chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	42502952	42502953	T	C	35	GENIC	homozygous	112493690
15	42503162	42503163	C	T	37	GENIC	homozygous	112493692
15	42504517	42504518	T	C	41	GENIC	homozygous	112493698
15	42504704	42504705	C	T	32	GENIC	homozygous	112493700
15	42504829	42504830	A	G	36	GENIC	homozygous	112493702
15	42505112	42505113	A	G	31	GENIC	homozygous	112493704
15	42506985	42506986	T	A	38	GENIC	homozygous	112493706
15	42507260	42507261	C	G	24	GENIC	homozygous	112493708
15	42507476	42507477	T	C	46	GENIC	homozygous	112493710
15	42507672	42507673	A	G	33	GENIC	homozygous	112493712
15	42508426	42508427	A	G	29	GENIC	homozygous	112493714
15	42510807	42510808	G	T	32	GENIC	homozygous	112493719
15	42510978	42510979	C	T	32	GENIC	homozygous	112493721
15	42511800	42511801	T	A	34	GENIC	homozygous	112493723
15	42512368	42512369	T	C	31	GENIC	homozygous	112493727
15	42512498	42512499	A	C	29	GENIC	homozygous	112493729
15	42513094	42513095	G	A	29	GENIC	homozygous	112493731
15	42515096	42515097	T	C	24	GENIC	homozygous	112493735
15	42515625	42515626	T	A	36	GENIC	homozygous	112493737
15	42515697	42515698	A	G	39	GENIC	homozygous	112493739
15	42517306	42517307	G	C	40	GENIC	homozygous	112493741
15	42517788	42517789	C	T	28	GENIC	homozygous	112493743