chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	62353116	62353117	C	A	34	GENIC	homozygous	51472192
10	62354507	62354508	C	T	35	GENIC	homozygous	51900485
10	62354582	62354583	T	C	34	GENIC	homozygous	51472193
10	62354668	62354669	G	-	22	GENIC	homozygous	51900487
10	62354700	62354701	A	T	38	GENIC	homozygous	51472195
10	62354784	62354785	C	T	41	GENIC	homozygous	51900489
10	62355208	62355209	A	G	45	GENIC	homozygous	51900491
10	62356101	62356102	G	A	38	GENIC	homozygous	51900493
10	62356185	62356186	C	T	41	GENIC	homozygous	51900495
10	62356599	62356600	G	A	22	GENIC	homozygous	51900497
10	62358398	62358399	C	-	6	GENIC	homozygous	51472198
10	62359124	62359125	G	A	26	GENIC	possibly homozygous	51900499
10	62359125	62359126	T	C	26	GENIC	possibly homozygous	51900501
10	62359220	62359221	G	A	32	GENIC	homozygous	51900503
10	62359295	62359296	C	T	22	GENIC	homozygous	51900505
10	62359304	62359305	G	-	17	GENIC	homozygous	51472199
10	62359322	62359323	A	ACGCG	12	GENIC	homozygous	51900507
10	62359353	62359355	CT	--	19	GENIC	homozygous	51472201
10	62359366	62359367	A	C	21	GENIC	possibly homozygous	51472202
10	62359416	62359417	G	C	28	GENIC	homozygous	51472203
10	62359513	62359514	G	-	37	GENIC	homozygous	51900509
10	62359519	62359520	G	A	37	GENIC	homozygous	51472204
10	62359530	62359531	T	C	35	GENIC	homozygous	51900511
10	62359570	62359571	G	T	30	GENIC	homozygous	51900513
10	62360074	62360075	G	T	32	GENIC	possibly homozygous	51900515
10	62360407	62360408	G	A	41	GENIC	homozygous	51900517
10	62360905	62360906	C	T	43	GENIC	homozygous	51900519