chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	173233691	173233692	A	T	11	GENIC	homozygous	109168563
1	173233912	173233913	G	A	28	GENIC	homozygous	109168565
1	173234048	173234049	A	G	22	GENIC	homozygous	109168567
1	173234983	173234984	T	C	26	GENIC	homozygous	109168569
1	173235214	173235215	G	T	29	GENIC	homozygous	108387899
1	173237489	173237490	C	T	17	GENIC	homozygous	108387901
1	173237572	173237573	T	G	19	GENIC	homozygous	108387903
1	173238154	173238155	T	C	41	GENIC	homozygous	109168571
1	173241377	173241378	A	C	16	GENIC	homozygous	108387907
1	173241429	173241430	A	G	22	GENIC	homozygous	108387909
1	173242185	173242186	A	G	29	GENIC	homozygous	108387913
1	173242422	173242423	T	A	32	GENIC	homozygous	109168573
1	173242426	173242427	T	G	31	GENIC	homozygous	109168575
1	173244322	173244323	C	T	11	GENIC	homozygous	109168580
1	173247418	173247419	G	A	34	GENIC	homozygous	109168588
1	173248612	173248613	A	G	17	GENIC	homozygous	109168592
1	173248734	173248735	A	G	27	GENIC	homozygous	109168594
1	173249089	173249090	G	A	28	GENIC	homozygous	109168596
1	173250782	173250783	A	G	32	GENIC	homozygous	109168602
1	173251543	173251544	G	A	33	GENIC	homozygous	109168606
1	173253964	173253965	T	C	22	GENIC	homozygous	108387939
1	173258071	173258072	G	A	26	GENIC	homozygous	108387941
1	173258537	173258538	T	G	31	GENIC	homozygous	109168616
1	173259393	173259394	C	T	27	GENIC	homozygous	108387945