chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	40441649	40441650	T	A	21	GENIC	homozygous	116927639
10	40441660	40441661	C	T	17	GENIC	homozygous	116569260
10	40443489	40443490	T	C	29	GENIC	homozygous	116569262
10	40445186	40445187	C	A	20	GENIC	homozygous	116927641
10	40446610	40446611	C	T	22	GENIC	homozygous	116927643
10	40446844	40446845	C	T	28	GENIC	homozygous	116927645
10	40447474	40447475	A	G	37	GENIC	homozygous	116569278
10	40449212	40449213	C	G	33	GENIC	homozygous	116927647
10	40449483	40449484	A	T	41	GENIC	homozygous	116927649
10	40449612	40449613	T	C	34	GENIC	homozygous	116569280
10	40449639	40449640	G	C	35	GENIC	homozygous	116569282
10	40449961	40449962	A	C	26	GENIC	homozygous	116569284
10	40450040	40450041	A	T	34	GENIC	homozygous	116927651
10	40450189	40450190	G	A	43	GENIC	homozygous	116569286
10	40450385	40450386	A	G	28	GENIC	homozygous	116569288
10	40450626	40450627	C	A	20	GENIC	homozygous	116569290
10	40450648	40450649	A	G	21	GENIC	homozygous	116569292