chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	92074355	92074356	T	C	20	GENIC	homozygous	114578933
13	92079835	92079836	T		17	GENIC	homozygous	129085277
13	92076176	92076177	C		13	GENIC	homozygous	129085274
13	92079807	92079807		A	13	GENIC	homozygous	129085275
13	92079817	92079817		T	16	GENIC	homozygous	129085276
13	92079734	92079735	G	C	20	GENIC	homozygous	114425023
13	92079842	92079843	G	A	18	GENIC	homozygous	114425025
13	92079843	92079844	A	G	18	GENIC	homozygous	114425027
13	92079866	92079867	T		18	GENIC	homozygous	129085278
13	92079882	92079882		G	20	GENIC	homozygous	129085279
13	92079914	92079915	T		24	GENIC	homozygous	129085280
13	92079992	92079993	T	C	27	GENIC	homozygous	114425029
13	92079993	92079994	C	T	27	GENIC	homozygous	114425031
13	92079998	92079999	C		29	GENIC	homozygous	129085281
13	92080147	92080147		T	19	GENIC	homozygous	129085282
13	92080196	92080198	AC		16	GENIC	homozygous	129085283
13	92087695	92087696	G	C	13	GENIC	homozygous	123783959