chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	76637992	76637993	C	G	26	GENIC	homozygous	110409581
18	76638119	76638120	C	T	26	GENIC	homozygous	110870155
18	76638248	76638249	A	G	13	GENIC	homozygous	110409583
18	76638266	76638267	C	T	15	GENIC	homozygous	110409585
18	76639243	76639244	C	T	27	GENIC	homozygous	110409589
18	76639252	76639253	T	C	27	GENIC	homozygous	110409591
18	76639466	76639467	T	C	27	GENIC	homozygous	110409593
18	76639785	76639786	T	G	25	GENIC	homozygous	110409595
18	76641039	76641040	T	C	30	GENIC	homozygous	110409597
18	76644008	76644009	C	T	20	GENIC	homozygous	110409599
18	76646691	76646692	T	C	22	GENIC	homozygous	110870157
18	76649042	76649043	C	T	15	GENIC	homozygous	110409603
18	76650326	76650327	A	G	17	GENIC	homozygous	110732989
18	76640353	76640354	G	A	8	GENIC	homozygous	119502340
18	76642339	76642340	T	C	17	GENIC	homozygous	131762189
18	76644952	76644952		ATGTGTTCTGTGTGCATGC	24	GENIC	homozygous	131758423
18	76646076	76646078	TT		15	GENIC	homozygous	131758424
18	76659020	76659021	T	C	19	GENIC	homozygous	110870159
18	76660312	76660313	A		22	GENIC	homozygous	129554769
18	76660360	76660361	A		21	GENIC	homozygous	129554770