chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	54269687	54269688	G	T	38	GENIC	homozygous	53698465
8	54270202	54270203	G	A	23	GENIC	homozygous	53340156
8	54270222	54270223	C	CA	22	GENIC	homozygous	52636896
8	54270601	54270602	C	T	18	GENIC	homozygous	53698466
8	54270659	54270660	A	-	7	GENIC	homozygous	53698467
8	54271105	54271106	C	T	25	GENIC	homozygous	53698468
8	54271369	54271370	C	T	21	GENIC	homozygous	53698469
8	54271400	54271401	C	T	19	GENIC	homozygous	53340158
8	54273120	54273121	T	C	34	GENIC	homozygous	53698470
8	54273417	54273420	TAT	---	4	GENIC	homozygous	53698471
8	54273813	54273814	G	A	5	GENIC	homozygous	53698472
8	54274290	54274291	C	-	16	GENIC	possibly homozygous	52636898
8	54274651	54274667	GTGTGTGTGTGTGTGT	----------------	4	GENIC	homozygous	53698473
8	54274874	54274875	T	C	45	GENIC	homozygous	52976896
8	54275031	54275032	T	C	38	GENIC	homozygous	53698474
8	54275308	54275309	C	T	48	GENIC	homozygous	53698475
8	54275453	54275454	C	T	40	GENIC	homozygous	53698476
8	54276882	54276883	T	TAAA	13	GENIC	homozygous	53646407
8	54277000	54277001	G	T	33	GENIC	homozygous	52976900
8	54277156	54277157	A	G	45	GENIC	homozygous	53340170
8	54277484	54277485	C	T	38	GENIC	homozygous	53698477