chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	142108366	142108367	A		11	GENIC	homozygous	131025758
7	142108595	142108596	T	C	15	GENIC	homozygous	116097456
7	142113026	142113026		A	15	GENIC	heterozygous	131025759
7	142116047	142116048	C	T	11	GENIC	homozygous	115941387
7	142111295	142111296	A	G	20	GENIC	homozygous	116097458
7	142114193	142114194	C	T	14	GENIC	homozygous	116097460
7	142116249	142116250	T	C	19	GENIC	homozygous	115941388
7	142116258	142116259	C	T	19	GENIC	homozygous	115941389
7	142116946	142116947	A	G	17	GENIC	homozygous	115941391
7	142116993	142116994	T	G	17	GENIC	homozygous	116097462
7	142117902	142117903	T	C	12	GENIC	homozygous	116097464
7	142117905	142117909	GTGT		12	GENIC	homozygous	131025760
7	142117968	142117969	C	T	12	GENIC	homozygous	122877561
7	142117989	142117995	GTGCGC		12	GENIC	homozygous	131025761
7	142118001	142118002	G	A	13	GENIC	homozygous	122877563
7	142118004	142118005	C	T	13	GENIC	homozygous	116097470
7	142118015	142118019	GTGC		12	GENIC	homozygous	131025762
7	142118023	142118025	GC		15	GENIC	homozygous	131025763
7	142118028	142118029	T	C	16	GENIC	homozygous	122877566
7	142119389	142119390	A	G	6	GENIC	homozygous	115941394
7	142119769	142119770	C	G	20	GENIC	homozygous	115941396
7	142117444	142117444		A	12	GENIC	heterozygous	131875198