chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43083531830835319TC41GENIChomozygous134819670
43095039030950392CA49GENICheterozygous132294998
43097323730973238CA23GENICheterozygous132465202
43097550830975509T30GENICheterozygous130294229
43100852331008524GC20GENICheterozygous133731673
43100852631008527TC18GENICheterozygous133886850
43102279231022792CTTT29GENIChomozygous130648230
43103080031030801CA30GENIChomozygous112567767
43103413831034139GC9GENIChomozygous112567773
43104826531048266AG38GENICpossibly homozygous112567775
43105480731054808CG14GENICheterozygous128121333
43106924031069241TC54GENIChomozygous112567777
43107190531071906CG21GENIChomozygous112567779
43107650031076501TG49GENICheterozygous134127987
43107650731076508AT49GENICheterozygous132613352
43111172231111723GC35GENICpossibly homozygous112567789
43103425431034254AC5GENIChomozygous129901393
43100853331008537ATTG20GENICheterozygous134816369
43103390031033900TG17GENICheterozygous128018969
43111290331112905TT52GENIChomozygous128018970