chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	45762000	45762001	G	T	25	GENIC	homozygous	116931032
10	45764787	45764788	T	C	12	GENIC	homozygous	116584426
10	45766214	45766215	G	C	24	GENIC	homozygous	116584432
10	45766473	45766474	G	C	24	GENIC	homozygous	116584434
10	45766924	45766925	A	C	16	GENIC	homozygous	116877338
10	45766948	45766949	T	A	15	GENIC	homozygous	116931034
10	45766953	45766954	A	G	16	GENIC	homozygous	116877340
10	45770919	45770920	A	T	23	GENIC	homozygous	116931036
10	45775097	45775098	G	A	25	GENIC	homozygous	116931038
10	45780337	45780338	C	T	12	GENIC	homozygous	116877346
10	45781101	45781102	C	T	13	GENIC	homozygous	116931040
10	45781562	45781563	C	T	18	GENIC	homozygous	116584456
10	45787945	45787946	G	A	22	GENIC	homozygous	116931042
10	45788305	45788306	A	C	21	GENIC	homozygous	116931044
10	45790485	45790486	A	G	27	GENIC	homozygous	116931046
10	45791312	45791313	A	G	32	GENIC	homozygous	116771938
10	45792734	45792735	G	A	21	GENIC	homozygous	117993384
10	45795615	45795616	G	A	27	GENIC	homozygous	116584478
10	45796109	45796110	T	C	25	GENIC	homozygous	116931048