chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 19,14653911,14653912,G,T,35,GENIC,homozygous,971331396 19,14654618,14654619,C,T,29,GENIC,homozygous,971331397 19,14654824,14654825,G,A,29,GENIC,homozygous,971331398 19,14656129,14656130,C,T,29,GENIC,homozygous,971331399 19,14657553,14657554,A,G,42,GENIC,homozygous,971331400 19,14658363,14658364,T,C,32,GENIC,homozygous,971331401 19,14658871,14658872,A,G,29,GENIC,homozygous,971331402 19,14659256,14659257,A,T,30,GENIC,homozygous,971331403 19,14659420,14659421,A,G,34,GENIC,homozygous,971331404 19,14659786,14659787,A,T,39,GENIC,homozygous,971331405 19,14660773,14660774,A,G,35,GENIC,homozygous,971331406 19,14662466,14662467,A,C,29,GENIC,homozygous,971331407 19,14662467,14662468,G,A,29,GENIC,homozygous,971331408 19,14662927,14662928,T,C,32,GENIC,homozygous,971331409 19,14663545,14663546,A,G,33,GENIC,homozygous,971331410 19,14663776,14663777,T,C,35,GENIC,homozygous,971331411