chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	111676152	111676153	T	C	27	GENIC	homozygous	116648544
8	111676535	111676536	T	C	48	GENIC	homozygous	116648546
8	111676727	111676728	A	C	42	GENIC	homozygous	116648548
8	111677564	111677565	T	C	35	GENIC	homozygous	116648550
8	111677792	111677793	A	G	42	GENIC	homozygous	116648552
8	111678092	111678093	C	T	39	GENIC	homozygous	116648554
8	111678149	111678150	A	G	41	GENIC	homozygous	116648556
8	111678156	111678157	G	C	39	GENIC	homozygous	116648558
8	111679047	111679048	C	G	36	GENIC	possibly homozygous	116648560
8	111680019	111680020	T	C	45	GENIC	homozygous	116648562
8	111680058	111680059	T	C	43	GENIC	homozygous	116648564
8	111682019	111682020	A	G	28	GENIC	homozygous	116648566
8	111682251	111682252	A	G	32	GENIC	heterozygous	117057824
8	111682267	111682268	G	A	32	GENIC	homozygous	116648568
8	111682438	111682439	A	G	36	GENIC	homozygous	116648570
8	111683450	111683451	T	C	28	GENIC	homozygous	116648572
8	111684688	111684689	A	G	53	GENIC	homozygous	116648574
8	111684944	111684945	G	A	42	GENIC	homozygous	116648576
8	111685486	111685487	C	T	50	GENIC	homozygous	116648578
8	111685985	111685986	A	G	44	GENIC	homozygous	116648580