chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	74787729	74787730	G	T	21	GENIC	possibly homozygous	63940491
18	74797906	74797907	T	G	12	GENIC	homozygous	64068047
18	74797907	74797908	G	T	12	GENIC	homozygous	64068048
18	74798409	74798410	A	C	5	GENIC	homozygous	63940493
18	74798468	74798469	G	T	6	GENIC	homozygous	63940495
18	74829198	74829199	T	A	17	GENIC	heterozygous	64104607
18	74860193	74860194	G	A	30	GENIC	homozygous	64104783
18	74937537	74937538	T	C	21	GENIC	possibly homozygous	63940531
18	74937539	74937540	T	C	21	GENIC	possibly homozygous	63940533
18	74939707	74939708	T	C	7	GENIC	homozygous	63940555
18	74939713	74939714	G	C	7	GENIC	homozygous	63940557
18	74939729	74939730	G	T	5	GENIC	homozygous	63940559
18	74939739	74939740	T	C	4	GENIC	homozygous	63940561
18	74939741	74939742	G	C	4	GENIC	homozygous	63940563
18	74939747	74939748	C	A	3	GENIC	homozygous	63940565
18	74939753	74939754	A	C	3	GENIC	homozygous	63940567
18	74939754	74939755	G	T	3	GENIC	homozygous	63940569
18	74940916	74940917	C	T	4	GENIC	homozygous	63940581
18	74940943	74940944	A	T	3	GENIC	homozygous	64927968