chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 138947446 138947447 A ACTCTGCCTGAGCCAGGTTGACTCTCCCAAGAGCCCTCCCCATGGCCCCCTTCATTTCCTTGTTGCGGAAGCT 8 GENIC heterozygous 739733444 7 138947534 138947535 G A 47 GENIC possibly homozygous 622204552 7 138947567 138947568 A - 40 GENIC heterozygous 739733445 7 138947570 138947571 A AC 40 GENIC heterozygous 739733446 7 138947582 138947583 T C 42 GENIC homozygous 622204553 7 138947619 138947620 G T 50 GENIC homozygous 622204554 7 138948227 138948228 A AG 1 GENIC homozygous 739733447 7 138948229 138948230 T TTGAG 1 GENIC homozygous 739733448 7 138948233 138948234 G GT 1 GENIC homozygous 739733449 7 138948245 138948246 T - 1 GENIC homozygous 739733450 7 138948642 138948643 A G 12 GENIC possibly homozygous 622204555 7 138948653 138948654 A G 12 GENIC possibly homozygous 622204556 7 138948877 138948878 T A 16 GENIC homozygous 622204557 7 138948908 138948909 G C 20 GENIC homozygous 622204558 7 138948930 138948931 T C 17 GENIC homozygous 622204559 7 138948935 138948936 C G 18 GENIC homozygous 622204560 7 138949108 138949109 C A 25 GENIC homozygous 622204561 7 138949121 138949122 T C 27 GENIC homozygous 622204562 7 138949149 138949150 C T 27 GENIC homozygous 622204563 7 138949181 138949182 A G 30 GENIC homozygous 622204564 7 138949385 138949386 G C 26 GENIC homozygous 622204565 7 138949491 138949492 G T 26 GENIC homozygous 622204566