chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	96103851	96103852	C	T	29	GENIC	heterozygous	116853870
8	96103932	96103933	T	C	30	GENIC	heterozygous	117119856
8	96103951	96103952	T	A	24	GENIC	heterozygous	116853871
8	96103952	96103953	T	A	24	GENIC	heterozygous	116853872
8	96104073	96104074	T	G	25	GENIC	heterozygous	117119858
8	96104238	96104239	A	C	30	GENIC	heterozygous	117119860
8	96104381	96104382	A	C	24	GENIC	heterozygous	116853875
8	96104566	96104567	A	T	30	GENIC	heterozygous	117119862
8	96104686	96104687	C	T	20	GENIC	heterozygous	116853877
8	96105081	96105082	G	A	29	GENIC	heterozygous	116853881
8	96105107	96105108	G	A	29	GENIC	heterozygous	116853882
8	96105410	96105411	T	C	23	GENIC	homozygous	117119864
8	96106705	96106706	T	C	18	GENIC	homozygous	117119866
8	96105562	96105563	G	A	13	GENIC	homozygous	116588826
8	96105799	96105800	A	T	20	GENIC	homozygous	116588828
8	96108159	96108160	T	A	17	GENIC	homozygous	117119868
8	96108679	96108680	C	G	15	GENIC	homozygous	116588838
8	96117023	96117024	C	A	15	GENIC	possibly homozygous	117119873
8	96117243	96117244	G	A	22	GENIC	homozygous	117119875
8	96119795	96119796	C	A	34	GENIC	homozygous	116588864
8	96125322	96125323	T	C	25	GENIC	homozygous	116588880
8	96126281	96126282	T	C	16	GENIC	homozygous	116588882
8	96126295	96126296	T	C	18	GENIC	homozygous	116588884
8	96127201	96127202	G	A	25	GENIC	homozygous	116588886
8	96127516	96127517	A	T	25	GENIC	homozygous	117119882
8	96260716	96260717	A	G	23	GENIC	homozygous	116588890