chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	62381049	62381050	G	A	15	GENIC	homozygous	112672391
4	62382721	62382722	G	T	19	GENIC	homozygous	112672393
4	62383178	62383179	T	G	17	GENIC	possibly homozygous	112672395
4	62383310	62383311	A	G	24	GENIC	homozygous	112672397
4	62383350	62383351	T	C	25	GENIC	homozygous	112672399
4	62383519	62383520	A	G	36	GENIC	homozygous	112672401
4	62383539	62383540	T	C	43	GENIC	homozygous	112672403
4	62384278	62384279	G	A	24	GENIC	homozygous	113235790
4	62385156	62385157	G	C	27	GENIC	homozygous	112672405
4	62385985	62385986	G	A	32	GENIC	homozygous	113235791
4	62386384	62386385	G	A	24	GENIC	homozygous	113235792
4	62386664	62386665	T	G	8	GENIC	homozygous	112672412
4	62386888	62386889	C	T	18	GENIC	possibly homozygous	113235793
4	62387928	62387929	C	G	33	GENIC	homozygous	112672414
4	62388247	62388248	C	G	32	GENIC	homozygous	112672416
4	62388387	62388388	C	A	25	GENIC	homozygous	113235794
4	62388911	62388912	T	C	23	GENIC	homozygous	112672418
4	62388991	62388992	G	A	45	GENIC	homozygous	113235795
4	62390352	62390353	T	C	27	GENIC	homozygous	112672424
4	62391785	62391786	G	A	31	GENIC	homozygous	113235796
4	62391845	62391846	C	A	20	GENIC	homozygous	113235797