chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	10942936	10942937	A	C	27	GENIC	homozygous	142213361
10	10942975	10942976	T	C	33	GENIC	homozygous	142213362
10	10943057	10943058	T	C	27	GENIC	homozygous	142213363
10	10943366	10943367	T	C	18	GENIC	homozygous	142213364
10	10943374	10943375	T	C	19	GENIC	homozygous	142213365
10	10943813	10943814	A	G	20	GENIC	homozygous	142213367
10	10944478	10944479	T	G	24	GENIC	homozygous	142213368
10	10944519	10944520	G	A	23	GENIC	homozygous	144413729
10	10944615	10944616	A	T	20	GENIC	homozygous	144413730
10	10944698	10944699	A	G	21	GENIC	homozygous	142213371
10	10945021	10945022	C	A	21	GENIC	possibly homozygous	138724576
10	10945051	10945052	G	T	23	GENIC	homozygous	142213372
10	10945472	10945473	C	T	37	GENIC	homozygous	142213374
10	10945494	10945495	G		33	GENIC	homozygous	142195959
10	10945545	10945546	A	G	38	GENIC	homozygous	142213375
10	10945574	10945575	G	T	36	GENIC	homozygous	142213376
10	10945829	10945830	A	G	29	GENIC	homozygous	142213377
10	10946609	10946609		C	27	GENIC	homozygous	142195960
10	10947782	10947791	AGAGCAGTC		25	GENIC	homozygous	142195961
10	10947804	10947805	T	A	25	GENIC	homozygous	142213378
10	10949114	10949115	A	G	26	GENIC	homozygous	142213379
10	10949678	10949679	A	G	24	GENIC	homozygous	138724578
10	10950195	10950196	C	T	29	GENIC	homozygous	142213380
10	10950204	10950205	T	C	31	GENIC	homozygous	142213381
10	10950351	10950352	T	C	27	GENIC	homozygous	142213382
10	10950519	10950520	T	C	22	GENIC	homozygous	142213383
10	10949460	10949461	G	A	16	GENIC	homozygous	148050473
10	10945314	10945315	G		28	GENIC	homozygous	144411191
10	10947656	10947657	A		22	GENIC	homozygous	141094755
10	10948155	10948156	G	A	32	GENIC	homozygous	148050472
10	10945178	10945179	A		29	GENIC	heterozygous	403276143
10	10945178	10945179	A	C	29	GENIC	homozygous	154676620