chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	149183330	149183331	T	G	34	GENIC	homozygous	112880540
4	149184196	149184197	T	C	27	GENIC	homozygous	112880544
4	149184932	149184933	C	A	34	GENIC	homozygous	112880546
4	149185296	149185297	T	G	16	GENIC	homozygous	112880548
4	149185408	149185409	A	G	28	GENIC	homozygous	112880550
4	149185441	149185442	C	T	27	GENIC	homozygous	112880552
4	149186124	149186125	G	A	42	GENIC	homozygous	112880553
4	149186677	149186678	T	C	24	GENIC	homozygous	112880555
4	149187685	149187686	C	A	19	GENIC	homozygous	112880556
4	149188291	149188292	T	C	16	GENIC	homozygous	112880558
4	149190086	149190087	G	A	23	GENIC	homozygous	112880560
4	149190431	149190432	G	A	34	GENIC	homozygous	112880562
4	149190469	149190470	G	A	44	GENIC	homozygous	112880564
4	149190633	149190634	G	C	40	GENIC	homozygous	112880566
4	149191241	149191242	T	C	25	GENIC	homozygous	112880571
4	149191247	149191248	C	T	27	GENIC	homozygous	112880573
4	149191382	149191383	T	C	29	GENIC	homozygous	112880575
4	149191769	149191770	A	G	23	GENIC	homozygous	112880577
4	149191776	149191777	T	C	22	GENIC	homozygous	112880579
4	149191802	149191803	G	A	23	GENIC	homozygous	112880580
4	149191817	149191818	T	C	26	GENIC	homozygous	112880582
4	149191846	149191847	A	G	26	GENIC	homozygous	112880584