chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 49255337 49255379 GATGGGGAGGATGAGTATAGAGAGGAGGATGATGGGGAGGGT 3 GENIC homozygous 141001916 5 49255711 49255712 A C 14 GENIC homozygous 141003638 5 49255845 49255846 G A 22 GENIC homozygous 137459044 5 49255931 49255932 C T 17 GENIC homozygous 141003639 5 49256203 49256204 T A 14 GENIC homozygous 137459045 5 49256308 49256309 T C 21 GENIC homozygous 141003640 5 49256315 49256316 A C 21 GENIC homozygous 141003641 5 49256520 49256521 T C 25 GENIC possibly homozygous 141003642 5 49256543 49256544 G T 25 GENIC homozygous 141003643 5 49257702 49257703 T G 8 GENIC homozygous 141003644 5 49257717 49257718 G T 8 GENIC homozygous 141003645 5 49257972 49257974 CA 19 GENIC homozygous 141001917 5 49259919 49259951 CAGGATCACAGGATCTCAGGATCACAGGATCC 16 GENIC homozygous 141001918 5 49261092 49261093 C A 12 GENIC homozygous 141003646 5 49261776 49261777 G A 9 GENIC homozygous 141003647 5 49262087 49262088 C T 17 GENIC homozygous 141003648 5 49262353 49262354 C T 20 GENIC homozygous 137459052 5 49271219 49271220 T C 15 GENIC homozygous 141003649 5 49272170 49272171 C 12 GENIC homozygous 141001919 5 49273927 49273928 G C 13 GENIC homozygous 141003650 5 49274307 49274308 C T 14 GENIC homozygous 141003651 5 49274349 49274350 C G 14 GENIC homozygous 141003652 5 49274638 49274639 T C 17 GENIC homozygous 141003653 5 49276276 49276281 CTTAA 12 GENIC homozygous 141001920 5 49278482 49278483 T C 14 GENIC homozygous 141003654 5 49279285 49279286 T A 21 GENIC homozygous 141003655 5 49279374 49279375 G T 18 GENIC homozygous 141003656 5 49279919 49279920 A G 22 GENIC homozygous 141003657 5 49281343 49281344 C T 32 GENIC homozygous 141003658 5 49282627 49282628 A C 15 GENIC homozygous 137459059 5 49283468 49283469 A G 26 GENIC homozygous 141003659 5 49283539 49283540 T G 21 GENIC homozygous 154285790 5 49284994 49284995 T C 18 GENIC homozygous 137459061 5 49285295 49285296 A G 22 GENIC homozygous 141003660 5 49283539 49283540 T 21 GENIC heterozygous 403140328