chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	53247920	53247921	C	T	26	GENIC	homozygous	116820338
8	53248344	53248345	T	G	19	GENIC	homozygous	116820340
8	53248478	53248479	A	G	21	GENIC	homozygous	116820342
8	53248623	53248624	T	C	26	GENIC	homozygous	116820344
8	53248768	53248769	G	A	10	GENIC	homozygous	116820346
8	53248928	53248929	T	C	25	GENIC	homozygous	116820348
8	53249111	53249112	G	A	12	GENIC	homozygous	116820350
8	53249486	53249487	A	C	10	GENIC	homozygous	116820360
8	53249523	53249524	T	G	8	GENIC	homozygous	116820362
8	53249596	53249597	C	T	9	GENIC	homozygous	116820364
8	53250624	53250625	A	G	24	GENIC	homozygous	116820366
8	53251543	53251544	C	G	5	GENIC	homozygous	116820372
8	53264064	53264065	G	A	21	GENIC	homozygous	116820374
8	53264110	53264111	C	T	18	GENIC	homozygous	116820376
8	53270522	53270523	G	A	22	GENIC	homozygous	116820378
8	53273882	53273883	T	C	6	GENIC	homozygous	116820380
8	53273957	53273958	A	C	7	GENIC	homozygous	116820382
8	53275019	53275020	A	G	30	GENIC	homozygous	116820384
8	53275327	53275328	G	A	28	GENIC	homozygous	116820386
8	53276585	53276586	A	G	12	GENIC	homozygous	116820388
8	53277882	53277883	G	T	15	GENIC	homozygous	116820394