chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	196113766	196113767	G	C	10	GENIC	homozygous	110195835
2	196113992	196113993	T	A	15	GENIC	homozygous	110195836
2	196114050	196114051	C	A	20	GENIC	homozygous	110195837
2	196114455	196114456	A	G	27	GENIC	homozygous	110195838
2	196114580	196114581	C	T	25	GENIC	homozygous	110195839
2	196115014	196115015	C	T	21	GENIC	homozygous	110195840
2	196115043	196115044	A	G	24	GENIC	homozygous	110195841
2	196115061	196115062	A	G	27	GENIC	homozygous	110195842
2	196115403	196115404	C	G	29	GENIC	homozygous	110195844
2	196115445	196115446	A	C	26	GENIC	homozygous	110195845
2	196115693	196115694	G	A	22	GENIC	homozygous	110195846
2	196116180	196116181	A	G	27	GENIC	homozygous	110195847
2	196116713	196116714	A	G	25	GENIC	homozygous	110195848
2	196118270	196118271	T	C	28	GENIC	homozygous	110195850
2	196118374	196118375	T	C	30	GENIC	homozygous	110195851
2	196118473	196118474	T	C	29	GENIC	homozygous	110195852
2	196119177	196119178	G	A	32	GENIC	homozygous	110195853
2	196119759	196119760	T	G	31	GENIC	homozygous	110195854
2	196121203	196121204	G	A	19	GENIC	homozygous	110195855
2	196126236	196126237	G	A	28	GENIC	possibly homozygous	110195858
2	196129689	196129690	A	T	28	GENIC	homozygous	110617782
2	196130724	196130725	T	C	16	GENIC	homozygous	110195859
2	196132896	196132897	C	A	15	GENIC	homozygous	110195860
2	196136508	196136509	T	C	13	GENIC	homozygous	110195861
2	196139674	196139675	A	C	8	GENIC	homozygous	110195864