chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	37522595	37522596	A	G	33	GENIC	homozygous	114316208
13	37522750	37522751	A	G	35	GENIC	homozygous	114316209
13	37522926	37522927	T	C	20	GENIC	homozygous	114663318
13	37522931	37522932	A	G	16	GENIC	homozygous	114663320
13	37522948	37522949	C	T	17	GENIC	heterozygous	114920419
13	37523409	37523410	C	T	26	GENIC	homozygous	114316210
13	37523513	37523514	C	T	26	GENIC	homozygous	114316211
13	37523538	37523539	C	T	23	GENIC	homozygous	114316212
13	37524342	37524343	A	G	32	GENIC	homozygous	114316213
13	37524788	37524789	C	A	36	GENIC	homozygous	114316214
13	37524910	37524911	A	T	20	GENIC	homozygous	114316215
13	37524943	37524944	A	G	19	GENIC	homozygous	114316216
13	37525465	37525466	T	C	42	GENIC	homozygous	114316217
13	37525551	37525552	T	C	43	GENIC	homozygous	114316218
13	37525613	37525614	G	T	41	GENIC	homozygous	114663321
13	37526041	37526042	A	G	36	GENIC	homozygous	114316219
13	37526090	37526091	G	C	49	GENIC	homozygous	114316220
13	37526137	37526138	A	G	44	GENIC	homozygous	114663323
13	37526338	37526339	A	G	34	GENIC	homozygous	114316221
13	37528517	37528518	C	T	34	GENIC	homozygous	114316222
13	37530587	37530588	C	T	34	GENIC	homozygous	114663324
13	37532133	37532134	G	T	24	GENIC	possibly homozygous	114610010
13	37534003	37534004	T	C	34	GENIC	homozygous	114316225
13	37535290	37535291	T	C	20	GENIC	homozygous	114316226
13	37524112	37524113	C	T	35	GENIC	heterozygous	118566123