chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	11476483	11476484	T	C	28	GENIC	homozygous	112065625
3	11476775	11476776	T	A	25	GENIC	homozygous	112065627
3	11477467	11477468	C	T	37	GENIC	homozygous	112065629
3	11477870	11477871	C	T	25	GENIC	homozygous	112065631
3	11478187	11478188	G	A	16	GENIC	homozygous	112065633
3	11478789	11478790	T	C	35	GENIC	homozygous	112065635
3	11478995	11478996	T	C	33	GENIC	homozygous	112065637
3	11479084	11479085	A	G	26	GENIC	homozygous	112065639
3	11479143	11479144	A	G	27	GENIC	homozygous	112065641
3	11479221	11479222	A	G	24	GENIC	homozygous	111447222
3	11479258	11479259	A	G	19	GENIC	homozygous	112065643
3	11479313	11479314	C	G	17	GENIC	homozygous	112065645
3	11479692	11479693	C	T	40	GENIC	homozygous	112065647
3	11479767	11479768	C	T	32	GENIC	homozygous	112065649
3	11480160	11480161	G	T	24	GENIC	homozygous	112065651
3	11480461	11480462	A	G	32	GENIC	homozygous	111447228
3	11481164	11481165	A	G	29	GENIC	homozygous	112065653
3	11481627	11481628	C	T	16	GENIC	homozygous	112065655
3	11481758	11481759	C	G	15	GENIC	homozygous	112065657
3	11481977	11481978	A	G	31	GENIC	homozygous	112065659
3	11482390	11482391	G	A	27	GENIC	homozygous	112065661