chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	25130615	25130616	T	C	26	GENIC	homozygous	115289787
12	25130625	25130626	G	A	28	GENIC	homozygous	115369232
12	25130734	25130735	T	G	24	GENIC	homozygous	115289789
12	25131117	25131118	C	T	33	GENIC	homozygous	115369234
12	25131171	25131172	A	G	29	GENIC	homozygous	115289791
12	25131774	25131775	G	T	27	GENIC	homozygous	115289793
12	25131870	25131871	C	T	19	GENIC	homozygous	115369236
12	25132343	25132344	T	C	31	GENIC	homozygous	115369238
12	25133036	25133037	A	T	20	GENIC	homozygous	115289797
12	25133196	25133197	T	C	20	GENIC	homozygous	115289799
12	25133767	25133768	T	C	24	GENIC	homozygous	115289801
12	25134680	25134681	T	A	14	GENIC	homozygous	115369240
12	25134773	25134774	A	G	18	GENIC	homozygous	115289803
12	25136264	25136265	G	A	21	GENIC	homozygous	115289805
12	25136311	25136312	T	C	20	GENIC	homozygous	115289807
12	25137293	25137294	G	C	16	GENIC	homozygous	115369241
12	25138473	25138474	C	T	18	GENIC	homozygous	115289811
12	25139765	25139766	G	A	17	GENIC	homozygous	115470209
12	25140481	25140482	T	C	24	GENIC	homozygous	115369243
12	25140877	25140878	G	A	17	GENIC	homozygous	115422826
12	25140959	25140960	T	C	14	GENIC	homozygous	115289819
12	25141181	25141182	G	A	11	GENIC	homozygous	115369245
12	25142467	25142468	G	A	16	GENIC	homozygous	115369247
12	25142896	25142897	A	G	16	GENIC	homozygous	115289823