chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 9912012 9912013 T C 2 GENIC homozygous 51616110 10 9912020 9912021 T C 2 GENIC homozygous 51616111 10 9912107 9912108 G A 7 GENIC homozygous 52110797 10 9912459 9912460 A G 13 GENIC possibly homozygous 52027443 10 9913124 9913125 T G 3 GENIC homozygous 52027445 10 9913133 9913134 G T 1 GENIC homozygous 52110799 10 9913210 9913211 T C 8 GENIC heterozygous 51616113 10 9913344 9913345 A G 9 GENIC homozygous 51616114 10 9913697 9913698 G T 7 GENIC homozygous 51616115 10 9913699 9913700 G A 6 GENIC homozygous 52027451 10 9913824 9913825 A C 8 GENIC homozygous 51616116 10 9914118 9914119 C T 5 GENIC homozygous 52027455 10 9914140 9914141 G - 6 GENIC heterozygous 52027457 10 9914191 9914192 A G 11 GENIC homozygous 51616117 10 9914220 9914221 G T 18 GENIC homozygous 52027459 10 9914475 9914476 A G 10 GENIC possibly homozygous 51616118 10 9915254 9915255 T TC 9 GENIC homozygous 51616121 10 9916302 9916303 A - 6 GENIC heterozygous 52027461 10 9916450 9916451 T A 4 GENIC heterozygous 51616124 10 9917759 9917760 A G 3 GENIC homozygous 51616126 10 9918849 9918850 T C 4 GENIC homozygous 52027467 10 9913667 9913668 C A 8 GENIC possibly homozygous 51323666 10 9916592 9916593 T TC 8 GENIC homozygous 51323667 10 9918323 9918324 A G 6 GENIC homozygous 51323669 10 9918840 9918841 C T 6 GENIC homozygous 52027465 10 9918996 9918997 T C 6 GENIC heterozygous 52027469 10 9919164 9919165 T C 7 GENIC possibly homozygous 52027471