chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	261964159	261964160	A	AG	3	GENIC	homozygous	59539334
2	261964270	261964271	T	C	2	GENIC	homozygous	59539335
2	261964329	261964330	C	G	13	GENIC	homozygous	60090629
2	261964760	261964761	C	T	8	GENIC	possibly homozygous	59539336
2	261964874	261964875	T	TTTGG	1	GENIC	homozygous	59779963
2	261965348	261965349	C	T	6	GENIC	homozygous	60090630
2	261966066	261966067	A	-	4	GENIC	homozygous	59539344
2	261966134	261966135	G	A	18	GENIC	homozygous	60090632
2	261967672	261967673	G	A	11	GENIC	possibly homozygous	60090633
2	261968039	261968040	G	A	21	GENIC	possibly homozygous	60090634
2	261969383	261969385	AC	--	10	GENIC	homozygous	59539350
2	261970277	261970278	G	A	25	GENIC	possibly homozygous	60090635
2	261970338	261970339	T	C	22	GENIC	possibly homozygous	59539352
2	261970512	261970513	G	A	17	GENIC	possibly homozygous	59539353
2	261976291	261976292	C	T	19	GENIC	possibly homozygous	60090636
2	261976417	261976418	A	G	21	GENIC	homozygous	59539357
2	261976672	261976673	A	G	24	GENIC	homozygous	59539358
2	261977306	261977307	G	C	15	GENIC	homozygous	59539361
2	261978013	261978014	G	A	20	GENIC	possibly homozygous	59539364
2	261969463	261969464	T	TA	1	GENIC	homozygous	60465025
2	261975905	261975906	C	CTT	1	GENIC	homozygous	60465026