iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

Bfar

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs4163487	snp	A/G	0.274723	0.248775	intron-variant, missense	Bfar, 3110001I22Rik	Mm_Celera	16:13677895	TTCAGTTTGCGCTCC[A/G]GCAGAATTTACATGA	67118
rs4163488	snp	A/T	0.375	0.216506	intron-variant	Bfar	Mm_Celera	16:13696705	CCTTTATTCACTGAG[A/T]TATCTTGCCTAAGCT	67118
rs6389023	snp	G/T	0.244898	0.249948	intron-variant	Bfar	Mm_Celera	16:13690920	CACCATACATGGATG[G/T]TTTTAACAGTGAGTT	67118
rs6389537	snp	G/T	0.5	0	intron-variant	Bfar	Mm_Celera	16:13691008	GTTTTCTTTCTTTTA[G/T]AGATANNTATTTTTT	67118
rs6389550	snp	A/G	0.5	0	intron-variant	Bfar	GRCm38.p3	16:13691014	TTTCTTTTANAGATA[A/G]NTATTTTTTAAAATT	67118
rs6389551	snp	A/C	0.5	0	intron-variant	Bfar	Mm_Celera	16:13691015	TTCTTTTANAGATAN[A/C]TATTTTTTAAAATTT	67118
rs6389570	snp	C/T	0.5	0	intron-variant	Bfar	Mm_Celera	16:13691031	TATTTTTTAAAATTT[C/T]Atctatttttatatg	67118
rs6403876	snp	C/T	0.5	0	intron-variant	Bfar	Mm_Celera	16:13691299	ATCTCAGTACAATCA[C/T]TGTTTTGGGGTAttt	67118
rs6403919	snp	A/G	0.5	0	intron-variant	Bfar	Mm_Celera	16:13691321	GGGGTAttttttgaa[A/G]tggagatcttgatat	67118
rs13471626	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13703498	gaaggagagagtcag[A/G]gagaCTTGGTAATTC	67118
rs13471627	snp	A/T			missense	Bfar	Mm_Celera	16:13702238	AGGAAGTCCGACGGC[A/T]GGAAACCCAAGTGTT	67118
rs45670848	snp	A/G	0.277778	0.248452	intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678565	AATCCCAGCATCAAA[A/G]TGAATATTTTAAACC	67118
rs45799154	snp	C/T	0.277778	0.248452	intron-variant	Bfar	GRCm38.p3	16:13684562	TCCCCAAGCTCTTGT[C/T]GTCGTGGCCGCTGTG	67118
rs45928616	snp	C/G	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13701272	TTCCATGGCCAAGCT[C/G]AAGGTATAAAGCATA	67118
rs45977180	snp	A/G	0.493827	0.0552116	intron-variant	Bfar	GRCm38.p3	16:13679171	CCGGTTTGATTGTGA[A/G]TGTTCTCTGTGGAAC	67118
rs45990034	snp	A/G	0.391111	0.206368	intron-variant, utr-variant-3-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13678243	TGTATGGCTCAGTGT[A/G]CTTTACAGTTAGATT	67118
rs46017551	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13690344	GGTAAACCTGGGTTA[A/T]ACATCACACCCTGTC	67118
rs46019810	snp	A/G	0.142012	0.225474	intron-variant	Bfar	Mm_Celera	16:13690894	ATTCTCTACCACTGA[A/G]CTGTGTCTCCCACCA	67118
rs46027378	snp	A/G	0.489796	0.070696	intron-variant	Bfar, 3110001I22Rik	GRCm38.p3	16:13675033	ATGGTGAATGAGGGG[A/G]AAAATTCAGTTCAAT	67118
rs46044794	snp	A/C	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13694051	CAGGTCACAAATAAT[A/C]CACAGCTTCATCTTT	67118
rs46109823	snp	C/G	0.336735	0.234472	intron-variant	Bfar	Mm_Celera	16:13694103	TCATTGTGACGGTAT[C/G]AGTTGATTCTCCCCC	67118
rs46147051	snp	C/T	0.142012	0.225474	intron-variant, missense	Bfar	Mm_Celera	16:13688838	TAGATAAGTGGACGA[C/T]GGAAGAAGTTGTCCT	67118
rs46149705	snp	A/G	0.231111	0.249285	intron-variant	Bfar	Mm_Celera	16:13697851	TCACGGTAGTAAGCC[A/G]TGGCCCAGGATGTGA	67118
rs46245581	snp	A/G	0.32	0.24	intron-variant	Bfar	Mm_Celera	16:13693410	AAGTTGCTTGAGAGA[A/G]GTCTTGTTGTCTTTG	67118
