chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	69874494	69874495	T	C	35	GENIC	homozygous	51486880
10	69875004	69875005	C	T	43	GENIC	homozygous	51486882
10	69875027	69875028	C	T	37	GENIC	homozygous	51486884
10	69875500	69875501	G	A	33	GENIC	possibly homozygous	51486886
10	69876063	69876064	C	CAGCTTGTTGTGAGCT	18	GENIC	homozygous	51486888
10	69876067	69876068	A	T	30	GENIC	heterozygous	51486890
10	69876428	69876429	T	TATTG	36	GENIC	homozygous	51486892
10	69876771	69876772	G	A	58	GENIC	homozygous	51486894
10	69876850	69876851	T	C	57	GENIC	homozygous	51486896
10	69877041	69877042	A	AC	30	GENIC	homozygous	51486898
10	69877211	69877212	C	A	51	GENIC	possibly homozygous	51486900
10	69877358	69877359	G	C	41	GENIC	heterozygous	51486902
10	69877488	69877489	C	T	24	GENIC	homozygous	51486904
10	69877546	69877548	AA	--	19	GENIC	homozygous	51486906
10	69877572	69877573	A	G	28	GENIC	homozygous	51486908
10	69877635	69877636	C	T	40	GENIC	homozygous	51486910
10	69877748	69877749	T	G	48	GENIC	homozygous	51486912
10	69877943	69877945	GT	--	16	GENIC	homozygous	51486914
10	69878394	69878395	T	C	21	GENIC	homozygous	51486916
10	69879434	69879435	C	T	42	GENIC	possibly homozygous	51486918
10	69879478	69879479	T	C	59	GENIC	homozygous	51486920
10	69879812	69879818	CACCCC	------	9	GENIC	homozygous	51486922
10	69879827	69879828	A	-	8	GENIC	possibly homozygous	51486924
10	69880614	69880615	A	G	59	GENIC	homozygous	51486926
10	69880815	69880816	C	T	55	GENIC	possibly homozygous	51486928