chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	45323629	45323630	G	A	17	GENIC	homozygous	116583375
10	45326544	45326545	G	A	15	GENIC	homozygous	116583377
10	45327480	45327480		ACCT	16	GENIC	homozygous	128813927
10	45327573	45327574	C	T	21	GENIC	homozygous	116583379
10	45327733	45327739	CTCTCG		10	GENIC	homozygous	128813928
10	45329039	45329040	G		15	GENIC	homozygous	128813929
10	45329764	45329765	T	A	17	GENIC	homozygous	116583381
10	45329938	45329939	T	C	13	GENIC	homozygous	116583383
10	45330230	45330231	C	T	15	GENIC	homozygous	116583385
10	45332032	45332033	C	T	13	GENIC	homozygous	116583387
10	45332542	45332543	T	C	17	GENIC	homozygous	116583389
10	45332640	45332641	C	T	14	GENIC	homozygous	116583391
10	45333385	45333386	A	G	21	GENIC	homozygous	116583393
10	45330691	45330691		T	10	GENIC	possibly homozygous	128813931
10	45331613	45331613		G	18	GENIC	homozygous	128813932
10	45329919	45329920	T	A	17	GENIC	homozygous	128869007
10	45329925	45329926	T	A	17	GENIC	homozygous	132882973