chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	61404392	61404393	A	T	22	GENIC	homozygous	116612733
10	61404899	61404900	C	A	29	GENIC	homozygous	116612735
10	61406197	61406198	C	T	16	GENIC	homozygous	116612737
10	61406226	61406227	A	T	13	GENIC	homozygous	117295720
10	61407281	61407282	A	G	26	GENIC	homozygous	116612741
10	61411680	61411681	T	C	15	GENIC	homozygous	116612747
10	61411681	61411682	C	T	15	GENIC	homozygous	116612749
10	61411687	61411688	T	C	16	GENIC	homozygous	116612751
10	61412751	61412752	A	G	27	GENIC	homozygous	116612757
10	61413119	61413120	T	C	14	GENIC	homozygous	116612759
10	61413125	61413126	A	G	13	GENIC	homozygous	116612761
10	61413326	61413327	G	A	11	GENIC	homozygous	117295722
10	61414391	61414392	T	C	35	GENIC	homozygous	116612765
10	61414893	61414894	G	T	20	GENIC	homozygous	116612769
10	61415380	61415381	T	G	15	GENIC	homozygous	116612771
10	61416202	61416203	T	G	16	GENIC	homozygous	116790521
10	61416897	61416898	G	T	25	GENIC	homozygous	117295724
10	61418381	61418382	A	C	8	GENIC	homozygous	116612775
10	61419199	61419200	G	A	8	GENIC	homozygous	117295726
10	61419465	61419466	T	G	22	GENIC	homozygous	116612779
10	61419537	61419538	C	A	19	GENIC	homozygous	116790525
10	61419548	61419549	G	C	20	GENIC	homozygous	116790527
10	61419837	61419838	A	C	22	GENIC	homozygous	116612781
10	61419879	61419880	C	G	9	GENIC	homozygous	116612783
10	61420449	61420450	G	A	15	GENIC	homozygous	116612787