chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18694891186948912TC20GENIChomozygous108882976
18694942486949425CT17GENIChomozygous120560196
18695176386951764TC25GENIChomozygous108882981
18695421886954219GA24GENICpossibly homozygous120560198
18695467986954680GT20GENIChomozygous108882988
18695597486955975GT16GENICpossibly homozygous120560200
18695198586951986CT17GENIChomozygous120869394
18695934786959348GA8GENIChomozygous120869395
18695259686952596T14GENIChomozygous131259587
18695994286959950CTGACTGA21GENIChomozygous131259588
18696080386960804GA23GENIChomozygous120560202
18696323786963238AG19GENIChomozygous108883006
18696349786963498AC19GENIChomozygous108883007
18696350386963504TC19GENIChomozygous108883008
18696352786963527G15GENIChomozygous131259589
18696570786965708TG15GENIChomozygous120560204
18696579386965794CT15GENIChomozygous120560206
18696639086966391GA25GENIChomozygous120560208
18696652386966524AG24GENIChomozygous108883009
18696848486968485GC26GENIChomozygous108883010
18696933386969334TC15GENIChomozygous108883011
18696982886969828TATG13GENIChomozygous131259590
18697158786971588CA22GENIChomozygous108883012
18697176086971761TC15GENIChomozygous108883013
18697179386971794TC16GENIChomozygous108883014