chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	148767439	148767440	C	T	31	GENIC	homozygous	110050038
2	148768944	148768945	A	G	22	GENIC	homozygous	110050040
2	148768963	148768964	A	G	21	GENIC	homozygous	110050042
2	148768983	148768984	A	G	20	GENIC	homozygous	110050044
2	148769583	148769584	A	G	25	GENIC	homozygous	110050046
2	148770176	148770177	G	C	17	GENIC	homozygous	110050048
2	148770183	148770184	G	A	17	GENIC	homozygous	110050050
2	148770717	148770718	G	T	27	GENIC	homozygous	110050052
2	148771214	148771215	C	A	33	GENIC	homozygous	110050053
2	148771476	148771477	G	A	31	GENIC	homozygous	110050055
2	148771787	148771788	C	T	33	GENIC	homozygous	110050057
2	148771812	148771813	G	T	28	GENIC	homozygous	110050059
2	148772361	148772362	A	C	23	GENIC	homozygous	110050063
2	148773264	148773265	C	G	19	GENIC	homozygous	110050065
2	148773864	148773865	A	G	25	GENIC	homozygous	110050067
2	148774217	148774218	C	T	10	GENIC	homozygous	110050069
2	148774769	148774770	C	G	18	GENIC	homozygous	110050071
2	148775745	148775746	C	T	20	GENIC	homozygous	110050073
2	148776388	148776389	T	C	18	GENIC	homozygous	110050075
2	148776434	148776435	C	T	22	GENIC	homozygous	110050077
2	148776543	148776544	T	C	26	GENIC	homozygous	110050079
2	148779920	148779921	C	T	27	GENIC	homozygous	110050095