chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	154148178	154148179	T	C	18	GENIC	homozygous	108316032
1	154148417	154148418	T	A	29	GENIC	homozygous	108316034
1	154148863	154148864	G	A	22	GENIC	homozygous	108947442
1	154153070	154153071	G	A	27	GENIC	homozygous	108316042
1	154155137	154155138	C	A	25	GENIC	homozygous	108316046
1	154156909	154156910	A	G	34	GENIC	homozygous	108947443
1	154158221	154158222	C	A	23	GENIC	homozygous	108947444
1	154159100	154159101	C	T	27	GENIC	homozygous	108316052
1	154159305	154159306	T	C	13	GENIC	homozygous	108316054
1	154159607	154159608	A	G	29	GENIC	homozygous	108316056
1	154160358	154160359	G	A	15	GENIC	homozygous	108947445
1	154160555	154160556	A	G	20	GENIC	homozygous	108947446
1	154161133	154161134	T	G	10	GENIC	homozygous	108947447
1	154163729	154163730	T	C	36	GENIC	homozygous	108316064
1	154165762	154165763	G	A	27	GENIC	homozygous	108947448
1	154166546	154166547	C	T	33	GENIC	homozygous	108947449
1	154167027	154167028	A	C	25	GENIC	homozygous	108947450
1	154167196	154167197	G	C	30	GENIC	homozygous	108947451
1	154167941	154167942	A	T	22	GENIC	homozygous	108947452
1	154168510	154168511	G	A	23	GENIC	homozygous	108947453
1	154168673	154168674	C	A	29	GENIC	homozygous	108947454
1	154169531	154169532	T	C	25	GENIC	homozygous	108947455