chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 20,4892323,4892324,G,A,107,GENIC,heterozygous,783121268 20,4892334,4892335,G,C,116,GENIC,heterozygous,783121269 20,4892341,4892342,C,T,121,GENIC,heterozygous,783121270 20,4892393,4892394,A,G,123,GENIC,heterozygous,783121271 20,4892396,4892397,G,C,119,GENIC,heterozygous,783121272 20,4892497,4892498,G,T,83,GENIC,heterozygous,783121273 20,4892812,4892813,G,T,63,GENIC,heterozygous,783121274 20,4892878,4892879,T,C,103,GENIC,heterozygous,783121275 20,4892889,4892890,A,G,118,GENIC,heterozygous,783121276 20,4892897,4892898,T,A,122,GENIC,heterozygous,783121277 20,4892915,4892916,C,T,121,GENIC,heterozygous,783121278 20,4892930,4892931,G,C,123,GENIC,heterozygous,783121279 20,4892952,4892953,T,C,169,GENIC,heterozygous,783121280 20,4892962,4892963,A,T,174,GENIC,heterozygous,783121281 20,4892966,4892967,T,C,141,GENIC,heterozygous,783121282 20,4892968,4892969,A,G,179,GENIC,heterozygous,783121283 20,4892996,4892997,A,G,250,GENIC,heterozygous,783121284 20,4892997,4892998,A,G,193,GENIC,heterozygous,783121285 20,4893007,4893008,A,G,250,GENIC,heterozygous,783121286 20,4893058,4893059,T,C,249,GENIC,heterozygous,783121287 20,4893088,4893089,G,A,248,GENIC,heterozygous,783121288 20,4893110,4893111,C,T,248,GENIC,heterozygous,783121289 20,4893166,4893167,A,G,248,GENIC,heterozygous,783121290