rs46250200	snp	C/T	0.124444	0.216185	upstream-variant-2KB	Bfar, 3110001I22Rik, Parn	GRCm38.p3	16:13670047	ACTATGCATATCTAT[C/T]TCCCTTCTTGCTTAA	67118
rs46281976	snp	C/T	0.165289	0.235211	upstream-variant-2KB	Bfar, 3110001I22Rik	GRCm38.p3	16:13671104	GCCTCTGCTGGCTTA[C/T]AGGAGATAAGAGTTT	67118
rs46343127	snp	C/T	0.459184	0.136902	intron-variant, utr-variant-5-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13676937	ACATCTCCTAGAGTC[C/T]AGCCTATCTAGTGTG	67118
rs46548249	snp	C/T	0.152778	0.230321	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674625	TTTAGTCTTATTTTC[C/T]TTTTCCATAGCAGGG	67118
rs46571207	snp	A/T	0.408163	0.193609	intron-variant	Bfar	Mm_Celera	16:13680165	GGCTATGGAACCTAC[A/T]TGTTTCCACCTGTCA	67118
rs46605412	snp	C/G	0.336735	0.234472	intron-variant	Bfar	Mm_Celera	16:13700103	AGTAGACCAAGGTCA[C/G]AAAATGCTAGGACTA	67118
rs46616049	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13690480	TCTCTACCATTGAAA[C/T]CCTCCCCAGCCCTAG	67118
rs46637094	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13699165	CTGGCATGGGGGATG[A/G]GGTTGCCTAGCGCCC	67118
rs46701843	snp	C/T	0.426035	0.177515	intron-variant	Bfar	Mm_Celera	16:13693950	TAATTTTAATGGTTA[C/T]AACAAATCATGCTGC	67118
rs46869703	snp	A/G	0.489796	0.070696	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673706	TTAATCATCAAAGAC[A/G]GTTTGGATCTTGTGA	67118
rs46969771	snp	A/G	0.132653	0.220748	intron-variant	Bfar, 3110001I22Rik	GRCm38.p3	16:13676557	TGATATAACCAGCAC[A/G]GTATTGCTCTGGAGG	67118
rs47037279	snp	C/T	0.244898	0.249948	intron-variant	Bfar	Mm_Celera	16:13688473	CTTAAGTCCAGTCCT[C/T]TGAAGTTCTTAATGT	67118
rs47081610	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690163	GTGAAACCCTGTCTC[A/G]AGGGGAAAATAATAA	67118
rs47177442	snp	A/T	0.277778	0.248452	intron-variant	Bfar	GRCm38.p3	16:13684481	TAGCGGGTCTCATGC[A/T]GGAGGTGGTGTGCTT	67118
rs47227380	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13699221	AACCTCAGAGCATCT[A/G]GCATCCTCTTCTGGC	67118
rs47236061	snp	A/T	0.142012	0.225474	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676289	AACCATTGTTCTAGT[A/T]CCTTAATAGGCAAAA	67118
rs47385146	snp	A/G	0.132653	0.220748	intron-variant, utr-variant-5-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13676864	CCTCTAACTGCTCCT[A/G]TGGCAGCCTGCGTAC	67118
rs47452457	snp	C/T	0.244898	0.249948	utr-variant-5-prime	Bfar	Mm_Celera	16:13685119	CTATGTGTATGGATC[C/T]CAGAATTTGCTGAGA	67118
rs47468544	snp	C/T	0.231111	0.249285	intron-variant	Bfar	Mm_Celera	16:13698313	TGTATATGAATGTGA[C/T]ATTGGTGCATATGTG	67118
rs47501759	snp	A/G	0.132653	0.220748	utr-variant-5-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13672059	GCGGTGACAGAGTGG[A/G]TACCAGGACTAGTGG	67118
rs47544365	snp	C/T	0.152778	0.230321	upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670637	ATAGCTAAGTCTCCA[C/T]AGTCTTAAACTTTTT	67118
rs47564034	snp	A/C	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13698751	TTTGAAGGCAGCTAG[A/C]TATAACCAGGTGTTG	67118
rs47623983	snp	C/T	0.260355	0.249785	intron-variant	Bfar	Mm_Celera	16:13684329	CCAGGAGTGAATACA[C/T]GTGGCTTGTTATATC	67118
