chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 14,22932823,22932824,G,A,18,GENIC,homozygous,976966544 14,22933042,22933043,C,T,19,GENIC,homozygous,976966545 14,22934665,22934666,A,G,25,GENIC,homozygous,976966546 14,22935869,22935870,G,A,20,GENIC,heterozygous,976966547 14,22935871,22935872,T,A,15,GENIC,heterozygous,976966548 14,22936366,22936367,G,A,12,GENIC,homozygous,976966549 14,22937139,22937140,A,G,7,GENIC,possibly homozygous,976966550 14,22937397,22937398,G,A,21,GENIC,homozygous,976966551 14,22937646,22937647,T,A,33,GENIC,homozygous,976966552 14,22937683,22937684,T,C,31,GENIC,homozygous,976966553 14,22940949,22940950,A,G,24,GENIC,homozygous,976966554 14,22941343,22941344,C,A,27,GENIC,homozygous,976966555 14,22942777,22942778,C,A,13,GENIC,homozygous,976966556 14,22943895,22943896,A,G,30,GENIC,homozygous,976966557 14,22944029,22944030,T,A,31,GENIC,homozygous,976966558 14,22947519,22947520,C,A,16,GENIC,homozygous,976966559 14,22947521,22947522,A,C,15,GENIC,homozygous,976966560 14,22952359,22952360,C,G,31,GENIC,homozygous,976966561 14,22955522,22955523,C,T,43,GENIC,homozygous,976966562 14,22955579,22955580,G,T,47,GENIC,homozygous,976966563