chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	41020059	41020060	A	C	26	GENIC	homozygous	114768794
6	41020388	41020389	G	A	23	GENIC	homozygous	115205730
6	41020627	41020628	C	G	24	GENIC	homozygous	115205731
6	41021574	41021575	A	C	19	GENIC	homozygous	114768810
6	41021613	41021614	C	A	13	GENIC	homozygous	114768812
6	41021654	41021655	G	A	12	GENIC	homozygous	114768814
6	41022469	41022470	C	A	24	GENIC	homozygous	114768816
6	41023796	41023797	C	T	30	GENIC	homozygous	114768818
6	41023828	41023829	C	T	23	GENIC	homozygous	114768820
6	41023987	41023988	G	A	23	GENIC	homozygous	114768822
6	41024160	41024161	A	T	21	GENIC	homozygous	114768824
6	41024423	41024424	G	T	20	GENIC	homozygous	114768828
6	41024735	41024736	A	G	17	GENIC	homozygous	114768830
6	41026772	41026773	G	T	22	GENIC	possibly homozygous	114768834
6	41027806	41027807	C	G	21	GENIC	homozygous	118647884
6	41033488	41033488		TC	24	GENIC	homozygous	128331880
6	41036274	41036278	GACC		18	GENIC	homozygous	128331882
6	41038471	41038471		C	28	GENIC	homozygous	128331885
6	41039339	41039339		T	20	GENIC	possibly homozygous	131408010
6	41023788	41023789	T	C	29	GENIC	homozygous	118585368
6	41025162	41025163	T	A	18	GENIC	homozygous	118553043
6	41025163	41025164	A	T	18	GENIC	homozygous	118553044
6	41026515	41026516	C	T	18	GENIC	homozygous	115374685
6	41027020	41027021	G	A	22	GENIC	homozygous	115374687
6	41030329	41030330	A	G	18	GENIC	homozygous	115374689
6	41028511	41028513	GC		17	GENIC	homozygous	132092943
6	41034522	41034522		GG	25	GENIC	homozygous	132092944
6	41038361	41038365	AACC		28	GENIC	homozygous	132092945