chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5108702	5108703	T	C	22	GENIC	homozygous	109076889
20	5108974	5108975	C	T	25	GENIC	homozygous	109233836
20	5109119	5109120	C	T	24	GENIC	homozygous	109076893
20	5109310	5109311	G	C	24	GENIC	homozygous	109076895
20	5109566	5109567	A	G	27	GENIC	homozygous	109076897
20	5109660	5109661	A	G	28	GENIC	homozygous	109076899
20	5109705	5109706	T	G	21	GENIC	homozygous	109076901
20	5109726	5109727	T	G	26	GENIC	homozygous	109076903
20	5109750	5109751	C	T	21	GENIC	homozygous	109296825
20	5109758	5109759	A	G	18	GENIC	homozygous	109076905
20	5110085	5110086	C	T	27	GENIC	homozygous	109233837
20	5110196	5110197	A	G	32	GENIC	homozygous	109076907
20	5110695	5110696	T	A	31	GENIC	homozygous	109076909
20	5111006	5111007	T	C	26	GENIC	homozygous	109076915
20	5111453	5111454	C	T	21	GENIC	homozygous	109076921
20	5111690	5111691	A	T	23	GENIC	homozygous	109076923
20	5111863	5111864	C	T	23	GENIC	homozygous	109233838
20	5112085	5112086	T	C	30	GENIC	homozygous	109076925
20	5112487	5112488	C	T	16	GENIC	homozygous	109233839
20	5112498	5112499	G	A	15	GENIC	homozygous	109076931
20	5112508	5112509	C	T	16	GENIC	homozygous	109296827
20	5112637	5112638	T	C	9	GENIC	homozygous	109076935
20	5112927	5112928	A	G	10	GENIC	homozygous	109233840
20	5112938	5112939	C	G	8	GENIC	homozygous	109076939
20	5113027	5113028	T	C	10	GENIC	homozygous	109076941
20	5113033	5113034	C	T	11	GENIC	homozygous	109233841
20	5113261	5113262	G	A	9	GENIC	homozygous	109076943
20	5113349	5113350	C	T	9	GENIC	homozygous	109076945