rs47737883	snp	A/G	0.244898	0.249948	intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678815	CCCAACACAGCTTAA[A/G]GCAATCTGTTCAGAC	67118
rs47755656	snp	A/G	0.497778	0.0332592	intron-variant	Bfar, 3110001I22Rik	GRCm38.p3	16:13675375	TAAGAGATGACTAAA[A/G]GAGCCTGGTGGTGGT	67118
rs47781943	snp	C/T	0.132653	0.220748	intron-variant	Bfar	Mm_Celera	16:13678952	TGGAAATGCTTTCTG[C/T]CTTATTAATGGAAGA	67118
rs47788856	snp	A/T			intron-variant	Bfar	GRCm38.p3	16:13695617	CACCATGCTGCTAGG[A/T]CTACACGCCTTCCTC	67118
rs47809744	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13689920	CCCAGCAGCCACATG[G/T]TGGCTTACAACCATC	67118
rs47860036	snp	A/G	0.32	0.24	intron-variant	Bfar	Mm_Celera	16:13691657	AATAGTGTTCAGTTG[A/G]ATTTCCTTCTAGTTT	67118
rs47972379	snp	G/T	0.32	0.24	intron-variant	Bfar	Mm_Celera	16:13684424	ATTTTGTTGTATAGC[G/T]CTCCTAAGTAATTTA	67118
rs48005213	snp	C/T	0.244898	0.249948	intron-variant	Bfar	GRCm38.p3	16:13687336	CTGGTGGGTGTAGTC[C/T]CTGAATGCTATATCT	67118
rs48199348	snp	A/G	0.408163	0.193609	intron-variant	Bfar	Mm_Celera	16:13700464	ATAACTTCCAGATTA[A/G]TGTAGGATGAGAACA	67118
rs48243762	snp	A/G	0.277778	0.248452	downstream-variant-500B	Bfar	Mm_Celera	16:13703631	TTATAGAGAAATCTG[A/G]TTGCTAAGGAAATAG	67118
rs48253436	snp	A/G	0.132653	0.220748	intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678772	GACAGGCTTAGCCTA[A/G]TGCCCTTCTCAGCCT	67118
rs48290907	snp	A/C	0.336735	0.234472	intron-variant	Bfar	Mm_Celera	16:13679212	CTAACAGTTGGAGTT[A/C]ATGTCCCAGATAGTA	67118
rs48298575	snp	G/T	0.244898	0.249948	intron-variant	Bfar	Mm_Celera	16:13692306	ATTCATCAACACAGC[G/T]TTTAATGTTCAGCCT	67118
rs48304681	snp	C/T	0.142012	0.225474	utr-variant-5-prime	Bfar	Mm_Celera	16:13685075	AGACTTTATGATGCA[C/T]TGCAGCAGTGTCCTG	67118
rs48344242	snp	C/T	0.444444	0.157135	intron-variant	Bfar	GRCm38.p3	16:13698806	AAACGTAAAGCTCAT[C/T]CATCGACATTACTTG	67118
rs48371934	snp	C/T	0.336735	0.234472	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673972	ATCAGAGTAAACTTT[C/T]ATTCCTGGCAGGGCA	67118
rs48405547	snp	A/G	0.231111	0.249285	intron-variant	Bfar	Mm_Celera	16:13681933	TCCCATTAAGAGCAA[A/G]ACCTGAGAACTCCTG	67118
rs48483996	snp	C/T	0.132653	0.220748	intron-variant, missense	Bfar, 3110001I22Rik	GRCm38.p3	16:13677415	CAGAGCTTAGGAAGT[C/T]CGAGCATGCTCATTC	67118
rs48585717	snp	A/G	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13681337	ACCAGACAACTTAGA[A/G]CAGGAATGGACAAGT	67118
rs48602962	snp	C/T	0.142012	0.225474	upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671652	ACCCCAAATTCCGAC[C/T]CTATAAATAAAACTT	67118
rs48605896	snp	A/G	0.408163	0.193609	intron-variant	Bfar	Mm_Celera	16:13679958	AAGAGAGGATTGAAA[A/G]AAAAAGTTTTAGGCT	67118
rs48611555	snp	A/G	0.124444	0.216185	intron-variant	Bfar, 3110001I22Rik	GRCm38.p3	16:13675600	GAAAGTCCCGGAGGA[A/G]ACACCAAAGGAGGAC	67118
rs48665769	snp	A/G	0.336735	0.234472	intron-variant, missense	Bfar, 3110001I22Rik	Mm_Celera	16:13677565	GTTTAAACAAACTCA[A/G]AAGGCTTGATGAAAA	67118
rs48668766	snp	A/G	0.375	0.216506	intron-variant	Bfar	Mm_Celera	16:13679378	TATTTTATGTGTATT[A/G]AGATTTTTATTTTAG	67118
