chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	103545864	103545865	C	G	12	GENIC	homozygous	51588851
10	103545878	103545879	C	T	12	GENIC	homozygous	51588853
10	103547464	103547465	T	TC	21	GENIC	homozygous	51588855
10	103549345	103549346	T	-	10	GENIC	heterozygous	51588857
10	103557249	103557250	C	A	48	GENIC	heterozygous	51588863
10	103557296	103557297	G	A	45	GENIC	heterozygous	51588865
10	103557332	103557333	G	A	43	GENIC	heterozygous	51946049
10	103557441	103557442	T	C	35	GENIC	heterozygous	51588867
10	103557472	103557473	T	C	34	GENIC	heterozygous	51588869
10	103557507	103557508	G	A	32	GENIC	heterozygous	51588871
10	103557515	103557516	A	AC	27	GENIC	heterozygous	51588873
10	103557529	103557530	C	T	31	GENIC	heterozygous	51760861
10	103557530	103557531	G	A	30	GENIC	heterozygous	51946052
10	103557548	103557549	C	T	26	GENIC	heterozygous	51760863
10	103557549	103557550	A	G	27	GENIC	heterozygous	51760865
10	103557560	103557561	A	G	31	GENIC	heterozygous	51946055
10	103557566	103557567	T	C	33	GENIC	heterozygous	51946058