chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	126166284	126166285	A	C	56	GENIC	possibly homozygous	113996572
5	126166507	126166508	A	C	61	GENIC	homozygous	113996576
5	126166941	126166942	T	C	44	GENIC	homozygous	113996579
5	126167370	126167371	G	C	56	GENIC	homozygous	114137106
5	126167389	126167390	C	A	63	GENIC	homozygous	114137107
5	126168430	126168431	G	A	34	GENIC	homozygous	114137108
5	126168624	126168625	T	A	67	GENIC	homozygous	113996587
5	126169988	126169989	A	G	66	GENIC	homozygous	119016617
5	126173825	126173825		G	46	GENIC	homozygous	128235418
5	126178445	126178446	A	G	50	GENIC	homozygous	113996624
5	126182103	126182104	A	G	55	GENIC	homozygous	113996630
5	126182616	126182617	C		49	GENIC	homozygous	128235421
5	126186603	126186603		ATAAAG	48	GENIC	homozygous	128235422
5	126174360	126174361	G	A	42	GENIC	homozygous	119181875
5	126174554	126174555	G	A	51	GENIC	homozygous	119181876
5	126178292	126178293	G	A	56	GENIC	homozygous	119181877
5	126180713	126180714	C	T	52	GENIC	homozygous	119181878
5	126181528	126181529	A	C	55	GENIC	homozygous	119181879
5	126182937	126182938	G	A	57	GENIC	homozygous	119181880
5	126178649	126178649		AAGAAG	46	GENIC	homozygous	131648805