chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	33639254	33639255	G	C	11	GENIC	homozygous	113265568
4	33639693	33639694	G	A	4	GENIC	homozygous	113097194
4	33639710	33639711	C	T	3	GENIC	homozygous	113097196
4	33640009	33640010	C	T	15	GENIC	homozygous	113097204
4	33640231	33640232	T	G	14	GENIC	homozygous	113097208
4	33640419	33640420	C	G	21	GENIC	homozygous	113097210
4	33641762	33641763	C	T	17	GENIC	homozygous	113097212
4	33643253	33643254	G	A	14	GENIC	possibly homozygous	113265569
4	33643298	33643299	T	C	11	GENIC	homozygous	113097214
4	33643994	33643995	T	C	11	GENIC	homozygous	113097220
4	33644882	33644883	A	G	24	GENIC	homozygous	113097224
4	33644965	33644966	T	C	20	GENIC	homozygous	113097226
4	33644996	33644997	C	A	19	GENIC	homozygous	113097228
4	33645023	33645024	A	T	16	GENIC	homozygous	113097230
4	33645165	33645166	C	T	16	GENIC	homozygous	113097232
4	33645338	33645339	A	C	26	GENIC	homozygous	113097234
4	33645343	33645344	A	T	26	GENIC	homozygous	113097236
4	33645499	33645500	C	T	22	GENIC	homozygous	113097238
4	33645948	33645949	A	G	18	GENIC	homozygous	113097242
4	33644920	33644922	CT		19	GENIC	homozygous	130928011