chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	51480694	51480695	C	T	65	GENIC	homozygous	116594340
10	51481807	51481808	T	C	22	GENIC	homozygous	116594342
10	51481955	51481956	T	A	48	GENIC	homozygous	116594344
10	51482230	51482231	T	C	44	GENIC	homozygous	116594346
10	51482598	51482599	T	C	40	GENIC	homozygous	116594348
10	51483679	51483680	G	A	57	GENIC	homozygous	116594350
10	51484093	51484094	T	A	64	GENIC	homozygous	116594352
10	51489427	51489428	A	G	57	GENIC	homozygous	116594354
10	51489727	51489728	G	A	60	GENIC	homozygous	116594356
10	51491062	51491063	G	A	17	GENIC	homozygous	116933225
10	51491110	51491110		TGGG	10	GENIC	homozygous	128817073
10	51491112	51491112		T	10	GENIC	homozygous	128817074
10	51491115	51491115		G	9	GENIC	homozygous	128817075
10	51491116	51491116		T	9	GENIC	homozygous	128817076
10	51491118	51491118		GTGGT	9	GENIC	homozygous	128817077
10	51491119	51491119		GAGCGCTTGC	12	GENIC	homozygous	128817078
10	51491122	51491123	A	G	11	GENIC	homozygous	123358698
10	51491123	51491124	T	C	11	GENIC	homozygous	123358699
10	51491126	51491126		G	10	GENIC	homozygous	128817079
10	51491128	51491129	G		10	GENIC	homozygous	128817080
10	51491205	51491205		GTGTGGCTTGGGGAGGAACC	50	GENIC	homozygous	128817081
10	51495136	51495137	G	T	46	GENIC	possibly homozygous	116594358
10	51496075	51496075		G	59	GENIC	homozygous	128817082
10	51498746	51498747	A	G	65	GENIC	homozygous	116594360
10	51498981	51498982	A	C	56	GENIC	possibly homozygous	116777966
10	51500072	51500073	G	A	52	GENIC	homozygous	116594362
10	51495796	51495797	G	A	49	GENIC	homozygous	117994125