chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	115389384	115389385	T	C	60	GENIC	homozygous	112815428
4	115389598	115389599	T	C	45	GENIC	homozygous	112815430
4	115394356	115394357	G	T	50	GENIC	possibly homozygous	112815432
4	115394660	115394661	T	C	61	GENIC	homozygous	112815434
4	115395610	115395611	T	A	62	GENIC	possibly homozygous	112815436
4	115396016	115396017	C	A	36	GENIC	homozygous	112815438
4	115396105	115396106	T	C	60	GENIC	possibly homozygous	112815440
4	115396201	115396202	T	G	83	GENIC	heterozygous	112815442
4	115396210	115396211	G	C	81	GENIC	possibly homozygous	112815448
4	115401097	115401098	C	T	59	GENIC	homozygous	112815452
4	115401499	115401500	G	A	39	GENIC	homozygous	112815454
4	115404444	115404445	T	C	73	GENIC	homozygous	112815456
4	115405163	115405164	C	T	57	GENIC	homozygous	112815458
4	115406817	115406818	T	C	68	GENIC	homozygous	112815460
4	115410238	115410239	T	C	61	GENIC	homozygous	112815462
4	115410484	115410485	T	G	48	GENIC	possibly homozygous	112815464
4	115411250	115411251	T	C	65	GENIC	homozygous	112815466