chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	30308583	30308584	G	A	20	GENIC	homozygous	115562245
12	30308766	30308767	G	A	18	GENIC	homozygous	115562249
12	30309045	30309046	G	A	15	GENIC	homozygous	115601924
12	30309617	30309618	G	T	16	GENIC	homozygous	115562259
12	30309725	30309726	C	T	11	GENIC	homozygous	115562261
12	30309813	30309814	A	G	22	GENIC	homozygous	115562263
12	30309874	30309875	G	A	9	GENIC	homozygous	115562265
12	30309883	30309884	T	G	5	GENIC	homozygous	115562267
12	30309888	30309889	T	A	6	GENIC	homozygous	115562269
12	30310157	30310158	A	G	16	GENIC	homozygous	115562271
12	30310213	30310214	G	A	23	GENIC	homozygous	115562273
12	30310563	30310564	T	C	15	GENIC	homozygous	115562277
12	30310888	30310889	G	A	20	GENIC	homozygous	115562281
12	30311107	30311108	T	C	6	GENIC	homozygous	115582443
12	30311156	30311157	T	A	5	GENIC	homozygous	115562283
12	30311366	30311367	C	T	13	GENIC	homozygous	118341814
12	30311571	30311572	C	G	5	GENIC	homozygous	118341816
12	30312569	30312570	G	T	16	GENIC	homozygous	115582445
12	30312665	30312666	G	A	18	GENIC	heterozygous	115562291
12	30312790	30312791	A	G	7	GENIC	heterozygous	118341820
12	30313088	30313089	C	A	14	GENIC	homozygous	115304367
12	30310739	30310740	T	C	8	GENIC	homozygous	115374612
12	30313087	30313088	C	T	13	GENIC	homozygous	115304365
12	30313401	30313402	T	C	25	GENIC	homozygous	115562295
12	30313599	30313600	A	T	14	GENIC	homozygous	115562297
12	30313740	30313741	T	C	18	GENIC	homozygous	115562299
12	30313779	30313780	T	C	12	GENIC	homozygous	115562303
12	30313794	30313795	T	C	17	GENIC	homozygous	115601926
12	30313952	30313953	T	C	5	GENIC	homozygous	115582447
12	30313961	30313962	C	T	9	GENIC	heterozygous	115601928
12	30314218	30314219	G	A	8	GENIC	homozygous	115562305