chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39688826	39688827	G	A	17	GENIC	possibly homozygous	52963101
8	39690555	39690556	G	A	8	GENIC	homozygous	52591421
8	39690934	39690935	A	G	8	GENIC	homozygous	52591422
8	39691253	39691254	A	ATGTATGTGTGTGTG	2	GENIC	heterozygous	53378061
8	39691253	39691254	A	ATGTGTGTG	2	GENIC	heterozygous	53459974
8	39691742	39691743	C	T	3	GENIC	heterozygous	52963106
8	39692640	39692641	A	G	9	GENIC	homozygous	52591430
8	39695029	39695030	C	CTTTTT	1	GENIC	homozygous	53378069
8	39695107	39695108	T	C	11	GENIC	homozygous	52591447
8	39695400	39695401	G	A	9	GENIC	homozygous	52963111
8	39695767	39695768	T	C	7	GENIC	homozygous	52591450
8	39696400	39696401	G	GT	2	GENIC	heterozygous	52591452
8	39696568	39696569	A	G	8	GENIC	possibly homozygous	52591453
8	39696961	39696962	C	T	24	GENIC	possibly homozygous	52591454
8	39697481	39697482	A	G	13	GENIC	homozygous	52591455
8	39697811	39697812	C	T	8	GENIC	homozygous	52591456
8	39697844	39697845	C	T	16	GENIC	homozygous	52963115
8	39699119	39699120	A	G	13	GENIC	homozygous	52963116
8	39703868	39703869	C	-	6	GENIC	heterozygous	52963117