chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124473723124473724AC24GENIChomozygous964301169
7124473882124473883CT30GENIChomozygous964301170
7124476979124476980AG37GENIChomozygous964301171
7124477222124477223GT25GENIChomozygous964301172
7124479267124479268CT29GENIChomozygous964301173
7124481146124481147CT29GENIChomozygous964301174
7124481242124481243GA25GENIChomozygous964301175
7124481581124481582GA28GENIChomozygous964301176
7124482145124482146TC19GENIChomozygous964301177
7124482410124482411AG24GENIChomozygous964301178
7124482804124482805CT26GENIChomozygous964301179
7124482851124482852GA36GENIChomozygous964301180
7124483065124483066GA39GENIChomozygous964301181
7124483197124483198CT32GENIChomozygous964301182
7124483201124483202GA31GENIChomozygous964301183
7124483364124483365AG21GENIChomozygous964301184
7124483457124483458CT36GENIChomozygous964301185
7124483730124483731CT31GENIChomozygous964301186
7124483749124483750GA34GENIChomozygous964301187
7124483761124483762TC39GENIChomozygous964301188
7124484943124484944TC13GENIChomozygous964301189
7124485255124485256CG15GENIChomozygous964301190
7124485634124485635TC31GENIChomozygous964301191
7124486185124486186GC36GENIChomozygous964301192
7124486252124486253AC38GENIChomozygous964301193
7124486398124486399AC37GENIChomozygous964301194
7124487212124487213GA41GENIChomozygous964301195
7124487574124487575TC27GENIChomozygous964301196
7124487701124487702TC23GENIChomozygous964301197
7124488094124488095TA46GENIChomozygous964301198
7124488101124488102GT48GENIChomozygous964301199
7124489115124489116TC39GENIChomozygous964301200
7124489229124489230AG39GENIChomozygous964301201
7124489497124489498CT33GENIChomozygous964301202
7124489541124489542CG25GENIChomozygous964301203