chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	129479785	129479786	G	C	44	GENIC	homozygous	137620137
5	129479796	129479797	T	A	45	GENIC	homozygous	137620138
5	129481792	129481793	T	C	40	GENIC	homozygous	137620143
5	129483238	129483239	C	T	47	GENIC	homozygous	143959110
5	129481164	129481165	C	A	42	GENIC	homozygous	143959109
5	129487826	129487827	C	G	51	GENIC	homozygous	143959111
5	129480722	129480723	G	A	38	GENIC	homozygous	143959108
5	129488732	129488733	A	G	51	GENIC	homozygous	137620147
5	129490010	129490011	G	A	39	GENIC	homozygous	143959112
5	129490213	129490214	A	G	25	GENIC	homozygous	137620148
5	129490803	129490804	C	T	14	GENIC	heterozygous	143959113
5	129492324	129492325	A	G	42	GENIC	homozygous	137620154
5	129492648	129492649	C	T	46	GENIC	homozygous	143959114
5	129493965	129493966	A	G	44	GENIC	homozygous	137620157
5	129495783	129495784	C	T	48	GENIC	homozygous	143959115
5	129497257	129497258	C	T	47	GENIC	homozygous	143959116
5	129489317	129489318	A	G	18	GENIC	homozygous	154318249
5	129494831	129494832	A		13	GENIC	homozygous	137341063
5	129497494	129497494		ACTC	44	GENIC	homozygous	143943612