chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	263887426	263887427	A	G	22	GENIC	possibly homozygous	108634285
1	263887840	263887841	A	C	32	GENIC	homozygous	108634287
1	263888658	263888659	C	G	47	GENIC	homozygous	108634289
1	263889187	263889188	T	C	67	GENIC	homozygous	108634291
1	263889519	263889520	A	G	58	GENIC	homozygous	108634293
1	263890725	263890726	A	G	51	GENIC	homozygous	108634295
1	263891863	263891864	C	T	27	GENIC	homozygous	108634297
1	263892668	263892669	T	C	45	GENIC	homozygous	108634299
1	263892906	263892907	T	C	45	GENIC	homozygous	108634301
1	263893662	263893663	G	A	34	GENIC	homozygous	108634303
1	263895367	263895368	A	C	34	GENIC	homozygous	108634305
1	263895899	263895900	G	T	43	GENIC	homozygous	108634307
1	263895929	263895930	T	C	40	GENIC	homozygous	108634309
1	263898569	263898570	A	C	42	GENIC	homozygous	108634311
1	263900833	263900834	G	A	51	GENIC	heterozygous	108634313
1	263901150	263901151	T	C	45	GENIC	homozygous	108634315
1	263902638	263902639	G	A	39	GENIC	possibly homozygous	108634317
1	263903440	263903441	A	G	42	GENIC	homozygous	108634319
1	263903777	263903778	C	T	35	GENIC	homozygous	108634321
1	263905424	263905425	G	A	51	GENIC	homozygous	108634323
1	263906708	263906709	A	C	44	GENIC	homozygous	108634325
1	263906727	263906728	T	C	48	GENIC	homozygous	108634327
1	263910156	263910157	C	T	35	GENIC	homozygous	108634329