chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50532279	50532280	G	A	28	GENIC	homozygous	114340712
13	50532281	50532282	A	G	29	GENIC	homozygous	114340713
13	50533753	50533754	T	C	15	GENIC	homozygous	114340715
13	50534819	50534820	C	T	18	GENIC	homozygous	114340717
13	50536617	50536618	A	C	20	GENIC	homozygous	114340719
13	50537247	50537248	C	T	22	GENIC	homozygous	114340721
13	50537783	50537784	T	C	19	GENIC	homozygous	114340723
13	50537849	50537850	G	A	21	GENIC	homozygous	114340725
13	50538858	50538859	A	G	20	GENIC	homozygous	114340727
13	50538998	50538999	G	A	27	GENIC	homozygous	114340729
13	50542271	50542272	G	A	24	GENIC	homozygous	114340731
13	50545627	50545628	T	G	27	GENIC	homozygous	114340733
13	50546106	50546107	G	T	28	GENIC	homozygous	114340735
13	50546488	50546489	G	A	29	GENIC	homozygous	114340737
13	50548326	50548327	T	C	31	GENIC	homozygous	114340739
13	50549175	50549176	C	T	21	GENIC	homozygous	114340741
13	50549495	50549496	T	C	26	GENIC	homozygous	114340743
13	50550009	50550010	A	G	24	GENIC	homozygous	114340745