chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	265812073	265812074	T	C	41	GENIC	homozygous	108637307
1	265812439	265812440	T	C	43	GENIC	possibly homozygous	108637308
1	265813330	265813331	T	G	63	GENIC	homozygous	108637309
1	265813411	265813412	G	A	50	GENIC	homozygous	108637310
1	265813509	265813510	G	T	37	GENIC	homozygous	108637311
1	265813563	265813564	A	T	49	GENIC	homozygous	108637312
1	265813569	265813570	A	G	49	GENIC	homozygous	108637313
1	265813678	265813679	A	T	35	GENIC	homozygous	108637314
1	265813935	265813936	T	C	30	GENIC	homozygous	108637315
1	265814680	265814681	T	C	33	GENIC	possibly homozygous	108637316
1	265817456	265817457	A	G	53	GENIC	possibly homozygous	108637317
1	265818586	265818587	C	T	50	GENIC	homozygous	108637318
1	265819020	265819021	G	A	46	GENIC	homozygous	108637319
1	265819282	265819283	T	C	59	GENIC	homozygous	108637320
1	265819772	265819773	C	G	41	GENIC	homozygous	108637321
1	265819832	265819833	T	G	36	GENIC	homozygous	108637322
1	265819865	265819866	T	A	45	GENIC	homozygous	108637323
1	265820899	265820900	A	G	34	GENIC	homozygous	108637324
1	265820997	265820998	A	T	55	GENIC	possibly homozygous	108637325
1	265821200	265821201	G	A	53	GENIC	homozygous	108637326
1	265823543	265823544	A	G	60	GENIC	homozygous	108637327