chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	12016043	12016044	T	C	49	GENIC	homozygous	115256889
12	12019720	12019721	T	C	31	GENIC	homozygous	115256929
12	12020209	12020210	A	G	32	GENIC	homozygous	115256931
12	12020709	12020710	G	C	26	GENIC	homozygous	115256933
12	12020875	12020876	G	A	23	GENIC	heterozygous	123591962
12	12020899	12020900	A		25	GENIC	homozygous	128960194
12	12020911	12020912	A		23	GENIC	possibly homozygous	128960195
12	12022067	12022068	G	A	62	GENIC	homozygous	115256937
12	12022240	12022244	AAGA		41	GENIC	homozygous	128960196
12	12022324	12022325	T	A	43	GENIC	homozygous	115256939
12	12022430	12022431	C	G	43	GENIC	homozygous	115256941
12	12022435	12022436	T	C	43	GENIC	homozygous	115256943
12	12022561	12022562	A	G	34	GENIC	homozygous	115256945
12	12022628	12022629	C	G	36	GENIC	homozygous	115256947
12	12023841	12023841		CGCTGGCT	30	GENIC	homozygous	128960197
12	12024500	12024501	T	C	46	GENIC	homozygous	115256949
12	12024642	12024643	A		48	GENIC	homozygous	128960198
12	12025313	12025314	G	A	52	GENIC	homozygous	115445143