chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	113531956	113531957	C	G	10	GENIC	homozygous	113557222
14	113533611	113533612	G	A	29	GENIC	homozygous	113557224
14	113540553	113540554	C	T	19	GENIC	homozygous	113557226
14	113541006	113541007	T	C	27	GENIC	homozygous	113557228
14	113541082	113541083	G	T	20	GENIC	homozygous	113557230
14	113541309	113541310	C	T	17	GENIC	homozygous	113557232
14	113544101	113544102	G	A	17	GENIC	homozygous	113557234
14	113544204	113544205	A	C	8	GENIC	homozygous	113557236
14	113544933	113544934	A	G	27	GENIC	homozygous	113557238
14	113544941	113544942	C	A	26	GENIC	homozygous	113557240
14	113545196	113545197	A	G	23	GENIC	homozygous	113557242
14	113547706	113547707	G	A	20	GENIC	homozygous	113557244
14	113549446	113549447	A	C	31	GENIC	homozygous	113557246
14	113556302	113556303	G	T	19	GENIC	homozygous	113557248
14	113556303	113556304	G	A	19	GENIC	homozygous	113557250
14	113556304	113556305	G	T	19	GENIC	homozygous	113557252
14	113559595	113559596	G	A	22	GENIC	homozygous	113557256
14	113555237	113555238	G	A	7	GENIC	homozygous	113699697
14	113555238	113555239	T	C	7	GENIC	homozygous	113699699