chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	14573239	14573239		C	8	GENIC	homozygous	130277554
3	14573689	14573691	CC		4	GENIC	homozygous	129887714
3	14573667	14573668	G		1	GENIC	homozygous	129887711
3	14573678	14573679	C		3	GENIC	homozygous	129887712
3	14573687	14573687		G	4	GENIC	homozygous	129887713
3	14573703	14573704	C		6	GENIC	homozygous	129887715
3	14573705	14573706	A		6	GENIC	homozygous	129887716
3	14573716	14573717	A		7	GENIC	homozygous	129887717
3	14573727	14573728	C		8	GENIC	homozygous	129887718
3	14573731	14573733	CA		9	GENIC	homozygous	129887719
3	14573734	14573734		T	9	GENIC	homozygous	129887720
3	14574228	14574229	C	A	37	GENIC	homozygous	111880008
3	14574357	14574358	T	A	52	GENIC	homozygous	111880010
3	14574403	14574404	A	G	53	GENIC	homozygous	111880012
3	14574425	14574426	A	G	54	GENIC	homozygous	111880014
3	14574523	14574524	A	G	45	GENIC	homozygous	111453432
3	14574534	14574535	G	A	47	GENIC	homozygous	112407506
3	14574835	14574836	T	C	39	GENIC	homozygous	111880024
3	14574630	14574631	T	G	46	GENIC	homozygous	111880018
3	14574692	14574693	C	G	51	GENIC	homozygous	112407508
3	14574704	14574705	C	T	47	GENIC	homozygous	111880020
3	14574811	14574812	A	C	46	GENIC	homozygous	111880022
3	14573698	14573699	C	G	5	GENIC	homozygous	129894048
3	14573722	14573723	T	G	7	GENIC	homozygous	129894049
3	14574191	14574192	T		34	GENIC	homozygous	132821232
3	14574836	14574837	T	C	38	GENIC	homozygous	111880026
3	14574868	14574869	C	T	44	GENIC	homozygous	111880028
3	14574926	14574927	C	A	45	GENIC	homozygous	111880030
3	14574998	14574999	C	T	48	GENIC	homozygous	111880032
3	14575231	14575232	A	T	38	GENIC	homozygous	111880034
3	14575312	14575313	C	A	33	GENIC	homozygous	111880036
3	14575348	14575349	A	T	38	GENIC	homozygous	111880038
3	14574839	14574842	TGA		40	GENIC	homozygous	132038870
3	14575427	14575428	C	T	30	GENIC	homozygous	119774622