chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	17615986	17615987	T	C	33	GENIC	homozygous	113362766
14	17617028	17617029	C	A	8	GENIC	homozygous	113362768
14	17621063	17621064	T	C	15	GENIC	homozygous	113362770
14	17621382	17621383	T	C	19	GENIC	homozygous	113362772
14	17622565	17622566	T	A	15	GENIC	homozygous	113362774
14	17623031	17623032	C	T	15	GENIC	homozygous	113362776
14	17624364	17624365	C	T	24	GENIC	homozygous	113362779
14	17624390	17624391	T	C	24	GENIC	homozygous	113662487
14	17625885	17625886	A	G	10	GENIC	homozygous	113362781
14	17629810	17629811	A	G	20	GENIC	homozygous	113362783
14	17629837	17629838	T	C	16	GENIC	possibly homozygous	113362785
14	17629841	17629842	T	C	17	GENIC	homozygous	113362787
14	17629925	17629926	A	G	18	GENIC	homozygous	113362789
14	17630522	17630523	T	A	9	GENIC	homozygous	113362791
14	17630650	17630651	T	G	4	GENIC	homozygous	113362793
14	17624426	17624427	C	G	17	GENIC	possibly homozygous	113784139