chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154485851744858517C15GENIChomozygous129251805
154485852544858527GC14GENIChomozygous129251806
154485853044858531G14GENIChomozygous129251807
154485853344858534A14GENIChomozygous129251808
154485855144858551C12GENIChomozygous129251809
154485856444858564C19GENIChomozygous129251810
154485857044858571C21GENIChomozygous129251811
154485863244858632A17GENIChomozygous129251812
154485863444858634TC17GENIChomozygous129251813
154485864144858642G16GENIChomozygous129251814
154485864544858646C16GENIChomozygous129251815
154485865444858654C15GENIChomozygous129251816
154485867744858678G15GENIChomozygous129251817
154485868044858681C15GENIChomozygous129251818
154485869044858691T15GENIChomozygous129251819
154485874544858746A22GENIChomozygous129251820
154485875644858757A25GENIChomozygous129251821
154485876244858762CC23GENIChomozygous129251822
154485876844858769GC25GENIChomozygous124070888
154485879244858792G21GENIChomozygous129251823
154485879644858800TTCC20GENIChomozygous129251824
154485880644858806T20GENIChomozygous129251825
154485881544858815T19GENIChomozygous129251826
154485885444858855GA16GENIChomozygous112499491
154485891144858912C10GENIChomozygous129251827
154485893844858938T11GENIChomozygous129251828
154485897644858976C15GENIChomozygous129251829
154485904744859047G16GENIChomozygous129251830
154485905644859056G15GENIChomozygous129251831
154485910044859100G7GENIChomozygous129251832
154485910744859107G8GENIChomozygous129251833
154485911644859116GGG9GENIChomozygous129251834
154485914644859147A14GENIChomozygous129251835
154485914444859145TA14GENIChomozygous112851957