chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10645111	10645112	T	C	13	GENIC	homozygous	46059628
19	10645197	10645198	A	G	12	GENIC	heterozygous	46059630
19	10645262	10645263	T	G	17	GENIC	possibly homozygous	46486199
19	10645670	10645671	C	G	13	GENIC	homozygous	46486202
19	10645771	10645772	G	A	19	GENIC	homozygous	46486204
19	10645792	10645793	A	G	20	GENIC	homozygous	46486206
19	10646216	10646217	T	C	7	GENIC	homozygous	46059633
19	10646265	10646266	G	A	5	GENIC	homozygous	46059634
19	10646435	10646436	T	C	13	GENIC	homozygous	46486208
19	10646737	10646738	T	C	2	GENIC	homozygous	46059639
19	10646745	10646746	T	A	4	GENIC	heterozygous	46059640
19	10647177	10647192	GGGGGGGGGGGGTGG	---------------	3	GENIC	heterozygous	46486212
19	10647405	10647406	T	TC	14	GENIC	homozygous	46059643
19	10648324	10648325	C	CA	10	INTERGENIC	homozygous	46486214
19	10648379	10648380	G	C	22	INTERGENIC	possibly homozygous	46059648
19	10651296	10651297	A	C	23	INTERGENIC	homozygous	46059650
19	10651595	10651596	C	T	15	INTERGENIC	homozygous	46059651
19	10651834	10651835	C	T	10	INTERGENIC	homozygous	46059653
19	10652232	10652233	T	G	12	INTERGENIC	homozygous	46059658
19	10653254	10653255	T	C	8	INTERGENIC	homozygous	46059661
19	10653256	10653257	C	CG	8	INTERGENIC	heterozygous	46486216