chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50533753	50533754	T	C	46	GENIC	homozygous	114340715
13	50534819	50534820	C	T	29	GENIC	homozygous	114340717
13	50536617	50536618	A	C	22	GENIC	homozygous	114340719
13	50537247	50537248	C	T	32	GENIC	homozygous	114340721
13	50537783	50537784	T	C	43	GENIC	homozygous	114340723
13	50537849	50537850	G	A	42	GENIC	homozygous	114340725
13	50538858	50538859	A	G	25	GENIC	homozygous	114340727
13	50538998	50538999	G	A	27	GENIC	homozygous	114340729
13	50542271	50542272	G	A	16	GENIC	homozygous	114340731
13	50541831	50541832	G	A	47	GENIC	possibly homozygous	118450634
13	50545627	50545628	T	G	20	GENIC	homozygous	114340733
13	50549175	50549176	C	T	35	GENIC	homozygous	114340741
13	50544734	50544735	A	G	8	GENIC	homozygous	114720341
13	50546106	50546107	G	T	23	GENIC	homozygous	114340735
13	50546488	50546489	G	A	21	GENIC	homozygous	114340737
13	50548326	50548327	T	C	33	GENIC	homozygous	114340739
13	50549495	50549496	T	C	31	GENIC	homozygous	114340743
13	50550009	50550010	A	G	19	GENIC	homozygous	114340745