chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	107550924	107550925	G	A	25	GENIC	homozygous	115471724
6	107551212	107551213	G	A	28	GENIC	homozygous	115471726
6	107551405	107551406	A	G	20	GENIC	homozygous	115471728
6	107551446	107551447	C	A	30	GENIC	homozygous	115471730
6	107551528	107551529	G	A	30	GENIC	homozygous	115471732
6	107551535	107551536	C	T	32	GENIC	homozygous	115471734
6	107551564	107551565	A	C	25	GENIC	homozygous	115471736
6	107551717	107551718	C	G	37	GENIC	homozygous	115471738
6	107553034	107553035	T	A	15	GENIC	homozygous	115471740
6	107553093	107553094	G	A	24	GENIC	homozygous	115471742
6	107553288	107553289	C	T	21	GENIC	homozygous	115471744
6	107553615	107553616	T	C	33	GENIC	homozygous	115471746
6	107553903	107553904	T	C	41	GENIC	homozygous	115471748
6	107554452	107554453	G	C	20	GENIC	homozygous	115471750
6	107554648	107554649	A	G	21	GENIC	homozygous	115471752
6	107555274	107555275	C	T	18	GENIC	heterozygous	115471754
6	107555363	107555364	A	G	25	GENIC	heterozygous	115471756
6	107556600	107556601	A	G	27	GENIC	homozygous	115471758
6	107556696	107556697	G	A	37	GENIC	homozygous	115471760
6	107557092	107557093	T	A	21	GENIC	homozygous	115471762
6	107557265	107557266	A	G	27	GENIC	homozygous	115471764
6	107557647	107557648	T	G	23	GENIC	homozygous	115471766