chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	107840468	107840469	A	C	20	GENIC	homozygous	113956444
5	107842559	107842560	C	T	41	GENIC	possibly homozygous	113956445
5	107842620	107842621	C	T	48	GENIC	homozygous	113956446
5	107845237	107845238	T	C	48	GENIC	homozygous	113956447
5	107845283	107845284	G	A	45	GENIC	homozygous	113956448
5	107848543	107848544	T	C	57	GENIC	homozygous	113956449
5	107849329	107849330	A	G	18	GENIC	homozygous	113956450
5	107850487	107850488	G	C	41	GENIC	homozygous	113956451
5	107852132	107852133	A	G	39	GENIC	homozygous	113956452
5	107853578	107853579	C	T	28	GENIC	homozygous	113956453
5	107854716	107854717	T	C	45	GENIC	homozygous	113956454
5	107855008	107855009	G	T	46	GENIC	possibly homozygous	113956455
5	107855284	107855285	T	G	45	GENIC	homozygous	113956456
5	107856002	107856003	C	T	22	GENIC	possibly homozygous	113956457
5	107857364	107857365	T	C	29	GENIC	homozygous	113956458