chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121407471314074714TC7GENIChomozygous50064203
121407702614077027CCTT1GENIChomozygous50365263
121407839014078391TC13GENICpossibly homozygous50064261
121407887914078880AG15GENICpossibly homozygous50064263
121407937914079380GC13GENIChomozygous50064265
121408073714080738GA26GENICpossibly homozygous50064277
121408091014080914AAGA----5GENICheterozygous50064279
121408099414080995TA28GENIChomozygous50064281
121408110014081101CG6GENIChomozygous50064283
121408110514081106TC7GENIChomozygous50064285
121408122714081229AA--2GENIChomozygous50064287
121408123114081232AG3GENIChomozygous50503906
121408129814081299CG14GENIChomozygous50064289
121408317014083171TC11GENIChomozygous50064293
121408331214083313A-8GENICheterozygous50064295
121408398314083984GA4GENIChomozygous50400517