chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 24181726 24181727 G A 21 GENIC homozygous 991644614 11 24182790 24182791 G A 17 GENIC homozygous 991644615 11 24184004 24184005 G T 20 GENIC homozygous 991644616 11 24184007 24184008 T G 22 GENIC homozygous 991644617 11 24184459 24184460 C A 14 GENIC homozygous 991644618 11 24184907 24184908 A G 12 GENIC homozygous 991644619 11 24185318 24185319 C A 28 GENIC homozygous 991644620 11 24185670 24185671 T C 32 GENIC homozygous 991644621 11 24186683 24186684 A T 18 GENIC homozygous 991644622 11 24186841 24186842 G A 18 GENIC homozygous 991644623 11 24186930 24186931 C T 17 GENIC homozygous 991644624 11 24187185 24187186 A C 12 GENIC homozygous 991644625 11 24187616 24187617 C T 26 GENIC homozygous 991644626 11 24187969 24187970 C T 25 GENIC homozygous 991644627 11 24188161 24188162 G A 20 GENIC homozygous 991644628 11 24188628 24188629 A C 29 GENIC homozygous 991644629 11 24189688 24189689 T C 22 GENIC homozygous 991644630 11 24190552 24190553 C T 27 GENIC homozygous 991644631 11 24190555 24190556 G A 28 GENIC homozygous 991644632 11 24190710 24190711 A T 13 GENIC homozygous 991644633 11 24192049 24192050 A G 6 GENIC homozygous 991644634 11 24192062 24192063 C G 6 GENIC homozygous 991644635 11 24192093 24192094 G T 2 GENIC homozygous 991644636 11 24192103 24192104 C G 2 GENIC homozygous 991644637 11 24192104 24192105 G C 2 GENIC homozygous 991644638 11 24192654 24192655 C T 23 GENIC homozygous 991644639 11 24192822 24192823 C T 23 GENIC homozygous 991644640