chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	11392728	11392729	C	T	30	GENIC	homozygous	111446864
3	11393346	11393347	G	A	29	GENIC	homozygous	111446866
3	11398213	11398214	T	G	38	GENIC	homozygous	111446868
3	11398297	11398298	A	G	32	GENIC	homozygous	111446870
3	11400709	11400710	G	A	41	GENIC	homozygous	111446872
3	11400819	11400820	C	T	45	GENIC	possibly homozygous	111446874
3	11400829	11400830	T	C	45	GENIC	homozygous	111446876
3	11400936	11400937	C	T	43	GENIC	homozygous	111446878
3	11401160	11401161	A	G	17	GENIC	homozygous	111446880
3	11401381	11401382	A	G	30	GENIC	possibly homozygous	111446882
3	11401638	11401639	T	C	36	GENIC	homozygous	111446884
3	11402110	11402111	C	T	26	GENIC	possibly homozygous	111446886
3	11402814	11402815	G	A	36	GENIC	homozygous	111446888
3	11402927	11402928	T	A	38	GENIC	heterozygous	111446890
3	11403482	11403483	G	C	43	GENIC	homozygous	111446892
3	11403935	11403936	G	A	34	GENIC	homozygous	111446894
3	11405029	11405030	T	G	56	GENIC	homozygous	111446896
3	11405506	11405507	G	A	25	GENIC	homozygous	111446898
3	11406186	11406187	A	G	44	GENIC	homozygous	111446900
3	11406528	11406529	T	G	35	GENIC	homozygous	111446902
3	11406704	11406705	G	A	24	GENIC	heterozygous	111446904
3	11406752	11406753	A	G	24	GENIC	homozygous	111446906
3	11408880	11408881	G	A	32	GENIC	homozygous	111446908