chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	47621249	47621250	A	G	50	GENIC	homozygous	60697861
1	47625577	47625578	A	ATTTT	6	GENIC	heterozygous	60697862
1	47625594	47625595	G	T	34	GENIC	heterozygous	61290430
1	47627351	47627352	C	T	69	GENIC	homozygous	60697863
1	47627845	47627846	C	A	54	GENIC	homozygous	60697864
1	47627846	47627847	A	G	54	GENIC	homozygous	60697865
1	47628165	47628166	T	C	61	GENIC	homozygous	60697866
1	47629878	47629879	C	CAAA	15	GENIC	homozygous	60697867
1	47629896	47629897	G	A	40	GENIC	heterozygous	60697868
1	47630241	47630242	A	G	60	GENIC	homozygous	60697869
1	47632167	47632168	T	C	58	GENIC	homozygous	60697870
1	47633228	47633230	AG	--	11	GENIC	heterozygous	60697871
1	47633233	47633234	G	A	47	GENIC	heterozygous	60697872
1	47633599	47633600	T	C	52	GENIC	homozygous	60697873
1	47634300	47634301	G	A	54	GENIC	homozygous	60697874
1	47635171	47635175	ACAC	----	31	GENIC	heterozygous	61290431
1	47635173	47635175	AC	--	31	GENIC	heterozygous	60697875
1	47638405	47638406	A	G	32	GENIC	homozygous	60697876
1	47638908	47638909	A	ACATG	36	GENIC	possibly homozygous	60697877
1	47640604	47640606	AC	--	38	GENIC	homozygous	60697878
1	47640944	47640945	T	-	29	GENIC	heterozygous	60697879
1	47641124	47641125	T	TAC	33	GENIC	possibly homozygous	60697880
1	47641176	47641180	GTGT	----	38	GENIC	homozygous	60697881
1	47641717	47641719	GG	--	22	GENIC	homozygous	60697882