chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	84058470	84058471	T	C	29	GENIC	homozygous	117594488
9	84068495	84068495		C	19	GENIC	homozygous	128728640
9	84068502	84068502		CC	20	GENIC	homozygous	128728641
9	84068509	84068509		C	19	GENIC	homozygous	128728642
9	84082127	84082128	C	A	52	GENIC	homozygous	117594490
9	84082127	84082127		TGGTG	53	GENIC	homozygous	128728643
9	84089054	84089054		G	29	GENIC	homozygous	128728644
9	84089089	84089090	G		33	GENIC	homozygous	128728645
9	84089125	84089126	G	T	32	GENIC	homozygous	117594492
9	84089153	84089154	T	G	39	GENIC	homozygous	117594494
9	84089166	84089167	T		41	GENIC	homozygous	128728646
9	84089232	84089233	T		33	GENIC	homozygous	128728647
9	84089251	84089251		G	30	GENIC	homozygous	128728648
9	84089263	84089264	G		34	GENIC	homozygous	128728649
9	84089293	84089293		C	33	GENIC	homozygous	128728650
9	84089312	84089312		G	36	GENIC	homozygous	128728651
9	84089342	84089343	T		37	GENIC	homozygous	128728652
9	84089351	84089352	C		41	GENIC	homozygous	128728653
9	84089368	84089369	A		41	GENIC	homozygous	128728654
9	84089458	84089459	A		38	GENIC	homozygous	128728655
9	84089463	84089464	T		37	GENIC	homozygous	128728656
9	84089500	84089501	T	A	26	GENIC	homozygous	120406790
9	84089528	84089529	G		16	GENIC	homozygous	128728657
9	84089499	84089500	A	T	26	GENIC	homozygous	117849971