chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	26137408	26137409	A	G	41	GENIC	homozygous	148012281
6	26137444	26137445	A	G	46	GENIC	homozygous	146155248
6	26137679	26137680	G	A	48	GENIC	homozygous	146155249
6	26139430	26139430		CTGC	53	GENIC	possibly homozygous	148006830
6	26139687	26139691	GTGG		30	GENIC	possibly homozygous	148006831
6	26140030	26140031	G	A	38	GENIC	homozygous	148012282
6	26141358	26141359	C	T	49	GENIC	homozygous	148012283
6	26141637	26141638	T	C	52	GENIC	homozygous	146155259
6	26143155	26143156	G	T	21	GENIC	homozygous	148012284
6	26143437	26143438	G	A	38	GENIC	homozygous	148012285
6	26143455	26143456	G	A	40	GENIC	homozygous	148012286
6	26143822	26143823	G	A	24	GENIC	homozygous	148012287
6	26143835	26143836	C	T	27	GENIC	homozygous	148012288
6	26143975	26143976	G	A	34	GENIC	homozygous	148012289
6	26144535	26144536	G	A	33	GENIC	homozygous	148012290