chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	38916385	38916386	C	T	22	GENIC	homozygous	50195934
12	38916399	38916400	A	G	20	GENIC	homozygous	50195936
12	38916457	38916458	C	A	21	GENIC	homozygous	50195938
12	38916470	38916472	GG	--	20	GENIC	homozygous	50511123
12	38916483	38916484	G	A	15	GENIC	homozygous	50195942
12	38917512	38917513	G	A	32	GENIC	homozygous	50195944
12	38917523	38917524	G	A	29	GENIC	homozygous	50195946
12	38917595	38917596	T	TG	11	GENIC	homozygous	50195948
12	38918044	38918045	A	G	24	GENIC	homozygous	50195950
12	38918171	38918172	G	GGA	18	GENIC	homozygous	50195954
12	38918839	38918840	G	C	23	GENIC	homozygous	50195956
12	38918851	38918852	T	C	32	GENIC	homozygous	50195958
12	38918987	38918988	T	C	30	GENIC	homozygous	50195960
12	38919823	38919824	A	G	12	GENIC	homozygous	50195962
12	38920289	38920290	C	T	32	GENIC	homozygous	50195964
12	38920873	38920875	CA	--	33	GENIC	homozygous	50195966
12	38920959	38920960	G	A	30	GENIC	homozygous	50195968
12	38921116	38921117	A	G	22	GENIC	homozygous	50195970
12	38921329	38921330	G	GCGCGCACACA	15	GENIC	heterozygous	50195974
12	38922013	38922014	T	C	27	GENIC	homozygous	50195978
12	38922037	38922038	A	G	26	GENIC	homozygous	50195980
12	38922277	38922278	G	A	27	GENIC	homozygous	50195982
12	38922524	38922525	T	C	29	GENIC	homozygous	50195984
12	38922526	38922527	T	A	29	GENIC	homozygous	50195985
12	38922535	38922536	T	C	32	GENIC	homozygous	50195987
12	38922544	38922545	G	A	29	GENIC	homozygous	50195989
12	38922630	38922631	C	T	31	GENIC	homozygous	50195991
12	38921329	38921330	G	GCGCGCGCACA	15	GENIC	possibly homozygous	50599001
12	38923083	38923084	T	TCC	8	GENIC	homozygous	50195993
12	38923242	38923243	A	AG	30	GENIC	homozygous	50195995
12	38923369	38923370	C	-	24	GENIC	homozygous	50195997
12	38923517	38923518	C	A	22	GENIC	homozygous	50195999
12	38923830	38923831	G	A	17	GENIC	homozygous	50196003