chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	45470418	45470419	A	G	12	GENIC	homozygous	50216397
12	45470531	45470532	G	A	22	GENIC	homozygous	50216398
12	45470547	45470548	A	T	23	GENIC	homozygous	50453281
12	45470700	45470701	T	TAA	25	GENIC	homozygous	50216400
12	45470713	45470714	G	A	24	GENIC	homozygous	50216401
12	45471134	45471135	T	C	20	GENIC	homozygous	50216402
12	45471391	45471392	T	C	16	GENIC	homozygous	50216403
12	45471453	45471454	T	C	13	GENIC	homozygous	50216404
12	45471576	45471577	G	T	22	GENIC	homozygous	50216405
12	45471617	45471618	A	AT	16	GENIC	possibly homozygous	50216406
12	45472080	45472083	AGA	---	37	GENIC	homozygous	50453282
12	45472304	45472305	G	GA	12	GENIC	heterozygous	50453283
12	45472609	45472610	A	T	20	GENIC	homozygous	50216409
12	45472780	45472781	A	AAAGGTAG	32	GENIC	homozygous	50216410
12	45472781	45472782	C	CAAG	32	GENIC	homozygous	50216411
12	45473217	45473218	A	T	23	GENIC	homozygous	50386298
12	45473592	45473593	C	T	33	GENIC	homozygous	50216412
12	45474747	45474748	T	A	8	GENIC	homozygous	50216413
12	45474899	45474902	GAC	---	13	GENIC	homozygous	50453284
12	45475310	45475311	G	A	10	GENIC	homozygous	50216414
12	45475602	45475603	G	A	31	GENIC	homozygous	50216415
12	45475878	45475879	T	TCATG	56	GENIC	homozygous	50216416
12	45476125	45476126	G	GCACA	23	GENIC	possibly homozygous	50216417
12	45476125	45476126	G	GCA	23	GENIC	heterozygous	50216418
12	45476225	45476228	TTG	---	20	GENIC	homozygous	50216419
12	45476363	45476364	A	G	27	GENIC	homozygous	50216421
12	45476625	45476626	T	C	29	GENIC	homozygous	50216423
12	45476812	45476813	T	C	19	GENIC	homozygous	50216424
12	45476920	45476921	T	C	27	GENIC	homozygous	50216427
12	45470671	45470672	T	TTATA	25	GENIC	homozygous	50545403
12	45470672	45470673	G	GGGTACTT	24	GENIC	homozygous	50545404
12	45471770	45471771	C	CTTTTTT	9	GENIC	homozygous	50545405