chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 24181726 24181727 G A 11 GENIC homozygous 935907436 11 24182790 24182791 G A 27 GENIC possibly homozygous 935907437 11 24184004 24184005 G T 31 GENIC homozygous 935907438 11 24184007 24184008 T G 31 GENIC homozygous 935907439 11 24184459 24184460 C A 29 GENIC homozygous 935907440 11 24184907 24184908 A G 14 GENIC homozygous 935907441 11 24185318 24185319 C A 18 GENIC homozygous 935907442 11 24185670 24185671 T C 18 GENIC homozygous 935907443 11 24186683 24186684 A T 23 GENIC homozygous 935907444 11 24186841 24186842 G A 12 GENIC homozygous 935907445 11 24186930 24186931 C T 23 GENIC homozygous 935907446 11 24187185 24187186 A C 17 GENIC homozygous 935907447 11 24187616 24187617 C T 32 GENIC homozygous 935907448 11 24187969 24187970 C T 25 GENIC homozygous 935907449 11 24188161 24188162 G A 22 GENIC homozygous 935907450 11 24189688 24189689 T C 24 GENIC homozygous 935907451 11 24190552 24190553 C T 29 GENIC homozygous 935907452 11 24190555 24190556 G A 24 GENIC homozygous 935907453 11 24190710 24190711 A T 26 GENIC homozygous 935907454 11 24192822 24192823 C T 13 GENIC homozygous 935907455