chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	115045146	115045147	T	TTTCCA	26	GENIC	homozygous	54657025
6	115046105	115046106	A	G	29	GENIC	homozygous	54657027
6	115046469	115046470	A	C	34	GENIC	homozygous	54657029
6	115046730	115046731	T	TACCAATGCCTTCCTTCATA	40	GENIC	homozygous	55531482
6	115046833	115046834	T	C	31	GENIC	homozygous	54657035
6	115046835	115046836	T	A	31	GENIC	homozygous	54657037
6	115047003	115047005	TT	--	32	GENIC	homozygous	54657039
6	115047396	115047397	C	T	29	GENIC	homozygous	54657041
6	115048071	115048072	A	G	30	GENIC	possibly homozygous	54657043
6	115048337	115048338	A	C	29	GENIC	homozygous	54657045
6	115048749	115048750	A	T	37	GENIC	homozygous	54657047
6	115054494	115054495	C	-	12	GENIC	homozygous	54657049
6	115056182	115056183	G	A	24	GENIC	homozygous	54657056
6	115053567	115053573	GTGTGT	------	14	GENIC	homozygous	55975920