chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 138947446 138947447 A ACTCTGCCTGAGCCAGGTTGACTCTCCCAAGAGCCCTCCCCATGGCCCCCTTCATTTCCTTGTTGCGGAAGCT 15 GENIC heterozygous 701074381 7 138947534 138947535 G A 51 GENIC homozygous 550916086 7 138947567 138947568 A - 52 GENIC heterozygous 701074382 7 138947570 138947571 A AC 52 GENIC heterozygous 701074383 7 138947582 138947583 T C 66 GENIC homozygous 550916087 7 138947619 138947620 G T 70 GENIC homozygous 550916088 7 138948227 138948228 A AG 5 GENIC homozygous 701074384 7 138948229 138948230 T TTGAG 5 GENIC homozygous 701074385 7 138948233 138948234 G GT 5 GENIC homozygous 701074386 7 138948245 138948246 T - 1 GENIC homozygous 701074387 7 138948642 138948643 A G 9 GENIC homozygous 550916089 7 138948653 138948654 A G 8 GENIC homozygous 550916090 7 138948877 138948878 T A 15 GENIC homozygous 550916091 7 138948908 138948909 G C 16 GENIC homozygous 550916092 7 138948930 138948931 T C 20 GENIC homozygous 550916093 7 138948935 138948936 C G 22 GENIC homozygous 550916094 7 138949108 138949109 C A 22 GENIC homozygous 550916095 7 138949121 138949122 T C 25 GENIC homozygous 550916096 7 138949149 138949150 C T 29 GENIC homozygous 550916097 7 138949181 138949182 A G 24 GENIC homozygous 550916098 7 138949385 138949386 G C 30 GENIC homozygous 550916099 7 138949491 138949492 G T 29 GENIC homozygous 550916100