chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	14573929	14573930	C	T	6	GENIC	homozygous	112407501
3	14574184	14574185	G	A	13	GENIC	homozygous	112407504
3	14574357	14574358	T	A	23	GENIC	homozygous	111880010
3	14574403	14574404	A	G	27	GENIC	homozygous	111880012
3	14574425	14574426	A	G	26	GENIC	homozygous	111880014
3	14574523	14574524	A	G	19	GENIC	homozygous	111453432
3	14574534	14574535	G	A	18	GENIC	homozygous	112407506
3	14574630	14574631	T	G	22	GENIC	possibly homozygous	111880018
3	14574692	14574693	C	G	16	GENIC	homozygous	112407508
3	14574704	14574705	C	T	16	GENIC	homozygous	111880020
3	14574811	14574812	A	C	14	GENIC	homozygous	111880022
3	14574835	14574836	T	C	8	GENIC	homozygous	111880024
3	14574836	14574837	T	C	8	GENIC	homozygous	111880026
3	14574868	14574869	C	T	5	GENIC	homozygous	111880028
3	14574926	14574927	C	A	8	GENIC	homozygous	111880030
3	14574998	14574999	C	T	11	GENIC	homozygous	111880032
3	14575107	14575108	C	T	16	GENIC	homozygous	112407510
3	14575231	14575232	A	T	8	GENIC	homozygous	111880034
3	14575255	14575256	G	A	7	GENIC	homozygous	112407512
3	14575257	14575258	G	A	7	GENIC	homozygous	112407514
3	14575312	14575313	C	A	5	GENIC	homozygous	111880036
3	14575348	14575349	A	T	4	GENIC	homozygous	111880038