chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	141099160	141099161	C	A	30	GENIC	homozygous	108260084
1	141099809	141099810	G	A	46	GENIC	homozygous	108936393
1	141101245	141101246	A	C	37	GENIC	homozygous	108260086
1	141102193	141102194	C	A	35	GENIC	homozygous	108260088
1	141102413	141102414	A	C	33	GENIC	homozygous	108260090
1	141102481	141102482	A	T	20	GENIC	homozygous	108936394
1	141104298	141104299	T	C	32	GENIC	homozygous	108260096
1	141104542	141104543	A	G	30	GENIC	homozygous	108260098
1	141104681	141104682	C	T	34	GENIC	homozygous	108936396
1	141103747	141103747		TGGCCTTGTTGGAGTGGGTG	34	GENIC	homozygous	127438799
1	141103952	141103953	G		10	GENIC	homozygous	127438800
1	141104725	141104725		A	40	GENIC	homozygous	127438801
1	141102147	141102147		A	27	GENIC	homozygous	132534145
1	141105789	141105790	C	T	30	GENIC	homozygous	108936397
1	141108119	141108120	C	T	43	GENIC	homozygous	108260106
1	141109086	141109087	G	C	48	GENIC	homozygous	108936398