chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182974103129741032C-16GENICheterozygous762229329
182974598429745985TTTC8GENICpossibly homozygous762229332
182978296129782962CG8GENIChomozygous658624083
182978579529785796TTCA16GENICheterozygous762229334
182978580129785802T-16GENICheterozygous762229335
182978939829789399GGC34GENIChomozygous762229336
182979098629790987CCTCTG50GENICheterozygous762229337
182979098829790989AAC50GENICheterozygous762229338
182979099029790992GG--53GENICheterozygous762229339
182979374829793754TTTTTT------10GENICheterozygous762229340
182979374929793754TTTTT-----10GENICheterozygous762229341
182979375129793754TTT---10GENICheterozygous762229342
182981177129811772GGGTGTTACAATGTTAAGTAACAACGCGCTTAATAACAAGGGGTATGGGACAGTAGAGAGAACAGATGTCTA38GENICheterozygous762229343
182982079529820796CCAAA6GENICheterozygous762229344
182983627229836273TC18GENIChomozygous658624084
182983991729839918A-4GENICheterozygous762229345
182984950629849508TG--7GENICheterozygous762229348
182988488529884886CCT5GENICheterozygous762229349
182989305729893058CT43GENIChomozygous658624085
182990534129905342AATGTG7GENICheterozygous762229352
182990534229905344TG--7GENICheterozygous762229351
182990716129907162AATG18GENICheterozygous762229354
182990716229907164TG--18GENICheterozygous762229353
182992377629923777GGT9GENICheterozygous762229355