chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	92074355	92074356	T	C	25	GENIC	homozygous	114578933
13	92076176	92076177	C		13	GENIC	homozygous	129085274
13	92079734	92079735	G	C	30	GENIC	homozygous	114425023
13	92079807	92079807		A	32	GENIC	homozygous	129085275
13	92079817	92079817		T	32	GENIC	homozygous	129085276
13	92079835	92079836	T		33	GENIC	homozygous	129085277
13	92079842	92079843	G	A	31	GENIC	homozygous	114425025
13	92079843	92079844	A	G	31	GENIC	homozygous	114425027
13	92079866	92079867	T		30	GENIC	homozygous	129085278
13	92079882	92079882		G	30	GENIC	homozygous	129085279
13	92079914	92079915	T		25	GENIC	homozygous	129085280
13	92079992	92079993	T	C	23	GENIC	homozygous	114425029
13	92079993	92079994	C	T	23	GENIC	homozygous	114425031
13	92079998	92079999	C		22	GENIC	homozygous	129085281
13	92080147	92080147		T	40	GENIC	homozygous	129085282
13	92080196	92080198	AC		35	GENIC	homozygous	129085283