chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157143793157143794TC15GENIChomozygous112905582
4157143867157143868AG9GENIChomozygous112905584
4157144034157144035TC14GENIChomozygous112905586
4157144099157144100CT16GENIChomozygous112905588
4157144164157144165CT17GENIChomozygous112905590
4157144997157144998TC20GENIChomozygous112905592
4157145282157145283GA16GENIChomozygous112905596
4157145362157145363TC22GENIChomozygous112905598
4157145639157145640AG18GENIChomozygous112905599
4157145756157145757GA20GENIChomozygous112905601
4157145862157145863GA22GENIChomozygous112905603
4157146025157146026AT15GENIChomozygous112905605
4157146155157146156GA26GENIChomozygous112905607
4157146176157146177TC25GENIChomozygous112905609
4157146181157146182AT25GENIChomozygous112905611
4157146555157146556CT7GENIChomozygous112905615
4157147329157147330TC20GENIChomozygous112905617
4157148213157148214GA19GENIChomozygous112905619
4157148569157148570TG20GENIChomozygous112905621
4157148660157148661CT12GENIChomozygous112905623
4157149886157149887GC31GENICheterozygous112905625
4157149933157149934GA33GENICheterozygous112905626
4157150241157150242TA19GENIChomozygous126027595
4157150840157150841AG34GENICheterozygous112905630
4157150960157150961GA27GENICheterozygous112905632
4157150963157150964AC27GENICheterozygous112905634
4157151034157151035AG21GENICheterozygous113062844
4157151038157151039CT21GENICheterozygous113062846
4157151039157151040AG21GENICheterozygous113062848
4157151062157151063TG24GENICheterozygous112905636
4157151108157151109AG25GENICheterozygous112905638
4157151133157151134AG28GENICheterozygous112905640
4157153831157153832CT17GENIChomozygous112905642
4157153977157153978TC14GENIChomozygous112905644
4157152403157152404T8GENIChomozygous128096035