chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	26772383	26772383		AAGG	30	GENIC	homozygous	141320589
2	26772847	26772848	G	A	22	GENIC	homozygous	141360217
2	26773894	26773895	T	G	31	GENIC	homozygous	141360225
2	26773948	26773949	T	C	37	GENIC	homozygous	141360226
2	26776045	26776049	GTCG		55	GENIC	homozygous	141320594
2	26778274	26778275	A	G	35	GENIC	homozygous	141360229
2	26778820	26778828	CTCTCTCA		20	GENIC	heterozygous	145201464
2	26778905	26778905		G	12	GENIC	homozygous	141320595
2	26779365	26779366	G	T	44	GENIC	homozygous	144589858
2	26779121	26779121		AA	39	GENIC	homozygous	144575767
2	26773240	26773241	G	A	54	GENIC	homozygous	144589856
2	26777071	26777072	G	A	52	GENIC	homozygous	144589857
2	26779610	26779611	C	T	39	GENIC	homozygous	141360230
2	26779676	26779677	C	T	49	GENIC	homozygous	144589859
2	26780350	26780350		G	8	GENIC	heterozygous	145129236
2	26780351	26780351		G	8	GENIC	heterozygous	144575768
2	26780398	26780399	T	G	33	GENIC	homozygous	136054511
2	26782676	26782677	A	G	44	GENIC	homozygous	141360233
2	26783084	26783085	C	T	52	GENIC	homozygous	144589860
2	26783338	26783339	G	A	34	GENIC	homozygous	144589861
2	26780326	26780326		C	9	GENIC	heterozygous	140967053