chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	48034526	48034527	T	C	25	GENIC	homozygous	58801911
2	48035248	48035249	T	A	29	GENIC	homozygous	61343699
2	48036168	48036169	T	C	39	GENIC	homozygous	58801912
2	48036901	48036902	T	C	29	GENIC	homozygous	58801915
2	48037074	48037075	C	A	24	GENIC	homozygous	58801918
2	48038026	48038027	T	-	18	GENIC	possibly homozygous	58801927
2	48039227	48039228	A	G	37	GENIC	homozygous	58801940
2	48040469	48040470	G	A	36	GENIC	homozygous	59802836
2	48040607	48040608	G	A	28	GENIC	homozygous	59802837
2	48041650	48041651	T	C	17	GENIC	homozygous	58801951
2	48042522	48042523	A	C	25	GENIC	homozygous	58801953
2	48042689	48042690	G	A	22	GENIC	homozygous	59802838
2	48043207	48043208	G	A	30	GENIC	homozygous	58801955
2	48043211	48043212	C	G	27	GENIC	homozygous	58801957
2	48043289	48043290	C	T	32	GENIC	homozygous	58801959
2	48043324	48043325	G	T	29	GENIC	homozygous	58801961
2	48043777	48043778	C	CGTGTGTGTGTGT	1	GENIC	homozygous	60539379
2	48043940	48043941	G	A	26	GENIC	homozygous	59802840
2	48043946	48043947	T	C	28	GENIC	homozygous	58801963
2	48044133	48044134	A	AATTT	32	GENIC	homozygous	59802841