chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	104191886	104191887	A	G	5	GENIC	homozygous	111663783
3	104229164	104229165	A	T	13	GENIC	homozygous	111663840
3	104283632	104283633	C	G	23	GENIC	homozygous	111663888
3	104284977	104284978	C	T	21	GENIC	homozygous	111663889
3	104286228	104286229	A	C	16	GENIC	homozygous	111663890
3	104286428	104286429	T	G	26	GENIC	homozygous	111663891
3	104346953	104346954	T	C	12	GENIC	homozygous	111663958
3	104346957	104346958	A	C	9	GENIC	homozygous	111663959
3	104346965	104346966	A	C	4	GENIC	homozygous	111663960
3	104346969	104346970	T	C	3	GENIC	homozygous	112255564
3	104432251	104432252	C	A	10	GENIC	homozygous	111663965
3	104432269	104432270	T	G	10	GENIC	homozygous	111663966
3	104432281	104432282	G	C	10	GENIC	homozygous	111663967
3	104432316	104432317	C	A	5	GENIC	homozygous	111663968
3	104453426	104453427	C	A	24	GENIC	homozygous	111663970
3	104514512	104514513	A	G	18	GENIC	heterozygous	111663973
3	104547766	104547767	A	T	2	GENIC	homozygous	112255565
3	104596890	104596891	A	C	24	GENIC	heterozygous	112255566
3	104603250	104603251	G	T	31	GENIC	homozygous	111664111
3	104603299	104603300	A	C	28	GENIC	homozygous	111664112
3	104603464	104603465	C	T	16	GENIC	homozygous	111664113
3	104604730	104604731	G	T	13	GENIC	homozygous	111664114
3	104625777	104625778	G	T	18	GENIC	homozygous	111664144
3	104625799	104625800	G	A	16	GENIC	homozygous	111664145
3	104625803	104625804	C	A	18	GENIC	homozygous	111664146