chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	11476483	11476484	T	C	54	GENIC	homozygous	112065625
3	11476775	11476776	T	A	47	GENIC	homozygous	112065627
3	11477467	11477468	C	T	62	GENIC	homozygous	112065629
3	11477870	11477871	C	T	42	GENIC	homozygous	112065631
3	11478187	11478188	G	A	26	GENIC	homozygous	112065633
3	11478789	11478790	T	C	47	GENIC	possibly homozygous	112065635
3	11478995	11478996	T	C	41	GENIC	homozygous	112065637
3	11479084	11479085	A	G	47	GENIC	possibly homozygous	112065639
3	11479143	11479144	A	G	47	GENIC	possibly homozygous	112065641
3	11479258	11479259	A	G	50	GENIC	homozygous	112065643
3	11479313	11479314	C	G	49	GENIC	homozygous	112065645
3	11479692	11479693	C	T	28	GENIC	homozygous	112065647
3	11479767	11479768	C	T	45	GENIC	homozygous	112065649
3	11478425	11478427	CT		32	GENIC	homozygous	130900649
3	11478827	11478839	TCAACCAGACTC		46	GENIC	homozygous	130900650
3	11479221	11479222	A	G	48	GENIC	homozygous	111447222
3	11480803	11480804	T		49	GENIC	homozygous	130900651
3	11481758	11481759	C	G	48	GENIC	homozygous	112065657
3	11480461	11480462	A	G	45	GENIC	homozygous	111447228
3	11481164	11481165	A	G	38	GENIC	homozygous	112065653
3	11481627	11481628	C	T	42	GENIC	homozygous	112065655
3	11481843	11481843		CCCCG	20	GENIC	possibly homozygous	130900652
3	11481977	11481978	A	G	39	GENIC	homozygous	112065659
3	11482390	11482391	G	A	45	GENIC	homozygous	112065661
3	11482608	11482609	A		51	GENIC	homozygous	130900653