chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14948797	14948797		CCTCTT	54	GENIC	possibly homozygous	142197048
10	14949103	14949104	T	G	55	GENIC	homozygous	142219179
10	14949106	14949107	G		53	GENIC	possibly homozygous	142197049
10	14949663	14949663		ATT	57	GENIC	homozygous	142197050
10	14949666	14949666		GAA	56	GENIC	homozygous	142197051
10	14949668	14949671	TTC		60	GENIC	homozygous	142197052
10	14949674	14949676	AA		58	GENIC	homozygous	142197053
10	14949681	14949682	A	C	61	GENIC	homozygous	142219180
10	14949684	14949685	T	C	61	GENIC	homozygous	142219181
10	14950704	14950705	A	C	68	GENIC	homozygous	142219182
10	14951153	14951154	C	T	77	GENIC	homozygous	142219183
10	14953671	14953672	C	T	78	GENIC	homozygous	142219184
10	14956400	14956401	G	A	55	GENIC	homozygous	142219185
10	14956565	14956565		CT	29	GENIC	homozygous	142197054
10	14957877	14957878	G	A	81	GENIC	homozygous	142219186
10	14951839	14951840	G	T	17	GENIC	homozygous	154679353
10	14951839	14951840	G		17	GENIC	heterozygous	403277091