chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	107289109	107289110	G	A	35	GENIC	heterozygous	52788657
8	107289200	107289201	C	T	50	GENIC	heterozygous	52788658
8	107289280	107289281	T	C	56	GENIC	heterozygous	52788659
8	107290948	107290949	A	C	15	GENIC	heterozygous	52788667
8	107291106	107291117	CTGAAAAGCTG	-----------	32	GENIC	heterozygous	52788669
8	107291122	107291130	GGACTGAA	--------	32	GENIC	heterozygous	52788670
8	107291134	107291135	T	A	35	GENIC	heterozygous	52788671
8	107301939	107301940	A	G	9	GENIC	heterozygous	52788779
8	107301967	107301968	A	G	13	GENIC	heterozygous	52788780
8	107308867	107308868	C	T	18	GENIC	heterozygous	53162326
8	107308966	107308967	C	T	12	GENIC	heterozygous	53162330
8	107318414	107318415	C	T	11	GENIC	heterozygous	52789021
8	107322219	107322222	CTC	---	8	GENIC	heterozygous	52789098
8	107325738	107325739	C	T	9	GENIC	heterozygous	52789151
8	107325749	107325750	C	T	12	GENIC	heterozygous	52789152
8	107325794	107325795	T	C	15	GENIC	heterozygous	52789153
8	107326472	107326473	C	T	5	GENIC	heterozygous	52789163
8	107329840	107329841	A	C	25	GENIC	heterozygous	52789181
8	107348904	107348905	T	C	57	INTERGENIC	heterozygous	52789228
8	107353062	107353063	C	CT	18	INTERGENIC	heterozygous	52789260
8	107358971	107358972	T	TG	13	GENIC	heterozygous	52789274
8	107359432	107359433	C	T	16	GENIC	heterozygous	52789275
8	107362168	107362169	A	G	16	GENIC	heterozygous	52789281
8	107364126	107364127	G	A	37	GENIC	heterozygous	52789285
8	107376191	107376192	T	C	13	GENIC	heterozygous	52789310
8	107376332	107376333	A	C	12	GENIC	heterozygous	52789311