chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	46485711	46485712	T	G	21	GENIC	homozygous	54876787
6	46485907	46485908	A	T	23	GENIC	homozygous	54876788
6	46486115	46486116	T	TC	18	GENIC	homozygous	54876789
6	46486543	46486544	G	C	27	GENIC	homozygous	54876790
6	46487298	46487299	C	T	30	GENIC	homozygous	54876791
6	46487401	46487402	C	T	36	GENIC	homozygous	54876792
6	46487709	46487710	C	CT	16	GENIC	possibly homozygous	54876793
6	46487787	46487788	A	G	18	GENIC	homozygous	54876794
6	46487854	46487855	G	-	10	GENIC	homozygous	54876795
6	46488142	46488143	C	T	7	GENIC	homozygous	54876798
6	46488589	46488590	A	G	21	GENIC	homozygous	54876799
6	46488649	46488650	C	G	18	GENIC	homozygous	54876800
6	46488701	46488702	T	C	23	GENIC	homozygous	54876801
6	46488948	46488949	G	A	30	GENIC	homozygous	54876802
6	46489100	46489101	G	C	29	GENIC	homozygous	54876803
6	46489719	46489720	C	T	22	GENIC	homozygous	54876804
6	46489750	46489751	C	G	23	GENIC	homozygous	54876805
6	46489800	46489801	A	G	26	GENIC	homozygous	54876806
6	46489815	46489816	C	T	24	GENIC	homozygous	54876807
6	46489905	46489906	G	-	21	GENIC	homozygous	54876808
6	46489926	46489927	C	T	22	GENIC	homozygous	54876809
6	46488137	46488138	A	ACGCG	8	GENIC	homozygous	55497711