chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242322324232233TC6GENIChomozygous616658050
1242327264232727AG8GENIChomozygous616658051
1242328904232891TTCCCTCC5GENIChomozygous741238911
1242336624233668GTGTGT------15GENIChomozygous741238912
1242338354233836GC24GENIChomozygous616658052
1242338884233889GA19GENIChomozygous616658053
1242340884234089TC24GENICpossibly homozygous616658054
1242343054234306TC16GENIChomozygous616658055
1242344524234453TC11GENIChomozygous616658056
1242346594234660A-3GENICheterozygous741238914
1242346614234666ACACA-----3GENICheterozygous741238916
1242348524234867AAAAAAAGAAAGAAA---------------11GENIChomozygous741238918
1242350874235088TG25GENIChomozygous616658057
1242355454235546GC24GENIChomozygous616658058
1242358524235853CA26GENIChomozygous616658059
1242359274235928TC25GENIChomozygous616658060
1242359854235986TC24GENIChomozygous616658061
1242373164237317GT16GENIChomozygous616658062
1242374124237413TTGGTTATTCAACTCGACCTTTGAA20GENIChomozygous741238919
1242374454237446AAT12GENIChomozygous741238920
1242374524237453GA12GENIChomozygous616658063
1242396454239646TA13GENIChomozygous616658064
1242401504240151CCT13GENIChomozygous741238921
1242415714241573GT--4GENIChomozygous741238923
1242420704242071T-19GENIChomozygous741238924
1242430894243091GT--3GENICheterozygous741238926
1242440344244035TTTC6GENICheterozygous741238928
1242440824244083AAGTGT8GENIChomozygous741238934
1242445504244551CCTTTTTT4GENICheterozygous741238937
1242445504244551CCTTTTTTT4GENICheterozygous741238938
1242455704245571TTAC16GENIChomozygous741238939
1242484834248484CA13GENIChomozygous616658065
1242492094249211AC--1GENIChomozygous741238941
1242519794251980AG7GENIChomozygous616658066
1242547014254709TACATACA--------15GENICheterozygous741238942
1242547054254709TACA----15GENICpossibly homozygous741238943
1242555614255562CT23GENIChomozygous616658067
1242570074257008GA12GENIChomozygous616658068
1242590844259085GA11GENIChomozygous616658069