chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87150302271503023GT11GENIChomozygous52673646
87150302471503025GT10GENIChomozygous52673647
87150309071503091G-27GENIChomozygous52673648
87150416571504166GGT21GENIChomozygous52673649
87150675271506753CCT5GENIChomozygous52673650
87151485071514851CCTG27GENICheterozygous53517654
87151486371514865TG--27GENICheterozygous53446720
87152449971524501GT--17GENICheterozygous53469728
87152542271525423GT16GENIChomozygous52673656
87152863971528640TC5GENICheterozygous53394252
87152866471528665C-2GENIChomozygous53446722
87154131571541317CA--23GENICheterozygous53469730
87154519371545194CA7GENIChomozygous52673660
87154636371546364GGCACA19GENICpossibly homozygous53563260
87154665171546652AAGGGAGAAGGAGGAGGAAGAAGAGGTGAGGAAGGGGAGGGAGGAGG27GENIChomozygous53394294
87154677071546771AAGC24GENIChomozygous52673662
87154802671548028CA--12GENICheterozygous53517656
87155367171553673AC--8GENICheterozygous53394302
87151020671510207TTA14GENICheterozygous53570344
87152449771524501GTGT----17GENICheterozygous53570345
87155949071559491A-11GENICheterozygous53570346
87158376571583766GGCA5GENICheterozygous53394338
87158454071584541CCAAAAAAAAAAAAAAAAAAAA4GENIChomozygous53394346
87158527971585280GC19GENIChomozygous52673664
87159005071590051T-32GENICheterozygous53570347
87159005371590055CA--32GENICheterozygous53570348
87159005671590064CATGGACC--------30GENICheterozygous53570349
87159008471590094TCATACTTTA----------26GENICheterozygous53570350
87159049871590499T-32GENIChomozygous52673665
87159050171590502GGA32GENIChomozygous52673666
87159050471590505GT32GENIChomozygous52673667
87159813471598135CCTTTTTTTT13GENICheterozygous53394397
87159813571598136T-13GENICheterozygous53364360
87159979671599802CACACA------17GENICheterozygous53394399
87159979871599802CACA----17GENICheterozygous53394400
87160345471603455TTACAC12GENICheterozygous53394407
87160345571603457AC--12GENICheterozygous52673668