chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	40017132	40017133	A	G	26	GENIC	homozygous	116801811
8	40017487	40017488	T	A	21	GENIC	homozygous	116801813
8	40017786	40017787	A	T	20	GENIC	homozygous	116801815
8	40017817	40017817		TGCCTCTATGGG	18	GENIC	homozygous	128585048
8	40018275	40018276	C	T	18	GENIC	homozygous	116801817
8	40018903	40018904	T	C	15	GENIC	homozygous	116801819
8	40019636	40019637	G	A	15	GENIC	homozygous	116801821
8	40020039	40020040	C	T	29	GENIC	homozygous	116801823
8	40020152	40020153	A	G	24	GENIC	homozygous	116801825
8	40020405	40020406	C	T	22	GENIC	homozygous	116801827
8	40021852	40021853	A	G	12	GENIC	homozygous	116801829
8	40022007	40022008	G	A	16	GENIC	homozygous	116801831
8	40022177	40022178	G	A	23	GENIC	homozygous	116463710
8	40022330	40022331	T	C	26	GENIC	homozygous	116801833
8	40022483	40022484	A	G	24	GENIC	homozygous	116463711
8	40022662	40022663	T	C	25	GENIC	homozygous	116801835
8	40022895	40022896	A	G	22	GENIC	homozygous	116463712