chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242322324232233TC21GENIChomozygous50002798
1242327264232727AG21GENIChomozygous50002799
1242328904232891TTCCCTCC11GENIChomozygous50002800
1242336614233662AAGTGTGTGTGTGTGTGT12GENICheterozygous50555772
1242336624233668GTGTGT------12GENICpossibly homozygous50526413
1242338354233836GC30GENIChomozygous50002802
1242338884233889GA25GENIChomozygous50002803
1242340884234089TC30GENIChomozygous50002804
1242343054234306TC23GENIChomozygous50002805
1242344524234453TC27GENIChomozygous50002806
1242346594234660A-4GENICheterozygous50002807
1242346614234664ACA---7GENICheterozygous50555775
1242348524234867AAAAAAAGAAAGAAA---------------11GENIChomozygous50002809
1242350874235088TG26GENIChomozygous50002810
1242355454235546GC23GENIChomozygous50002811
1242358524235853CA15GENIChomozygous50002812
1242359274235928TC30GENIChomozygous50002813
1242359854235986TC21GENIChomozygous50002814
1242373164237317GT28GENIChomozygous50002815
1242374124237413TTGGTTATTCAACTCGACCTTTGAA31GENIChomozygous50002816
1242374454237446AAT32GENIChomozygous50002817
1242374524237453GA29GENIChomozygous50002818
1242396454239646TA35GENIChomozygous50002819
1242401504240151CCT24GENIChomozygous50002820
1242415714241573GT--6GENIChomozygous50526415
1242420704242071T-25GENIChomozygous50002822
1242440344244035TTTC8GENICpossibly homozygous50002823
1242440824244083AAGTGT4GENICheterozygous50002824
1242445504244551CCTTTTTT7GENICheterozygous50002825
1242445504244551CCTTTTTTT7GENICheterozygous50526419
1242455704245571TTAC20GENIChomozygous50002826
1242484574248458CCT3GENICheterozygous50559705
1242484834248484CA5GENIChomozygous50002828
1242492094249211AC--4GENICheterozygous50526423
1242519794251980AG26GENIChomozygous50002830
1242547054254709TACA----11GENIChomozygous50394265
1242555614255562CT31GENIChomozygous50002832
1242570074257008GA26GENIChomozygous50002833
1242590844259085GA26GENIChomozygous50002834