chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	42965190	42965191	C	G	18	INTERGENIC	homozygous	109706269
19	42965436	42965437	A	G	19	INTERGENIC	homozygous	109783540
19	42965586	42965587	C	A	13	INTERGENIC	homozygous	109706271
19	42965662	42965663	G	A	23	INTERGENIC	homozygous	109706273
19	42965995	42965996	C	T	18	INTERGENIC	homozygous	109706275
19	42966198	42966199	A	G	16	INTERGENIC	homozygous	109706277
19	42966660	42966661	G	A	15	INTERGENIC	homozygous	109706279
19	42966814	42966815	G	A	21	INTERGENIC	homozygous	109706281
19	42966888	42966889	C	T	27	INTERGENIC	homozygous	109706283
19	42967480	42967481	A	G	24	INTERGENIC	homozygous	109706285
19	42967883	42967884	C	T	27	INTERGENIC	homozygous	109706287
19	42968517	42968518	A	G	9	INTERGENIC	homozygous	109870242
19	42969249	42969250	T	A	11	INTERGENIC	homozygous	109706289
19	42969328	42969329	T	C	18	INTERGENIC	homozygous	109706291
19	42970591	42970592	G	A	21	INTERGENIC	homozygous	109706293
19	42970654	42970655	A	G	22	INTERGENIC	homozygous	109706295
19	42970842	42970843	G	A	6	INTERGENIC	homozygous	109706297
19	42971184	42971185	C	T	16	INTERGENIC	homozygous	109706299
19	42971193	42971194	C	T	15	INTERGENIC	homozygous	109706301
19	42971412	42971413	G	A	16	INTERGENIC	homozygous	109706303
19	42971657	42971658	T	G	20	INTERGENIC	homozygous	109706305