chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 153561408 153561409 A T 6 GENIC homozygous 896616481 X 153561689 153561690 G T 6 GENIC homozygous 896616480 X 153563062 153563063 G C 10 GENIC heterozygous 896616479 X 153568757 153568758 G T 3 GENIC heterozygous 895729733 X 153719311 153719312 G A 6 GENIC homozygous 896616478 X 153719364 153719365 A T 12 GENIC homozygous 896616477 X 153719374 153719375 A T 11 GENIC homozygous 896616476 X 153719399 153719400 T A 4 GENIC homozygous 896616475 X 153719436 153719437 C T 12 GENIC homozygous 896616474 X 153719484 153719485 A G 7 GENIC homozygous 896616473 X 153719485 153719486 G A 7 GENIC homozygous 896616472 X 153719491 153719492 T C 8 GENIC homozygous 896616471 X 153719493 153719494 C T 7 GENIC homozygous 896616470 X 153723221 153723222 T C 11 GENIC homozygous 896616469 X 153730957 153730958 C G 9 GENIC heterozygous 896616468 X 153730959 153730960 T C 9 GENIC heterozygous 896616467 X 153731005 153731006 A T 14 GENIC heterozygous 896616466 X 153755316 153755317 G C 12 GENIC homozygous 896616465 X 153802093 153802094 G T 10 GENIC heterozygous 896616464 X 153817525 153817526 G A 11 GENIC homozygous 896616463 X 153913999 153914000 A G 13 GENIC heterozygous 896616461 X 153914008 153914009 A T 17 GENIC heterozygous 896616460 X 153914489 153914490 A G 14 GENIC homozygous 896616459