chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	53287308	53287309	T	C	30	GENIC	heterozygous	50345041
12	53287312	53287313	C	T	31	GENIC	heterozygous	50388367
12	53287329	53287330	C	CA	32	GENIC	heterozygous	50414098
12	53287349	53287350	C	CT	36	GENIC	heterozygous	50256021
12	53287410	53287411	C	CT	33	GENIC	heterozygous	50256023
12	53287451	53287452	T	C	35	GENIC	heterozygous	50256027
12	53287471	53287472	C	CT	33	GENIC	heterozygous	50256029
12	53287478	53287479	A	G	44	GENIC	heterozygous	50256031
12	53287482	53287483	A	-	38	GENIC	heterozygous	50256033
12	53287513	53287514	C	CA	39	GENIC	heterozygous	50256037
12	53287526	53287527	T	C	43	GENIC	heterozygous	50414104
12	53288478	53288479	A	C	36	GENIC	homozygous	50256039
12	53289252	53289253	T	C	21	GENIC	homozygous	50256041
12	53289909	53289910	T	C	47	GENIC	homozygous	50256043
12	53290335	53290336	G	A	35	GENIC	homozygous	50256045
12	53290594	53290595	A	C	30	GENIC	homozygous	50256047