chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	13937011	13937012	A	G	20	GENIC	homozygous	111452046
3	13937317	13937318	A	G	15	GENIC	homozygous	111452047
3	13937702	13937703	T	C	13	GENIC	homozygous	111452048
3	13938597	13938598	A	G	38	GENIC	homozygous	111452050
3	13939043	13939044	T	C	21	GENIC	homozygous	111452051
3	13939530	13939531	G	T	29	GENIC	homozygous	111452052
3	13939890	13939891	G	A	34	GENIC	homozygous	111452053
3	13940012	13940013	T	C	39	GENIC	homozygous	111452054
3	13940369	13940370	C	T	16	GENIC	possibly homozygous	111452055
3	13940495	13940496	A	G	21	GENIC	homozygous	111452056
3	13940600	13940601	T	C	34	GENIC	possibly homozygous	111452058
3	13943880	13943881	G	A	36	GENIC	homozygous	111452063
3	13944099	13944100	G	T	40	GENIC	homozygous	111452064
3	13944559	13944560	G	A	40	GENIC	homozygous	111452065
3	13944770	13944771	C	T	26	GENIC	homozygous	111452066
3	13945281	13945282	G	A	28	GENIC	homozygous	111452067
3	13945806	13945807	C	T	32	GENIC	possibly homozygous	111452068
3	13946770	13946771	A	G	39	GENIC	homozygous	111452074
3	13946803	13946804	C	T	40	GENIC	homozygous	111452075
3	13947734	13947735	T	G	25	GENIC	homozygous	111452078
3	13948157	13948158	T	A	41	GENIC	homozygous	111452079
3	13949115	13949116	G	A	29	GENIC	possibly homozygous	111452081
3	13949368	13949369	C	T	36	GENIC	homozygous	111452082
3	13949766	13949767	G	C	32	GENIC	homozygous	111452083
3	13951066	13951067	T	C	38	GENIC	homozygous	111452086
3	13952434	13952435	G	A	36	GENIC	homozygous	111452087
3	13953282	13953283	A	G	33	GENIC	homozygous	111452088
3	13953474	13953475	T	C	38	GENIC	homozygous	111452089