chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	118161056	118161057	T	A	34	GENIC	homozygous	116673189
8	118166915	118166916	C	T	33	GENIC	homozygous	116673193
8	118167052	118167053	T	C	25	GENIC	homozygous	116673195
8	118167649	118167650	T	C	35	GENIC	homozygous	116673197
8	118170343	118170344	G	A	35	GENIC	homozygous	116673199
8	118171107	118171108	A	G	32	GENIC	homozygous	116673201
8	118171420	118171421	G	A	17	GENIC	homozygous	116673203
8	118175426	118175427	C	T	40	GENIC	homozygous	116673205
8	118178403	118178404	A	G	20	GENIC	homozygous	116673209
8	118179554	118179555	G	A	20	GENIC	homozygous	116673211
8	118179605	118179606	A	C	23	GENIC	homozygous	116673213
8	118179766	118179767	G	A	13	GENIC	homozygous	116673215
8	118182231	118182232	C	T	17	GENIC	homozygous	116673217
8	118185764	118185765	G	A	16	GENIC	homozygous	116673219
8	118186299	118186300	G	T	14	GENIC	homozygous	116673221
8	118190683	118190684	T	C	29	GENIC	homozygous	116673225
8	118190891	118190892	A	G	14	GENIC	homozygous	116673227
8	118190968	118190969	C	G	17	GENIC	homozygous	116673229
8	118191706	118191707	C	G	27	GENIC	homozygous	116673231
8	118194412	118194413	A	G	13	GENIC	homozygous	116673239