chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	26772383	26772383		AAGG	27	GENIC	homozygous	141320589
2	26772847	26772848	G	A	15	GENIC	homozygous	141360217
2	26773894	26773895	T	G	23	GENIC	homozygous	141360225
2	26773948	26773949	T	C	23	GENIC	homozygous	141360226
2	26776045	26776049	GTCG		37	GENIC	homozygous	141320594
2	26773240	26773241	G	A	51	GENIC	homozygous	144589856
2	26777071	26777072	G	A	45	GENIC	homozygous	144589857
2	26778274	26778275	A	G	37	GENIC	homozygous	141360229
2	26778905	26778905		G	11	GENIC	homozygous	141320595
2	26779365	26779366	G	T	37	GENIC	homozygous	144589858
2	26778827	26778828	A		7	GENIC	possibly homozygous	402995107
2	26778827	26778828	A	T	7	GENIC	heterozygous	402995108
2	26779610	26779611	C	T	38	GENIC	homozygous	141360230
2	26779676	26779677	C	T	33	GENIC	homozygous	144589859
2	26782676	26782677	A	G	36	GENIC	homozygous	141360233
2	26783084	26783085	C	T	26	GENIC	homozygous	144589860
2	26783338	26783339	G	A	41	GENIC	homozygous	144589861
2	26779121	26779121		AA	34	GENIC	homozygous	144575767
2	26780351	26780351		G	6	GENIC	heterozygous	144575768
2	26780326	26780326		C	6	GENIC	heterozygous	140967053
2	26780398	26780399	T	G	20	GENIC	homozygous	136054511