chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	49369542	49369543	G	C	9	GENIC	homozygous	112641575
4	49369571	49369572	C	T	7	GENIC	homozygous	112641577
4	49370407	49370408	G	A	10	GENIC	homozygous	112641579
4	49371418	49371419	G	A	17	GENIC	homozygous	112641581
4	49372049	49372050	A	G	21	GENIC	homozygous	112641583
4	49372697	49372698	A	G	10	GENIC	homozygous	112641585
4	49373534	49373535	A	G	19	GENIC	homozygous	112641587
4	49373732	49373733	G	A	23	GENIC	homozygous	112641589
4	49374001	49374002	G	T	24	GENIC	homozygous	112641591
4	49374711	49374712	T	C	21	GENIC	homozygous	112641593
4	49376881	49376882	C	T	21	GENIC	homozygous	112641595
4	49378460	49378461	G	T	15	GENIC	homozygous	112641597
4	49378613	49378614	A	G	10	GENIC	homozygous	112641599
4	49378714	49378715	C	T	6	GENIC	homozygous	119337650
4	49378716	49378717	C	T	6	GENIC	homozygous	119337652
4	49381804	49381805	A	C	26	GENIC	homozygous	112641601
4	49382114	49382115	A	T	9	GENIC	homozygous	112641603
4	49386813	49386814	A	G	30	GENIC	homozygous	112641605