chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5108702	5108703	T	C	43	GENIC	homozygous	109076889
20	5109055	5109056	A	C	50	GENIC	possibly homozygous	109076891
20	5109119	5109120	C	T	40	GENIC	homozygous	109076893
20	5109310	5109311	G	C	41	GENIC	homozygous	109076895
20	5109566	5109567	A	G	82	GENIC	homozygous	109076897
20	5109660	5109661	A	G	62	GENIC	homozygous	109076899
20	5109705	5109706	T	G	53	GENIC	homozygous	109076901
20	5109726	5109727	T	G	60	GENIC	homozygous	109076903
20	5109758	5109759	A	G	68	GENIC	homozygous	109076905
20	5110196	5110197	A	G	63	GENIC	homozygous	109076907
20	5110695	5110696	T	A	43	GENIC	homozygous	109076909
20	5110945	5110946	C	T	35	GENIC	homozygous	109076913
20	5111006	5111007	T	C	57	GENIC	homozygous	109076915
20	5111173	5111174	C	T	36	GENIC	homozygous	109076917
20	5111262	5111263	C	T	24	GENIC	homozygous	109076919
20	5111453	5111454	C	T	46	GENIC	homozygous	109076921
20	5111690	5111691	A	T	27	GENIC	homozygous	109076923
20	5112472	5112473	A	G	50	GENIC	homozygous	109076929
20	5112498	5112499	G	A	45	GENIC	homozygous	109076931
20	5112607	5112608	A	G	28	GENIC	possibly homozygous	109076933
20	5112637	5112638	T	C	36	GENIC	homozygous	109076935
20	5112824	5112825	G	C	68	GENIC	homozygous	109076937
20	5112927	5112928	A	G	56	GENIC	homozygous	109233840
20	5112938	5112939	C	G	45	GENIC	homozygous	109076939
20	5113027	5113028	T	C	32	GENIC	homozygous	109076941
20	5113261	5113262	G	A	43	GENIC	homozygous	109076943
20	5113349	5113350	C	T	56	GENIC	homozygous	109076945