chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	21931901	21931902	A	C	11	GENIC	homozygous	120187282
2	21932087	21932088	T	C	8	GENIC	homozygous	120187283
2	21932303	21932304	T	C	4	GENIC	homozygous	109635677
2	21934730	21934731	A	G	6	GENIC	homozygous	109635693
2	21936101	21936102	A	G	18	GENIC	homozygous	109635721
2	21936552	21936553	A	C	10	GENIC	homozygous	109635738
2	21937608	21937609	A	G	19	GENIC	homozygous	109635754
2	21941015	21941016	A	G	11	GENIC	homozygous	109635775
2	21941240	21941241	C	T	19	GENIC	homozygous	120187292
2	21941823	21941824	T	C	12	GENIC	homozygous	109635779
2	21945780	21945781	A	G	29	GENIC	homozygous	120187293
2	21945901	21945902	A	G	16	GENIC	homozygous	109635805
2	21946978	21946979	A	T	15	GENIC	homozygous	109635813
2	21947349	21947350	G	T	11	GENIC	homozygous	109635816
2	21947603	21947604	G	A	20	GENIC	homozygous	120187294
2	21947901	21947902	A	G	23	GENIC	homozygous	109635820
2	21949335	21949336	G	A	23	GENIC	homozygous	109635822
2	21949947	21949948	G	T	19	GENIC	homozygous	120187295
2	21953048	21953049	G	C	8	GENIC	homozygous	109635828
2	21958148	21958149	G	T	25	GENIC	homozygous	120187296
2	21944181	21944182	T	A	11	GENIC	homozygous	125786219