chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
168168975681689757TC46GENIChomozygous111877758
168169049981690500CT55GENIChomozygous111877760
168169169681691697AG38GENIChomozygous112378446
168169170481691705AG37GENIChomozygous119134460
168169170681691707AG36GENIChomozygous119134461
168169232581692326TC24GENIChomozygous119134462
168169354981693550CT45GENIChomozygous111877762
168169538281695383CG48GENIChomozygous111877764
168169181181691812GT7GENIChomozygous112179953
168169782481697825GA64GENIChomozygous111877766
168169825581698263ACACAGAC50GENIChomozygous129387399
168169553381695533ACAC28GENIChomozygous129387398
168169179181691791T12GENIChomozygous129387396
168169372181693723AA4GENIChomozygous129387397
168170066881700669TA55GENICpossibly homozygous111877768
168170130881701309TC54GENIChomozygous111877770
168170303981703040AG46GENIChomozygous111877772
168170442181704422CT62GENIChomozygous111877774
168170466881704669AG57GENIChomozygous111877776
168170689381706894CT44GENIChomozygous111877778
168170742781707432ATAAA33GENIChomozygous129387400
168170767381707676TTG32GENIChomozygous129387401
168170808481708084AT60GENIChomozygous129387402
168170939381709394CT61GENIChomozygous111877788
168170697581706976TC35GENIChomozygous111877780
168170704181707042CT34GENIChomozygous111877782
168170912081709121CT59GENIChomozygous111877784
168170914081709141CT60GENIChomozygous111877786
168170452681704527TG63GENIChomozygous112436594
168170965581709656TG70GENIChomozygous111877790
168171143481711435AG58GENIChomozygous111877792
168171240881712409AC57GENIChomozygous111877794
168171243181712432TC50GENIChomozygous111877796
168171245581712456AG52GENIChomozygous111877798
168171353181713532AT51GENIChomozygous111877800
168171425081714251TC37GENIChomozygous111877802