chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14034061	14034062	T	C	20	GENIC	possibly homozygous	51622644
10	14034338	14034339	A	-	5	GENIC	homozygous	51622646
10	14034627	14034628	G	A	8	GENIC	possibly homozygous	51622647
10	14034869	14034870	C	A	10	GENIC	possibly homozygous	51622648
10	14037333	14037334	G	C	19	GENIC	homozygous	51622651
10	14039205	14039206	T	C	23	GENIC	possibly homozygous	51622652
10	14043753	14043754	A	G	19	GENIC	heterozygous	51622655
10	14044236	14044237	T	C	19	GENIC	possibly homozygous	51622656
10	14044937	14044941	TTTG	----	5	GENIC	homozygous	51622657
10	14045329	14045330	G	A	19	GENIC	heterozygous	51622658
10	14045400	14045401	T	TTCCTGGGAGC	2	GENIC	homozygous	51622659