chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	148767439	148767440	C	T	46	GENIC	homozygous	110050038
2	148768944	148768945	A	G	44	GENIC	homozygous	110050040
2	148768963	148768964	A	G	40	GENIC	homozygous	110050042
2	148768983	148768984	A	G	41	GENIC	homozygous	110050044
2	148769583	148769584	A	G	53	GENIC	homozygous	110050046
2	148770053	148770054	G	C	25	GENIC	possibly homozygous	110596554
2	148770176	148770177	G	C	38	GENIC	homozygous	110050048
2	148770183	148770184	G	A	37	GENIC	homozygous	110050050
2	148770717	148770718	G	T	41	GENIC	homozygous	110050052
2	148771214	148771215	C	A	42	GENIC	homozygous	110050053
2	148771476	148771477	G	A	43	GENIC	homozygous	110050055
2	148771787	148771788	C	T	62	GENIC	homozygous	110050057
2	148771812	148771813	G	T	49	GENIC	possibly homozygous	110050059
2	148772286	148772287	A	G	46	GENIC	homozygous	110050061
2	148772361	148772362	A	C	51	GENIC	possibly homozygous	110050063
2	148773264	148773265	C	G	39	GENIC	homozygous	110050065
2	148773864	148773865	A	G	45	GENIC	heterozygous	110050067
2	148774217	148774218	C	T	57	GENIC	homozygous	110050069
2	148774769	148774770	C	G	28	GENIC	homozygous	110050071
2	148775745	148775746	C	T	54	GENIC	homozygous	110050073
2	148776388	148776389	T	C	52	GENIC	homozygous	110050075
2	148776434	148776435	C	T	42	GENIC	homozygous	110050077
2	148776543	148776544	T	C	52	GENIC	homozygous	110050079
2	148777428	148777429	A	G	21	GENIC	heterozygous	110050081
2	148777942	148777943	C	T	71	GENIC	heterozygous	110050087
2	148778069	148778070	G	A	44	GENIC	homozygous	110050089
2	148778078	148778079	A	T	46	GENIC	homozygous	110050091
2	148778265	148778266	C	T	28	GENIC	homozygous	110050093
2	148779920	148779921	C	T	55	GENIC	homozygous	110050095
2	148780550	148780551	A	G	58	GENIC	possibly homozygous	110050096
2	148780615	148780616	A	G	31	GENIC	heterozygous	110596562
2	148777699	148777700	T	C	15	GENIC	heterozygous	110891968