chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	53625238	53625243	CTGTA		22	GENIC	homozygous	128818013
10	53632889	53632890	C	G	34	GENIC	heterozygous	117994484
10	53632908	53632909	A	G	32	GENIC	heterozygous	117994485
10	53632909	53632910	T	C	32	GENIC	heterozygous	117994486
10	53632912	53632913	C		32	GENIC	heterozygous	128818014
10	53632918	53632918		CAATC	28	GENIC	heterozygous	128818015
10	53633004	53633005	C	A	33	GENIC	heterozygous	117994487
10	53633010	53633011	C	T	34	GENIC	heterozygous	117994488
10	53633019	53633020	A	G	34	GENIC	heterozygous	117994489
10	53633023	53633024	A	G	35	GENIC	heterozygous	117994490
10	53633024	53633025	A	C	35	GENIC	heterozygous	117994491
10	53633058	53633059	G	A	40	GENIC	heterozygous	117994492
10	53633113	53633114	T	A	46	GENIC	heterozygous	117295412
10	53633103	53633104	C	T	48	GENIC	heterozygous	117295403
10	53633108	53633109	G	A	48	GENIC	heterozygous	117295405
10	53633109	53633110	T	C	48	GENIC	heterozygous	117295407
10	53633110	53633111	G	A	48	GENIC	heterozygous	117295410
10	53633115	53633116	G	T	46	GENIC	heterozygous	117295414
10	53633127	53633128	G	C	42	GENIC	heterozygous	117994493