chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	135566179	135566180	C	T	28	GENIC	homozygous	56938446
4	135566242	135566243	A	C	33	GENIC	homozygous	56938447
4	135566982	135566983	A	G	34	GENIC	homozygous	56938448
4	135567045	135567046	C	A	34	GENIC	possibly homozygous	56938449
4	135567135	135567136	G	T	28	GENIC	homozygous	56938450
4	135567136	135567137	G	A	28	GENIC	homozygous	56938451
4	135567332	135567333	A	T	36	GENIC	homozygous	56938452
4	135567419	135567420	A	G	31	GENIC	homozygous	56938453
4	135567438	135567439	A	G	30	GENIC	homozygous	56938454
4	135567514	135567515	G	A	41	GENIC	homozygous	56938455
4	135567527	135567528	A	G	43	GENIC	homozygous	56938456
4	135567556	135567557	T	C	37	GENIC	homozygous	56938457
4	135567662	135567663	A	G	37	GENIC	homozygous	56938458
4	135567802	135567803	A	G	28	GENIC	homozygous	56938459
4	135568512	135568513	C	T	23	GENIC	homozygous	56938460
4	135568805	135568806	T	G	23	GENIC	homozygous	56938461
4	135568832	135568833	A	C	35	GENIC	homozygous	56938462
4	135568903	135568904	G	T	40	GENIC	homozygous	56938463