chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	13655973	13655974	A	C	24	GENIC	homozygous	115261345
12	13657023	13657024	C	T	37	GENIC	homozygous	115261351
12	13657601	13657602	A	G	26	GENIC	homozygous	115510022
12	13657723	13657724	G	T	16	GENIC	homozygous	115482440
12	13659995	13659996	C	G	11	GENIC	homozygous	118245512
12	13661422	13661423	A	G	39	GENIC	homozygous	115261353
12	13661546	13661547	C	T	34	GENIC	homozygous	115467842
12	13661554	13661555	C	A	32	GENIC	homozygous	115521354
12	13661638	13661639	C	T	35	GENIC	homozygous	118245513
12	13662705	13662706	A	C	24	GENIC	homozygous	118245514
12	13662735	13662736	A	T	14	GENIC	possibly homozygous	118245515
12	13662741	13662742	C	G	14	GENIC	homozygous	118245516
12	13662807	13662808	C	G	22	GENIC	homozygous	115261355
12	13663223	13663224	C	G	29	GENIC	homozygous	115261357
12	13663289	13663290	A	C	12	GENIC	homozygous	115522389
12	13663292	13663293	A	C	12	GENIC	homozygous	115522390
12	13666197	13666198	T	A	24	GENIC	homozygous	115261359
12	13666620	13666621	A	G	24	GENIC	homozygous	115261363
12	13666719	13666720	C	T	27	GENIC	homozygous	118245517
12	13668051	13668052	C	G	32	GENIC	homozygous	115261365
12	13668578	13668579	A	C	26	GENIC	homozygous	115261367
12	13662670	13662671	G	T	19	GENIC	homozygous	118292353