chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	62006732	62006733	G	C	22	GENIC	homozygous	49780013
13	62006810	62006811	A	ATAAAAGACATAGAC	17	GENIC	homozygous	49780015
13	62008223	62008224	G	T	12	GENIC	homozygous	49780026
13	62008236	62008237	G	GT	11	GENIC	homozygous	49780027
13	62008270	62008271	G	T	8	GENIC	homozygous	50059502
13	62008272	62008273	T	-	8	GENIC	homozygous	49780031
13	62008274	62008275	C	A	7	GENIC	homozygous	50495842
13	62008284	62008285	G	A	8	GENIC	homozygous	49780032
13	62008286	62008287	T	C	9	GENIC	homozygous	49780033
13	62008320	62008321	G	-	17	GENIC	homozygous	49780034
13	62008330	62008331	A	-	17	GENIC	homozygous	49780035
13	62008337	62008338	C	A	17	GENIC	homozygous	49780036
13	62008351	62008352	G	A	19	GENIC	homozygous	49780037
13	62037353	62037354	C	CGTGTGTG	3	GENIC	heterozygous	50581789
13	62037353	62037354	C	CGTGTGTGTG	3	GENIC	heterozygous	50581790
13	62039373	62039374	T	TCCC	2	GENIC	homozygous	50520154
13	62046295	62046296	A	G	51	GENIC	heterozygous	49780209
13	62046388	62046389	A	G	26	GENIC	heterozygous	49780211
13	62046397	62046399	AA	--	27	GENIC	heterozygous	49780212
13	62046400	62046401	A	T	26	GENIC	heterozygous	49780213
13	62046517	62046518	T	-	34	GENIC	heterozygous	50520155
13	62046519	62046526	ATAAAGA	-------	35	GENIC	heterozygous	50520156
13	62046549	62046550	G	GTGTGTATA	44	GENIC	heterozygous	49780221
13	62046901	62046902	A	-	41	GENIC	heterozygous	49780232
13	62060366	62060367	T	TCC	2	GENIC	heterozygous	50581796
13	62086196	62086202	ACACAT	------	13	GENIC	heterozygous	50617394
13	62086202	62086204	AC	--	6	GENIC	heterozygous	50581797
13	62087777	62087779	CA	--	9	GENIC	homozygous	50581798
13	62092473	62092474	A	AG	14	GENIC	homozygous	49780480