chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	117700532	117700533	A	T	31	GENIC	homozygous	116672152
8	117701145	117701146	A	G	41	GENIC	homozygous	116672154
8	117701290	117701291	A	G	32	GENIC	homozygous	116672156
8	117702377	117702378	C	T	22	GENIC	homozygous	116672158
8	117702413	117702414	A	G	26	GENIC	homozygous	116672160
8	117704582	117704583	C	A	27	GENIC	homozygous	116672176
8	117704714	117704715	G	A	23	GENIC	homozygous	116672178
8	117706643	117706644	A	G	32	GENIC	homozygous	116672180
8	117707459	117707460	A	C	26	GENIC	homozygous	116672182
8	117708270	117708271	G	A	27	GENIC	homozygous	116672184
8	117709062	117709063	C	T	24	GENIC	homozygous	116672186
8	117709511	117709512	C	T	31	GENIC	homozygous	116672188
8	117710241	117710242	C	T	30	GENIC	homozygous	116672190
8	117710469	117710470	C	T	24	GENIC	homozygous	116672192
8	117711094	117711095	C	G	28	GENIC	homozygous	116672194
8	117711896	117711897	G	C	4	GENIC	homozygous	116672198
8	117712042	117712043	T	C	20	GENIC	homozygous	116672200
8	117715505	117715506	A	G	30	GENIC	homozygous	116672202
8	117715842	117715843	T	C	29	GENIC	homozygous	116672204
8	117716765	117716766	A	G	33	GENIC	homozygous	116672206
8	117716825	117716826	T	C	27	GENIC	homozygous	116672208
8	117716935	117716936	C	A	41	GENIC	homozygous	116672210
8	117717055	117717056	A	G	24	GENIC	homozygous	116672212
8	117718283	117718284	T	C	27	GENIC	homozygous	116672220
8	117720757	117720758	T	C	26	GENIC	homozygous	116672222
8	117723251	117723252	A	G	27	GENIC	homozygous	116672224