chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 108892487 108892488 T C 53 GENIC homozygous 112642703 15 108893582 108893583 T C 46 GENIC homozygous 112642705 15 108893674 108893675 C T 33 GENIC homozygous 112642707 15 108893762 108893763 A C 41 GENIC possibly homozygous 113080421 15 108893765 108893766 A C 43 GENIC heterozygous 112642709 15 108893964 108893965 C T 46 GENIC homozygous 112865621 15 108894621 108894622 T C 39 GENIC possibly homozygous 112642711 15 108895108 108895109 T C 61 GENIC homozygous 112642713 15 108895471 108895472 T C 38 GENIC homozygous 112642715 15 108895977 108895978 T C 53 GENIC homozygous 112642717 15 108896318 108896319 G A 56 GENIC homozygous 112642719 15 108896716 108896717 A G 40 GENIC possibly homozygous 112642721 15 108896808 108896809 G A 27 GENIC heterozygous 112642723 15 108896810 108896811 G A 27 GENIC homozygous 112642725 15 108898766 108898767 A G 43 GENIC homozygous 112642727 15 108898891 108898892 A G 35 GENIC possibly homozygous 112642730 15 108899054 108899055 T C 45 GENIC homozygous 112642732 15 108899535 108899536 G A 35 GENIC homozygous 112642734 15 108901061 108901062 A T 43 GENIC homozygous 112642736 15 108901355 108901356 C T 67 GENIC homozygous 112865623 15 108901824 108901825 T G 47 GENIC homozygous 112642739 15 108904357 108904358 A G 56 GENIC homozygous 112642745 15 108904397 108904398 G T 54 GENIC homozygous 112865627 15 108904689 108904690 G T 62 GENIC homozygous 112865629 15 108905657 108905658 T C 36 GENIC homozygous 112642748 15 108906724 108906725 A G 38 GENIC homozygous 112642750 15 108907099 108907100 G C 22 GENIC homozygous 112642752 15 108904888 108904889 A T 42 GENIC homozygous 113013393 15 108904916 108904917 C G 40 GENIC homozygous 113013395