chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	107010232	107010233	A	C	18	GENIC	homozygous	138409459
8	107010811	107010812	C	T	14	GENIC	homozygous	138409460
8	107011758	107011759	T	G	12	GENIC	heterozygous	154542703
8	107012251	107012252	T	G	22	GENIC	homozygous	138409461
8	107012964	107012965	A	T	21	GENIC	homozygous	138409463
8	107014462	107014463	A	G	26	GENIC	homozygous	138409465
8	107014690	107014691	C	A	25	GENIC	homozygous	138409466
8	107010586	107010587	A	G	10	GENIC	homozygous	142099094
8	107011065	107011066	G	A	19	GENIC	homozygous	142099095
8	107011096	107011097	A	C	20	GENIC	homozygous	142099096
8	107013226	107013227	G	A	17	GENIC	homozygous	142099097
8	107011758	107011759	T		12	GENIC	homozygous	403248264
8	107015408	107015409	G	A	29	GENIC	homozygous	138409467
8	107015880	107015881	G	A	16	GENIC	homozygous	138409468
8	107016158	107016162	CTCA		9	GENIC	heterozygous	142030147
8	107014979	107014983	TTCC		19	GENIC	homozygous	138263139
8	107011758	107011762	TTGG		12	GENIC	homozygous	138263137
8	107012895	107012895		A	20	GENIC	homozygous	138263138