chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	96103851	96103852	C	T	26	GENIC	heterozygous	116853870
8	96103951	96103952	T	A	26	GENIC	heterozygous	116853871
8	96103952	96103953	T	A	26	GENIC	heterozygous	116853872
8	96103985	96103986	C	T	27	GENIC	heterozygous	116853873
8	96104099	96104100	C	T	25	GENIC	heterozygous	116853874
8	96104381	96104382	A	C	39	GENIC	heterozygous	116853875
8	96104684	96104685	C	T	28	GENIC	heterozygous	116853876
8	96104686	96104687	C	T	27	GENIC	heterozygous	116853877
8	96104794	96104795	G	A	28	GENIC	heterozygous	116853878
8	96104831	96104832	A	G	27	GENIC	heterozygous	116853879
8	96104877	96104878	A		30	GENIC	heterozygous	131051722
8	96104890	96104891	A	G	30	GENIC	heterozygous	118108734
8	96104919	96104920	G	C	34	GENIC	heterozygous	116853880
8	96105081	96105082	G	A	22	GENIC	heterozygous	116853881
8	96105107	96105108	G	A	22	GENIC	heterozygous	116853882
8	96123921	96123922	G	A	16	GENIC	heterozygous	116588872
8	96123936	96123937	A	C	16	GENIC	heterozygous	116588874
8	96123947	96123948	C	G	16	GENIC	heterozygous	116588876