chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	119139994	119139995	G	C	6	GENIC	homozygous	109994931
2	119140160	119140161	T	C	8	GENIC	homozygous	109994933
2	119141029	119141030	G	A	22	GENIC	homozygous	109994935
2	119141846	119141847	T	C	12	GENIC	homozygous	109994937
2	119141855	119141856	T	C	13	GENIC	homozygous	109994939
2	119142964	119142965	T	G	19	GENIC	homozygous	109994941
2	119143442	119143443	T	A	20	GENIC	homozygous	109994943
2	119144693	119144694	T	C	15	GENIC	homozygous	109994945
2	119145037	119145038	G	T	18	GENIC	homozygous	109994947
2	119145892	119145893	T	C	11	GENIC	homozygous	109994948
2	119146227	119146228	C	T	13	GENIC	homozygous	109994950
2	119146621	119146622	C	T	24	GENIC	homozygous	109994952
2	119147235	119147236	C	T	20	GENIC	homozygous	109994954
2	119147659	119147660	A	T	28	GENIC	homozygous	109994956
2	119147710	119147711	A	T	27	GENIC	possibly homozygous	109994958
2	119147791	119147792	A	G	15	GENIC	homozygous	109994960
2	119150449	119150450	G	A	13	GENIC	homozygous	109994970
2	119151107	119151108	C	G	11	GENIC	homozygous	109994972
2	119152021	119152022	T	C	9	GENIC	homozygous	109994977
2	119152110	119152111	T	C	16	GENIC	homozygous	109994979
2	119152285	119152286	C	T	18	GENIC	homozygous	109994981
2	119152410	119152411	A	G	8	GENIC	homozygous	109994983