chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	1305283	1305284	A	G	63	GENIC	homozygous	139419707
14	1306761	1306762	G	T	69	GENIC	homozygous	139419708
14	1312747	1312748	G	A	54	GENIC	homozygous	139419709
14	1314434	1314435	G	A	44	GENIC	homozygous	139419710
14	1314954	1314955	A	G	33	GENIC	homozygous	139419711
14	1315250	1315251	A	G	45	GENIC	homozygous	139419712
14	1315272	1315273	C	G	47	GENIC	homozygous	139419713
14	1316622	1316623	C	T	78	GENIC	homozygous	139419714
14	1317015	1317016	C	T	52	GENIC	homozygous	139419715
14	1317174	1317175	T	C	91	GENIC	homozygous	139419716
14	1318648	1318649	C	T	36	GENIC	possibly homozygous	139419717
14	1319325	1319325		C	49	GENIC	homozygous	139373265
14	1312562	1312562		CAGA	50	GENIC	homozygous	139373262
14	1312624	1312624		AGAC	51	GENIC	possibly homozygous	139373263
14	1318645	1318645		AC	36	GENIC	possibly homozygous	139373264
14	1317651	1317652	C	T	61	GENIC	homozygous	147602709
14	1312441	1312442	A		51	GENIC	homozygous	403348352
14	1312441	1312442	A	G	51	GENIC	heterozygous	403348353