rs48722655	snp	A/G	0.297521	0.245442	intron-variant	Bfar, 3110001I22Rik	GRCm38.p3	16:13676636	CTATTGAGGGACAAG[A/G]CCAACCTGGGAGGGT	67118
rs48842361	snp	A/G	0.444444	0.157135	upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670572	TTTACCAACTTGAAA[A/G]GAACACTCTCATTTA	67118
rs48877736	snp	A/T	0.18	0.24	utr-variant-3-prime	Bfar	Mm_Celera	16:13703007	GAGAAAACTTCAGGC[A/T]AAGAGACAGTGCTGC	67118
rs48917079	snp	A/G	0.132653	0.220748	intron-variant	Bfar	Mm_Celera	16:13695064	AGATAACTGACACAT[A/G]TACACAAACACCCAC	67118
rs49044297	snp	A/G	0.260355	0.249785	intron-variant	Bfar	Mm_Celera	16:13700476	TTAATGTAGGATGAG[A/G]ACATTGGGCTACCTA	67118
rs49090431	snp	C/T	0.391111	0.206368	downstream-variant-500B	Bfar	Mm_Celera	16:13703745	GCTTAGAGATTTCTA[C/T]AGGAAGGGACGAGTC	67118
rs49096758	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13690353	GGGTTATACATCACA[C/T]CCTGTCTCAAAAAAA	67118
rs49161310	snp	A/G	0.152778	0.230321	intron-variant	Bfar	Mm_Celera	16:13692378	AGTGTGTAAGCACGC[A/G]TTGTCTGCATCCTGT	67118
rs49277348	snp	C/T	0.124444	0.216185	intron-variant	Bfar	Mm_Celera	16:13698293	CTTATTTTTGACTTT[C/T]TGTGTGTATATGAAT	67118
rs49383365	snp	C/T	0.408163	0.193609	intron-variant	Bfar	Mm_Celera	16:13697781	AGATTTGGCAGAACC[C/T]CTAAAGAGTAGTAGT	67118
rs49492871	snp	C/T	0.336735	0.234472	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673529	AACTGAGTCTAGAAA[C/T]CTGGACTTATGCAAA	67118
rs49551488	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13695630	GGACTACACGCCTTC[C/T]TCACCATGCTGCTAG	67118
rs49571937	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13689976	TAGCTACATAGTATG[C/T]TCATATACGTAAAAT	67118
rs49644714	snp	A/G	0.336735	0.234472	intron-variant	Bfar	Mm_Celera	16:13701010	CCCAGAGATGCAAAT[A/G]CTCTCCTCGGGGCTG	67118
rs49819365	snp	C/T	0.408163	0.193609	downstream-variant-500B	Bfar	Mm_Celera	16:13704093	TAGCTTCCGTTAGAG[C/T]GGGCATGCTCAGATC	67118
rs49876216	snp	A/G	0.124444	0.216185	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676331	CTAGGTCACGTGTAT[A/G]ATTCAAGATTGGTTA	67118
rs49886524	snp	A/C	0.391111	0.206368	synonymous-codon	Bfar	Mm_Celera	16:13697386	TCTCAAGAGCTCACC[A/C]AGACTTGGCTTGCTA	67118
rs49946225	snp	A/C/T	0.277778	0.248452	intron-variant	Bfar	Mm_Celera	16:13679903	GTCATCTCTTCAGAC[A/C/T]CAAAGTGGGGTTGTT	67118
rs50068107	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690164	TGAAACCCTGTCTCG[A/G]GGGGAAAATAATAAT	67118
rs50119351	snp	C/T	0.124444	0.216185	intron-variant	Bfar	GRCm38.p3	16:13699501	TTAGGTTTCTAATGC[C/T]GTGCTAAAACACTGT	67118
rs50128825	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13690173	GTCTCGAGGGGAAAA[A/T]AATAATAATAATAGT	67118
rs50363818	snp	G/T	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13698237	AATCTTCCACAACTC[G/T]ACAATAAACATCTCA	67118
rs50432716	snp	C/G	0.391111	0.206368	synonymous-codon	Bfar	Mm_Celera	16:13698950	GTACCAGCTGATCGC[C/G]GAGTTTGCCTGGGAC	67118
rs50538488	snp	A/G	0.336735	0.234472	intron-variant	Bfar	Mm_Celera	16:13693472	CCTGGAGCTACCACT[A/G]TAAAGGTAAAATGGC	67118
rs50599551	snp	A/G	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13693196	TTCCTGTTGATAGTC[A/G]CAATTTTTCTGTTGT	67118
