chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	126901949	126901950	G	A	28	GENIC	homozygous	119409587
4	126905311	126905312	C	T	16	GENIC	possibly homozygous	119409588
4	126905371	126905372	T	G	18	GENIC	homozygous	113302650
4	126906203	126906204	C	T	33	GENIC	possibly homozygous	119409589
4	126908259	126908260	G	A	30	GENIC	possibly homozygous	119409590
4	126909404	126909405	A	C	17	GENIC	possibly homozygous	119409591
4	126913301	126913302	T	C	29	GENIC	homozygous	119409592
4	126913452	126913453	T	C	18	GENIC	homozygous	113302668
4	126913889	126913890	A	G	21	GENIC	homozygous	113302669
4	126921865	126921866	A	G	31	GENIC	homozygous	113302673
4	126922472	126922473	A	G	32	GENIC	homozygous	113302676
4	126923977	126923978	A	G	20	GENIC	homozygous	113302680
4	126924062	126924063	A	G	17	GENIC	homozygous	113302681
4	126924285	126924286	C	T	31	GENIC	possibly homozygous	119409593
4	126924291	126924292	T	C	31	GENIC	possibly homozygous	119409594
4	126927626	126927627	T	C	39	GENIC	possibly homozygous	119409595