chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	47459082	47459085	GTG		17	GENIC	homozygous	144438752
13	47460289	47460290	C	T	23	GENIC	homozygous	139289166
13	47460353	47460354	T	A	21	GENIC	homozygous	139289167
13	47460392	47460393	G	A	18	GENIC	homozygous	139289168
13	47460521	47460522	T	A	27	GENIC	homozygous	139289169
13	47460870	47460871	T	G	26	GENIC	homozygous	139289170
13	47460934	47460935	G	A	26	GENIC	homozygous	139289171
13	47461071	47461072	C	T	25	GENIC	homozygous	139289172
13	47461188	47461189	T	C	29	GENIC	homozygous	139289173
13	47461194	47461195	A	G	29	GENIC	homozygous	139289174
13	47462582	47462583	G	A	30	GENIC	homozygous	139289175
13	47463800	47463801	T	C	18	GENIC	homozygous	139289177
13	47466485	47466486	T		18	GENIC	homozygous	139171931
13	47466991	47466992	T	C	25	GENIC	homozygous	139289186
13	47467345	47467346	A	G	21	GENIC	homozygous	139289188
13	47471837	47471838	A	G	23	GENIC	homozygous	139289190
13	47472400	47472404	GTGG		28	GENIC	homozygous	139171937
13	47473762	47473763	G	A	32	GENIC	homozygous	144444728
13	47467773	47467774	A	G	17	GENIC	homozygous	144444725
13	47468471	47468472	A	G	25	GENIC	homozygous	144444726
13	47470768	47470769	C	G	23	GENIC	homozygous	144444727
13	47473772	47473773	T	G	29	GENIC	homozygous	139289191
13	47474284	47474291	CGTGCGT		14	GENIC	homozygous	144438753
13	47474298	47474299	T		14	GENIC	heterozygous	404022974
13	47474298	47474299	T	G	14	GENIC	homozygous	404022975
13	47474294	47474295	T		13	GENIC	heterozygous	404022972
13	47474294	47474295	T	G	13	GENIC	homozygous	404022973
13	47474336	47474337	C	T	16	GENIC	homozygous	139289192
13	47475254	47475255	A	G	29	GENIC	homozygous	139289193