rs50616396	snp	C/G	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13700400	AGGCCAGAGAGACAT[C/G]ATGTGAATTTTATAG	67118
rs50637453	snp	C/T	0.408163	0.193609	utr-variant-3-prime	Bfar	Mm_Celera	16:13703115	ACCAGGCCGAGTCTT[C/T]TTAGATGACTGAGCA	67118
rs50823047	snp	C/T	0.260355	0.249785	intron-variant	Bfar	Mm_Celera	16:13681800	GCAAGACCTAAGCTA[C/T]CATTTTCTCAACCTG	67118
rs50892295	snp	C/T	0.493827	0.0552116	intron-variant	Bfar	Mm_Celera	16:13693134	CTCTAGTTCATTCCA[C/T]CTTTTTGATGGAATT	67118
rs50925512	snp	C/T	0.336735	0.234472	upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671062	GCTAACTGACTGTCT[C/T]CTCCTAAATCGGGTT	67118
rs50933803	snp	C/T	0.391111	0.206368	intron-variant	Bfar	Mm_Celera	16:13697625	AGAAAGTGTGACCCT[C/T]TCCTGGAAGCCAACT	67118
rs50960448	snp	A/T	0.408163	0.193609	intron-variant	Bfar	Mm_Celera	16:13680243	TTTAATGTACATTGG[A/T]GGTGTGTCCATGTGA	67118
rs51001317	snp	C/G	0.277778	0.248452	intron-variant	Bfar	Mm_Celera	16:13687196	GAAAAAGACTTGTAC[C/G]TAAATATCTCATTTG	67118
rs51018010	snp	G/T	0.124444	0.216185	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672934	AAACCTGATGGGAAA[G/T]CTGTACTCTGTCCAG	67118
rs51163027	snp	A/T	0.152778	0.230321	intron-variant	Bfar	Mm_Celera	16:13685887	ACACTTCTTTCTGAT[A/T]TATGCTTATGAGTAA	67118
rs51207248	snp	C/G	0.124444	0.216185	utr-variant-3-prime	Bfar	GRCm38.p3	16:13703328	ATGACCGTTATGCCC[C/G]TGTAGACATAGTGTA	67118
rs51308592	snp	A/T	0.132653	0.220748	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13675969	TGAATCATGTTAGCA[A/T]TTCTGCTTTTGGCAG	67118
rs51498227	snp	C/T	0.231111	0.249285	intron-variant	Bfar	Mm_Celera	16:13699405	TTTGTGTCCAGGAGG[C/T]AGTCTTCATTTCATA	67118
rs51551592	snp	C/T	0.124444	0.216185	intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673216	AGCCCAGGTTGGCCT[C/T]GCTCTGAAGACTTAA	67118
rs51622285	snp	C/T	0.277778	0.248452	downstream-variant-500B	Bfar	Mm_Celera	16:13703616	ATACAAATACAACCT[C/T]TATAGAGAAATCTGA	67118
rs51675784	snp	C/T	0.408163	0.193609	intron-variant	Bfar	Mm_Celera	16:13693774	CAAGAAAAACGTAGA[C/T]TAGCTAGGTAGAATG	67118
rs51676741	snp	A/G	0.152778	0.230321	intron-variant	Bfar	Mm_Celera	16:13692172	AGTCACTTTATTTCT[A/G]AAACCAGGTTTTGAT	67118
rs51918924	snp	A/G	0.152778	0.230321	intron-variant	Bfar	Mm_Celera	16:13686669	GCCTTGGAGGCTCTC[A/G]TTCTTTTTCTTCTTA	67118
rs51919140	snp	A/G	0.391111	0.206368	utr-variant-3-prime	Bfar	Mm_Celera	16:13703308	AGTATGGAGTAAGCT[A/G]AAGGATGACCGTTAT	67118
rs51978395	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13699503	AGGTTTCTAATGCCG[C/T]GCTAAAACACTGTGA	67118
rs52011591	snp	A/T	0.142012	0.225474	upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671409	GCAAACAGTTTATTA[A/T]ATCAGAACTGAGAAA	67118
rs52049870	snp	A/G	0.336735	0.234472	upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671107	TCTGCTGGCTTATAG[A/G]AGATAAGAGTTTAAA	67118
rs52147376	snp	A/G	0.124444	0.216185	upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671331	CCGAGTTGGCTATTA[A/G]CACGTTTTTATAAAG	67118
rs52178058	snp	C/T	0.244898	0.249948	intron-variant	Bfar	Mm_Celera	16:13687872	CAAGACTTGAGAAAC[C/T]ATGTCTGCACTGTTA	67118
