chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	60619492	60619493	A	G	35	GENIC	possibly homozygous	110369511
18	60619754	60619755	G	T	26	GENIC	possibly homozygous	119496424
18	60620465	60620466	T	C	64	GENIC	homozygous	110369513
18	60620560	60620561	G	T	51	GENIC	homozygous	110369515
18	60620603	60620604	T	C	51	GENIC	homozygous	110369517
18	60621069	60621070	G	A	47	GENIC	homozygous	110369519
18	60621383	60621384	T	A	45	GENIC	homozygous	110369521
18	60621387	60621388	A	G	42	GENIC	homozygous	110369523
18	60622829	60622830	T	C	37	GENIC	homozygous	110369525
18	60623204	60623205	C	A	42	GENIC	homozygous	110369527
18	60623296	60623297	T	C	42	GENIC	heterozygous	119496425
18	60623305	60623306	C	T	45	GENIC	heterozygous	119496426
18	60625800	60625801	T	C	32	GENIC	homozygous	110369529
18	60626632	60626633	T	C	24	GENIC	homozygous	110369531
18	60627484	60627485	T	C	61	GENIC	homozygous	110369533
18	60628464	60628465	A	C	71	GENIC	homozygous	110369535
18	60628800	60628801	A	G	50	GENIC	homozygous	110369537