chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14032439	14032440	C	T	34	GENIC	homozygous	51982582
10	14034061	14034062	T	C	28	GENIC	homozygous	51622644
10	14034627	14034628	G	A	13	GENIC	homozygous	51622647
10	14035315	14035316	C	CAAAA	18	GENIC	possibly homozygous	52356527
10	14036759	14036760	A	-	15	GENIC	possibly homozygous	51622650
10	14037333	14037334	G	C	29	GENIC	homozygous	51622651
10	14038073	14038074	A	T	33	GENIC	homozygous	51810025
10	14039205	14039206	T	C	25	GENIC	homozygous	51622652
10	14040127	14040128	G	GGGC	22	GENIC	homozygous	51810027
10	14040129	14040130	T	TGGCC	22	GENIC	homozygous	51810031
10	14041046	14041054	GTGTGTGT	--------	5	GENIC	heterozygous	52481274
10	14041052	14041054	GT	--	5	GENIC	heterozygous	52481278
10	14041114	14041115	A	ATGTGTGTGTAGTATGTGG	14	GENIC	homozygous	52313039
10	14042089	14042090	C	T	43	GENIC	homozygous	51810033
10	14044937	14044941	TTTG	----	11	GENIC	homozygous	51622657
10	14045400	14045401	T	TTCCTGGAGC	34	GENIC	homozygous	51810035