chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	115045146	115045147	T	TTTCCA	37	GENIC	homozygous	54657025
6	115046105	115046106	A	G	36	GENIC	homozygous	54657027
6	115046469	115046470	A	C	82	GENIC	homozygous	54657029
6	115046727	115046728	A	AACCAATG	15	GENIC	homozygous	54657031
6	115046730	115046731	T	TTCCTTCATA	9	GENIC	homozygous	54657033
6	115046833	115046834	T	C	34	GENIC	homozygous	54657035
6	115046835	115046836	T	A	36	GENIC	homozygous	54657037
6	115047003	115047005	TT	--	55	GENIC	homozygous	54657039
6	115047396	115047397	C	T	62	GENIC	homozygous	54657041
6	115048071	115048072	A	G	56	GENIC	possibly homozygous	54657043
6	115048337	115048338	A	C	75	GENIC	homozygous	54657045
6	115048749	115048750	A	T	77	GENIC	homozygous	54657047
6	115054494	115054495	C	-	31	GENIC	homozygous	54657049
6	115054864	115054865	C	-	19	GENIC	heterozygous	54657050
6	115054864	115054865	C	CT	5	GENIC	heterozygous	54657052
6	115054865	115054866	T	-	5	GENIC	heterozygous	54657054
6	115056182	115056183	G	A	47	GENIC	possibly homozygous	54657056