chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	87259645	87259646	G	A	12	GENIC	homozygous	113358405
4	87260360	87260361	C	A	17	GENIC	homozygous	113358407
4	87260800	87260801	G	A	19	GENIC	homozygous	112767795
4	87263201	87263202	A	G	25	GENIC	homozygous	112767801
4	87263603	87263604	A	G	42	GENIC	homozygous	112767805
4	87263633	87263634	G	A	38	GENIC	homozygous	113358409
4	87263934	87263935	G	A	15	GENIC	homozygous	113358411
4	87264893	87264894	A	G	24	GENIC	possibly homozygous	113358413
4	87265561	87265562	C	T	14	GENIC	homozygous	113358415
4	87266658	87266659	T	C	8	GENIC	homozygous	113130365
4	87267067	87267068	G	A	26	GENIC	homozygous	113358419
4	87267670	87267671	C	G	19	GENIC	heterozygous	113040608
4	87267680	87267681	G	C	20	GENIC	heterozygous	113358421
4	87268959	87268960	C	T	13	GENIC	homozygous	113358423
4	87270594	87270595	C	A	18	GENIC	homozygous	112767809
4	87272662	87272663	A	G	26	GENIC	homozygous	112767811
4	87273347	87273348	C	A	21	GENIC	homozygous	113358425
4	87276505	87276506	T	C	20	GENIC	homozygous	112767815
4	87276829	87276830	G	A	19	GENIC	homozygous	112767817