chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	50410098	50410099	T	C	20	GENIC	homozygous	115352211
12	50410853	50410854	G	T	29	GENIC	homozygous	115352213
12	50411067	50411068	C	T	43	GENIC	homozygous	115352215
12	50411448	50411449	C	G	7	GENIC	homozygous	118274617
12	50411485	50411486	A	T	6	GENIC	homozygous	118274618
12	50411597	50411598	C	T	3	GENIC	homozygous	118328046
12	50411629	50411630	C	T	12	GENIC	homozygous	118274620
12	50411667	50411668	T	C	10	GENIC	homozygous	118306577
12	50412543	50412544	A	G	37	GENIC	homozygous	115352218
12	50413136	50413137	G	T	29	GENIC	homozygous	115352220
12	50413510	50413511	C	T	37	GENIC	homozygous	115352222
12	50414268	50414269	A	G	38	GENIC	homozygous	115352224