chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	92628469	92628470	C	T	6	GENIC	homozygous	116823463
10	92630864	92630865	C	G	9	GENIC	homozygous	116823465
10	92631030	92631031	T	C	15	GENIC	homozygous	116681019
10	92629351	92629352	G	A	7	GENIC	homozygous	116681012
10	92630547	92630548	G	A	4	GENIC	homozygous	116681014
10	92631214	92631215	T	C	12	GENIC	homozygous	116681021
10	92631223	92631224	T	C	13	GENIC	homozygous	116681023
10	92631422	92631423	G	C	8	GENIC	homozygous	116681025
10	92631450	92631451	T	C	10	GENIC	homozygous	116681028
10	92631531	92631532	A	G	15	GENIC	homozygous	116681030
10	92631794	92631795	T	C	10	GENIC	homozygous	116681034
10	92631875	92631876	C	T	16	GENIC	homozygous	116681036
10	92631876	92631877	T	C	16	GENIC	homozygous	116681038
10	92631929	92631930	C	A	15	GENIC	homozygous	116681040
10	92632006	92632007	G	C	6	GENIC	homozygous	116681042
10	92632165	92632166	T	A	2	GENIC	homozygous	116823467
10	92632168	92632169	C	T	2	GENIC	homozygous	116823469
10	92632169	92632170	T	C	2	GENIC	homozygous	116823471
10	92634545	92634546	G	A	15	GENIC	homozygous	116823473
10	92634768	92634769	T	C	16	GENIC	homozygous	116681046
10	92634841	92634842	A	G	4	GENIC	homozygous	116823475
10	92635919	92635920	C	T	6	GENIC	homozygous	116823477
10	92635922	92635923	A	G	6	GENIC	homozygous	116681052
10	92637258	92637259	T	C	9	GENIC	homozygous	116681064
10	92637758	92637759	C	T	10	GENIC	homozygous	116823479