chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	54073768	54073769	C	A	8	GENIC	homozygous	52976697
8	54073946	54073947	C	CAT	11	GENIC	homozygous	52636105
8	54075170	54075171	G	A	20	GENIC	homozygous	52976698
8	54075464	54075465	C	T	15	GENIC	homozygous	52976699
8	54075616	54075617	G	A	19	GENIC	heterozygous	52976701
8	54075723	54075724	C	A	16	GENIC	homozygous	52976702
8	54077274	54077275	G	A	3	GENIC	heterozygous	52976704
8	54077435	54077436	C	T	8	GENIC	possibly homozygous	52976705
8	54077770	54077771	T	C	20	GENIC	homozygous	52636109
8	54078430	54078431	T	-	2	GENIC	homozygous	52976706
8	54078849	54078850	C	CTCTCTG	2	GENIC	heterozygous	53363882
8	54080135	54080136	C	T	10	GENIC	homozygous	52976709
8	54080650	54080651	T	C	18	GENIC	possibly homozygous	52636121
8	54080731	54080732	T	C	18	GENIC	possibly homozygous	52636123
8	54080927	54080928	T	A	38	GENIC	possibly homozygous	52976710
8	54082175	54082176	A	G	21	GENIC	possibly homozygous	52976711
8	54083251	54083252	C	T	29	GENIC	homozygous	52976712
8	54083565	54083566	T	TGAGCTGGC	3	GENIC	homozygous	52976713
8	54083567	54083568	A	C	7	GENIC	homozygous	53363883
8	54083617	54083618	G	A	23	GENIC	possibly homozygous	52976714
8	54084554	54084555	A	G	17	GENIC	homozygous	52636133
8	54085162	54085163	C	A	18	GENIC	homozygous	52976717
8	54086136	54086137	A	AAT	14	GENIC	possibly homozygous	52636141
8	54086735	54086736	A	AT	3	GENIC	homozygous	52976718