chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	63616127	63616128	T	G	37	GENIC	homozygous	51672433
10	63616950	63616953	TTT	---	7	GENIC	heterozygous	52381118
10	63617224	63617225	C	CGA	11	GENIC	homozygous	51672435
10	63617888	63617889	G	GTTTGT	13	GENIC	homozygous	51672443
10	63619603	63619604	A	C	14	GENIC	homozygous	51672445
10	63621518	63621519	C	T	23	GENIC	homozygous	51672447
10	63619563	63619564	C	G	11	GENIC	homozygous	51475133
10	63621926	63621927	T	A	27	GENIC	homozygous	51672451
10	63622117	63622118	A	C	14	GENIC	homozygous	51475138
10	63622138	63622139	A	G	15	GENIC	homozygous	51672454
10	63626047	63626048	T	G	18	GENIC	homozygous	51672456
10	63626448	63626449	T	C	13	GENIC	homozygous	51672458
10	63626818	63626819	A	G	7	GENIC	homozygous	51475140
10	63627853	63627854	C	G	28	GENIC	homozygous	51672460
10	63628454	63628455	C	CCCTCCTGTGATGTTAAGAT	12	GENIC	homozygous	51672462
10	63628576	63628577	T	G	13	GENIC	homozygous	51672464
10	63630423	63630424	A	C	22	GENIC	homozygous	51672466
10	63631950	63631951	G	T	12	GENIC	homozygous	51475143
10	63632070	63632071	T	G	18	GENIC	homozygous	51672468
10	63632141	63632142	G	A	19	GENIC	homozygous	51672470
10	63633397	63633398	A	AG	8	GENIC	homozygous	51475146