chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14217079	14217080	A	-	28	GENIC	homozygous	51622874
10	14218258	14218259	T	G	32	GENIC	homozygous	51622875
10	14218600	14218601	T	C	31	GENIC	homozygous	51329145
10	14219473	14219474	A	G	16	GENIC	homozygous	51622877
10	14219648	14219649	A	T	35	GENIC	homozygous	51622878
10	14219789	14219790	T	C	40	GENIC	homozygous	51622879
10	14220061	14220062	T	C	27	GENIC	homozygous	51622880
10	14221193	14221194	T	C	30	GENIC	homozygous	51622881
10	14222353	14222354	G	A	36	GENIC	homozygous	51622882
10	14222436	14222437	C	CT	28	GENIC	possibly homozygous	51810352
10	14223120	14223121	G	A	37	GENIC	homozygous	51810354
10	14223121	14223122	C	T	36	GENIC	homozygous	51810356
10	14224476	14224477	C	CTTTTT	18	GENIC	homozygous	51329147
10	14227096	14227097	T	C	11	GENIC	homozygous	51622890
10	14227117	14227118	T	-	5	GENIC	homozygous	51810360
10	14227144	14227145	C	CT	4	GENIC	homozygous	51622892
10	14228030	14228031	A	C	29	GENIC	homozygous	51622893
10	14228068	14228077	GTGCAATGA	---------	23	GENIC	homozygous	51622894
10	14228310	14228311	T	C	26	GENIC	homozygous	51622895
10	14228471	14228472	T	A	27	GENIC	homozygous	51810362
10	14228603	14228604	T	-	20	GENIC	possibly homozygous	51810364
10	14228670	14228671	C	A	14	GENIC	homozygous	51810366
10	14228688	14228689	G	T	15	GENIC	homozygous	51810368
10	14229328	14229329	T	G	34	GENIC	homozygous	51622896
10	14229603	14229604	T	C	28	GENIC	homozygous	51810370
10	14229638	14229639	C	T	30	GENIC	homozygous	51810372
10	14229966	14229967	C	G	22	GENIC	homozygous	51810374
10	14229967	14229968	C	T	23	GENIC	homozygous	51810376
10	14230126	14230127	G	A	16	GENIC	homozygous	51810380
10	14230297	14230298	A	G	32	GENIC	homozygous	51810382