chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79944427999444281CA--33GENICheterozygous694172212
79944861199448612AAC14GENICheterozygous694172213
79945328599453286TTC21GENIChomozygous694172214
79948248699482487A-12GENICheterozygous694172215
79948269199482692C-4GENICheterozygous694172216
79948362799483631GTGT----14GENICheterozygous694172218
79948623599486237AC--12GENICheterozygous694172219
79949002399490027TTTG----15GENICheterozygous694172220
79949943399499434CCA22GENIChomozygous694172221
79951214299512143TTAC12GENICheterozygous694172222
79951328099513282TT--13GENIChomozygous694172224
79951330299513303TTG17GENIChomozygous694172225
79951330699513307TTC19GENIChomozygous694172226
79952499599524996A-20GENICheterozygous694172227
79952853099528531GGACAC7GENICheterozygous694172228
79952887299528873CCT12GENICheterozygous694172229
79953727099537271T-18GENICheterozygous694172230
79953727999537280T-15GENICheterozygous694172231
79953728699537287AAC14GENICheterozygous694172232
79953734599537349GATG----12GENIChomozygous694172233
79954621999546220A-21GENICheterozygous694172235
79954937899549379C-22GENIChomozygous694172236
79955361499553615TTCA20GENIChomozygous694172237
79955447499554475T-4GENICheterozygous694172238
79955447599554476C-4GENIChomozygous694172239
79955448799554489TG--6GENIChomozygous694172240
79955452199554523TA--5GENIChomozygous694172241
79955453199554533TT--5GENIChomozygous694172242
79955456099554561CA5GENIChomozygous531087557
79955784899557849GGA18GENICheterozygous694172243