chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10942563	10942563		C	60	GENIC	possibly homozygous	142195958
10	10942565	10942566	A	C	61	GENIC	possibly homozygous	144413728
10	10942936	10942937	A	C	80	GENIC	homozygous	142213361
10	10942975	10942976	T	C	92	GENIC	possibly homozygous	142213362
10	10943057	10943058	T	C	90	GENIC	possibly homozygous	142213363
10	10943366	10943367	T	C	60	GENIC	homozygous	142213364
10	10943374	10943375	T	C	61	GENIC	homozygous	142213365
10	10943813	10943814	A	G	49	GENIC	homozygous	142213367
10	10944478	10944479	T	G	63	GENIC	homozygous	142213368
10	10944519	10944520	G	A	55	GENIC	homozygous	144413729
10	10944615	10944616	A	T	60	GENIC	homozygous	144413730
10	10944698	10944699	A	G	60	GENIC	homozygous	142213371
10	10945051	10945052	G	T	63	GENIC	homozygous	142213372
10	10945053	10945054	G	A	61	GENIC	homozygous	142213373
10	10945472	10945473	C	T	67	GENIC	homozygous	142213374
10	10945494	10945495	G		66	GENIC	homozygous	142195959
10	10945545	10945546	A	G	63	GENIC	homozygous	142213375
10	10945574	10945575	G	T	63	GENIC	homozygous	142213376
10	10945829	10945830	A	G	47	GENIC	homozygous	142213377
10	10946609	10946609		C	53	GENIC	homozygous	142195960
10	10947656	10947657	A		47	GENIC	possibly homozygous	141094755
10	10947782	10947791	AGAGCAGTC		60	GENIC	homozygous	142195961
10	10947804	10947805	T	A	59	GENIC	homozygous	142213378
10	10949114	10949115	A	G	55	GENIC	possibly homozygous	142213379
10	10950195	10950196	C	T	71	GENIC	homozygous	142213380
10	10950204	10950205	T	C	69	GENIC	homozygous	142213381
10	10950351	10950352	T	C	59	GENIC	homozygous	142213382
10	10950519	10950520	T	C	50	GENIC	homozygous	142213383
10	10945021	10945022	C	A	65	GENIC	homozygous	138724576
10	10945178	10945179	A	C	63	GENIC	homozygous	154676620
10	10949678	10949679	A	G	50	GENIC	homozygous	138724578
10	10945178	10945179	A		63	GENIC	heterozygous	403276143
10	10945314	10945315	G		43	GENIC	homozygous	144411191