chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	71941577	71941578	T	C	36	GENIC	homozygous	114384895
13	72040553	72040554	A	G	27	GENIC	homozygous	114385193
13	72073411	72073412	C	T	33	GENIC	homozygous	114968873
13	72119290	72119291	C	T	16	GENIC	homozygous	114385461
13	72119293	72119294	C	A	18	GENIC	homozygous	114385463
13	72119331	72119332	C	A	19	GENIC	homozygous	114385465
13	72119393	72119394	C	G	16	GENIC	homozygous	114385467
13	72137396	72137397	G	C	14	GENIC	homozygous	114566067
13	72137421	72137422	G	T	18	GENIC	homozygous	114385469
13	72137427	72137428	G	T	18	GENIC	homozygous	114385470
13	72137430	72137431	G	T	18	GENIC	homozygous	114385472
13	72138216	72138217	C	A	30	GENIC	homozygous	114385474
13	72275781	72275782	T	A	9	GENIC	homozygous	114385513
13	72275785	72275786	A	G	9	GENIC	homozygous	114385515
13	72323823	72323824	T	C	30	GENIC	homozygous	114385633
13	72395229	72395230	C	A	36	GENIC	homozygous	114385909
13	72395257	72395258	C	G	38	GENIC	homozygous	114385911
13	72395275	72395276	G	A	37	GENIC	homozygous	114385913
13	72395336	72395337	G	T	41	GENIC	homozygous	114385915
13	72395338	72395339	G	C	41	GENIC	homozygous	114385917
13	72395370	72395371	G	A	34	GENIC	homozygous	114385919
13	72444655	72444656	A	G	25	GENIC	homozygous	114386153
13	72482297	72482298	G	A	29	GENIC	homozygous	114639166