chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	156200949	156200950	A	G	62	GENIC	homozygous	135716288
1	156201644	156201645	T	C	43	GENIC	homozygous	135716289
1	156202758	156202759	A	T	21	GENIC	homozygous	135716290
1	156203441	156203442	G	A	49	GENIC	homozygous	135716291
1	156204376	156204377	C	T	65	GENIC	homozygous	135716292
1	156204661	156204662	G	A	55	GENIC	homozygous	135716293
1	156205454	156205455	C		18	GENIC	heterozygous	402969228
1	156205454	156205455	C	A	18	GENIC	heterozygous	402969229
1	156206431	156206432	T	G	46	GENIC	homozygous	135716294
1	156207277	156207278	A	G	32	GENIC	homozygous	135716295
1	156210741	156210742	A	G	50	GENIC	homozygous	135716296
1	156210753	156210754	G	A	49	GENIC	homozygous	135716297
1	156213500	156213501	G		6	GENIC	homozygous	402969230
1	156213500	156213501	G	T	6	GENIC	heterozygous	402969231
1	156213997	156213998	T	A	59	GENIC	homozygous	135716298
1	156214704	156214705	C	G	47	GENIC	homozygous	135716299
1	156216263	156216264	C	T	53	GENIC	homozygous	135716300
1	156216982	156216983	T	C	47	GENIC	homozygous	135716301
1	156217508	156217509	G	T	43	GENIC	homozygous	135716302
1	156206386	156206389	ATT		37	GENIC	homozygous	135438913
1	156214923	156214924	T		42	GENIC	homozygous	135438914