chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	145472369	145472370	T	C	17	GENIC	homozygous	112870906
4	145472937	145472938	A		16	GENIC	homozygous	128087995
4	145472965	145472966	C	A	17	GENIC	homozygous	113179000
4	145473165	145473166	T	A	24	GENIC	homozygous	113179001
4	145473627	145473627		A	23	GENIC	homozygous	130938720
4	145476316	145476316		G	8	GENIC	homozygous	130938721
4	145476319	145476319		GGG	8	GENIC	homozygous	130938722
4	145476776	145476777	G	T	17	GENIC	homozygous	113179002
4	145477153	145477154	T	C	19	GENIC	homozygous	113179003
4	145477809	145477810	G	A	15	GENIC	homozygous	113179004
4	145477850	145477851	A	G	17	GENIC	homozygous	113179005
4	145479385	145479386	C	T	7	GENIC	homozygous	113179006
4	145480529	145480530	T	C	16	GENIC	homozygous	112870909
4	145481733	145481734	C	T	19	GENIC	homozygous	112870910
4	145481748	145481749	C	G	18	GENIC	homozygous	112870911
4	145482481	145482484	AAC		7	GENIC	homozygous	130938723
4	145485656	145485657	C	T	16	GENIC	homozygous	112870914
4	145485793	145485794	G	T	12	GENIC	possibly homozygous	112870915
4	145485847	145485848	A	T	14	GENIC	homozygous	113179007
4	145486088	145486089	C	G	16	GENIC	homozygous	113179008
4	145486325	145486326	G	T	24	GENIC	homozygous	112870917
4	145486784	145486785	G	C	11	GENIC	homozygous	112870918
4	145486793	145486794	G	C	10	GENIC	homozygous	112870919