chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	206928946	206928947	T	C	33	GENIC	homozygous	111161307
2	206929083	206929084	G	C	36	GENIC	homozygous	110216594
2	206929524	206929525	T	C	37	GENIC	homozygous	110216595
2	206932034	206932035	A	T	41	GENIC	homozygous	111282634
2	206933955	206933956	C	A	22	GENIC	homozygous	111282636
2	206934078	206934079	C	A	23	GENIC	homozygous	111282638
2	206935662	206935663	A	G	26	GENIC	possibly homozygous	110216598
2	206935686	206935687	A	C	25	GENIC	homozygous	120325028
2	206937543	206937544	A	G	14	GENIC	possibly homozygous	111161317
2	206938395	206938396	T	C	28	GENIC	homozygous	111282643
2	206939389	206939390	C	T	24	GENIC	homozygous	111282645
2	206940499	206940500	G	A	12	GENIC	homozygous	120325029
2	206941344	206941345	A	G	17	GENIC	homozygous	120325030
2	206948100	206948101	A	G	18	GENIC	homozygous	110216606
2	206965563	206965564	T	C	22	GENIC	homozygous	110216619
2	206966129	206966130	A	G	26	GENIC	possibly homozygous	120325031
2	206982808	206982809	T	C	14	GENIC	homozygous	110216638
2	206982825	206982826	C	T	14	GENIC	homozygous	120325032
2	206983655	206983656	A	G	22	GENIC	homozygous	110216639
2	206989150	206989151	A	G	23	GENIC	homozygous	110216645
2	206989157	206989158	C	G	22	GENIC	homozygous	110216646