chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	59167690	59167691	T	C	23	GENIC	homozygous	113820336
5	59170352	59170353	C	T	23	GENIC	homozygous	113820348
5	59171212	59171213	G	A	26	GENIC	homozygous	113820350
5	59171549	59171550	A	G	22	GENIC	homozygous	113820352
5	59171910	59171911	T	A	23	GENIC	homozygous	113820354
5	59172532	59172533	G	T	21	GENIC	homozygous	119163464
5	59173524	59173525	A	T	30	GENIC	homozygous	119163466
5	59174087	59174088	G	A	20	GENIC	homozygous	114118273
5	59174169	59174170	G	A	28	GENIC	homozygous	119163468
5	59177007	59177008	G	A	30	GENIC	homozygous	119163470
5	59178266	59178267	T	C	23	GENIC	homozygous	114118281
5	59178293	59178294	T	C	18	GENIC	homozygous	114118283
5	59184448	59184449	C	G	31	GENIC	homozygous	114206396
5	59184492	59184493	G	A	26	GENIC	homozygous	113820370
5	59185101	59185102	A	C	20	GENIC	homozygous	113820372
5	59185642	59185643	A	G	17	GENIC	homozygous	113820374
5	59188584	59188585	A	G	28	GENIC	homozygous	113820380
5	59190557	59190558	C	T	27	GENIC	homozygous	113820382
5	59191285	59191286	A	G	17	GENIC	homozygous	113820384
5	59191681	59191682	A	G	10	GENIC	homozygous	113820386
5	59192315	59192316	T	C	24	GENIC	possibly homozygous	113820390
5	59193417	59193418	G	A	30	GENIC	homozygous	119163472
5	59193441	59193442	T	G	30	GENIC	homozygous	119163474