chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	81932202	81932203	C	T	12	GENIC	homozygous	144135916
14	81932366	81932367	C	T	22	GENIC	homozygous	144135917
14	81932383	81932384	G	C	22	GENIC	homozygous	144135918
14	81932499	81932500	G	A	9	GENIC	possibly homozygous	144135919
14	81932567	81932568	T	C	13	GENIC	homozygous	147050935
14	81932567	81932568	T		13	GENIC	heterozygous	403852701
14	81955672	81955673	G	A	21	GENIC	possibly homozygous	403364202
14	81932584	81932584		AGAGAC	11	GENIC	homozygous	147043462
14	81932701	81932702	A		8	GENIC	homozygous	144107314
14	81932706	81932707	A		8	GENIC	homozygous	144107315
14	81955672	81955673	G		21	GENIC	heterozygous	403364203
14	82013572	82013573	C	T	21	GENIC	homozygous	139576611
14	82013590	82013590		ATCGTGTACACCAGC	21	GENIC	homozygous	139406710
14	82014174	82014175	C	T	25	GENIC	homozygous	139576612
14	82015204	82015205	G	A	27	GENIC	homozygous	139576613
14	82015449	82015450	G	A	19	GENIC	homozygous	139576614
14	82015847	82015848	T	C	16	GENIC	homozygous	139576615
14	82018042	82018043	C	T	15	GENIC	homozygous	139576616
14	82018118	82018119	T	C	21	GENIC	homozygous	139576617
14	82018468	82018469	A	G	22	GENIC	homozygous	139576618
14	82018825	82018826	G	A	18	GENIC	homozygous	139576619
14	82019799	82019800	T	C	22	GENIC	homozygous	139576620