chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	90561371	90561372	G	GT	19	GENIC	homozygous	50131503
13	90566441	90566443	AA	--	26	GENIC	heterozygous	50618701
13	90566442	90566443	A	-	26	GENIC	possibly homozygous	50596694
13	90581897	90581898	C	CT	16	GENIC	homozygous	49858903
13	90581910	90581911	G	GA	16	GENIC	homozygous	49858904
13	90581914	90581915	C	-	15	GENIC	homozygous	49858905
13	90581923	90581924	C	A	17	GENIC	homozygous	50497287
13	90581924	90581925	A	T	17	GENIC	homozygous	50497288
13	90603032	90603033	G	GGTGCTTT	24	GENIC	homozygous	49858908
13	90614750	90614751	C	-	14	GENIC	homozygous	49858909
13	90630634	90630635	C	-	4	GENIC	heterozygous	50497290
13	90652744	90652745	G	GGA	2	GENIC	homozygous	49960835
13	90660367	90660369	TC	--	6	GENIC	heterozygous	50530018
13	90662159	90662160	A	AC	15	GENIC	homozygous	49858912
13	90666686	90666687	A	ATT	10	GENIC	homozygous	49858913
13	90667544	90667545	A	AGTGT	7	GENIC	heterozygous	50553532
13	90667549	90667551	GT	--	7	GENIC	heterozygous	50553533
13	90667587	90667589	GA	--	17	GENIC	heterozygous	50530024
13	90670814	90670815	G	GAA	3	GENIC	homozygous	50566354
13	90675988	90675990	TC	--	3	GENIC	homozygous	49858921
13	90683343	90683345	GT	--	3	GENIC	heterozygous	50530026
13	90685467	90685468	T	-	7	GENIC	heterozygous	50131519
13	90696340	90696342	AC	--	7	GENIC	heterozygous	50553537