chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	17210769	17210770	G	C	46	GENIC	homozygous	113809491
14	17211123	17211124	A	T	40	GENIC	homozygous	113361677
14	17211351	17211352	C	T	45	GENIC	homozygous	113809493
14	17211504	17211505	C	T	46	GENIC	homozygous	113809495
14	17211562	17211563	T	A	50	GENIC	homozygous	113361679
14	17212056	17212057	G	C	48	GENIC	possibly homozygous	113809497
14	17212433	17212434	G	A	52	GENIC	homozygous	113809499
14	17212435	17212436	C	T	52	GENIC	homozygous	113809501
14	17212509	17212510	A	T	53	GENIC	homozygous	113809503
14	17212671	17212672	C	A	53	GENIC	homozygous	113809505
14	17212774	17212775	G	C	71	GENIC	homozygous	113809507