rs52268407	snp	C/G	0.244898	0.249948	intron-variant	Bfar	Mm_Celera	16:13685000	ACTTGAGTAGAATGA[C/G]AGTAATCTTACACAG	67118
rs52277947	snp	A/G	0.152778	0.230321	intron-variant	Bfar	GRCm38.p3	16:13685021	TCTTACACAGCGACC[A/G]TTCATTCATCCTGTT	67118
rs52415055	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13699319	AAAATAAAGTCTTTT[A/T]AAAAAATTCTACCTT	67118
rs52489466	snp	A/G	0.142012	0.225474	intron-variant	Bfar	Mm_Celera	16:13681661	CCCAAGTTATCAGAG[A/G]CTACTCTTTTAAACC	67118
rs52531729	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13700068	TTGTCCTGCTTTGTA[A/G]CTCTGTCTAGCTACT	67118
rs211741364	snp	A/T			intron-variant, utr-variant-5-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13676933	GTTCACATCTCCTAG[A/T]GTCTAGCCTATCTAG	67118
rs211798191	snp	C/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676225	TATGGTTGGGGGTCA[C/T]CACACATGAGGAACT	67118
rs211798459	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13686553	CAACCACTGAGCCAT[C/T]TCTCCAGCCCTTGAT	67118
rs211842035	in-del	-/AA			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674111	GAGGAACATTTGAAG[-/AA]AAAAAAAAAAAACAC	67118
rs211863078	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13685498	AGATTACTCTAGGAG[A/C]TTGGAACCAAAAGCC	67118
rs211960452	in-del	-/AG			intron-variant	Bfar	Mm_Celera	16:13685823	TCCATGGGAAGAAAC[-/AG]AGATACATTTCTGGT	67118
rs211977620	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13696176	TTAACATGTAGCCCT[C/G]GCTGTCCTAGAGCTC	67118
rs212034943	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13696853	CGAACACAGAAATCC[A/G]ACTGCCTCTGCCTCC	67118
rs212087826	in-del	-/GCCC			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13675758	CTGCAAATATTTAGA[-/GCCC]CACTTTGCAGCTATT	67118
rs212291997	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674188	TTAGTAATAGAAGGA[A/G]CTCCTGTGAGTTGTG	67118
rs212310452	in-del	-/AAACAAAC			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671283	GAAACCCTGTCTCGA[-/AAACAAAC]AAACAAACAAACAAA	67118
rs212421386	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13682967	TGCCCTCTTCTGTAC[A/G]TCTGAAGTCAGCTAC	67118
rs212482724	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13682143	GGCCAAGAACTCAGA[C/T]ACTCAAATGCCTCTG	67118
rs212543791	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13692658	AATCACCTTCCTGCT[C/T]ACTGTGTAACTTAAG	67118
rs212586333	in-del	-/ACAG			intron-variant	Bfar	Mm_Celera	16:13681337	ACCAGACAACTTAGA[-/ACAG]GAATGGACAAGTTCA	67118
rs212942793	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13680870	CAAAGAGCTTGCTCT[C/T]CTTTCCTCCTATATA	67118
rs213005315	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13680304	GACTGCTGTGAGTTG[G/T]CGAGTGGGTGCTGGG	67118
rs213011289	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13691615	ACCGCTGAGCCATCT[C/T]TCCAGCCCCACAACG	67118
rs213077713	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690701	GGAGAAAGGCGGGAA[A/G]GGAATGGGGAGTGGG	67118
rs213096973	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13701417	GCTCCAGGCAAACAG[A/G]CTACCACAATGTTTC	67118
