chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	2430185	2430186	A	G	42	GENIC	homozygous	115357404
12	2430429	2430430	A	G	39	GENIC	homozygous	115357405
12	2430763	2430764	C	T	18	GENIC	homozygous	115357406
12	2431329	2431330	G	A	41	GENIC	homozygous	115357407
12	2431547	2431548	T	C	44	GENIC	possibly homozygous	115357408
12	2433512	2433513	A	G	42	GENIC	homozygous	115357409
12	2434232	2434233	G	A	14	GENIC	possibly homozygous	115535436
12	2435229	2435230	A	C	69	GENIC	homozygous	115357410
12	2435238	2435239	C	G	75	GENIC	possibly homozygous	115357411
12	2435391	2435392	A	C	32	GENIC	homozygous	115234417
12	2435504	2435505	A	G	7	GENIC	homozygous	115678389
12	2435641	2435642	T	A	44	GENIC	homozygous	115357413
12	2435738	2435739	T	A	37	GENIC	homozygous	115357414
12	2435937	2435938	C	T	29	GENIC	homozygous	115234419
12	2436095	2436096	C	G	4	GENIC	homozygous	115357415
12	2436486	2436487	T	C	45	GENIC	homozygous	115357416
12	2436647	2436648	A	C	29	GENIC	homozygous	118328769
12	2436747	2436748	C	T	47	GENIC	possibly homozygous	115357417
12	2437143	2437144	T	C	38	GENIC	possibly homozygous	115357418
12	2438011	2438012	T	A	30	GENIC	homozygous	115357419
12	2438216	2438217	A	C	36	GENIC	homozygous	115357420
12	2438499	2438500	A	G	41	GENIC	homozygous	115357421
12	2438710	2438711	C	T	38	GENIC	homozygous	115357422