chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	140107794	140107795	C	A	30	GENIC	homozygous	111752222
3	140108166	140108167	T	C	37	GENIC	homozygous	111752224
3	140108369	140108370	C	T	33	GENIC	homozygous	111752228
3	140108405	140108406	T	G	34	GENIC	homozygous	112166913
3	140108992	140108993	C	T	21	GENIC	homozygous	112166915
3	140109707	140109708	C	T	26	GENIC	homozygous	112166919
3	140112195	140112196	A	T	28	GENIC	homozygous	112166921
3	140112918	140112919	A	G	30	GENIC	homozygous	111752236
3	140113216	140113217	G	A	29	GENIC	homozygous	112166923
3	140113544	140113545	G	A	30	GENIC	homozygous	111752239
3	140114039	140114040	A	G	28	GENIC	homozygous	111752243
3	140114246	140114247	T	C	19	GENIC	homozygous	111752244
3	140114744	140114745	T	C	13	GENIC	homozygous	111752246
3	140117248	140117249	G	T	21	GENIC	homozygous	111752250
3	140119408	140119409	A	G	28	GENIC	homozygous	111752256
3	140119679	140119680	G	A	19	GENIC	homozygous	111752258
3	140119896	140119897	T	C	21	GENIC	homozygous	111752262
3	140120418	140120419	C	T	12	GENIC	homozygous	112166925
3	140120856	140120857	C	T	28	GENIC	homozygous	112166927
3	140121166	140121167	A	G	26	GENIC	homozygous	111752264
3	140123648	140123649	A	T	11	GENIC	heterozygous	119704575
3	140123653	140123654	A	T	10	GENIC	heterozygous	119704576
3	140123851	140123852	C	T	15	GENIC	homozygous	111752266