chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	75772222	75772223	C	T	44	GENIC	homozygous	147168979
18	75772984	75772985	A	G	45	GENIC	homozygous	147168980
18	75774045	75774046	T	C	48	GENIC	homozygous	147168981
18	75774123	75774124	T	A	43	GENIC	homozygous	147168982
18	75774511	75774512	A	G	39	GENIC	homozygous	147168983
18	75776066	75776067	G	C	48	GENIC	homozygous	147168984
18	75776109	75776110	T	C	47	GENIC	homozygous	147168985
18	75776162	75776163	G	A	57	GENIC	homozygous	147168986
18	75776245	75776246	C	T	53	GENIC	homozygous	147168987
18	75776436	75776437	A	G	53	GENIC	homozygous	147168988
18	75776612	75776613	C	T	53	GENIC	homozygous	147168989
18	75777029	75777030	G	A	15	GENIC	homozygous	147168990
18	75777104	75777105	G	A	18	GENIC	homozygous	147168991
18	75777311	75777312	C	T	52	GENIC	homozygous	147168992
18	75777433	75777434	G	A	56	GENIC	homozygous	147168993
18	75778269	75778270	G	A	43	GENIC	homozygous	147168994
18	75778326	75778327	T		43	GENIC	possibly homozygous	141146592
18	75778432	75778434	AT		29	GENIC	homozygous	147158178
18	75779288	75779289	T	G	33	GENIC	homozygous	147168995
18	75779316	75779316		GT	27	GENIC	homozygous	147158179
18	75781334	75781335	G	A	45	GENIC	homozygous	147168996
18	75783838	75783839	C	G	55	GENIC	homozygous	147168997
18	75784494	75784495	A	G	46	GENIC	homozygous	147168998
18	75785228	75785229	T	C	56	GENIC	homozygous	147168999
18	75787212	75787213	C	T	57	GENIC	homozygous	147169000
18	75787558	75787559	G	C	62	GENIC	homozygous	147169001
18	75778435	75778436	C		34	GENIC	heterozygous	403674225
18	75778435	75778436	C	G	34	GENIC	possibly homozygous	155056203