chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116863452368634524CA19GENIChomozygous804232816
116863478768634788GA17GENIChomozygous804232817
116863759168637592CT19GENICpossibly homozygous804232818
116864157868641579AG13GENIChomozygous804232819
116865279668652797GA11GENIChomozygous804232820
116865328768653288GA5GENIChomozygous804232821
116865397368653974CT16GENIChomozygous804232822
116865398268653983CG16GENIChomozygous804232823
116865399068653991CT14GENIChomozygous804232824
116865562068655621AG36GENIChomozygous804232825
116865587468655875AT8GENIChomozygous804232826
116865589268655893GA5GENIChomozygous804232827
116865603868656039AT7GENIChomozygous804232828
116865604568656046GT7GENIChomozygous804232829
116865607968656080GA4GENIChomozygous804232830
116865609768656098CG5GENIChomozygous804232831
116866274368662744TG34GENIChomozygous804232832
116866420368664204CT12GENIChomozygous804232833
116867016268670163CT90GENICheterozygous804232834
116867032968670330GA66GENICheterozygous804232835
116867418468674185GT15GENIChomozygous804232836
116867690268676903TC12GENIChomozygous804232837
116867795668677957CT15GENIChomozygous804232838
116868111468681115GA31GENIChomozygous804232839
116868458968684590AG13GENIChomozygous804232840
116868618468686185AG27GENIChomozygous804232841