chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	75846037	75846038	C		19	GENIC	homozygous	137317980
5	75846638	75846639	T	C	18	GENIC	homozygous	137513360
5	75846852	75846853	A	T	13	GENIC	homozygous	137513361
5	75852437	75852438	C	G	14	GENIC	homozygous	137513362
5	75852739	75852740	A	G	10	GENIC	possibly homozygous	137513363
5	75852741	75852742	G	A	10	GENIC	possibly homozygous	137513364
5	75853378	75853379	T	A	13	GENIC	homozygous	137513365
5	75853744	75853745	G	A	14	GENIC	homozygous	137513366
5	75853782	75853783	G	T	14	GENIC	homozygous	137513367
5	75853788	75853789	C	A	13	GENIC	homozygous	137513368
5	75853790	75853790		ATGCTAAAT	13	GENIC	homozygous	137317982
5	75854053	75854054	T	C	21	GENIC	homozygous	137513369
5	75856416	75856417	G	A	18	GENIC	homozygous	137513370
5	75856584	75856585	C	A	27	GENIC	homozygous	137513371
5	75857562	75857563	C	T	18	GENIC	homozygous	137513372
5	75858887	75858888	A	G	21	GENIC	homozygous	137513373
5	75859265	75859266	T		18	GENIC	homozygous	137317983