chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	41020059	41020060	A	C	33	GENIC	homozygous	114768794
6	41020388	41020389	G	A	33	GENIC	homozygous	115205730
6	41021613	41021614	C	A	25	GENIC	homozygous	114768812
6	41021574	41021575	A	C	25	GENIC	homozygous	114768810
6	41021654	41021655	G	A	33	GENIC	homozygous	114768814
6	41022469	41022470	C	A	21	GENIC	homozygous	114768816
6	41023796	41023797	C	T	28	GENIC	homozygous	114768818
6	41023828	41023829	C	T	29	GENIC	homozygous	114768820
6	41023987	41023988	G	A	31	GENIC	homozygous	114768822
6	41024160	41024161	A	T	44	GENIC	homozygous	114768824
6	41024423	41024424	G	T	30	GENIC	homozygous	114768828
6	41024735	41024736	A	G	25	GENIC	homozygous	114768830
6	41025162	41025163	T	A	10	GENIC	homozygous	118553043
6	41025163	41025164	A	T	10	GENIC	homozygous	118553044
6	41026772	41026773	G	T	20	GENIC	homozygous	114768834
6	41026515	41026516	C	T	26	GENIC	homozygous	115374685
6	41027020	41027021	G	A	15	GENIC	homozygous	115374687
6	41030329	41030330	A	G	37	GENIC	homozygous	115374689