chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	90561371	90561372	G	GT	12	GENIC	heterozygous	50131503
13	90563869	90563871	TT	--	15	GENIC	heterozygous	50603157
13	90563870	90563871	T	-	15	GENIC	heterozygous	50603158
13	90565261	90565262	T	TTTCTTCTTC	5	GENIC	heterozygous	50530010
13	90581897	90581898	C	CT	13	GENIC	homozygous	49858903
13	90581910	90581911	G	GA	15	GENIC	homozygous	49858904
13	90581914	90581915	C	-	16	GENIC	homozygous	49858905
13	90581923	90581924	C	A	15	GENIC	homozygous	50497287
13	90581924	90581925	A	T	15	GENIC	homozygous	50497288
13	90583616	90583617	C	-	8	GENIC	heterozygous	49858907
13	90585246	90585248	GT	--	21	GENIC	heterozygous	50613147
13	90592263	90592265	GT	--	28	GENIC	heterozygous	50497289
13	90603032	90603033	G	GGTGCTTT	18	GENIC	homozygous	49858908
13	90614750	90614751	C	-	32	GENIC	homozygous	49858909
13	90644674	90644676	AT	--	19	GENIC	heterozygous	50606877
13	90649257	90649259	TG	--	17	GENIC	heterozygous	50553530
13	90652744	90652745	G	GGA	4	GENIC	heterozygous	49960835
13	90652745	90652747	GA	--	4	GENIC	heterozygous	50553531
13	90660365	90660369	TCTC	----	17	GENIC	heterozygous	50530016
13	90660367	90660369	TC	--	17	GENIC	heterozygous	50530018
13	90662159	90662160	A	AC	12	GENIC	homozygous	49858912
13	90665119	90665120	A	ATG	32	GENIC	possibly homozygous	50466785
13	90665120	90665122	TG	--	32	GENIC	heterozygous	50530020
13	90666686	90666687	A	ATT	22	GENIC	homozygous	49858913
13	90667549	90667551	GT	--	12	GENIC	heterozygous	50553533
13	90672095	90672096	A	ATC	9	GENIC	heterozygous	50606879
13	90672214	90672216	GT	--	12	GENIC	heterozygous	50553535
13	90674938	90674940	CA	--	20	GENIC	heterozygous	50606880
13	90683341	90683345	GTGT	----	16	GENIC	possibly homozygous	49858922
13	90685467	90685468	T	-	3	GENIC	homozygous	50131519
13	90690463	90690464	C	CGT	7	GENIC	heterozygous	50566355