chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1190497763190497764GA53GENIChomozygous143808532
1190498586190498587AG55GENIChomozygous141289585
1190503591190503592CG50GENICheterozygous135772862
1190503594190503595CT50GENICheterozygous135772863
1190508295190508296GA50GENIChomozygous143808533
1190508537190508538CA59GENICpossibly homozygous143808534
1190510265190510266AG51GENIChomozygous141289595
1190510565190510566CT41GENIChomozygous141289596
1190510674190510675CG29GENIChomozygous143808535
1190513451190513452TG60GENIChomozygous143808536
1190513540190513541CG55GENIChomozygous141289598
1190513565190513566TC49GENIChomozygous143808537
1190515068190515069TC49GENIChomozygous141289602
1190517877190517878CT63GENIChomozygous143808538
1190519727190519728TA41GENIChomozygous143808539
1190520500190520501CT42GENIChomozygous153897061
1190520500190520501C42GENICheterozygous402976469
1190521006190521007GA55GENIChomozygous143808540
1190521853190521854AG47GENIChomozygous143808541
1190522361190522362CT51GENIChomozygous143808542
1190522609190522610CT50GENIChomozygous135772865
1190522674190522675AG57GENIChomozygous135772866
1190522783190522784GC55GENIChomozygous141289606
1190522789190522790CT55GENIChomozygous141289607
1190511563190511563ATGGCCCTATGGTGTGTC52GENIChomozygous141177610