chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	1470219	1470220	T	C	9	GENIC	homozygous	117974635
10	1470228	1470229	A	C	9	GENIC	homozygous	117974636
10	1470262	1470263	A	G	7	GENIC	possibly homozygous	117974638
10	1470268	1470269	C	T	7	GENIC	possibly homozygous	117974640
10	1470294	1470295	A	C	11	GENIC	possibly homozygous	117974642
10	1470346	1470347	T	C	15	GENIC	heterozygous	117974644
10	1476299	1476300	T	G	13	GENIC	homozygous	116975167
10	1476477	1476478	T	C	4	GENIC	homozygous	116975170
10	1476544	1476545	T	C	24	GENIC	homozygous	116910609
10	1476668	1476669	T	G	13	GENIC	homozygous	117974650
10	1490196	1490197	C	G	30	GENIC	heterozygous	117974652
10	1490197	1490198	T	G	30	GENIC	heterozygous	117974654
10	1492883	1492884	A	G	30	GENIC	heterozygous	118059890
10	1494848	1494849	C	T	41	GENIC	heterozygous	117974656
10	1476795	1476796	A	C	18	GENIC	homozygous	117215028