chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14105925	14105926	T	C	31	GENIC	homozygous	51810147
10	14106005	14106006	C	A	25	GENIC	homozygous	51622751
10	14106440	14106441	T	C	23	GENIC	homozygous	51810149
10	14106477	14106478	G	C	22	GENIC	homozygous	51810151
10	14106850	14106854	TGTA	----	29	GENIC	homozygous	51810153
10	14107616	14107617	A	G	27	GENIC	homozygous	51810155
10	14108392	14108393	G	GA	17	GENIC	homozygous	51810157
10	14108942	14108943	C	CA	12	GENIC	heterozygous	51810159
10	14108944	14108948	AAAC	----	12	GENIC	homozygous	51622753
10	14108947	14108948	C	CA	8	GENIC	homozygous	51622754
10	14108957	14108959	AC	--	14	GENIC	heterozygous	51810161
10	14109038	14109039	A	G	26	GENIC	homozygous	51810163
10	14109271	14109272	C	A	27	GENIC	homozygous	51810165
10	14109282	14109283	T	A	27	GENIC	homozygous	51810167
10	14109649	14109650	C	CA	8	GENIC	homozygous	51622755
10	14109751	14109752	A	-	20	GENIC	homozygous	51622756
10	14109899	14109900	G	T	22	GENIC	homozygous	51622757
10	14111304	14111305	G	A	15	GENIC	homozygous	51810170
10	14111355	14111356	G	A	13	GENIC	homozygous	51810172
10	14111419	14111420	C	CAA	5	GENIC	heterozygous	51329123