chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	113318890	113318891	C	A	13	GENIC	homozygous	112008181
3	113319621	113319622	C	T	6	GENIC	heterozygous	111676989
3	113320014	113320015	C	T	17	GENIC	homozygous	112008183
3	113320488	113320489	C	T	11	GENIC	heterozygous	111677015
3	113320531	113320532	C	A	12	GENIC	heterozygous	111677016
3	113320559	113320560	G	T	15	GENIC	heterozygous	111677018
3	113321043	113321044	G	A	16	GENIC	homozygous	112008206
3	113321345	113321346	C	T	12	GENIC	homozygous	112008208
3	113321444	113321445	C	G	11	GENIC	heterozygous	111677026
3	113321596	113321597	G	A	13	GENIC	heterozygous	111677034
3	113321921	113321922	T	C	25	GENIC	homozygous	112008218
3	113322235	113322236	A	G	18	GENIC	homozygous	112008220
3	113322553	113322554	G	A	17	GENIC	homozygous	112008228
3	113322591	113322592	A	T	20	GENIC	homozygous	112008230
3	113322691	113322692	T	C	11	GENIC	homozygous	112008232
3	113322845	113322846	A	G	11	GENIC	homozygous	112008234
3	113323304	113323305	A	G	22	GENIC	homozygous	112008238
3	113323684	113323685	C	T	15	GENIC	homozygous	112008256
3	113324342	113324343	T	C	20	GENIC	homozygous	111677073
3	113324386	113324387	A	G	15	GENIC	heterozygous	111677075
3	113324423	113324424	A	C	9	GENIC	heterozygous	111677076