chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10644298	10644299	G	A	4	GENIC	heterozygous	46059619
19	10644365	10644366	T	C	11	GENIC	homozygous	46059620
19	10644516	10644517	C	T	15	GENIC	possibly homozygous	46059621
19	10644613	10644614	C	T	11	GENIC	possibly homozygous	46059622
19	10644622	10644623	A	G	9	GENIC	homozygous	46059623
19	10644673	10644674	T	C	22	GENIC	homozygous	46059624
19	10644705	10644706	G	A	13	GENIC	homozygous	46059625
19	10644973	10644974	C	T	6	GENIC	homozygous	46059626
19	10645000	10645001	C	T	7	GENIC	possibly homozygous	46059627
19	10645111	10645112	T	C	2	GENIC	homozygous	46059628
19	10645129	10645130	G	A	2	GENIC	homozygous	46059629
19	10645197	10645198	A	G	7	GENIC	homozygous	46059630
19	10645670	10645671	C	T	9	GENIC	homozygous	46059631
19	10646057	10646058	C	T	8	GENIC	possibly homozygous	46059632
19	10646216	10646217	T	C	9	GENIC	homozygous	46059633
19	10646265	10646266	G	A	2	GENIC	homozygous	46059634
19	10646278	10646279	A	C	3	GENIC	homozygous	46059635
19	10646377	10646378	G	A	2	GENIC	heterozygous	46059638
19	10646737	10646738	T	C	1	GENIC	homozygous	46059639
19	10646745	10646746	T	A	3	GENIC	heterozygous	46059640
19	10647405	10647406	T	TC	8	GENIC	possibly homozygous	46059643
19	10647671	10647672	T	C	7	GENIC	homozygous	46059644
19	10647680	10647681	T	C	8	GENIC	homozygous	46059645
19	10648205	10648206	T	G	5	INTERGENIC	homozygous	46059646
19	10648321	10648322	A	ACC	1	INTERGENIC	homozygous	46059647
19	10648379	10648380	G	C	6	INTERGENIC	heterozygous	46059648
19	10651296	10651297	A	C	12	INTERGENIC	homozygous	46059650
19	10651595	10651596	C	T	12	INTERGENIC	possibly homozygous	46059651
19	10651834	10651835	C	T	15	INTERGENIC	homozygous	46059653
19	10652232	10652233	T	G	7	INTERGENIC	homozygous	46059658
19	10652578	10652579	C	A	12	INTERGENIC	possibly homozygous	46059659
19	10653062	10653063	G	A	7	INTERGENIC	possibly homozygous	46059660
19	10653254	10653255	T	C	5	INTERGENIC	homozygous	46059661
19	10653377	10653378	C	A	9	INTERGENIC	heterozygous	46059662