chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1241372221241372223GT--19GENICheterozygous765901573
1241372966241372967GGGTGTGT6GENICheterozygous765901577
1241372967241372969GT--6GENICheterozygous765901576
1241378706241378707TTGATA23GENICpossibly homozygous765901580
1241378790241378794TAGA----7GENIChomozygous765901583
1241378870241378871GGTAGA16GENIChomozygous765901587
1241394163241394164GGAA4GENICheterozygous765901590
1241394655241394656AAAACAGGAAGGGCAGAGAAAGAAAAGGCCTTCTTGAGAAAAAATAACTACAAAGTTGTCCTGTTGCCCGGCACTCAAATTTACACTGTGTGCATGGAGG54GENIChomozygous765901591
1241394726241394727T-22GENIChomozygous765901592
1241398965241398969AGAG----3GENICheterozygous765901593
1241399145241399149GAAA----15GENIChomozygous765901595
1241409751241409752C-18GENIChomozygous765901598
1241412965241412973ACACACAC--------9GENICheterozygous765901599
1241412967241412973ACACAC------9GENICheterozygous765901600
1241412969241412973ACAC----9GENICheterozygous765901601
1241413436241413437TTCAACTACCCTTCCATTCCTGTACAA50GENIChomozygous765901602
1241437652241437654TG--10GENICheterozygous765901603
1241466659241466661AC--14GENICheterozygous765901606
1241473559241473560A-9GENICheterozygous765901611
1241474207241474209CA--7GENICheterozygous765901613
1241484441241484445TCTC----4GENIChomozygous765901614
1241497763241497765GG--22GENICheterozygous765901615
1241519600241519601T-15GENICheterozygous765901616
1241537079241537081AC--15GENICheterozygous765901617