212
1232553281232553282AG18GENIChomozygous61121197
1232553314232553315GA27GENIChomozygous61121199
1232553354232553355GA29GENIChomozygous61121201
1232553390232553391CG24GENIChomozygous61121203