chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	111078934	111078935	T	C	18	GENIC	homozygous	112004672
3	111079157	111079158	T	C	22	GENIC	homozygous	111673833
3	111079610	111079611	T	C	18	GENIC	homozygous	111673834
3	111079690	111079691	A	G	19	GENIC	homozygous	112004674
3	111079775	111079776	G	A	23	GENIC	homozygous	112004676
3	111080067	111080068	T	C	21	GENIC	homozygous	112004678
3	111080250	111080251	T	C	24	GENIC	homozygous	112004680
3	111080285	111080286	T	A	15	GENIC	homozygous	112004682
3	111080888	111080889	A	G	38	GENIC	homozygous	112004684
3	111081308	111081309	T	G	31	GENIC	homozygous	112004688
3	111081394	111081395	A	C	33	GENIC	homozygous	112004690
3	111082203	111082204	A	G	34	GENIC	homozygous	112004694
3	111082651	111082652	T	C	29	GENIC	homozygous	112004696
3	111083029	111083030	G	A	18	GENIC	homozygous	112004698
3	111083525	111083526	A	G	35	GENIC	homozygous	112004700
3	111084033	111084034	A	G	27	GENIC	homozygous	112004702
3	111084038	111084039	A	C	25	GENIC	homozygous	112004704
3	111084751	111084752	T	C	24	GENIC	homozygous	112004710
3	111084945	111084946	C	T	18	GENIC	homozygous	112004714
3	111086802	111086803	T	C	33	GENIC	homozygous	112004720
3	111087249	111087250	G	T	27	GENIC	homozygous	111673843