chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5158120835158120836AG5GENIChomozygous114070892
5158121952158121953CA38GENIChomozygous118847144
5158123525158123526TC30GENIChomozygous114070895
5158123659158123660AG37GENIChomozygous114070896
5158125991158125992AG37GENIChomozygous114070897
5158128335158128336CT30GENIChomozygous114070903
5158129275158129276TC21GENIChomozygous114070904
5158129406158129407GT31GENIChomozygous114070905
5158129660158129661CT36GENIChomozygous114070906
5158130388158130389GA24GENIChomozygous114070907
5158130857158130858CG18GENIChomozygous114070908
5158131205158131206AG31GENIChomozygous114070909
5158131283158131284CT22GENIChomozygous114070910
5158131824158131825GA12GENICpossibly homozygous114070911
5158132557158132558GA32GENIChomozygous114070913
5158132729158132730TC23GENIChomozygous114070914
5158133538158133539CT20GENIChomozygous114070915