chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242322324232233TC10GENIChomozygous646373353
1242327264232727AG5GENIChomozygous646373354
1242328904232891TTCCCTCC4GENIChomozygous754943757
1242336624233668GTGTGT------18GENIChomozygous754943758
1242338354233836GC20GENIChomozygous646373355
1242338884233889GA23GENIChomozygous646373356
1242340884234089TC24GENIChomozygous646373357
1242343054234306TC28GENIChomozygous646373358
1242344524234453TC20GENIChomozygous646373359
1242346604234667AACACAC-------6GENICheterozygous754943760
1242346614234666ACACA-----6GENICheterozygous754943761
1242348524234867AAAAAAAGAAAGAAA---------------12GENIChomozygous754943763
1242350874235088TG43GENIChomozygous646373360
1242355454235546GC43GENIChomozygous646373361
1242358524235853CA26GENIChomozygous646373362
1242359274235928TC24GENIChomozygous646373363
1242359854235986TC30GENIChomozygous646373364
1242373164237317GT22GENIChomozygous646373365
1242374124237413TTGGTTATTCAACTCGACCTTTGAA22GENIChomozygous754943764
1242374454237446AAT19GENIChomozygous754943765
1242374524237453GA19GENIChomozygous646373366
1242396454239646TA20GENIChomozygous646373367
1242401504240151CCT15GENIChomozygous754943766
1242415714241573GT--3GENIChomozygous754943768
1242420704242071T-26GENIChomozygous754943769
1242430864243087AAGTGT1GENIChomozygous754943772
1242440344244035TTTCTCTCTC2GENIChomozygous754943775
1242440824244083AAGTGTGT10GENICpossibly homozygous754943780
1242440824244083AAGTGTGTGTGTGTGT10GENICheterozygous754943781
1242445504244551CCTTTTTT2GENICheterozygous754943782
1242445504244551CCTTTTTTT2GENICheterozygous754943783
1242455704245571TTAC26GENIChomozygous754943784
1242472674247268AT20GENIChomozygous646373368
1242484834248484CA4GENIChomozygous646373369
1242491914249193AA--8GENICheterozygous754943785
1242519794251980AG6GENIChomozygous646373370
1242547014254709TACATACA--------16GENIChomozygous754943786
1242555614255562CT21GENIChomozygous646373371
1242570074257008GA21GENIChomozygous646373372
1242590844259085GA17GENIChomozygous646373373