chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 1,82401050,82401051,G,T,25,GENIC,heterozygous,927011184 1,82401308,82401309,G,T,60,GENIC,heterozygous,927011185 1,82401384,82401385,G,A,45,GENIC,heterozygous,927011186 1,82401417,82401418,G,A,43,GENIC,heterozygous,927011187 1,82401448,82401449,G,T,30,GENIC,heterozygous,927011188 1,82401451,82401452,T,-,30,GENIC,heterozygous,927202628 1,82401647,82401648,A,G,54,GENIC,heterozygous,927011189 1,82401716,82401717,A,-,33,GENIC,heterozygous,927202629 1,82401717,82401718,A,G,33,GENIC,heterozygous,927011190 1,82401783,82401784,A,C,24,GENIC,heterozygous,927011191 1,82401799,82401800,G,A,22,GENIC,heterozygous,927011192 1,82401838,82401839,G,A,21,GENIC,heterozygous,927011193 1,82401955,82401956,T,C,38,GENIC,heterozygous,927011194 1,82402123,82402124,C,T,43,GENIC,heterozygous,927011195 1,82402474,82402475,T,C,32,GENIC,heterozygous,927011196 1,82402513,82402514,G,A,29,GENIC,heterozygous,927011197 1,82402675,82402676,C,G,40,GENIC,heterozygous,927011198 1,82402693,82402694,C,G,37,GENIC,heterozygous,927011199 1,82402694,82402695,A,T,37,GENIC,heterozygous,927011200 1,82402744,82402745,A,G,32,GENIC,heterozygous,927011201 1,82402828,82402829,G,C,43,GENIC,heterozygous,927011202 1,82402882,82402883,A,T,46,GENIC,heterozygous,927011203 1,82402930,82402931,A,G,40,GENIC,heterozygous,927011204 1,82403051,82403052,C,T,17,GENIC,heterozygous,927011205 1,82410738,82410739,C,CAG,19,GENIC,heterozygous,927202630 1,82410739,82410740,C,A,18,GENIC,heterozygous,927011206 1,82415759,82415760,T,C,32,GENIC,heterozygous,927011207