chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109803424	109803425	A	G	14	GENIC	homozygous	116719121
10	109805182	109805183	G	A	23	GENIC	homozygous	116909769
10	109805336	109805337	T	C	12	GENIC	homozygous	116719123
10	109806708	109806709	T	C	21	GENIC	homozygous	116719125
10	109806825	109806826	G	A	27	GENIC	homozygous	116719127
10	109807251	109807252	C	G	23	GENIC	homozygous	116909770
10	109808018	109808019	A	G	24	GENIC	homozygous	116719129
10	109808148	109808149	A	T	16	GENIC	homozygous	116719131
10	109808369	109808370	T	C	16	GENIC	homozygous	116719133
10	109809128	109809129	C	T	19	GENIC	homozygous	116719135
10	109809149	109809150	T	C	19	GENIC	homozygous	116719137
10	109809559	109809560	C	A	20	GENIC	homozygous	116719139
10	109810385	109810386	A	G	13	GENIC	homozygous	116719141
10	109810682	109810683	T	C	13	GENIC	homozygous	116719143
10	109809226	109809226		T	14	GENIC	homozygous	128860726
10	109809289	109809289		TGTGTGCA	19	GENIC	homozygous	132148075