chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	101527439	101527440	G	A	50	GENIC	homozygous	113941716
5	101530646	101530647	G	A	44	GENIC	possibly homozygous	113941718
5	101531995	101531996	C	T	54	GENIC	homozygous	113941720
5	101533001	101533002	G	A	34	GENIC	homozygous	113941722
5	101533949	101533950	A	G	10	GENIC	homozygous	113941724
5	101534961	101534962	G	A	48	GENIC	homozygous	113941726
5	101536413	101536414	A	G	56	GENIC	homozygous	113941728
5	101537721	101537722	C	T	49	GENIC	homozygous	113941730
5	101537231	101537231		T	37	GENIC	possibly homozygous	128218252
5	101538630	101538630		T	40	GENIC	homozygous	128218253
5	101540003	101540011	TTAGTCCA		47	GENIC	homozygous	128218254
5	101540939	101540940	A	C	36	GENIC	homozygous	113941732
5	101541910	101541911	T	C	38	GENIC	homozygous	113941734
5	101542569	101542573	TTAC		57	GENIC	homozygous	128218255
5	101542929	101542930	C	A	52	GENIC	possibly homozygous	113941736
5	101544453	101544454	G	A	38	GENIC	homozygous	113941738
5	101546369	101546370	T	A	50	GENIC	possibly homozygous	113941740
5	101546370	101546371	T	C	49	GENIC	possibly homozygous	113941741
5	101551693	101551694	C	T	45	GENIC	homozygous	113941743
5	101553993	101553994	G	A	51	GENIC	homozygous	113941745