chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	71094656	71094657	T	G	20	GENIC	homozygous	117965336
8	71096593	71096594	A	C	26	GENIC	possibly homozygous	118149661
8	71098072	71098073	T	C	12	GENIC	homozygous	117917402
8	71098073	71098074	C	T	12	GENIC	homozygous	117917403
8	71098079	71098080	G	A	10	GENIC	homozygous	117917404
8	71104919	71104920	A	G	33	GENIC	possibly homozygous	117965341
8	71106845	71106846	A	T	23	GENIC	homozygous	118149663
8	71107855	71107856	A	C	24	GENIC	homozygous	117965345
8	71108960	71108961	A	G	28	GENIC	homozygous	117965346
8	71108989	71108990	C	T	25	GENIC	homozygous	117965347
8	71109130	71109131	T	C	37	GENIC	homozygous	117965348
8	71109275	71109276	T	G	27	GENIC	possibly homozygous	117965349
8	71109367	71109368	A	T	29	GENIC	possibly homozygous	117965350
8	71109616	71109617	G	C	20	GENIC	possibly homozygous	117965351
8	71110691	71110692	C	T	16	GENIC	possibly homozygous	117965353
8	71110699	71110700	A	C	16	GENIC	possibly homozygous	117965354
8	71111510	71111511	G	A	27	GENIC	possibly homozygous	117965356
8	71111960	71111961	A	T	20	GENIC	homozygous	117965357
8	71112113	71112114	T	C	23	GENIC	homozygous	117965358
8	71112460	71112461	G	A	28	GENIC	homozygous	118149665
8	71112505	71112506	T	G	31	GENIC	possibly homozygous	117965359
8	71113435	71113436	C	T	37	GENIC	possibly homozygous	117965361
8	71114601	71114602	C	T	24	GENIC	possibly homozygous	117965363
8	71114965	71114966	A	G	22	GENIC	possibly homozygous	117965364
8	71115308	71115309	G	A	30	GENIC	possibly homozygous	118149667
8	71115560	71115561	C	T	20	GENIC	homozygous	117965366
8	71115816	71115817	A	G	16	GENIC	homozygous	117965367
8	71115890	71115891	C	T	28	GENIC	homozygous	117965368
8	71116077	71116078	A	G	19	GENIC	homozygous	117965369
8	71116155	71116156	A	G	24	GENIC	possibly homozygous	117965370
8	71117208	71117209	A	C	36	GENIC	homozygous	117965371
8	71117733	71117734	A	G	29	GENIC	possibly homozygous	117965372
8	71118073	71118074	C	T	29	GENIC	possibly homozygous	117965373