chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	100167478	100167479	A	G	31	GENIC	possibly homozygous	113537159
4	100167531	100167532	C	T	40	GENIC	homozygous	113537161
4	100167537	100167538	A	G	43	GENIC	homozygous	113537163
4	100168292	100168293	C	T	37	GENIC	homozygous	113537165
4	100168894	100168895	C	T	31	GENIC	homozygous	113537167
4	100169886	100169887	C	A	16	GENIC	homozygous	113537169
4	100170254	100170255	G	T	26	GENIC	homozygous	113537171
4	100171003	100171004	T	C	19	GENIC	homozygous	113537173
4	100172373	100172374	C	T	35	GENIC	homozygous	113537175
4	100172441	100172442	C	T	33	GENIC	homozygous	113537177
4	100172745	100172746	C	A	29	GENIC	homozygous	113537179
4	100173159	100173160	A	G	27	GENIC	homozygous	113537181
4	100173420	100173421	T	C	26	GENIC	homozygous	112798239
4	100173501	100173502	T	G	22	GENIC	homozygous	112798241
4	100173507	100173508	G	A	25	GENIC	homozygous	113537183
4	100173798	100173799	A	G	35	GENIC	homozygous	113537185
4	100174035	100174036	G	A	30	GENIC	homozygous	113537187
4	100175830	100175831	A	G	29	GENIC	homozygous	112798251