chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	30654351	30654352	A	G	32	GENIC	homozygous	117498395
9	30654353	30654354	T	C	33	GENIC	homozygous	117498397
9	30654354	30654355	C	T	33	GENIC	homozygous	117498399
9	30654355	30654356	A	G	32	GENIC	homozygous	117498401
9	30654383	30654384	C	T	28	GENIC	homozygous	117304907
9	30752445	30752446	G	A	20	GENIC	homozygous	117305113
9	30772323	30772324	A	C	8	GENIC	homozygous	117492203
9	30778593	30778594	C	T	13	GENIC	homozygous	117305206
9	30778606	30778607	G	A	18	GENIC	homozygous	117305207
9	30778617	30778618	T	G	20	GENIC	homozygous	117498823
9	30778618	30778619	C	T	21	GENIC	homozygous	117498825
9	30778627	30778628	T	G	22	GENIC	homozygous	117305208
9	30778641	30778642	G	T	25	GENIC	homozygous	117498829
9	30779901	30779902	A	G	30	GENIC	homozygous	117305210
9	30857433	30857434	G	T	21	GENIC	homozygous	117305377
9	30857585	30857586	G	C	20	GENIC	homozygous	117499103