chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	44011182	44011184	TT		26	GENIC	homozygous	132707042
12	44016887	44016888	A	G	40	GENIC	homozygous	115390202
12	44011192	44011193	T	G	28	GENIC	homozygous	115443413
12	44011736	44011737	G	C	37	GENIC	homozygous	115443414
12	44012248	44012249	A	T	48	GENIC	homozygous	115443415
12	44014654	44014655	C	T	25	GENIC	homozygous	115443416
12	44011676	44011677	T	C	36	GENIC	homozygous	115336608
12	44012288	44012289	A	G	39	GENIC	homozygous	115336610
12	44012506	44012506		T	10	GENIC	heterozygous	132167339
12	44018694	44018695	G	A	32	GENIC	homozygous	115443417
12	44020947	44020948	A	G	21	GENIC	homozygous	115390208
12	44021630	44021631	G	A	37	GENIC	homozygous	115390210
12	44022382	44022383	A	T	39	GENIC	homozygous	115390212
12	44022390	44022391	A		31	GENIC	homozygous	131119315
12	44029184	44029185	T	C	17	GENIC	homozygous	115336614
12	44022487	44022490	GCG		42	GENIC	homozygous	128993922
12	44029184	44029184		GGGCA	15	GENIC	homozygous	128993923