chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1241354610241354611T-29GENICheterozygous748076013
1241358390241358391AAAC9GENICheterozygous748076016
1241358399241358401AC--9GENICheterozygous748076015
1241372221241372223GT--13GENICheterozygous748076018
1241372967241372969GT--10GENICheterozygous748076021
1241378706241378707TTGATA7GENIChomozygous748076025
1241378870241378871GGTAGA3GENIChomozygous748076028
1241389939241389940GGATAC15GENICpossibly homozygous748076032
1241394163241394164GGAA6GENICheterozygous748076034
1241394655241394656AAAACAGGAAGGGCAGAGAAAGAAAAGGCCTTCTTGAGAAAAAATAACTACAAAGTTGTCCTGTTGCCCGGCACTCAAATTTACACTGTGTGCATGGAGG31GENIChomozygous748076035
1241394726241394727T-17GENIChomozygous748076036
1241398965241398969AGAG----6GENICheterozygous748076037
1241399141241399149GAAAGAAA--------9GENIChomozygous748076038
1241409751241409752C-10GENICheterozygous748076042
1241412967241412973ACACAC------17GENICheterozygous748076044
1241412969241412973ACAC----17GENICheterozygous748076045
1241413436241413437TTCAACTACCCTTCCATTCCTGTACAA19GENIChomozygous748076046
1241437652241437654TG--16GENICheterozygous748076047
1241474207241474209CA--12GENICheterozygous748076051
1241524135241524136A-15GENICheterozygous748076052
1241529285241529287CT--8GENICheterozygous748076053
1241534693241534694C-3GENICheterozygous748076055
1241537079241537081AC--13GENICheterozygous748076056
1241538999241539000T-20GENICheterozygous748076059