chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 12,41703599,41703600,T,G,32,GENIC,heterozygous,926488916 12,41703654,41703655,T,C,17,GENIC,heterozygous,926488917 12,41703711,41703712,G,A,16,GENIC,heterozygous,926488918 12,41703992,41703993,A,G,23,GENIC,heterozygous,926488919 12,41703995,41703996,T,C,21,GENIC,heterozygous,926488920 12,41704366,41704367,C,CT,40,GENIC,heterozygous,926627629 12,41705465,41705466,A,G,33,GENIC,heterozygous,926488921 12,41705897,41705898,G,A,19,GENIC,heterozygous,926488922