chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140271040140271041G44GENIChomozygous128528971
7140271730140271731GC47GENIChomozygous115938437
7140272914140272915GA43GENIChomozygous115938439
7140273125140273126CG61GENICpossibly homozygous115938440
7140273218140273219CT67GENICpossibly homozygous115938441
7140273537140273538GT53GENIChomozygous115938442
7140274024140274025TC47GENIChomozygous115938443
7140274492140274493CT42GENIChomozygous115938444
7140277556140277557CT59GENIChomozygous115938445
7140278138140278139GA51GENIChomozygous115938446
7140279085140279085CCGT56GENIChomozygous128528972
7140280669140280669ACCCTCCAGCCTGT46GENIChomozygous128528973
7140284162140284163C33GENICheterozygous128528974
7140284400140284401AG59GENIChomozygous115938449
7140286052140286054CG48GENIChomozygous128528975
7140287170140287171TC52GENIChomozygous115938450
7140288110140288111T60GENIChomozygous128528976
7140290325140290326TA40GENIChomozygous115938451
7140290426140290427CT43GENIChomozygous115938452