chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	1305185	1305186	T	C	36	GENIC	homozygous	144947084
14	1305283	1305284	A	G	43	GENIC	homozygous	139419707
14	1305465	1305466	A	G	34	GENIC	homozygous	145832391
14	1305934	1305935	A	G	39	GENIC	homozygous	144947085
14	1306761	1306762	G	T	43	GENIC	homozygous	139419708
14	1306799	1306800	G	A	44	GENIC	homozygous	145832392
14	1307368	1307369	G	A	36	GENIC	homozygous	144947086
14	1307706	1307707	C	T	34	GENIC	homozygous	144947087
14	1307846	1307847	T	C	40	GENIC	homozygous	144947088
14	1309200	1309201	C	T	33	GENIC	homozygous	145832393
14	1311693	1311694	C	T	51	GENIC	homozygous	145832394
14	1312441	1312442	A	G	42	GENIC	heterozygous	403348353
14	1306337	1306338	C	A	41	GENIC	heterozygous	154821915
14	1306337	1306338	C	G	41	GENIC	homozygous	154821916
14	1312441	1312442	A		42	GENIC	homozygous	403348352
14	1312747	1312748	G	A	64	GENIC	homozygous	139419709
14	1314434	1314435	G	A	28	GENIC	homozygous	139419710
14	1314954	1314955	A	G	39	GENIC	homozygous	139419711
14	1315250	1315251	A	G	29	GENIC	homozygous	139419712
14	1315272	1315273	C	G	37	GENIC	homozygous	139419713
14	1316622	1316623	C	T	30	GENIC	homozygous	139419714
14	1316810	1316810		GTTTT	28	GENIC	homozygous	145824501
14	1307286	1307288	TT		27	GENIC	possibly homozygous	144938378
14	1307509	1307510	A		10	GENIC	homozygous	145824500
14	1312624	1312624		AGAC	42	GENIC	homozygous	139373263
14	1317015	1317016	C	T	45	GENIC	homozygous	139419715
14	1317128	1317129	A	T	41	GENIC	homozygous	145832395
14	1317174	1317175	T	C	32	GENIC	homozygous	139419716
14	1319325	1319325		C	37	GENIC	homozygous	139373265