chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	11607337	11607338	G	T	64	GENIC	possibly homozygous	112065900
3	11607485	11607486	G	A	51	GENIC	homozygous	112065902
3	11607930	11607931	A	T	41	GENIC	homozygous	111447606
3	11608676	11608677	A	T	41	GENIC	homozygous	111447609
3	11608776	11608777	C	T	8	GENIC	homozygous	112065904
3	11608805	11608806	T	C	7	GENIC	homozygous	112065906
3	11609000	11609001	C	T	34	GENIC	homozygous	112065908
3	11609727	11609728	A	T	45	GENIC	homozygous	121931772
3	11609729	11609730	C	T	46	GENIC	homozygous	121931773
3	11610205	11610206	G	T	54	GENIC	homozygous	112065910
3	11610800	11610801	A	G	45	GENIC	homozygous	112065912
3	11611249	11611250	T	C	37	GENIC	possibly homozygous	112065914
3	11611380	11611381	T	A	40	GENIC	possibly homozygous	112065916
3	11611617	11611618	C	T	50	GENIC	homozygous	112065918
3	11612236	11612237	G	A	43	GENIC	homozygous	112065924
3	11609726	11609726		TGG	42	GENIC	homozygous	130900671
3	11613520	11613521	G	T	21	GENIC	homozygous	112065926
3	11613524	11613525	T	C	21	GENIC	homozygous	112065928
3	11613541	11613542	C	T	26	GENIC	homozygous	112065930
3	11613566	11613567	G	A	29	GENIC	homozygous	112065932
3	11613596	11613597	T	C	31	GENIC	homozygous	112065934
3	11613605	11613606	G	A	31	GENIC	homozygous	112065936
3	11613618	11613619	C	T	37	GENIC	homozygous	112065938
3	11614275	11614276	C	A	46	GENIC	homozygous	112065940
3	11615559	11615560	C	T	30	GENIC	homozygous	112065942
3	11616081	11616082	A	C	49	GENIC	homozygous	112065944
3	11617483	11617484	C	G	59	GENIC	homozygous	112065946
3	11617893	11617894	T	C	42	GENIC	homozygous	112065948
3	11617920	11617921	G	A	40	GENIC	homozygous	112065950
3	11619091	11619091		GGTGACCTA	45	GENIC	homozygous	127849727
3	11619258	11619259	G	A	60	GENIC	homozygous	112065952