chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	45241699	45241700	G	A	21	GENIC	possibly homozygous	52615621
8	45241745	45241746	A	G	37	GENIC	homozygous	52615623
8	45241753	45241754	C	CA	36	GENIC	homozygous	52615625
8	45241866	45241867	G	A	28	GENIC	homozygous	52615627
8	45242104	45242105	T	TG	22	GENIC	homozygous	52615629
8	45242178	45242179	T	C	13	GENIC	homozygous	52615631
8	45242629	45242630	G	A	35	GENIC	homozygous	52615633
8	45242757	45242758	G	A	37	GENIC	homozygous	52615635
8	45242840	45242841	G	A	29	GENIC	homozygous	52615637
8	45242848	45242849	A	C	31	GENIC	possibly homozygous	52615639
8	45242940	45242941	C	T	28	GENIC	homozygous	52615641
8	45242976	45242977	G	A	31	GENIC	homozygous	52615643
8	45242985	45242986	T	C	29	GENIC	homozygous	52615645
8	45243130	45243131	A	G	34	GENIC	homozygous	52615647
8	45243311	45243312	G	A	47	GENIC	homozygous	52615649
8	45243577	45243578	A	G	52	GENIC	homozygous	52615651
8	45243783	45243784	T	TACAC	8	GENIC	homozygous	52615653
8	45243787	45243788	C	CACAG	27	GENIC	heterozygous	52615655
8	45244540	45244542	GG	--	33	GENIC	homozygous	52615657
8	45244674	45244675	A	AC	21	GENIC	homozygous	52615659
8	45244720	45244721	T	C	32	GENIC	homozygous	52615661
8	45244816	45244817	T	C	47	GENIC	homozygous	52615663
8	45245980	45245981	T	TA	18	GENIC	possibly homozygous	52615665
8	45246564	45246565	A	G	42	GENIC	homozygous	52615667
8	45246614	45246615	C	T	54	GENIC	homozygous	52615669
8	45247248	45247249	A	G	39	GENIC	homozygous	52615671
8	45247252	45247253	A	T	40	GENIC	homozygous	52615673