chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91041570	91041576	TTTGTT		43	GENIC	homozygous	131902759
10	91042057	91042058	G	T	47	GENIC	homozygous	116821622
10	91042604	91042605	T	C	50	GENIC	homozygous	116905267
10	91042815	91042816	C	T	44	GENIC	homozygous	116821624
10	91043967	91043968	C	T	55	GENIC	homozygous	116821626
10	91044572	91044593	GGTCCTGAGCTAGGGTAAGAC		52	GENIC	homozygous	131902760
10	91044862	91044863	T	C	44	GENIC	homozygous	116821628
10	91044945	91044945		A	40	GENIC	possibly homozygous	131902761
10	91045124	91045125	C	A	58	GENIC	homozygous	116821630
10	91045782	91045783	T	A	60	GENIC	possibly homozygous	116905271
10	91045977	91045978	A	G	53	GENIC	homozygous	116821638
10	91046099	91046100	T	G	57	GENIC	homozygous	116821640
10	91044273	91044274	C	T	57	GENIC	homozygous	117088087
10	91043021	91043022	G	A	56	GENIC	homozygous	117088085