chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	210862939	210862940	C	T	12	GENIC	homozygous	110223767
2	210863834	210863835	C	T	16	GENIC	homozygous	110223768
2	210864181	210864182	C	T	13	GENIC	homozygous	110223769
2	210866014	210866015	C	T	17	GENIC	homozygous	120158821
2	210866873	210866874	G	C	14	GENIC	homozygous	110223770
2	210868180	210868181	T	C	10	GENIC	homozygous	110223771
2	210868196	210868197	G	A	13	GENIC	homozygous	110223772
2	210868577	210868578	T	G	13	GENIC	homozygous	110223773
2	210869050	210869051	T	C	14	GENIC	homozygous	110223774
2	210869137	210869138	T	A	15	GENIC	homozygous	110223775
2	210869232	210869233	T	C	18	GENIC	homozygous	110223776
2	210869281	210869282	A	G	21	GENIC	homozygous	110223777
2	210869312	210869313	T	C	20	GENIC	homozygous	110223778
2	210870174	210870175	A	G	21	GENIC	homozygous	110223779
2	210870517	210870518	T	C	10	GENIC	homozygous	110223780
2	210870691	210870692	A	T	23	GENIC	homozygous	110223781
2	210870835	210870836	A	G	21	GENIC	homozygous	110223782
2	210871160	210871161	C	T	19	GENIC	homozygous	110223783
2	210871220	210871221	T	A	14	GENIC	homozygous	110223784
2	210871323	210871324	T	C	20	GENIC	homozygous	110223785