chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	30488843	30488844	G	C	21	GENIC	homozygous	111521816
3	30489034	30489035	G	A	18	GENIC	homozygous	111521818
3	30489036	30489037	G	C	18	GENIC	homozygous	111521820
3	30489039	30489040	G	C	17	GENIC	homozygous	119648423
3	30489040	30489041	C	A	17	GENIC	homozygous	119648424
3	30489108	30489109	C	T	18	GENIC	homozygous	111521822
3	30489129	30489130	C	A	20	GENIC	homozygous	111521824
3	30490377	30490378	G	A	30	GENIC	homozygous	111521826
3	30491168	30491169	G	A	16	GENIC	homozygous	111521828
3	30491397	30491398	A	C	18	GENIC	homozygous	119724492
3	30493535	30493536	A	G	34	GENIC	homozygous	111521830
3	30494837	30494838	T	A	17	GENIC	homozygous	111521832
3	30495446	30495447	C	T	16	GENIC	homozygous	111521836
3	30495836	30495837	C	T	23	GENIC	homozygous	111521838
3	30496143	30496144	G	A	32	GENIC	homozygous	111521840
3	30496418	30496419	T	C	30	GENIC	homozygous	111521842
3	30497134	30497135	T	A	29	GENIC	homozygous	111521844
3	30497840	30497841	G	A	35	GENIC	homozygous	111521846