chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	69874494	69874495	T	C	11	GENIC	possibly homozygous	51486880
10	69875004	69875005	C	T	3	GENIC	homozygous	51486882
10	69875027	69875028	C	T	4	GENIC	homozygous	51486884
10	69875500	69875501	G	A	14	GENIC	possibly homozygous	51486886
10	69876428	69876429	T	TATTG	7	GENIC	homozygous	51486892
10	69876771	69876772	G	A	12	GENIC	possibly homozygous	51486894
10	69876850	69876851	T	C	11	GENIC	possibly homozygous	51486896
10	69877041	69877042	A	AC	5	GENIC	heterozygous	51486898
10	69877044	69877045	T	C	5	GENIC	heterozygous	52764264
10	69877211	69877212	C	A	12	GENIC	homozygous	51486900
10	69877488	69877489	C	T	11	GENIC	homozygous	51486904
10	69877635	69877636	C	T	18	GENIC	homozygous	51486910
10	69877748	69877749	T	G	10	GENIC	possibly homozygous	51486912
10	69877943	69877945	GT	--	7	GENIC	possibly homozygous	51486914
10	69878394	69878395	T	C	8	GENIC	homozygous	51486916
10	69879434	69879435	C	T	10	GENIC	heterozygous	51486918
10	69879478	69879479	T	C	6	GENIC	homozygous	51486920
10	69880614	69880615	A	G	10	GENIC	homozygous	51486926
10	69880815	69880816	C	T	5	GENIC	homozygous	51486928