chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	14683658	14683659	T	C	21	GENIC	homozygous	50068620
12	14685124	14685125	G	A	17	GENIC	possibly homozygous	50068622
12	14690463	14690464	T	A	21	GENIC	possibly homozygous	50068628
12	14697039	14697040	C	CAAGTTCTGATTTCTGTAAAACTAAGAAGGATGTTCTCCTGCAGCAGG	18	GENIC	possibly homozygous	50503954
12	14697083	14697084	T	C	25	GENIC	possibly homozygous	50068656
12	14700285	14700286	T	TTGTC	9	GENIC	homozygous	50068664
12	14700499	14700500	G	C	4	GENIC	heterozygous	50068666
12	14700636	14700637	C	CTTTTTTT	1	GENIC	homozygous	50503955
12	14701225	14701226	G	C	15	GENIC	homozygous	50068672
12	14704132	14704133	T	TA	14	GENIC	possibly homozygous	50068674
12	14704150	14704151	G	T	9	GENIC	homozygous	50068676
12	14704153	14704154	C	T	8	GENIC	homozygous	50068678