chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	30487981	30487982	G	A	22	GENIC	homozygous	112268042
3	30488099	30488100	T	A	12	GENIC	homozygous	112268043
3	30488843	30488844	G	C	23	GENIC	homozygous	111521816
3	30489034	30489035	G	A	13	GENIC	homozygous	111521818
3	30489036	30489037	G	C	13	GENIC	homozygous	111521820
3	30489039	30489040	G	C	13	GENIC	homozygous	119648423
3	30489040	30489041	C	A	13	GENIC	homozygous	119648424
3	30489129	30489130	C	A	30	GENIC	homozygous	111521824
3	30489812	30489813	G	A	27	GENIC	homozygous	112268045
3	30490047	30490048	G	C	35	GENIC	homozygous	112268046
3	30490274	30490275	C	T	19	GENIC	homozygous	112268047
3	30490554	30490555	T	C	24	GENIC	homozygous	112268048
3	30490703	30490704	T	C	32	GENIC	homozygous	112268049
3	30491168	30491169	G	A	32	GENIC	homozygous	111521828
3	30491385	30491386	T	A	27	GENIC	homozygous	112335125
3	30491613	30491614	C	T	24	GENIC	homozygous	112268050
3	30491900	30491901	T	A	17	GENIC	homozygous	112268053
3	30491990	30491991	A	T	19	GENIC	homozygous	112268054
3	30492120	30492121	C	G	22	GENIC	homozygous	112268055
3	30492220	30492221	G	A	27	GENIC	homozygous	112268056
3	30492639	30492640	T	C	29	GENIC	homozygous	112268058
3	30492952	30492953	A	G	18	GENIC	homozygous	112268059
3	30492954	30492955	G	A	16	GENIC	homozygous	119700254
3	30493845	30493846	A	G	10	GENIC	homozygous	112268060
3	30494107	30494108	T	C	15	GENIC	homozygous	112268061
3	30494192	30494193	T	C	15	GENIC	homozygous	112268062
3	30494815	30494816	C	T	29	GENIC	homozygous	112268063
3	30494837	30494838	T	A	32	GENIC	homozygous	111521832
3	30496361	30496362	C	T	35	GENIC	homozygous	112268064
3	30496418	30496419	T	C	44	GENIC	homozygous	111521842
3	30497134	30497135	T	A	25	GENIC	homozygous	111521844