chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	54131944	54131945	G	GCTCTCTCT	4	GENIC	homozygous	53431442
8	54132760	54132761	G	C	10	GENIC	homozygous	52636441
8	54132876	54132899	AGATAGTGGGGATGGTGCTCCCC	-----------------------	5	GENIC	homozygous	53431444
8	54132955	54132956	C	CTTTTT	2	GENIC	homozygous	53387446
8	54133702	54133703	C	T	20	GENIC	homozygous	52636453
8	54135236	54135237	G	A	29	GENIC	homozygous	52636455
8	54135240	54135241	A	G	30	GENIC	homozygous	52636457
8	54135491	54135492	A	C	22	GENIC	homozygous	52636461
8	54136719	54136723	GTGT	----	11	GENIC	heterozygous	53431446
8	54136721	54136723	GT	--	11	GENIC	heterozygous	53431448
8	54138241	54138242	G	GT	19	GENIC	homozygous	52636520
8	54139136	54139137	G	T	29	GENIC	homozygous	52976758
8	54134129	54134130	T	G	12	GENIC	homozygous	52976756
8	54139435	54139436	T	C	27	GENIC	homozygous	52976759
8	54139711	54139712	C	T	19	GENIC	homozygous	52976760
8	54140224	54140225	A	G	13	GENIC	homozygous	52976761
8	54140309	54140310	A	G	13	GENIC	homozygous	52976762
8	54140514	54140515	A	AAG	4	GENIC	homozygous	52976763
8	54140661	54140662	G	GC	8	GENIC	possibly homozygous	52976764
8	54141211	54141212	G	A	28	GENIC	homozygous	52636536
8	54141221	54141222	T	TTAACTAAC	12	GENIC	homozygous	52636538
8	54140661	54140662	G	GCC	8	GENIC	heterozygous	53550580