chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	85859457	85859458	G	A	59	GENIC	homozygous	49021347
14	85861118	85861119	G	A	38	GENIC	heterozygous	49021348
14	85861175	85861176	T	C	11	GENIC	heterozygous	49021349
14	85861179	85861180	A	G	12	GENIC	possibly homozygous	49021350
14	85861208	85861209	G	T	32	GENIC	heterozygous	49021351
14	85861226	85861227	A	G	37	GENIC	heterozygous	49021352
14	85861247	85861248	T	C	55	GENIC	heterozygous	49021353
14	85861251	85861252	A	G	55	GENIC	heterozygous	49021354
14	85861280	85861281	T	G	61	GENIC	heterozygous	49021355
14	85861325	85861326	T	C	57	GENIC	heterozygous	49021356
14	85861344	85861345	A	T	52	GENIC	heterozygous	49021357
14	85861352	85861353	A	T	56	GENIC	heterozygous	49021358
14	85861355	85861356	T	C	57	GENIC	heterozygous	49021359
14	85861359	85861360	A	G	61	GENIC	heterozygous	49021360
14	85862143	85862144	G	A	56	GENIC	homozygous	49021361
14	85862259	85862260	G	GA	26	GENIC	heterozygous	49021362
14	85863774	85863775	T	TAC	12	GENIC	heterozygous	49021363
14	85863774	85863775	T	TACAC	12	GENIC	heterozygous	49021364
14	85864002	85864003	C	CTTTT	17	GENIC	possibly homozygous	49021365
14	85864015	85864016	C	T	37	GENIC	heterozygous	49021366
14	85864769	85864770	T	G	44	GENIC	homozygous	49021367
14	85866474	85866475	A	G	44	GENIC	homozygous	49021368
14	85867331	85867332	C	T	53	GENIC	possibly homozygous	49021369
14	85867441	85867442	C	T	62	GENIC	homozygous	49021370
14	85867568	85867569	A	G	66	GENIC	homozygous	49021371
14	85867592	85867593	C	T	67	GENIC	homozygous	49021372
14	85868539	85868540	C	T	40	GENIC	homozygous	49021373