chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	263887426	263887427	A	G	19	GENIC	heterozygous	108634285
1	263887840	263887841	A	C	31	GENIC	homozygous	108634287
1	263888658	263888659	C	G	28	GENIC	homozygous	108634289
1	263889187	263889188	T	C	45	GENIC	homozygous	108634291
1	263889519	263889520	A	G	34	GENIC	homozygous	108634293
1	263890725	263890726	A	G	22	GENIC	homozygous	108634295
1	263892668	263892669	T	C	28	GENIC	homozygous	108634299
1	263892906	263892907	T	C	50	GENIC	homozygous	108634301
1	263893662	263893663	G	A	45	GENIC	homozygous	108634303
1	263895929	263895930	T	C	27	GENIC	homozygous	108634309
1	263897034	263897035	T	A	32	GENIC	homozygous	109217546
1	263897347	263897348	G	A	43	GENIC	heterozygous	109571718
1	263897389	263897390	C	A	50	GENIC	possibly homozygous	109217548
1	263898569	263898570	A	C	25	GENIC	homozygous	108634311
1	263900833	263900834	G	A	26	GENIC	heterozygous	108634313
1	263901150	263901151	T	C	37	GENIC	homozygous	108634315
1	263903440	263903441	A	G	35	GENIC	homozygous	108634319
1	263905424	263905425	G	A	31	GENIC	homozygous	108634323
1	263906708	263906709	A	C	24	GENIC	homozygous	108634325
1	263906727	263906728	T	C	29	GENIC	homozygous	108634327
1	263910156	263910157	C	T	32	GENIC	homozygous	108634329