chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	42501241	42501242	T	C	10	GENIC	homozygous	119034195
15	42502952	42502953	T	C	18	GENIC	homozygous	112493690
15	42503162	42503163	C	T	51	GENIC	possibly homozygous	112493692
15	42503179	42503180	G	A	52	GENIC	homozygous	112493694
15	42504285	42504286	C	T	41	GENIC	homozygous	112493696
15	42504517	42504518	T	C	54	GENIC	homozygous	112493698
15	42504704	42504705	C	T	60	GENIC	homozygous	112493700
15	42504829	42504830	A	G	54	GENIC	homozygous	112493702
15	42505112	42505113	A	G	43	GENIC	homozygous	112493704
15	42503770	42503771	G	A	48	GENIC	heterozygous	118915480
15	42503774	42503775	G	A	50	GENIC	heterozygous	118915481
15	42505337	42505338	C	T	53	GENIC	heterozygous	118915482
15	42506985	42506986	T	A	54	GENIC	homozygous	112493706
15	42507260	42507261	C	G	59	GENIC	possibly homozygous	112493708
15	42507476	42507477	T	C	53	GENIC	homozygous	112493710
15	42507672	42507673	A	G	56	GENIC	homozygous	112493712
15	42508426	42508427	A	G	56	GENIC	homozygous	112493714
15	42508821	42508822	G	T	59	GENIC	homozygous	112493716
15	42510807	42510808	G	T	38	GENIC	homozygous	112493719
15	42510978	42510979	C	T	50	GENIC	homozygous	112493721
15	42511800	42511801	T	A	53	GENIC	homozygous	112493723
15	42512029	42512030	T	C	40	GENIC	possibly homozygous	112493725
15	42512368	42512369	T	C	34	GENIC	homozygous	112493727
15	42512498	42512499	A	C	42	GENIC	homozygous	112493729
15	42513094	42513095	G	A	50	GENIC	homozygous	112493731
15	42513436	42513437	C	G	39	GENIC	homozygous	112493733
15	42513537	42513538	C	A	28	GENIC	homozygous	118915483
15	42515096	42515097	T	C	56	GENIC	homozygous	112493735
15	42515452	42515453	C	T	20	GENIC	homozygous	118956257
15	42515625	42515626	T	A	42	GENIC	homozygous	112493737
15	42515697	42515698	A	G	45	GENIC	homozygous	112493739
15	42517306	42517307	G	C	46	GENIC	homozygous	112493741
15	42517788	42517789	C	T	29	GENIC	possibly homozygous	112493743