chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	9792829	9792830	A	G	11	GENIC	homozygous	111443612
3	9793207	9793208	T	C	16	GENIC	homozygous	111443613
3	9794443	9794444	A	G	16	GENIC	homozygous	111443618
3	9794460	9794461	C	T	14	GENIC	homozygous	111443619
3	9794756	9794757	T	C	16	GENIC	homozygous	111443621
3	9794903	9794904	T	C	22	GENIC	homozygous	111443622
3	9795064	9795065	C	T	23	GENIC	homozygous	111443623
3	9795377	9795378	T	C	29	GENIC	homozygous	111443625
3	9795479	9795480	C	T	32	GENIC	homozygous	111443627
3	9795489	9795490	C	G	26	GENIC	homozygous	111443628
3	9795569	9795570	C	T	18	GENIC	homozygous	112065537
3	9796272	9796273	T	C	20	GENIC	homozygous	111443630
3	9796296	9796297	A	T	24	GENIC	homozygous	111443631
3	9796383	9796384	G	A	16	GENIC	homozygous	111443632
3	9796562	9796563	T	G	19	GENIC	homozygous	111443633
3	9796608	9796609	A	G	15	GENIC	homozygous	111443634
3	9796912	9796913	G	T	32	GENIC	homozygous	111443635
3	9797087	9797088	T	C	15	GENIC	homozygous	111443636
3	9797203	9797204	G	A	25	GENIC	homozygous	111443637
3	9797339	9797340	C	T	24	GENIC	homozygous	111443638
3	9797487	9797488	A	G	17	GENIC	homozygous	111443639
3	9798146	9798147	C	T	13	GENIC	homozygous	111443640
3	9798348	9798349	A	C	21	GENIC	homozygous	111443641
3	9798596	9798597	G	A	34	GENIC	homozygous	112065539
3	9798633	9798634	C	G	33	GENIC	homozygous	111443642
3	9798714	9798715	A	G	29	GENIC	homozygous	111443643
3	9798777	9798778	C	T	29	GENIC	homozygous	111443644