chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	110306549	110306550	T	C	54	GENIC	homozygous	138413615
8	110308294	110308295	T	G	52	GENIC	homozygous	138413616
8	110310886	110310887	A	G	48	GENIC	homozygous	138413617
8	110311881	110311882	T	C	38	GENIC	homozygous	138413618
8	110314351	110314352	A	G	43	GENIC	homozygous	138413619
8	110314798	110314799	C	T	41	GENIC	possibly homozygous	138413620
8	110318365	110318366	T	C	32	GENIC	homozygous	138413621
8	110325496	110325497	G	A	53	GENIC	homozygous	138413623
8	110325982	110325983	T	C	48	GENIC	homozygous	138413624
8	110334297	110334299	GC		36	GENIC	homozygous	142030637
8	110336414	110336415	T	C	53	GENIC	homozygous	138413625
8	110336522	110336523	T	C	48	GENIC	homozygous	138413626
8	110345171	110345171		TAGC	51	GENIC	homozygous	138264399
8	110318411	110318413	GC		18	GENIC	heterozygous	144814420
8	110323179	110323179		GGACCGAACCCAGGGCCTTGC	32	GENIC	homozygous	144814421
8	110325467	110325468	G	C	55	GENIC	homozygous	144829758
8	110336196	110336197	T	C	40	GENIC	homozygous	144829759
8	110336204	110336205	T	C	39	GENIC	homozygous	144829760
8	110341128	110341132	AATG		32	GENIC	homozygous	138264398
8	110342456	110342457	C	T	64	GENIC	homozygous	138413627
8	110345178	110345179	C	G	51	GENIC	homozygous	138413628
8	110348970	110348971	G	A	58	GENIC	homozygous	138413629
8	110350499	110350500	A	G	52	GENIC	homozygous	138413630
8	110351774	110351774		CAT	18	GENIC	homozygous	138264400
8	110351781	110351781		A	18	GENIC	homozygous	138264401
8	110351795	110351796	T	C	18	GENIC	homozygous	138413633
8	110351846	110351847	T		43	GENIC	homozygous	138264402
8	110352155	110352156	A	G	47	GENIC	homozygous	138413634
8	110354057	110354058	G	C	54	GENIC	possibly homozygous	138413635
8	110357087	110357088	T	G	73	GENIC	homozygous	138413636
8	110357535	110357536	T	C	76	GENIC	homozygous	144829761
8	110357831	110357832	A	G	73	GENIC	possibly homozygous	138413637
8	110358300	110358300		G	55	GENIC	homozygous	138264403
8	110360659	110360660	T		56	GENIC	homozygous	138264404