chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	42963815	42963816	C	G	40	INTERGENIC	heterozygous	119695732
19	42963917	42963918	G	C	59	INTERGENIC	heterozygous	119644837
19	42964943	42964944	G	A	43	INTERGENIC	possibly homozygous	110065731
19	42965190	42965191	C	G	40	INTERGENIC	homozygous	109706269
19	42965586	42965587	C	A	49	INTERGENIC	possibly homozygous	109706271
19	42965662	42965663	G	A	30	INTERGENIC	homozygous	109706273
19	42966198	42966199	A	G	43	INTERGENIC	homozygous	109706277
19	42966660	42966661	G	A	55	INTERGENIC	homozygous	109706279
19	42966814	42966815	G	A	32	INTERGENIC	possibly homozygous	109706281
19	42967480	42967481	A	G	35	INTERGENIC	homozygous	109706285
19	42967883	42967884	C	T	54	INTERGENIC	homozygous	109706287
19	42968517	42968518	A	G	56	INTERGENIC	homozygous	109870242
19	42968835	42968836	T	G	50	INTERGENIC	homozygous	110006341
19	42969249	42969250	T	A	28	INTERGENIC	homozygous	109706289
19	42969328	42969329	T	C	49	INTERGENIC	homozygous	109706291
19	42970591	42970592	G	A	33	INTERGENIC	homozygous	109706293
19	42970654	42970655	A	G	35	INTERGENIC	homozygous	109706295
19	42970842	42970843	G	A	30	INTERGENIC	homozygous	109706297
19	42971184	42971185	C	T	47	INTERGENIC	possibly homozygous	109706299
19	42971193	42971194	C	T	46	INTERGENIC	possibly homozygous	109706301
19	42965436	42965437	A	G	43	INTERGENIC	homozygous	109783540
19	42970145	42970146	C	T	33	INTERGENIC	homozygous	109783542
19	42971657	42971658	T	G	39	INTERGENIC	homozygous	109706305