chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 61365342 61365343 A T 18 GENIC homozygous 626849538 18 61365591 61365592 G T 13 GENIC homozygous 626849539 18 61366058 61366059 T C 27 GENIC homozygous 626849540 18 61366089 61366090 C G 29 GENIC homozygous 626849541 18 61366283 61366284 G A 28 GENIC homozygous 626849542 18 61366536 61366537 G A 30 GENIC homozygous 626849543 18 61366558 61366559 G A 30 GENIC homozygous 626849544 18 61366569 61366570 G T 26 GENIC homozygous 626849545 18 61366584 61366585 G GGTT 20 GENIC homozygous 743569917 18 61366628 61366641 ATTGGGCAATGTC ------------- 19 GENIC homozygous 743569918 18 61367207 61367208 A G 12 GENIC homozygous 626849546 18 61367288 61367289 A AC 12 GENIC homozygous 743569919 18 61367351 61367352 T A 14 GENIC homozygous 626849547 18 61367374 61367375 G GTT 14 GENIC homozygous 743569921 18 61367467 61367468 A G 19 GENIC homozygous 626849548 18 61367570 61367571 G T 19 GENIC homozygous 626849549 18 61368285 61368286 G C 28 GENIC homozygous 626849550 18 61368317 61368318 T G 28 GENIC homozygous 626849551 18 61368365 61368366 G T 26 GENIC homozygous 626849552 18 61368515 61368516 T C 25 GENIC homozygous 626849553 18 61368576 61368577 T C 22 GENIC homozygous 626849554 18 61368965 61368966 G C 29 GENIC homozygous 626849555