chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	53595888	53595889	T	C	49	GENIC	homozygous	116887332
10	53596200	53596201	T	C	40	GENIC	homozygous	116887334
10	53597930	53597931	T	C	20	GENIC	homozygous	116887336
10	53600029	53600030	T	C	26	GENIC	homozygous	116887338
10	53600073	53600074	A	G	25	GENIC	homozygous	116887340
10	53600376	53600377	G	C	29	GENIC	homozygous	116887342
10	53601096	53601097	C	T	20	GENIC	homozygous	116887344
10	53601524	53601525	T	C	20	GENIC	homozygous	116887346
10	53602896	53602897	T	C	20	GENIC	homozygous	116887348
10	53603902	53603903	A	G	46	GENIC	homozygous	116887350
10	53604160	53604161	A	G	35	GENIC	homozygous	116887352
10	53604497	53604498	G	T	28	GENIC	homozygous	117011128
10	53604896	53604897	G	A	33	GENIC	homozygous	116887356
10	53605117	53605118	T	C	25	GENIC	homozygous	116887360
10	53605274	53605275	T	C	16	GENIC	homozygous	116887362
10	53605952	53605953	A	G	17	GENIC	homozygous	116887364
10	53606461	53606462	A	G	29	GENIC	homozygous	116887366
10	53606719	53606720	C	T	23	GENIC	homozygous	116887368
10	53607446	53607447	A	G	35	GENIC	homozygous	116887370
10	53608104	53608105	C	G	37	GENIC	homozygous	116933687
10	53608437	53608438	A	G	22	GENIC	homozygous	116887372