chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	87190545	87190546	A	T	28	GENIC	possibly homozygous	116949188
10	87191348	87191349	T	C	39	GENIC	homozygous	116669130
10	87191830	87191831	C	G	28	GENIC	homozygous	116669132
10	87192035	87192036	C	G	40	GENIC	homozygous	116949190
10	87192490	87192491	T	C	28	GENIC	homozygous	116669134
10	87193003	87193004	C	G	43	GENIC	homozygous	116949192
10	87193209	87193210	G	C	47	GENIC	possibly homozygous	116949194
10	87193341	87193342	T	C	46	GENIC	homozygous	116949196
10	87193619	87193620	T	C	32	GENIC	homozygous	116949198
10	87193810	87193811	T	C	31	GENIC	homozygous	116949200
10	87194191	87194192	C	T	46	GENIC	homozygous	116949202
10	87194195	87194196	G	A	47	GENIC	homozygous	116949204
10	87194477	87194478	T	C	33	GENIC	homozygous	116949208
10	87194519	87194520	G	A	38	GENIC	homozygous	116949210
10	87194787	87194788	C	T	28	GENIC	homozygous	116949212
10	87194886	87194887	T	C	23	GENIC	homozygous	116949214
10	87194909	87194910	T	G	22	GENIC	homozygous	116949216