chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	12591542	12591543	G		23	GENIC	heterozygous	403258706
9	12591542	12591543	G	C	23	GENIC	heterozygous	403258707
9	12591544	12591545	G		23	GENIC	heterozygous	403258708
9	12591544	12591545	G	C	23	GENIC	heterozygous	403258709
9	12591546	12591547	G		23	GENIC	heterozygous	403258710
9	12591546	12591547	G	C	23	GENIC	heterozygous	403258711
9	12591548	12591549	G		23	GENIC	heterozygous	403258712
9	12591548	12591549	G	C	23	GENIC	heterozygous	403258713
9	12600888	12600889	G		18	GENIC	heterozygous	403258714
9	12600892	12600893	G	C	18	GENIC	heterozygous	403258719
9	12598043	12598044	C	T	66	GENIC	homozygous	144841166
9	12600888	12600889	G	C	18	GENIC	heterozygous	403258715
9	12600890	12600891	G		18	GENIC	heterozygous	403258716
9	12600890	12600891	G	C	18	GENIC	heterozygous	403258717
9	12600892	12600893	G		18	GENIC	heterozygous	403258718
9	12600894	12600895	G		18	GENIC	heterozygous	403258720
9	12600894	12600895	G	C	18	GENIC	heterozygous	403258721
9	12600896	12600897	G		18	GENIC	heterozygous	403258722
9	12600896	12600897	G	C	18	GENIC	heterozygous	403258723
9	12600898	12600899	G		18	GENIC	heterozygous	403258724
9	12600898	12600899	G	C	18	GENIC	heterozygous	403258725
9	12600902	12600903	G		19	GENIC	heterozygous	403832478
9	12600902	12600903	G	C	19	GENIC	heterozygous	403832479
9	12612311	12612312	T	G	51	GENIC	homozygous	144841167
9	12600900	12600901	G		18	GENIC	heterozygous	403627731
9	12607752	12607757	TGTTC		38	GENIC	homozygous	138447563
9	12600900	12600901	G	C	18	GENIC	heterozygous	403627732