chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	126884510	126884511	A	G	16	GENIC	homozygous	113302593
4	126885584	126885585	T	G	36	GENIC	homozygous	113302594
4	126885607	126885608	A	C	35	GENIC	homozygous	113302595
4	126886665	126886666	C	T	20	GENIC	homozygous	113302596
4	126887139	126887140	T	G	13	GENIC	homozygous	113302597
4	126887270	126887271	C	T	26	GENIC	homozygous	113302598
4	126887411	126887412	A	T	25	GENIC	homozygous	113302599
4	126887845	126887846	T	C	13	GENIC	homozygous	113302600
4	126887881	126887882	G	A	19	GENIC	homozygous	113302601
4	126888179	126888180	G	T	31	GENIC	homozygous	113302602
4	126888588	126888589	C	T	26	GENIC	homozygous	113302603
4	126889256	126889257	C	T	25	GENIC	homozygous	113302611
4	126889541	126889542	C	A	11	GENIC	homozygous	113302612
4	126890219	126890220	T	C	26	GENIC	homozygous	113302613
4	126890238	126890239	C	T	27	GENIC	homozygous	113302614
4	126890317	126890318	C	T	37	GENIC	homozygous	113302615
4	126890357	126890358	T	G	31	GENIC	homozygous	113302616
4	126891195	126891196	G	T	27	GENIC	homozygous	113302617
4	126891507	126891508	C	T	31	GENIC	homozygous	113302618
4	126891695	126891696	A	G	34	GENIC	homozygous	113302619
4	126892077	126892078	T	C	22	GENIC	homozygous	113302620
4	126893107	126893108	A	G	17	GENIC	homozygous	113302622
4	126893825	126893826	T	C	21	GENIC	homozygous	113302623
4	126897491	126897492	T	C	18	GENIC	homozygous	113302624