chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	59167690	59167691	T	C	33	GENIC	homozygous	113820336
5	59167967	59167968	T	C	31	GENIC	homozygous	113820338
5	59168603	59168604	C	T	25	GENIC	homozygous	113820340
5	59170056	59170057	A	C	71	GENIC	heterozygous	113820342
5	59170058	59170059	C	T	81	GENIC	heterozygous	113820344
5	59170070	59170071	C	T	79	GENIC	heterozygous	113820346
5	59170352	59170353	C	T	44	GENIC	homozygous	113820348
5	59171212	59171213	G	A	41	GENIC	homozygous	113820350
5	59171549	59171550	A	G	25	GENIC	homozygous	113820352
5	59171910	59171911	T	A	35	GENIC	homozygous	113820354
5	59174087	59174088	G	A	26	GENIC	homozygous	114118273
5	59176041	59176042	C	T	34	GENIC	homozygous	114118275
5	59176260	59176261	G	A	31	GENIC	homozygous	114118277
5	59178124	59178125	A	G	48	GENIC	homozygous	114118279
5	59178266	59178267	T	C	41	GENIC	homozygous	114118281
5	59178293	59178294	T	C	35	GENIC	homozygous	114118283
5	59179745	59179746	A	T	32	GENIC	homozygous	114118285
5	59181351	59181352	C	A	33	GENIC	possibly homozygous	114118287
5	59181590	59181591	T	C	25	GENIC	heterozygous	114118291
5	59182929	59182930	C	A	25	GENIC	homozygous	114118305
5	59183556	59183557	A	T	34	GENIC	possibly homozygous	113820366
5	59183799	59183800	T	C	22	GENIC	homozygous	114118311
5	59185101	59185102	A	C	29	GENIC	homozygous	113820372
5	59185642	59185643	A	G	20	GENIC	homozygous	113820374
5	59186702	59186703	T	G	13	GENIC	possibly homozygous	113820376
5	59187155	59187156	C	T	39	GENIC	homozygous	113820378
5	59188584	59188585	A	G	26	GENIC	homozygous	113820380
5	59190557	59190558	C	T	29	GENIC	homozygous	113820382
5	59190663	59190664	G	A	28	GENIC	homozygous	114118317
5	59191285	59191286	A	G	60	GENIC	homozygous	113820384
5	59191681	59191682	A	G	53	GENIC	homozygous	113820386
5	59192315	59192316	T	C	32	GENIC	homozygous	113820390