chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	101527439	101527440	G	A	11	GENIC	homozygous	113941716
5	101530646	101530647	G	A	12	GENIC	homozygous	113941718
5	101531995	101531996	C	T	22	GENIC	homozygous	113941720
5	101533001	101533002	G	A	16	GENIC	homozygous	113941722
5	101534961	101534962	G	A	24	GENIC	homozygous	113941726
5	101536413	101536414	A	G	7	GENIC	homozygous	113941728
5	101537721	101537722	C	T	15	GENIC	homozygous	113941730
5	101540939	101540940	A	C	14	GENIC	homozygous	113941732
5	101541910	101541911	T	C	22	GENIC	homozygous	113941734
5	101542929	101542930	C	A	16	GENIC	homozygous	113941736
5	101544453	101544454	G	A	8	GENIC	homozygous	113941738
5	101546369	101546370	T	A	11	GENIC	homozygous	113941740
5	101546370	101546371	T	C	10	GENIC	homozygous	113941741
5	101551693	101551694	C	T	15	GENIC	homozygous	113941743
5	101553993	101553994	G	A	10	GENIC	homozygous	113941745
5	101550275	101550276	G	A	9	GENIC	heterozygous	126199387