chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	26800459	26800460	T	C	39	GENIC	homozygous	115493794
6	26800843	26800844	T	G	40	GENIC	homozygous	115493796
6	26801250	26801251	A	G	39	GENIC	homozygous	115493798
6	26803027	26803028	G	A	52	GENIC	possibly homozygous	115448504
6	26803419	26803420	G	A	55	GENIC	homozygous	115493800
6	26803721	26803722	T	C	47	GENIC	homozygous	115448508
6	26803776	26803777	G	A	47	GENIC	homozygous	115448510
6	26803793	26803794	T	C	51	GENIC	homozygous	115448512
6	26803934	26803935	T	C	45	GENIC	homozygous	115448514
6	26804894	26804895	C	T	41	GENIC	homozygous	115493802
6	26804981	26804981		G	34	GENIC	possibly homozygous	131660464
6	26805593	26805594	T	C	38	GENIC	homozygous	115493804
6	26805931	26805932	G	T	38	GENIC	homozygous	115493806
6	26806085	26806086	A	C	37	GENIC	homozygous	115493808
6	26806361	26806362	A	C	35	GENIC	homozygous	115493810
6	26806513	26806514	T	C	37	GENIC	homozygous	115448522
6	26806762	26806763	G	A	39	GENIC	homozygous	115493812
6	26806832	26806833	A	T	49	GENIC	homozygous	115448524
6	26806995	26806996	C	T	13	GENIC	homozygous	115493814
6	26807033	26807034	T	C	22	GENIC	homozygous	115493816
6	26807285	26807286	C	G	45	GENIC	homozygous	115493818
6	26808159	26808160	A	C	50	GENIC	homozygous	115493820