chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 61365512 61365513 T C 3 GENIC homozygous 595394535 18 61365591 61365592 G T 16 GENIC homozygous 595394536 18 61366037 61366038 C G 27 GENIC possibly homozygous 595394537 18 61366058 61366059 T C 22 GENIC possibly homozygous 595394538 18 61366089 61366090 C G 16 GENIC possibly homozygous 595394539 18 61366218 61366219 T G 21 GENIC possibly homozygous 595394540 18 61366283 61366284 G A 13 GENIC possibly homozygous 595394541 18 61366536 61366537 G A 9 GENIC homozygous 595394542 18 61366558 61366559 G A 2 GENIC homozygous 597989898 18 61366569 61366570 G T 2 GENIC homozygous 597989899 18 61366628 61366641 ATTGGGCAATGTC ------------- 2 GENIC homozygous 726724559 18 61367046 61367047 G A 6 GENIC homozygous 595394543 18 61367207 61367208 A G 12 GENIC homozygous 595394544 18 61367288 61367289 A AC 11 GENIC homozygous 726724560 18 61367351 61367352 T A 11 GENIC possibly homozygous 595394545 18 61367467 61367468 A G 17 GENIC homozygous 595394546 18 61367570 61367571 G T 19 GENIC homozygous 595394547 18 61368285 61368286 G C 17 GENIC possibly homozygous 595394548 18 61368515 61368516 T C 16 GENIC homozygous 595394549 18 61368576 61368577 T C 19 GENIC possibly homozygous 595394550 18 61368965 61368966 G C 15 GENIC homozygous 595394551