chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	34008844	34008845	A	G	13	GENIC	homozygous	113728144
5	34010404	34010405	A	G	27	GENIC	homozygous	113728146
5	34014487	34014488	C	T	22	GENIC	homozygous	113728148
5	34015213	34015214	C	T	4	GENIC	homozygous	113728150
5	34015217	34015218	C	T	3	GENIC	homozygous	113728152
5	34015221	34015222	C	T	3	GENIC	homozygous	113728154
5	34015467	34015468	C	T	7	GENIC	homozygous	113728158
5	34015548	34015549	C	T	22	GENIC	homozygous	113728160
5	34015640	34015641	T	A	19	GENIC	homozygous	113728162
5	34015667	34015668	G	A	16	GENIC	homozygous	113728164
5	34015680	34015681	G	C	12	GENIC	homozygous	113728166
5	34015710	34015711	T	C	15	GENIC	homozygous	113728168
5	34015715	34015716	T	C	15	GENIC	homozygous	113728170
5	34016180	34016181	G	A	16	GENIC	homozygous	113728172
5	34016367	34016368	T	C	18	GENIC	homozygous	113728174
5	34019146	34019147	T	A	14	GENIC	homozygous	113728176
5	34019595	34019596	A	G	25	GENIC	possibly homozygous	113728178
5	34019769	34019770	T	C	16	GENIC	homozygous	113728180
5	34019796	34019797	C	T	13	GENIC	homozygous	113728182
5	34022023	34022024	A	G	17	GENIC	homozygous	113728184
5	34022377	34022378	C	G	26	GENIC	homozygous	113728186
5	34023200	34023201	G	A	50	GENIC	heterozygous	113728188
5	34023296	34023297	T	A	16	GENIC	homozygous	113728190