chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 61365342 61365343 A T 16 GENIC homozygous 561640477 18 61365591 61365592 G T 14 GENIC homozygous 559011854 18 61366058 61366059 T C 29 GENIC homozygous 559011855 18 61366089 61366090 C G 28 GENIC homozygous 559011856 18 61366283 61366284 G A 17 GENIC homozygous 559011857 18 61366536 61366537 G A 10 GENIC homozygous 559011858 18 61366558 61366559 G A 9 GENIC homozygous 561640478 18 61366569 61366570 G T 9 GENIC homozygous 561640479 18 61366584 61366585 G GGTT 10 GENIC homozygous 706362874 18 61366628 61366641 ATTGGGCAATGTC ------------- 14 GENIC homozygous 706362875 18 61367207 61367208 A G 11 GENIC homozygous 559011859 18 61367288 61367289 A AC 12 GENIC homozygous 706362876 18 61367351 61367352 T A 11 GENIC homozygous 559011860 18 61367374 61367375 G GTT 14 GENIC homozygous 706362878 18 61367467 61367468 A G 15 GENIC homozygous 559011861 18 61367570 61367571 G T 22 GENIC homozygous 559011862 18 61368285 61368286 G C 20 GENIC homozygous 559011863 18 61368317 61368318 T G 16 GENIC homozygous 559011864 18 61368365 61368366 G T 22 GENIC homozygous 559011865 18 61368515 61368516 T C 25 GENIC homozygous 559011866 18 61368576 61368577 T C 27 GENIC homozygous 559011867 18 61368965 61368966 G C 12 GENIC homozygous 559011868