chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	126196656	126196657	G	A	18	GENIC	homozygous	113996640
5	126198484	126198485	G	T	28	GENIC	homozygous	113996642
5	126198694	126198695	A	G	24	GENIC	homozygous	113996644
5	126206686	126206687	A	T	22	GENIC	homozygous	113996652
5	126208062	126208063	C	T	23	GENIC	homozygous	113996654
5	126208247	126208248	G	T	24	GENIC	homozygous	113996656
5	126208411	126208412	G	A	35	GENIC	homozygous	113996658
5	126208590	126208591	T	A	36	GENIC	homozygous	113996660
5	126209139	126209140	G	A	29	GENIC	homozygous	113996662
5	126209608	126209609	A	G	32	GENIC	homozygous	113996664
5	126209611	126209612	G	A	30	GENIC	homozygous	113996666
5	126209705	126209706	T	C	22	GENIC	homozygous	113996668
5	126209708	126209709	G	A	23	GENIC	homozygous	113996670
5	126209715	126209716	G	C	27	GENIC	homozygous	113996672
5	126209768	126209769	C	A	27	GENIC	homozygous	113996674
5	126210065	126210066	T	A	25	GENIC	homozygous	113996675
5	126210514	126210515	A	G	32	GENIC	homozygous	113996677
5	126210631	126210632	T	A	34	GENIC	homozygous	113996679
5	126210873	126210874	T	C	27	GENIC	homozygous	113996681
5	126211601	126211602	C	A	25	GENIC	homozygous	113996683
5	126212657	126212658	C	T	31	GENIC	homozygous	113996685
5	126212671	126212672	A	G	33	GENIC	homozygous	113996687
5	126215100	126215101	G	A	29	GENIC	homozygous	113996689
5	126216747	126216748	C	T	14	GENIC	homozygous	113996691
5	126218232	126218233	C	T	29	GENIC	homozygous	113996693
5	126219108	126219109	A	C	29	GENIC	homozygous	113996695
5	126219778	126219779	T	C	26	GENIC	homozygous	113996697
5	126220266	126220267	C	T	32	GENIC	homozygous	113996699
5	126220467	126220468	A	C	33	GENIC	homozygous	113996701