chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	126165286	126165286		G	18	GENIC	homozygous	132843587
5	126166284	126166285	A	C	18	GENIC	homozygous	113996572
5	126166353	126166354	C	T	18	GENIC	homozygous	119016615
5	126166507	126166508	A	C	15	GENIC	homozygous	113996576
5	126166941	126166942	T	C	23	GENIC	homozygous	113996579
5	126168508	126168508		A	10	GENIC	homozygous	132843588
5	126168624	126168625	T	A	27	GENIC	homozygous	113996587
5	126169113	126169114	C	T	16	GENIC	homozygous	119016616
5	126169988	126169989	A	G	24	GENIC	homozygous	119016617
5	126170176	126170177	T	G	25	GENIC	homozygous	119016618
5	126167389	126167390	C	A	24	GENIC	homozygous	114137107
5	126168430	126168431	G	A	18	GENIC	homozygous	114137108
5	126173281	126173282	C	T	27	GENIC	homozygous	119016619
5	126173825	126173825		G	20	GENIC	homozygous	128235418
5	126178247	126178248	A	C	29	GENIC	homozygous	119016620
5	126178445	126178446	A	G	20	GENIC	homozygous	113996624
5	126178670	126178671	A	C	23	GENIC	homozygous	119016621
5	126179112	126179113	A	G	18	GENIC	homozygous	113996626
5	126179863	126179864	C	G	20	GENIC	homozygous	113996628
5	126180718	126180719	G		26	GENIC	homozygous	132843590
5	126181144	126181145	C	T	26	GENIC	homozygous	119016622
5	126182014	126182015	G	A	27	GENIC	homozygous	119016623
5	126182103	126182104	A	G	20	GENIC	homozygous	113996630
5	126182616	126182617	C		18	GENIC	homozygous	128235421
5	126183898	126183899	C	T	29	GENIC	homozygous	119016624
5	126184187	126184188	C	T	22	GENIC	homozygous	119016625
5	126186543	126186544	G	A	21	GENIC	homozygous	119016626
5	126186603	126186603		ATAAAG	18	GENIC	homozygous	128235422
5	126187664	126187665	A	G	20	GENIC	homozygous	113996634