chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	168126610	168126611	C	A	57	GENIC	homozygous	114083380
5	168126777	168126778	G	A	46	GENIC	homozygous	119206943
5	168127183	168127184	A	C	49	GENIC	possibly homozygous	119252653
5	168127389	168127392	AAC		40	GENIC	possibly homozygous	132845787
5	168127730	168127731	C	A	40	GENIC	homozygous	119206944
5	168128029	168128030	T	C	54	GENIC	homozygous	114083382
5	168131414	168131415	G	A	46	GENIC	homozygous	119206945
5	168131868	168131869	C	T	55	GENIC	homozygous	114083386
5	168132020	168132021	C	T	44	GENIC	homozygous	114083388
5	168132075	168132076	C	T	56	GENIC	homozygous	119206946
5	168132288	168132289	A	G	52	GENIC	homozygous	114083390
5	168133726	168133727	C	T	36	GENIC	possibly homozygous	119206947
5	168134009	168134010	C	T	51	GENIC	homozygous	119206948
5	168134097	168134098	G	A	49	GENIC	possibly homozygous	119206949
5	168134590	168134591	G	A	40	GENIC	homozygous	119206950
5	168136058	168136059	G	A	65	GENIC	homozygous	114083394
5	168135594	168135594		T	48	GENIC	homozygous	128270264