chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	57021204	57021205	A	C	11	GENIC	homozygous	110363525
18	57021205	57021206	A	C	11	GENIC	homozygous	110363527
18	57021406	57021407	G	A	54	GENIC	homozygous	110363529
18	57022210	57022211	T	C	48	GENIC	homozygous	110363531
18	57022278	57022279	T	C	48	GENIC	homozygous	110363533
18	57022793	57022794	G	A	38	GENIC	homozygous	110363535
18	57023691	57023692	G	C	42	GENIC	homozygous	110363537
18	57023752	57023753	A	G	61	GENIC	homozygous	110363539
18	57025166	57025167	T	G	30	GENIC	homozygous	110363541
18	57026066	57026067	G	A	44	GENIC	homozygous	110363543
18	57026267	57026268	A	G	30	GENIC	homozygous	110363545
18	57026554	57026555	G	A	49	GENIC	homozygous	110363547
18	57027038	57027039	A	G	32	GENIC	homozygous	110363549
18	57027830	57027831	G	A	46	GENIC	homozygous	110363551
18	57027924	57027925	C	T	41	GENIC	homozygous	110363553
18	57028083	57028084	C	T	32	GENIC	homozygous	110363555
18	57029382	57029383	C	T	30	GENIC	homozygous	110363557
18	57029441	57029442	C	T	36	GENIC	homozygous	110363559
18	57029603	57029604	C	T	32	GENIC	homozygous	110363561
18	57029768	57029769	T	C	32	GENIC	homozygous	110363563
18	57030369	57030370	C	G	23	GENIC	homozygous	110363565
18	57030957	57030958	T	C	45	GENIC	homozygous	110363567