chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39688826	39688827	G	A	18	GENIC	homozygous	52963101
8	39690555	39690556	G	A	12	GENIC	homozygous	52591421
8	39690934	39690935	A	G	11	GENIC	homozygous	52591422
8	39691382	39691383	G	-	5	GENIC	homozygous	52963103
8	39691385	39691393	TTGTTTTG	--------	5	GENIC	homozygous	52963104
8	39691393	39691394	T	A	8	GENIC	homozygous	53378063
8	39691742	39691743	C	T	8	GENIC	homozygous	52963106
8	39692640	39692641	A	G	18	GENIC	homozygous	52591430
8	39695107	39695108	T	C	14	GENIC	homozygous	52591447
8	39695400	39695401	G	A	10	GENIC	homozygous	52963111
8	39695727	39695728	A	T	13	GENIC	homozygous	52963112
8	39695728	39695729	G	GGT	13	GENIC	homozygous	53378071
8	39695730	39695732	CT	--	13	GENIC	homozygous	53378073
8	39695767	39695768	T	C	14	GENIC	homozygous	52591450
8	39696568	39696569	A	G	14	GENIC	homozygous	52591453
8	39697481	39697482	A	G	10	GENIC	homozygous	52591455
8	39697844	39697845	C	T	7	GENIC	homozygous	52963115
8	39699119	39699120	A	G	14	GENIC	homozygous	52963116