chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	50832055	50832056	A	C	25	GENIC	homozygous	53116306
8	50832068	50832069	G	C	25	GENIC	homozygous	53116307
8	50832410	50832411	A	C	28	GENIC	homozygous	53116308
8	50832458	50832459	C	A	26	GENIC	homozygous	53116309
8	50832533	50832534	T	C	28	GENIC	homozygous	53116310
8	50832813	50832814	G	A	14	GENIC	homozygous	53116311
8	50832830	50832831	G	T	18	GENIC	homozygous	53116312
8	50832974	50832976	AC	--	1	GENIC	homozygous	53116313
8	50833224	50833225	T	C	17	GENIC	homozygous	53116317
8	50833428	50833429	T	A	24	GENIC	homozygous	53116318
8	50833443	50833444	T	C	28	GENIC	homozygous	53116319
8	50834932	50834933	G	A	36	GENIC	homozygous	53116320
8	50834955	50834956	A	G	41	GENIC	homozygous	53116321
8	50835656	50835657	A	G	41	GENIC	homozygous	53116322
8	50836281	50836282	C	T	43	GENIC	homozygous	53116323
8	50836705	50836706	A	C	25	GENIC	homozygous	53116324
8	50837281	50837282	C	G	23	GENIC	homozygous	53116325
8	50837283	50837284	G	C	22	GENIC	homozygous	53116326
8	50837286	50837287	T	-	22	GENIC	homozygous	53116327
8	50837402	50837403	G	A	25	GENIC	homozygous	53116328
8	50837621	50837622	T	C	20	GENIC	homozygous	53116329
8	50837772	50837773	A	G	30	GENIC	homozygous	53116330
8	50837937	50837938	C	T	25	GENIC	homozygous	53116331
8	50838386	50838387	T	C	21	GENIC	homozygous	53116332
8	50838410	50838412	GC	--	16	GENIC	homozygous	53116333
8	50838458	50838460	AA	--	8	GENIC	heterozygous	53116334
8	50838492	50838493	C	T	22	GENIC	homozygous	53116335
8	50838798	50838799	G	GTC	32	GENIC	homozygous	53116336
8	50839383	50839384	G	A	43	GENIC	homozygous	53116337
8	50839444	50839445	T	C	39	GENIC	homozygous	53116338
8	50836832	50836836	ACAC	----	14	GENIC	homozygous	52972476