chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116440435	116440436	A	G	77	GENIC	homozygous	116669365
8	116440845	116440847	TA		55	GENIC	possibly homozygous	128634995
8	116446650	116446651	A	G	48	GENIC	homozygous	116669367
8	116446979	116446980	G	A	33	GENIC	homozygous	116669369
8	116443385	116443386	C	A	10	GENIC	homozygous	116886467
8	116447427	116447428	T	C	51	GENIC	homozygous	116669371
8	116447513	116447514	T	C	63	GENIC	homozygous	116669373
8	116447898	116447899	T	C	63	GENIC	homozygous	116669375
8	116448516	116448517	C	T	75	GENIC	homozygous	116669377
8	116451919	116451920	A	C	61	GENIC	homozygous	116669379
8	116452714	116452715	A		70	GENIC	homozygous	128634996
8	116453888	116453889	G	A	68	GENIC	homozygous	116669381
8	116454335	116454348	CCTCTGGTCTACC		54	GENIC	homozygous	128634997
8	116455245	116455246	G	A	70	GENIC	homozygous	116669383
8	116455668	116455669	G	A	60	GENIC	homozygous	116669385
8	116457201	116457202	A	G	66	GENIC	homozygous	116669387
8	116461784	116461785	A	G	52	GENIC	homozygous	116669391
8	116462705	116462706	C	G	46	GENIC	homozygous	116669393
8	116463618	116463618		CACACACACAG	31	GENIC	homozygous	128634998
8	116463898	116463906	ACACACAC		23	GENIC	homozygous	128634999
8	116464151	116464152	T	C	58	GENIC	homozygous	116669399
8	116465370	116465371	T	C	55	GENIC	homozygous	116669401
8	116465391	116465392	G	A	51	GENIC	homozygous	116669403
8	116469257	116469258	G	A	22	GENIC	homozygous	116669405
8	116469314	116469315	G		34	GENIC	homozygous	130770183
8	116469315	116469316	A	C	34	GENIC	homozygous	118077637
8	116469327	116469328	C	G	37	GENIC	homozygous	116669407
8	116469270	116469271	T		22	GENIC	homozygous	131054188
8	116469274	116469275	G		24	GENIC	homozygous	131054189
8	116469294	116469295	A		27	GENIC	homozygous	131054190
8	116469299	116469300	G		29	GENIC	homozygous	131054191
8	116469331	116469331		C	37	GENIC	homozygous	129951163