chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87150302271503023GT11GENIChomozygous575367273
87150302471503025GT10GENIChomozygous575367274
87150309071503091G-27GENIChomozygous714637207
87150416571504166GGT21GENIChomozygous714637208
87150675271506753CCT5GENIChomozygous714637211
87151020671510207TTA14GENICheterozygous714637212
87151485071514851CCTG27GENICheterozygous714637216
87151486371514865TG--27GENICheterozygous714637215
87152449771524501GTGT----17GENICheterozygous714637219
87152449971524501GT--17GENICheterozygous714637220
87152542271525423GT16GENIChomozygous573979383
87152863971528640TC5GENICheterozygous573979384
87152866471528665C-2GENIChomozygous714637221
87154131571541317CA--23GENICheterozygous714637222
87154519371545194CA7GENIChomozygous575367275
87154636371546364GGCACA19GENICpossibly homozygous714637226
87154665171546652AAGGGAGAAGGAGGAGGAAGAAGAGGTGAGGAAGGGGAGGGAGGAGG27GENIChomozygous714637227
87154677071546771AAGC24GENIChomozygous714637228
87154802671548028CA--12GENICheterozygous714637229
87155367171553673AC--8GENICheterozygous714637231
87155949071559491A-11GENICheterozygous714637232
87158376571583766GGCA5GENICheterozygous714637234
87158454071584541CCAAAAAAAAAAAAAAAAAAAA4GENIChomozygous714637236
87158527971585280GC19GENIChomozygous575367276
87159005071590051T-32GENICheterozygous714637237
87159005371590055CA--32GENICheterozygous714637238
87159005671590064CATGGACC--------30GENICheterozygous714637239
87159008471590094TCATACTTTA----------26GENICheterozygous714637240
87159049871590499T-32GENIChomozygous714637241
87159050171590502GGA32GENIChomozygous714637242
87159050471590505GT32GENIChomozygous575367277
87159813471598135CCTTTTTTTT13GENICheterozygous714637244
87159813571598136T-13GENICheterozygous714637243
87159979671599802CACACA------17GENICheterozygous714637245
87159979871599802CACA----17GENICheterozygous714637246
87160345471603455TTACAC12GENICheterozygous714637249
87160345571603457AC--12GENICheterozygous714637248