chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91041419	91041420	G	A	29	GENIC	homozygous	116821620
10	91042057	91042058	G	T	28	GENIC	homozygous	116821622
10	91042815	91042816	C	T	22	GENIC	homozygous	116821624
10	91043967	91043968	C	T	41	GENIC	homozygous	116821626
10	91044862	91044863	T	C	45	GENIC	homozygous	116821628
10	91045124	91045125	C	A	31	GENIC	homozygous	116821630
10	91045481	91045482	G	A	38	GENIC	homozygous	116821632
10	91045772	91045773	G	A	23	GENIC	possibly homozygous	116821634
10	91045782	91045783	T	A	23	GENIC	homozygous	116905271
10	91045887	91045888	C	T	36	GENIC	homozygous	116821636
10	91045977	91045978	A	G	35	GENIC	homozygous	116821638
10	91046099	91046100	T	G	30	GENIC	homozygous	116821640
10	91047085	91047086	C	T	32	GENIC	homozygous	116821642