chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	58420895	58420896	C	T	10	GENIC	homozygous	119634490
19	58420896	58420897	A	G	10	GENIC	homozygous	119634491
19	58420969	58420970	A	T	25	GENIC	possibly homozygous	119634492
19	58420984	58420985	A	T	23	GENIC	homozygous	119634493
19	58420985	58420986	C	T	23	GENIC	homozygous	119634494
19	58421066	58421067	T	C	13	GENIC	homozygous	119634495
19	58421283	58421284	G	C	20	GENIC	possibly homozygous	119646683
19	58421302	58421303	A	G	28	GENIC	possibly homozygous	119634496
19	58421310	58421311	C	T	28	GENIC	possibly homozygous	119634497
19	58421336	58421337	T	C	31	GENIC	possibly homozygous	119634498
19	58421360	58421361	A	G	23	GENIC	possibly homozygous	119634499
19	58421396	58421397	G	A	12	GENIC	possibly homozygous	119634500
19	58421429	58421430	C	T	5	GENIC	heterozygous	119720292