chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157143793157143794TC19GENIChomozygous112905582
4157143867157143868AG21GENIChomozygous112905584
4157144034157144035TC25GENIChomozygous112905586
4157144099157144100CT18GENIChomozygous112905588
4157144164157144165CT13GENIChomozygous112905590
4157144997157144998TC12GENIChomozygous112905592
4157145282157145283GA22GENIChomozygous112905596
4157145362157145363TC22GENIChomozygous112905598
4157145639157145640AG21GENIChomozygous112905599
4157145756157145757GA18GENIChomozygous112905601
4157145862157145863GA18GENIChomozygous112905603
4157146025157146026AT18GENIChomozygous112905605
4157146155157146156GA21GENIChomozygous112905607
4157146176157146177TC20GENIChomozygous112905609
4157146181157146182AT19GENIChomozygous112905611
4157146555157146556CT13GENIChomozygous112905615
4157147329157147330TC26GENIChomozygous112905617
4157148213157148214GA20GENIChomozygous112905619
4157148569157148570TG13GENIChomozygous112905621
4157148660157148661CT20GENIChomozygous112905623
4157149886157149887GC29GENICheterozygous112905625
4157149933157149934GA33GENICheterozygous112905626
4157150830157150831GA28GENICheterozygous113184414
4157150840157150841AG31GENICheterozygous112905630
4157150960157150961GA26GENICheterozygous112905632
4157150963157150964AC24GENICheterozygous112905634
4157153977157153978TC21GENIChomozygous112905644
4157151062157151063TG22GENICheterozygous112905636
4157153831157153832CT21GENIChomozygous112905642
4157150241157150242TA16GENIChomozygous126027595
4157151034157151035AG22GENICheterozygous113062844
4157151038157151039CT22GENICheterozygous113062846
4157151039157151040AG22GENICheterozygous113062848
4157152403157152404T5GENIChomozygous128096035
4157146450157146450CTCC6GENICheterozygous132833763