chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5100827	5100828	T	C	4	GENIC	homozygous	125177124
20	5101170	5101171	A	G	8	GENIC	homozygous	125177126
20	5101195	5101196	C	T	9	GENIC	homozygous	125177127
20	5101397	5101398	T	C	5	GENIC	homozygous	125210370
20	5101453	5101454	G	T	15	GENIC	homozygous	125226363
20	5101580	5101581	G	A	15	GENIC	homozygous	125177128
20	5101739	5101740	A	G	12	GENIC	homozygous	125177129
20	5101748	5101749	G	A	9	GENIC	homozygous	125177130
20	5101828	5101829	T	C	12	GENIC	homozygous	125177131
20	5102059	5102060	T	C	24	GENIC	homozygous	125177132
20	5102218	5102219	T	C	15	GENIC	homozygous	125177134
20	5102306	5102307	C	T	9	GENIC	homozygous	125226364
20	5102352	5102353	T	G	10	GENIC	homozygous	125226365
20	5102575	5102576	A	G	11	GENIC	homozygous	125177137
20	5102724	5102725	G	A	10	GENIC	homozygous	125226366
20	5103303	5103304	G	A	5	GENIC	homozygous	125177139
20	5103311	5103312	G	A	5	GENIC	homozygous	125177140
20	5103794	5103795	T	C	8	GENIC	homozygous	125177143
20	5103547	5103548	T	C	4	GENIC	homozygous	125177141
20	5103697	5103698	T	C	18	GENIC	homozygous	125177142
20	5103845	5103846	G	A	14	GENIC	homozygous	125177144
20	5103908	5103909	C	T	8	GENIC	homozygous	125177145
20	5103939	5103940	T	G	11	GENIC	homozygous	125177146
20	5103964	5103965	C	T	19	GENIC	homozygous	125226367
20	5104315	5104316	A	T	5	GENIC	homozygous	125177148
20	5104374	5104375	A	G	18	GENIC	homozygous	125177149