rs213350028	snp	G/T			upstream-variant-2KB	Bfar, 3110001I22Rik, Parn	Mm_Celera	16:13670106	GTTCCAGGACAACCA[G/T]GGGTACACAGAGAAA	67118
rs213521117	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13679306	ATAAAGGAGTGAGTC[A/G]TACTTATTAAGTACT	67118
rs213575815	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13687820	CTTCAGTGGTGTCAT[A/G]ATGACCCCCATTTTA	67118
rs213637722	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13686944	ACCAAACTCACACAT[C/T]GGACACATATGTGAA	67118
rs213641945	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13698680	TGATAAATTTTTATT[C/T]AATTTAGCCATGCAC	67118
rs213682439	snp	C/T			intron-variant, synonymous-codon	Bfar, 3110001I22Rik	Mm_Celera	16:13677257	CTCTTCTTCCCATTA[C/T]TCAGAACAGCAGTCT	67118
rs214068612	snp	C/T			synonymous-codon	Bfar	Mm_Celera	16:13685246	CTCCTGCCACTGCTG[C/T]TACGACACCCTGGTT	67118
rs214127943	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13696718	AGTTATCTTGCCTAA[C/G]CTAATACTGTTTGTT	67118
rs214133529	in-del	-/TAAGAGCC			intron-variant	Bfar	Mm_Celera	16:13693630	CTCTCCAAAGGCTTG[-/TAAGAGCC]TTTATGGAAGGAACT	67118
rs214202421	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13696103	GCTGCTAGGACTACA[C/T]GCCTTCTTCACCATG	67118
rs214229492	in-del	-/G			intron-variant	Bfar	Mm_Celera	16:13701851	CCAGGGCTACATAGA[-/G]AAAAAACCTGTCTTG	67118
rs214262573	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13694269	TGCAAATAAAACGAT[C/T]GATCAGGTGGCTTTC	67118
rs214455576	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13684545	TACACAGGTGTCTTA[A/G]CTCCCCAAGCTCTTG	67118
rs214565422	in-del	-/GGCCAA			intron-variant	Bfar	Mm_Celera	16:13701263	TGCTGTGCTTTCCAT[-/GGCCAA]GCTCAAGGTATAAAG	67118
rs214713775	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13692592	GGTATCTCGTGGGGG[G/T]TTTTTGTTTGTTTGT	67118
rs214777214	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13692084	CTAATTAAAAAAAAA[A/T]AAAGCAATATGACAG	67118
rs214777251	snp	A/G			utr-variant-3-prime	Bfar	GRCm38.p3	16:13703430	GACAGACGGACAGAC[A/G]GACAGACAGAATGTA	67118
rs214841364	snp	A/C			utr-variant-3-prime	Bfar	Mm_Celera	16:13702999	TAAACTCAGAGAAAA[A/C]TTCAGGCTAAGAGAC	67118
rs214969240	snp	A/G			utr-variant-5-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13672020	GAAGCCTTGTCCTCT[A/G]CTTCCGCGGGGTCCT	67118
rs215050314	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13682045	GTCCTGAGTTCAATT[C/T]CCAGCAACCACTTGG	67118
rs215119310	snp	A/G			upstream-variant-2KB	Bfar, Parn	Mm_Celera	16:13669930	ACATCACACAGGTGA[A/G]CAGCCTTGGGAAGAT	67118
rs215353178	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13699938	TGTGCTATTCTGCCT[A/G]GATCTTTGTGTTTGT	67118
rs215412084	snp	C/T			synonymous-codon	Bfar	Mm_Celera	16:13698914	GTGGAGAGAATTCCT[C/T]GTCAAGTACTCCTTT	67118
rs215546411	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13681040	TCTGGCTGTCCTAGA[A/T]CTCACTCTGTAGACC	67118
rs215572413	in-del	-/TTG			intron-variant	Bfar	Mm_Celera	16:13686398	TTTGTTTTTGTTTTT[-/TTG]TTTTTTTTAATATAA	67118
rs215793269	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13690671	TAGAGAAGTAGAGGC[C/T]GGCCATGAACACATG	67118
