chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14216455	14216456	C	A	23	GENIC	homozygous	51622873
10	14217079	14217080	A	-	17	GENIC	homozygous	51622874
10	14218258	14218259	T	G	20	GENIC	possibly homozygous	51622875
10	14218600	14218601	T	C	16	GENIC	possibly homozygous	51329145
10	14218908	14218909	C	T	24	GENIC	homozygous	51622876
10	14219473	14219474	A	G	24	GENIC	possibly homozygous	51622877
10	14219648	14219649	A	T	8	GENIC	homozygous	51622878
10	14219789	14219790	T	C	22	GENIC	homozygous	51622879
10	14220061	14220062	T	C	17	GENIC	possibly homozygous	51622880
10	14221193	14221194	T	C	15	GENIC	heterozygous	51622881
10	14222353	14222354	G	A	11	GENIC	homozygous	51622882
10	14223483	14223484	G	A	6	GENIC	homozygous	51622883
10	14223638	14223639	G	A	17	GENIC	homozygous	51622884
10	14223705	14223706	C	-	15	GENIC	homozygous	51622885
10	14224024	14224025	C	T	21	GENIC	possibly homozygous	51622886
10	14224476	14224477	C	CTTTTT	3	GENIC	heterozygous	51329147
10	14225670	14225671	G	A	15	GENIC	possibly homozygous	51622888
10	14226319	14226320	T	-	22	GENIC	homozygous	51622889
10	14227096	14227097	T	C	9	GENIC	possibly homozygous	51622890
10	14228030	14228031	A	C	14	GENIC	homozygous	51622893
10	14228068	14228077	GTGCAATGA	---------	1	GENIC	homozygous	51622894
10	14228310	14228311	T	C	17	GENIC	heterozygous	51622895
10	14229328	14229329	T	G	22	GENIC	possibly homozygous	51622896
10	14229371	14229372	G	A	13	GENIC	heterozygous	51622897
10	14229677	14229678	G	A	24	GENIC	heterozygous	51622898