chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	126166284	126166285	A	C	53	GENIC	homozygous	113996572
5	126166507	126166508	A	C	24	GENIC	homozygous	113996576
5	126166941	126166942	T	C	41	GENIC	homozygous	113996579
5	126167370	126167371	G	C	41	GENIC	homozygous	114137106
5	126167389	126167390	C	A	40	GENIC	possibly homozygous	114137107
5	126168430	126168431	G	A	36	GENIC	homozygous	114137108
5	126168624	126168625	T	A	30	GENIC	homozygous	113996587
5	126171274	126171275	C	T	47	GENIC	possibly homozygous	113996595
5	126172079	126172080	G	A	52	GENIC	homozygous	114137109
5	126172207	126172208	A	T	61	GENIC	homozygous	113996599
5	126171453	126171454	T	C	41	GENIC	homozygous	113996597
5	126172528	126172529	C	T	33	GENIC	homozygous	113996601
5	126172645	126172646	T	C	28	GENIC	homozygous	113996603
5	126172774	126172775	G	A	47	GENIC	homozygous	113996605
5	126172934	126172935	T	C	29	GENIC	homozygous	113996607
5	126173208	126173209	A	G	27	GENIC	homozygous	113996609
5	126173476	126173477	T	C	34	GENIC	homozygous	113996613
5	126174024	126174025	A	G	19	GENIC	homozygous	113996615
5	126175600	126175601	C	T	33	GENIC	homozygous	113996617
5	126175784	126175785	A	G	35	GENIC	homozygous	113996618
5	126175867	126175868	C	T	37	GENIC	homozygous	113996620
5	126175903	126175904	A	G	32	GENIC	homozygous	113996622
5	126178445	126178446	A	G	34	GENIC	homozygous	113996624
5	126179112	126179113	A	G	47	GENIC	homozygous	113996626
5	126179863	126179864	C	G	31	GENIC	homozygous	113996628
5	126182103	126182104	A	G	44	GENIC	homozygous	113996630
5	126186983	126186984	A	C	28	GENIC	homozygous	113996632
5	126187664	126187665	A	G	40	GENIC	homozygous	113996634
5	126188582	126188583	G	A	32	GENIC	homozygous	113996636