chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	13655973	13655974	A	C	14	GENIC	homozygous	115261345
12	13657016	13657017	T	C	27	GENIC	homozygous	115261347
12	13657017	13657018	C	T	26	GENIC	homozygous	115261349
12	13657023	13657024	C	T	27	GENIC	homozygous	115261351
12	13657723	13657724	G	T	20	GENIC	homozygous	115482440
12	13660100	13660101	T	C	23	GENIC	homozygous	115362793
12	13660141	13660142	G	A	29	GENIC	homozygous	115467838
12	13661058	13661059	C	G	30	GENIC	homozygous	115467840
12	13661422	13661423	A	G	35	GENIC	homozygous	115261353
12	13662105	13662106	A	C	3	GENIC	homozygous	115445247
12	13662774	13662775	C	T	25	GENIC	homozygous	115445249
12	13662807	13662808	C	G	27	GENIC	homozygous	115261355
12	13663223	13663224	C	G	29	GENIC	homozygous	115261357
12	13666197	13666198	T	A	16	GENIC	homozygous	115261359
12	13661501	13661502	G	A	31	GENIC	homozygous	115417330
12	13662690	13662691	C	G	17	GENIC	homozygous	115559784
12	13666607	13666608	T	C	38	GENIC	homozygous	115261361
12	13666620	13666621	A	G	42	GENIC	homozygous	115261363
12	13667364	13667365	G	C	39	GENIC	homozygous	115505136
12	13668578	13668579	A	C	36	GENIC	homozygous	115261367