chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 24181726 24181727 G A 17 GENIC homozygous 938946727 11 24182790 24182791 G A 24 GENIC homozygous 938946728 11 24184004 24184005 G T 18 GENIC homozygous 938946729 11 24184007 24184008 T G 18 GENIC homozygous 938946730 11 24184459 24184460 C A 19 GENIC homozygous 938946731 11 24184907 24184908 A G 14 GENIC homozygous 938946732 11 24185670 24185671 T C 30 GENIC homozygous 938946733 11 24186683 24186684 A T 18 GENIC homozygous 938946734 11 24186841 24186842 G A 19 GENIC homozygous 938946735 11 24186930 24186931 C T 16 GENIC homozygous 938946736 11 24187185 24187186 A C 15 GENIC homozygous 938946737 11 24187616 24187617 C T 29 GENIC homozygous 938946738 11 24187969 24187970 C T 25 GENIC homozygous 938946739 11 24188161 24188162 G A 22 GENIC homozygous 938946740 11 24188628 24188629 A C 19 GENIC homozygous 938946741 11 24189688 24189689 T C 21 GENIC homozygous 938946742 11 24190552 24190553 C T 12 GENIC homozygous 938946743 11 24190555 24190556 G A 12 GENIC homozygous 938946744 11 24190710 24190711 A T 23 GENIC homozygous 938946745 11 24192103 24192104 C G 5 GENIC homozygous 938946746 11 24192104 24192105 G C 5 GENIC homozygous 938946747 11 24192654 24192655 C T 24 GENIC homozygous 938946748 11 24192822 24192823 C T 21 GENIC homozygous 938946749