chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124473723124473724AC20GENIChomozygous976132329
7124473882124473883CT12GENIChomozygous976132330
7124476979124476980AG11GENIChomozygous976132331
7124477222124477223GT16GENIChomozygous976132332
7124479267124479268CT22GENIChomozygous976132333
7124481146124481147CT19GENIChomozygous976132334
7124481242124481243GA14GENIChomozygous976132335
7124481581124481582GA16GENIChomozygous976132336
7124482145124482146TC14GENIChomozygous976132337
7124482410124482411AG15GENIChomozygous976132338
7124482804124482805CT26GENIChomozygous976132339
7124482851124482852GA18GENIChomozygous976132340
7124483065124483066GA18GENIChomozygous976132341
7124483197124483198CT22GENIChomozygous976132342
7124483201124483202GA20GENIChomozygous976132343
7124483364124483365AG24GENIChomozygous976132344
7124483457124483458CT36GENIChomozygous976132345
7124483730124483731CT22GENIChomozygous976132346
7124483749124483750GA19GENIChomozygous976132347
7124483761124483762TC20GENIChomozygous976132348
7124484943124484944TC15GENIChomozygous976132349
7124485255124485256CG7GENIChomozygous976132350
7124485634124485635TC13GENIChomozygous976132351
7124486185124486186GC16GENIChomozygous976132352
7124486252124486253AC18GENIChomozygous976132353
7124486398124486399AC19GENIChomozygous976132354
7124487212124487213GA14GENIChomozygous976132355
7124487574124487575TC20GENIChomozygous976132356
7124487701124487702TC21GENIChomozygous976132357
7124488094124488095TA15GENIChomozygous976132358
7124488101124488102GT13GENIChomozygous976132359
7124489115124489116TC23GENIChomozygous976132360
7124489229124489230AG24GENIChomozygous976132361
7124489497124489498CT11GENIChomozygous976132362
7124489541124489542CG20GENIChomozygous976132363