chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	63872170	63872171	T	C	21	GENIC	possibly homozygous	52004111
9	63873196	63873197	C	T	21	GENIC	possibly homozygous	52004112
9	63873985	63873986	T	G	22	GENIC	possibly homozygous	52004113
9	63874370	63874371	C	T	16	GENIC	possibly homozygous	52004114
9	63874709	63874710	C	T	9	GENIC	homozygous	52004115
9	63874801	63874802	T	TC	19	GENIC	possibly homozygous	52004116
9	63874848	63874849	T	C	13	GENIC	possibly homozygous	52004117
9	63878663	63878664	C	A	12	GENIC	possibly homozygous	52004121
9	63879699	63879700	G	GTGTTT	3	GENIC	heterozygous	52004122
9	63880350	63880351	G	C	17	GENIC	homozygous	52004123
9	63880784	63880785	C	CGTG	10	GENIC	heterozygous	52004124