chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	50447610	50447611	C	G	23	GENIC	homozygous	115352303
12	50447854	50447855	A	C	27	GENIC	homozygous	115352305
12	50448203	50448204	C	T	36	GENIC	homozygous	115352307
12	50448887	50448888	G	A	36	GENIC	possibly homozygous	115352309
12	50449464	50449465	G	A	17	GENIC	homozygous	115352312
12	50449595	50449596	T	G	23	GENIC	homozygous	115352316
12	50449652	50449653	T	G	16	GENIC	homozygous	115549459
12	50449660	50449661	T	C	14	GENIC	homozygous	115403598
12	50449708	50449709	T	C	20	GENIC	homozygous	115506205
12	50449782	50449783	C	A	21	GENIC	homozygous	115352318
12	50450002	50450003	G	A	36	GENIC	homozygous	115352320
12	50450474	50450475	G	T	18	GENIC	homozygous	115352322
12	50454080	50454081	T	C	24	GENIC	homozygous	115352326
12	50454134	50454135	T	C	19	GENIC	homozygous	115352328
12	50455084	50455085	C	T	22	GENIC	homozygous	115352332
12	50456620	50456621	T	G	25	GENIC	homozygous	115352334
12	50457476	50457477	A	G	32	GENIC	homozygous	115352336
12	50457877	50457878	A	G	21	GENIC	homozygous	115352338
12	50458258	50458259	A	G	48	GENIC	homozygous	115352340
12	50460710	50460711	T	C	22	GENIC	homozygous	115549463