Table I:

Genetic variation between C57BL/6 Reference and NOD/ShiLtJ strains within and +/− 1kb of Nfkbid (Chr 7: 30,120,157–30,129,171 (GRCm39))

Variant ID	Variant Class	Predicted Consequence	B6	NOD
rs3147809	SNP	upstream gene variant	T	C
rs3142468	SNP	upstream gene variant	A	G
rs8261832	SNP	intron variant	A	G
rs3147847	SNP	intron variant	T	G
rs3142508	SNP	intron variant	C	T
rs3147846	SNP	synonymous variant	T	C
rs3147845	SNP	intron variant	G	A
rs3142506	SNP	intron variant	G	A
rs3147844	SNP	synonymous variant	T	A
rs3142505	SNP	intron variant	A	G
rs3142504	SNP	intron variant	G	A
rs3147843	SNP	intron variant	C	T
rs3147842	SNP	intron variant	C	T
rs8261873	insertion	intron variant	-	T
rs3142503	SNP	intron variant	G	C
rs586927013	SNP	intron variant	G	A
rs258934926	SNP	intron variant	T	C
rs3142502	SNP	intron variant	G	A
rs3142501	SNP	intron variant	A	T
rs258679767	deletion	splice region variant	C	-
rs3147840	SNP	synonymous variant	C	T
rs3147839	SNP	synonymous variant	G	A
rs3147838	SNP	intron variant	C	T
rs3142500	SNP	non coding transcript exon variant	G	T
rs585933734	SNP	non coding transcript exon variant	G	A
rs3147837	SNP	intron variant	C	T
rs3142498	SNP	intron variant	A	G
rs3147836	SNP	intron variant	C	T
rs3147835	SNP	intron variant	C	G
rs3147834	SNP	intron variant	T	C
rs3142497	SNP	intron variant	G	A
rs3142496	SNP	intron variant	C	T
rs3142495	SNP	intron variant	T	G
rs3142494	SNP	synonymous variant	A	G
rs3142493	SNP	intron variant	A	G
rs252747946	SNP	intron variant	G	C
rs225186782	SNP	intron variant	G	A
rs46738579	SNP	intron variant	T	G
rs8261888	SNP	intron variant	C	T
rs8261887	SNP	intron variant	C	G
rs8261886	SNP	intron variant	T	C
rs8261885	SNP	intron variant	G	A
rs32265778	SNP	intron variant	A	T
rs263326630	deletion	intron variant	TGATCTTAAATG	-
rs3142492	SNP	splice region variant	C	T
rs3147832	SNP	3' UTR variant	C	T
rs3142491	SNP	3' UTR variant	G	A