chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	25130615	25130616	T	C	24	GENIC	homozygous	115289787
12	25130734	25130735	T	G	24	GENIC	homozygous	115289789
12	25130778	25130779	A	G	26	GENIC	homozygous	115485342
12	25131117	25131118	C	T	26	GENIC	homozygous	115369234
12	25131171	25131172	A	G	26	GENIC	homozygous	115289791
12	25131774	25131775	G	T	27	GENIC	homozygous	115289793
12	25131870	25131871	C	T	23	GENIC	homozygous	115369236
12	25132343	25132344	T	C	30	GENIC	homozygous	115369238
12	25133036	25133037	A	T	33	GENIC	homozygous	115289797
12	25133767	25133768	T	C	24	GENIC	homozygous	115289801
12	25134773	25134774	A	G	18	GENIC	homozygous	115289803
12	25136264	25136265	G	A	20	GENIC	homozygous	115289805
12	25136311	25136312	T	C	26	GENIC	homozygous	115289807
12	25137466	25137467	G	C	21	GENIC	homozygous	115485344
12	25138473	25138474	C	T	28	GENIC	homozygous	115289811
12	25138579	25138580	G	A	24	GENIC	homozygous	115485345
12	25139499	25139500	C	A	22	GENIC	homozygous	115485346
12	25139765	25139766	G	A	5	GENIC	homozygous	115470209
12	25139962	25139963	A	T	18	GENIC	homozygous	115485347
12	25140481	25140482	T	C	17	GENIC	homozygous	115369243
12	25140975	25140976	C	T	20	GENIC	homozygous	115485348
12	25142896	25142897	A	G	23	GENIC	homozygous	115289823
12	25143151	25143152	A	T	8	GENIC	homozygous	115485349
12	25143247	25143248	G	T	12	GENIC	homozygous	115485350
12	25143254	25143255	T	A	14	GENIC	homozygous	115485351