chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	37522595	37522596	A	G	21	GENIC	homozygous	114316208
13	37522750	37522751	A	G	25	GENIC	homozygous	114316209
13	37523409	37523410	C	T	59	GENIC	homozygous	114316210
13	37523513	37523514	C	T	34	GENIC	homozygous	114316211
13	37523538	37523539	C	T	30	GENIC	homozygous	114316212
13	37524342	37524343	A	G	40	GENIC	homozygous	114316213
13	37524788	37524789	C	A	50	GENIC	homozygous	114316214
13	37524910	37524911	A	T	40	GENIC	homozygous	114316215
13	37524943	37524944	A	G	38	GENIC	homozygous	114316216
13	37525465	37525466	T	C	45	GENIC	homozygous	114316217
13	37525551	37525552	T	C	32	GENIC	homozygous	114316218
13	37526041	37526042	A	G	53	GENIC	homozygous	114316219
13	37526090	37526091	G	C	59	GENIC	homozygous	114316220
13	37526338	37526339	A	G	39	GENIC	homozygous	114316221
13	37528517	37528518	C	T	60	GENIC	homozygous	114316222
13	37528658	37528659	G	A	49	GENIC	homozygous	114316223
13	37529163	37529164	T	C	45	GENIC	homozygous	114316224
13	37534003	37534004	T	C	36	GENIC	homozygous	114316225
13	37535290	37535291	T	C	25	GENIC	homozygous	114316226