chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 61365512 61365513 T C 14 GENIC homozygous 591993242 18 61365591 61365592 G T 21 GENIC homozygous 591993243 18 61366037 61366038 C G 43 GENIC homozygous 591993244 18 61366058 61366059 T C 42 GENIC homozygous 591993245 18 61366089 61366090 C G 39 GENIC homozygous 591993246 18 61366218 61366219 T G 41 GENIC homozygous 591993247 18 61366283 61366284 G A 40 GENIC homozygous 591993248 18 61366536 61366537 G A 43 GENIC homozygous 591993249 18 61366558 61366559 G A 44 GENIC homozygous 594710584 18 61366569 61366570 G T 42 GENIC homozygous 594710585 18 61366584 61366585 G GGT 30 GENIC possibly homozygous 725050031 18 61366584 61366585 G GGTT 30 GENIC heterozygous 725050032 18 61366628 61366641 ATTGGGCAATGTC ------------- 35 GENIC homozygous 725050033 18 61367046 61367047 G A 19 GENIC homozygous 591993250 18 61367207 61367208 A G 22 GENIC homozygous 591993251 18 61367288 61367289 A AC 9 GENIC homozygous 725050034 18 61367351 61367352 T A 18 GENIC homozygous 591993252 18 61367374 61367375 G GTT 13 GENIC heterozygous 725050036 18 61367374 61367375 G GTTT 13 GENIC possibly homozygous 725050037 18 61367467 61367468 A G 27 GENIC homozygous 591993253 18 61367570 61367571 G T 31 GENIC homozygous 591993254 18 61368285 61368286 G C 35 GENIC homozygous 591993255 18 61368515 61368516 T C 33 GENIC homozygous 591993256 18 61368576 61368577 T C 39 GENIC homozygous 591993257 18 61368965 61368966 G C 27 GENIC homozygous 591993258