chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 12,40696133,40696134,C,A,11,GENIC,homozygous,933050211 12,40696151,40696152,G,A,10,GENIC,homozygous,933050212 12,40696216,40696217,T,C,14,GENIC,homozygous,933050213 12,40696648,40696649,A,T,13,GENIC,homozygous,933050214 12,40697020,40697021,A,C,11,GENIC,homozygous,933050215 12,40697446,40697447,T,C,11,GENIC,homozygous,933050216 12,40697467,40697468,C,T,10,GENIC,homozygous,933050217 12,40697524,40697525,C,A,9,GENIC,homozygous,933050218 12,40699564,40699565,C,A,9,GENIC,homozygous,933050219 12,40700278,40700279,G,T,16,GENIC,homozygous,933050220 12,40700652,40700653,C,G,14,GENIC,homozygous,933050221 12,40701317,40701318,C,A,7,GENIC,homozygous,933050222 12,40701563,40701564,G,A,9,GENIC,homozygous,933050223 12,40705325,40705326,A,G,3,GENIC,homozygous,933050224 12,40706564,40706565,T,G,9,GENIC,homozygous,933050225 12,40706860,40706861,T,G,5,GENIC,homozygous,933050226 12,40707476,40707477,C,T,9,GENIC,homozygous,933050227