chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	22447524	22447525	C	T	92	GENIC	homozygous	117926681
8	22449633	22449634	C	T	69	GENIC	homozygous	117926682
8	22449673	22449674	G	A	72	GENIC	homozygous	117926683
8	22449693	22449694	G	A	71	GENIC	homozygous	117926684
8	22449767	22449768	T	G	71	GENIC	homozygous	117926685
8	22449935	22449936	T	C	70	GENIC	homozygous	117926686
8	22450191	22450192	T	C	84	GENIC	homozygous	117926687
8	22450417	22450418	G		60	GENIC	homozygous	131044244
8	22450429	22450430	A	G	59	GENIC	homozygous	117926688
8	22451597	22451598	T	C	37	GENIC	possibly homozygous	131057931
8	22452070	22452071	C	A	45	GENIC	homozygous	131057932
8	22452076	22452077	T	C	44	GENIC	homozygous	116438850
8	22452094	22452095	T	C	47	GENIC	homozygous	116438851
8	22452158	22452159	T	G	59	GENIC	possibly homozygous	116438852
8	22452295	22452296	C	T	58	GENIC	homozygous	117926689
8	22452361	22452362	G	A	78	GENIC	homozygous	116438853
8	22452478	22452479	C	T	70	GENIC	homozygous	117937511
8	22453312	22453313	C	T	99	GENIC	homozygous	117926690
8	22453362	22453363	C	T	113	GENIC	homozygous	117926691
8	22454276	22454277	C	G	75	GENIC	homozygous	117926695
8	22453437	22453438	A	G	109	GENIC	homozygous	117926692
8	22453712	22453713	T	C	98	GENIC	homozygous	117926693
8	22454245	22454246	A	G	75	GENIC	homozygous	117926694