chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10645111	10645112	T	C	33	GENIC	possibly homozygous	46059628
19	10645197	10645198	A	G	32	GENIC	homozygous	46059630
19	10645262	10645263	T	G	42	GENIC	homozygous	46486199
19	10645771	10645772	G	A	16	GENIC	homozygous	46486204
19	10645792	10645793	A	G	22	GENIC	homozygous	46486206
19	10646103	10646104	C	T	26	GENIC	possibly homozygous	46788841
19	10646216	10646217	T	C	20	GENIC	possibly homozygous	46059633
19	10646737	10646738	T	C	31	GENIC	homozygous	46059639
19	10646745	10646746	T	A	33	GENIC	homozygous	46059640
19	10647194	10647202	GGGTGGGA	--------	8	GENIC	homozygous	46059642
19	10647405	10647406	T	TC	23	GENIC	homozygous	46059643
19	10647823	10647824	C	T	24	GENIC	homozygous	46279901
19	10648205	10648206	T	G	15	INTERGENIC	homozygous	46059646
19	10648321	10648322	A	ACC	6	INTERGENIC	heterozygous	46059647
19	10648379	10648380	G	C	18	INTERGENIC	possibly homozygous	46059648
19	10649129	10649130	C	T	22	INTERGENIC	homozygous	46788843
19	10649597	10649598	G	A	21	INTERGENIC	homozygous	46788845
19	10649779	10649780	C	T	9	INTERGENIC	homozygous	46556264
19	10650462	10650463	T	TCTC	36	INTERGENIC	homozygous	46279903
19	10650657	10650658	A	G	41	INTERGENIC	homozygous	46788847
19	10650673	10650675	TT	--	30	INTERGENIC	homozygous	46788849
19	10650922	10650923	G	A	34	INTERGENIC	homozygous	46788851
19	10651296	10651297	A	C	31	INTERGENIC	homozygous	46059650
19	10651547	10651548	G	A	17	INTERGENIC	homozygous	46788853
19	10651834	10651835	C	T	25	INTERGENIC	homozygous	46059653
19	10652209	10652210	C	T	26	INTERGENIC	homozygous	46788855
19	10653576	10653577	C	T	34	INTERGENIC	homozygous	46788857
19	10654476	10654477	G	A	36	INTERGENIC	homozygous	46788859