chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	104301940	104301941	T	C	45	GENIC	homozygous	117631212
9	104301945	104301946	G	T	43	GENIC	homozygous	117631214
9	104301949	104301950	T	C	46	GENIC	homozygous	117631216
9	104301950	104301951	A	T	45	GENIC	homozygous	117631218
9	104327490	104327490		AAAG	40	GENIC	homozygous	128740054
9	104331612	104331613	G	C	44	GENIC	homozygous	117631414
9	104331779	104331780	T	C	3	GENIC	homozygous	117787589
9	104331778	104331779	C	G	3	GENIC	homozygous	117787588
9	104331794	104331795	G	A	9	GENIC	homozygous	117631416
9	104331802	104331803	T	A	10	GENIC	homozygous	117408886
9	104331805	104331806	G	T	12	GENIC	homozygous	117408888
9	104331838	104331839	C	T	13	GENIC	homozygous	117408890
9	104331840	104331841	C	G	13	GENIC	homozygous	117408892
9	104331851	104331852	A		16	GENIC	homozygous	128740056
9	104342693	104342694	G	C	28	GENIC	homozygous	117631434
9	104342694	104342695	A	T	28	GENIC	homozygous	117408916
9	104342699	104342700	G	C	27	GENIC	homozygous	117408918
9	104342719	104342720	A	C	28	GENIC	homozygous	117408919
9	104342721	104342722	A	T	27	GENIC	homozygous	117408921
9	104342732	104342732		CT	26	GENIC	homozygous	128740062
9	104342734	104342736	GG		26	GENIC	homozygous	128740063
9	104342743	104342744	T	A	27	GENIC	homozygous	117408923
9	104342744	104342745	C	A	27	GENIC	homozygous	117631436
9	104342755	104342756	G	A	23	GENIC	homozygous	117408927
9	104342765	104342766	C	A	19	GENIC	homozygous	117408929
9	104348835	104348836	T	A	17	GENIC	homozygous	117408945
9	104349015	104349016	T	C	26	GENIC	homozygous	117631452
9	104349035	104349036	A		24	GENIC	homozygous	128740068
9	104349038	104349039	C		24	GENIC	homozygous	128740069
9	104349042	104349043	C		24	GENIC	homozygous	128740070