chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	214375846	214375847	T	C	32	GENIC	homozygous	108990366
1	214375847	214375848	T	C	32	GENIC	homozygous	108990367
1	214375955	214375956	T	C	37	GENIC	homozygous	108532379
1	214377230	214377231	G	A	17	GENIC	homozygous	108990368
1	214377429	214377430	C	T	25	GENIC	homozygous	108990369
1	214377502	214377503	T	C	32	GENIC	homozygous	108532380
1	214377709	214377710	T	G	37	GENIC	homozygous	108532382
1	214378464	214378465	C	T	28	GENIC	homozygous	108532385
1	214378647	214378648	G	A	17	GENIC	homozygous	108532386
1	214379284	214379285	A	G	34	GENIC	homozygous	108990370
1	214379430	214379431	A	G	33	GENIC	homozygous	108532387
1	214379707	214379708	G	C	31	GENIC	homozygous	108532388
1	214379953	214379954	A	G	25	GENIC	homozygous	108532389
1	214380033	214380034	C	G	27	GENIC	homozygous	108532390
1	214380178	214380179	A	G	12	GENIC	homozygous	108532391
1	214380679	214380680	A	C	12	GENIC	homozygous	108990371
1	214381137	214381138	C	T	29	GENIC	homozygous	108990372
1	214381179	214381180	C	T	32	GENIC	homozygous	108532392
1	214381761	214381762	C	T	15	GENIC	homozygous	108532393
1	214381939	214381940	G	T	6	GENIC	homozygous	108532394
1	214381944	214381945	G	T	6	GENIC	homozygous	108532395
1	214382007	214382008	A	G	13	GENIC	homozygous	108532396
1	214382137	214382138	T	A	17	GENIC	homozygous	108532397
1	214382436	214382437	G	A	13	GENIC	homozygous	108532398
1	214382788	214382789	T	C	17	GENIC	homozygous	108532400
1	214383824	214383825	T	C	30	GENIC	homozygous	108990375
1	214385259	214385260	G	T	29	GENIC	homozygous	108990376