chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242322324232233TC22GENIChomozygous50002798
1242327264232727AG22GENIChomozygous50002799
1242328904232891TTCCCTCC9GENIChomozygous50002800
1242336624233668GTGTGT------16GENIChomozygous50526413
1242338354233836GC30GENIChomozygous50002802
1242338884233889GA32GENIChomozygous50002803
1242340884234089TC22GENIChomozygous50002804
1242343054234306TC25GENIChomozygous50002805
1242344524234453TC23GENIChomozygous50002806
1242346594234660A-1GENIChomozygous50002807
1242348524234867AAAAAAAGAAAGAAA---------------7GENIChomozygous50002809
1242350874235088TG39GENIChomozygous50002810
1242355454235546GC62GENIChomozygous50002811
1242358524235853CA49GENIChomozygous50002812
1242359274235928TC54GENIChomozygous50002813
1242359854235986TC46GENIChomozygous50002814
1242373164237317GT29GENIChomozygous50002815
1242374124237413TTGGTTATTCAACTCGACCTTTGAA40GENIChomozygous50002816
1242374454237446AAT33GENIChomozygous50002817
1242374524237453GA32GENIChomozygous50002818
1242396454239646TA25GENICpossibly homozygous50002819
1242401504240151CCT15GENIChomozygous50002820
1242415714241573GT--6GENIChomozygous50526415
1242420704242071T-26GENIChomozygous50002822
1242430894243091GT--4GENICheterozygous50526417
1242440344244035TTTC6GENICheterozygous50002823
1242440824244083AAGTGT4GENIChomozygous50002824
1242445504244551CCTTTTTT2GENICheterozygous50002825
1242445504244551CCTTTTTTT2GENICheterozygous50526419
1242455704245571TTAC41GENIChomozygous50002826
1242484834248484CA7GENIChomozygous50002828
1242491904249191G-12GENICheterozygous50526421
1242492094249211AC--4GENIChomozygous50526423
1242519794251980AG29GENIChomozygous50002830
1242555614255562CT27GENIChomozygous50002832
1242570074257008GA21GENIChomozygous50002833
1242590844259085GA24GENIChomozygous50002834
1242547054254709TACA----19GENIChomozygous50394265