chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	44011190	44011191	T	G	10	GENIC	homozygous	115390198
12	44011676	44011677	T	C	17	GENIC	homozygous	115336608
12	44012288	44012289	A	G	18	GENIC	homozygous	115336610
12	44016186	44016187	A	T	21	GENIC	homozygous	115390200
12	44016887	44016888	A	G	21	GENIC	homozygous	115390202
12	44017080	44017081	C	A	16	GENIC	homozygous	115390204
12	44017648	44017649	A	G	22	GENIC	homozygous	115390206
12	44020947	44020948	A	G	9	GENIC	homozygous	115390208
12	44021630	44021631	G	A	21	GENIC	homozygous	115390210
12	44022382	44022383	A	T	18	GENIC	homozygous	115390212
12	44029184	44029185	T	C	2	GENIC	homozygous	115336614
12	44013973	44013977	ACAT		13	GENIC	heterozygous	131119311
12	44013979	44013981	AT		12	GENIC	heterozygous	131119312
12	44018568	44018568		ATCAATCT	14	GENIC	homozygous	131119313
12	44022390	44022391	A		16	GENIC	homozygous	131119315
12	44022487	44022490	GCG		21	GENIC	homozygous	128993922
12	44029184	44029184		GGGCA	2	GENIC	homozygous	128993923