chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	53595888	53595889	T	C	15	GENIC	homozygous	116887332
10	53596200	53596201	T	C	14	GENIC	homozygous	116887334
10	53597930	53597931	T	C	27	GENIC	homozygous	116887336
10	53600029	53600030	T	C	28	GENIC	homozygous	116887338
10	53600073	53600074	A	G	35	GENIC	homozygous	116887340
10	53600376	53600377	G	C	32	GENIC	homozygous	116887342
10	53601096	53601097	C	T	27	GENIC	homozygous	116887344
10	53601524	53601525	T	C	12	GENIC	homozygous	116887346
10	53602828	53602829	A	G	15	GENIC	homozygous	117078809
10	53602896	53602897	T	C	14	GENIC	homozygous	116887348
10	53603902	53603903	A	G	26	GENIC	homozygous	116887350
10	53604160	53604161	A	G	42	GENIC	homozygous	116887352
10	53604349	53604350	A	G	25	GENIC	homozygous	116887354
10	53604896	53604897	G	A	33	GENIC	homozygous	116887356
10	53605006	53605007	C	A	26	GENIC	homozygous	116887358
10	53605117	53605118	T	C	33	GENIC	homozygous	116887360
10	53605274	53605275	T	C	38	GENIC	homozygous	116887362
10	53605952	53605953	A	G	30	GENIC	homozygous	116887364
10	53606461	53606462	A	G	19	GENIC	homozygous	116887366
10	53606719	53606720	C	T	20	GENIC	homozygous	116887368
10	53607446	53607447	A	G	31	GENIC	homozygous	116887370
10	53608104	53608105	C	G	25	GENIC	homozygous	116933687
10	53608437	53608438	A	G	42	GENIC	homozygous	116887372