chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	263887426	263887427	A	G	29	GENIC	heterozygous	108634285
1	263887840	263887841	A	C	51	GENIC	homozygous	108634287
1	263888658	263888659	C	G	65	GENIC	homozygous	108634289
1	263889187	263889188	T	C	51	GENIC	homozygous	108634291
1	263889519	263889520	A	G	60	GENIC	homozygous	108634293
1	263890725	263890726	A	G	61	GENIC	possibly homozygous	108634295
1	263891863	263891864	C	T	70	GENIC	homozygous	108634297
1	263892668	263892669	T	C	58	GENIC	homozygous	108634299
1	263892906	263892907	T	C	69	GENIC	homozygous	108634301
1	263893662	263893663	G	A	57	GENIC	homozygous	108634303
1	263895367	263895368	A	C	72	GENIC	possibly homozygous	108634305
1	263895899	263895900	G	T	40	GENIC	homozygous	108634307
1	263895929	263895930	T	C	34	GENIC	homozygous	108634309
1	263898569	263898570	A	C	62	GENIC	homozygous	108634311
1	263900833	263900834	G	A	35	GENIC	heterozygous	108634313
1	263901150	263901151	T	C	47	GENIC	homozygous	108634315
1	263902638	263902639	G	A	55	GENIC	homozygous	108634317
1	263903440	263903441	A	G	54	GENIC	possibly homozygous	108634319
1	263903777	263903778	C	T	62	GENIC	possibly homozygous	108634321
1	263904194	263904195	T	C	76	GENIC	heterozygous	108782880
1	263904270	263904271	C	G	106	GENIC	heterozygous	108782881
1	263905424	263905425	G	A	46	GENIC	homozygous	108634323
1	263906708	263906709	A	C	83	GENIC	homozygous	108634325
1	263906727	263906728	T	C	76	GENIC	homozygous	108634327
1	263910156	263910157	C	T	34	GENIC	homozygous	108634329