chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5133764195133764196CT36GENIChomozygous118845666
5133764214133764215AG33GENIChomozygous114531586
5133767104133767105CA8GENIChomozygous119017876
5133767109133767110GC8GENIChomozygous114015004
5133768298133768299AT19GENIChomozygous114015007
5133768803133768804AT21GENIChomozygous114015008
5133769201133769202AG28GENIChomozygous114015010
5133770408133770409GA25GENIChomozygous114015015
5133771473133771474CT18GENIChomozygous114015016
5133771717133771718AT6GENIChomozygous114015017
5133773808133773809AG15GENIChomozygous114015019
5133776043133776044AG10GENIChomozygous114015023
5133776384133776385GA22GENICpossibly homozygous114531588
5133777109133777110CT22GENIChomozygous114531590
5133777854133777855GT27GENIChomozygous114015024
5133783540133783541CG20GENIChomozygous114015027
5133785987133785988AG12GENIChomozygous114015032