chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	122782201	122782202	C	T	45	GENIC	possibly homozygous	110002260
2	122782743	122782744	A	G	52	GENIC	homozygous	110002261
2	122783857	122783858	A	G	33	GENIC	homozygous	110002262
2	122784354	122784355	G	A	41	GENIC	homozygous	110002263
2	122784454	122784455	T	A	32	GENIC	homozygous	110002264
2	122784629	122784630	A	G	57	GENIC	homozygous	110002265
2	122784927	122784928	T	C	41	GENIC	homozygous	110002266
2	122785086	122785087	T	C	36	GENIC	homozygous	110002267
2	122785240	122785241	C	T	57	GENIC	homozygous	110002268
2	122785763	122785764	T	C	52	GENIC	homozygous	110002269
2	122786556	122786557	G	A	56	GENIC	homozygous	110002270
2	122786607	122786608	T	G	49	GENIC	heterozygous	110002271
2	122786856	122786857	T	C	38	GENIC	homozygous	110002272
2	122786869	122786870	C	T	46	GENIC	homozygous	110002273
2	122795240	122795241	A	C	46	GENIC	homozygous	110002274
2	122795475	122795476	A	G	48	GENIC	homozygous	110002275
2	122796891	122796892	T	C	50	GENIC	homozygous	110002276
2	122798250	122798251	T	C	46	GENIC	homozygous	110002277
2	122804066	122804067	T	C	61	GENIC	homozygous	110002278
2	122804349	122804350	G	A	47	GENIC	homozygous	110002279
2	122804403	122804404	C	A	51	GENIC	possibly homozygous	110002280
2	122804960	122804961	G	C	57	GENIC	homozygous	110002281