chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13797721	13797722	T	C	28	GENIC	homozygous	116859588
10	13797770	13797771	G	T	33	GENIC	homozygous	116859590
10	13798215	13798216	G	A	22	GENIC	homozygous	116736410
10	13798221	13798222	A	T	21	GENIC	homozygous	116736411
10	13798517	13798518	T	C	13	GENIC	homozygous	116736412
10	13799089	13799090	T	C	24	GENIC	homozygous	116736413
10	13799869	13799870	T	C	22	GENIC	homozygous	116736414
10	13800432	13800433	A	G	16	GENIC	homozygous	116736415
10	13800577	13800578	C	A	22	GENIC	homozygous	116736416
10	13800744	13800745	G	A	20	GENIC	homozygous	116736417
10	13803040	13803041	T	C	27	GENIC	homozygous	116736418
10	13804586	13804587	G	A	17	GENIC	homozygous	116736419
10	13804722	13804723	T	G	25	GENIC	homozygous	116736420
10	13804926	13804927	C	T	24	GENIC	homozygous	116736421
10	13805037	13805038	C	T	24	GENIC	homozygous	116736422
10	13805597	13805598	G	A	19	GENIC	homozygous	116736424
10	13805863	13805864	T	C	31	GENIC	homozygous	116736425
10	13805921	13805922	C	T	32	GENIC	homozygous	116736426
10	13807927	13807928	G	T	32	GENIC	homozygous	116736428
10	13808266	13808267	C	T	25	GENIC	homozygous	116736429
10	13808538	13808539	C	T	26	GENIC	homozygous	116736430
10	13808558	13808559	G	A	26	GENIC	homozygous	116859592
10	13808958	13808959	C	T	23	GENIC	homozygous	116736431
10	13809328	13809329	C	T	30	GENIC	homozygous	116736432
10	13809849	13809850	T	C	27	GENIC	homozygous	116736433
10	13810037	13810038	T	C	23	GENIC	homozygous	116736434