chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	41020059	41020060	A	C	28	GENIC	homozygous	114768794
6	41020388	41020389	G	A	23	GENIC	homozygous	115205730
6	41021384	41021385	C	T	25	GENIC	homozygous	114768808
6	41024423	41024424	G	T	28	GENIC	homozygous	114768828
6	41024735	41024736	A	G	22	GENIC	homozygous	114768830
6	41025162	41025163	T	A	16	GENIC	homozygous	118553043
6	41025163	41025164	A	T	16	GENIC	homozygous	118553044
6	41026772	41026773	G	T	23	GENIC	homozygous	114768834
6	41030931	41030932	G	C	22	GENIC	homozygous	114768846
6	41030942	41030943	G	A	26	GENIC	homozygous	114768848
6	41031264	41031265	G	A	31	GENIC	homozygous	115205732
6	41031539	41031540	T	C	28	GENIC	homozygous	114768850
6	41031547	41031548	G	A	29	GENIC	homozygous	114768852
6	41038364	41038365	C	A	29	GENIC	homozygous	114768854