chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	79691675	79691676	T	A	55	GENIC	homozygous	116844704
8	79691759	79691759		AGTGTATGG	44	GENIC	homozygous	132667577
8	79695698	79695699	T	C	57	GENIC	homozygous	116844706
8	79698343	79698344	A	C	64	GENIC	homozygous	116844708
8	79698718	79698719	G	T	51	GENIC	homozygous	117948449
8	79693997	79693998	C	T	60	GENIC	homozygous	117948446
8	79695540	79695541	C	A	59	GENIC	homozygous	117948447
8	79698648	79698649	T	C	45	GENIC	homozygous	117948448
8	79695660	79695670	CCTGTATATT		52	GENIC	homozygous	131050500
8	79697208	79697208		T	39	GENIC	homozygous	131050502
8	79699162	79699163	A	G	55	GENIC	homozygous	117948450
8	79699863	79699864	G	T	61	GENIC	possibly homozygous	118104441
8	79699891	79699892	T	C	63	GENIC	possibly homozygous	118104443
8	79700241	79700242	A	G	43	GENIC	homozygous	117928479
8	79700295	79700296	T	G	43	GENIC	homozygous	117948451
8	79703791	79703792	T	C	40	GENIC	homozygous	118119812
8	79705161	79705162	C	T	46	GENIC	homozygous	117948452
8	79705761	79705762	C	T	40	GENIC	homozygous	117948453
8	79705894	79705895	A	G	26	GENIC	homozygous	116844710
8	79706357	79706358	G	T	45	GENIC	homozygous	117948454
8	79706878	79706879	T	C	57	GENIC	homozygous	117948455
8	79707006	79707007	C	T	56	GENIC	homozygous	117948456
8	79707432	79707432		A	49	GENIC	homozygous	132123043
8	79707654	79707655	C	T	46	GENIC	homozygous	117948458
8	79708440	79708441	A	G	32	GENIC	homozygous	116844713
8	79709326	79709327	A	G	30	GENIC	homozygous	116844714
8	79711046	79711062	CAGTAATCCTCCGAGG		53	GENIC	homozygous	131050504
8	79714424	79714425	T	C	41	GENIC	possibly homozygous	116844715
8	79714452	79714453	T	G	36	GENIC	possibly homozygous	117948459
8	79714502	79714503	G	T	34	GENIC	homozygous	116844716
8	79706981	79706986	GGCTG		54	GENIC	homozygous	133191616
8	79709891	79709915	GGGTGAGGGTGGGTGGGTGGGCAG		18	GENIC	homozygous	133191617
8	79708517	79708518	A	C	5	GENIC	heterozygous	132129285