chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	45323629	45323630	G	A	16	GENIC	homozygous	116583375
10	45326544	45326545	G	A	21	GENIC	homozygous	116583377
10	45327480	45327480		ACCT	23	GENIC	homozygous	128813927
10	45327573	45327574	C	T	29	GENIC	homozygous	116583379
10	45327733	45327739	CTCTCG		9	GENIC	homozygous	128813928
10	45329039	45329040	G		18	GENIC	homozygous	128813929
10	45329764	45329765	T	A	15	GENIC	homozygous	116583381
10	45329938	45329939	T	C	18	GENIC	homozygous	116583383
10	45330230	45330231	C	T	17	GENIC	homozygous	116583385
10	45330691	45330691		T	25	GENIC	heterozygous	128813931
10	45331613	45331613		G	18	GENIC	homozygous	128813932
10	45332032	45332033	C	T	37	GENIC	homozygous	116583387
10	45332542	45332543	T	C	30	GENIC	homozygous	116583389
10	45332640	45332641	C	T	31	GENIC	homozygous	116583391
10	45333385	45333386	A	G	23	GENIC	homozygous	116583393
10	45329919	45329920	T	A	21	GENIC	homozygous	128869007