rs215876249	in-del	-/A			intron-variant	Bfar	Mm_Celera	16:13699692	CTCTTTTTTGAGGGG[-/A]AAAAAAAAATCAGTT	67118
rs216232703	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674374	CATGATGGTGTCCCA[A/G]CATTTAACAAGCCAA	67118
rs216235707	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13679548	AACAGTGTAGTTATT[A/T]ATAGTAATAAATAAA	67118
rs216286257	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673423	GCTTTATGTAATCCA[A/G]GCTGGCCAAGAATAA	67118
rs216310039	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13689897	TTCCAGAGGTCCTGA[A/G]TTCAATTCCCAGCAG	67118
rs216358478	snp	G/T			intron-variant, utr-variant-3-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13678084	CAGTTAAACATCTAG[G/T]AAACATCTGAAATGG	67118
rs216387655	in-del	-/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670647	TCCATAGTCTTAAAC[-/T]TTTTTTTTCTTTTTC	67118
rs216539750	snp	G/T			downstream-variant-500B	Bfar	Mm_Celera	16:13703864	CTTCCTTCCCATGAG[G/T]AGGTAGGGGCTGGCT	67118
rs216583146	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13685783	GTTACAGGCACAGGC[C/T]GACATGCCTAGCTGA	67118
rs216651101	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13696892	GGGATTAAAGGCGTG[C/T]GCCACCACTGCCCAG	67118
rs216743729	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671971	GCGGGAGCTGATCGT[A/G]GTCGGCCCCTAGGCC	67118
rs216798352	snp	A/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671169	CTGGTGGCGCATGCC[A/T]TTAATCCCAGCACTT	67118
rs216851920	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13681010	TGGTTTTCCGAGACA[A/G]TGTTTCTCTGTAGTT	67118
rs216917985	snp	C/T			intron-variant, missense	Bfar, 3110001I22Rik	Mm_Celera	16:13677069	GTCATCCTTGGTCAC[C/T]GTCCAGGATCAGTGT	67118
rs216991297	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13686892	GGAGGGGAGATCAGA[G/T]TCCTGAAAGTTGTCA	67118
rs217153823	in-del	-/TTT			intron-variant	Bfar	Mm_Celera	16:13686394	TGGTTTTTGTTTTTG[-/TTT]TTTTTTTTTTAATAT	67118
rs217188824	snp	G/T			upstream-variant-2KB	Bfar, Parn	Mm_Celera	16:13669859	CGAACATCTCCCCCA[G/T]GATGCTGACCTTCAG	67118
rs217246245	in-del	-/T			intron-variant	Bfar	Mm_Celera	16:13685561	CTTCCGTTTTATTTA[-/T]TTTTTTTAGGCAAGA	67118
rs217247236	in-del	-/TTCT			intron-variant	Bfar	Mm_Celera	16:13687892	TGCACTGTTACGGGA[-/TTCT]TTCTTTCTCTTCTTT	67118
rs217276990	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13679514	TCTGATGCCCTCTTC[A/T]GGTGTGTCTGAAGAC	67118
rs217311313	snp	A/T			intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678492	ATGTATCTGTGAGGT[A/T]CTGGGGATTACGCTC	67118
rs217448540	in-del	-/GGTA			intron-variant	Bfar	Mm_Celera	16:13694812	CAGGCTTGCCAAAAT[-/GGTA]GGTAGGGTTTAGGTC	67118
rs217499125	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13683282	CCAAAAACCCCTTCC[C/T]TCTGTAACTTGTCTT	67118
rs217596094	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13694099	ATCCTCATTGTGACG[G/T]TATGAGTTGATTCTC	67118
rs217607831	in-del	-/TT			intron-variant	Bfar	Mm_Celera	16:13683036	TATGTATAATAATAA[-/TT]ATTTTTAAAAAATGT	67118
rs217762947	in-del	-/T			intron-variant	Bfar	Mm_Celera	16:13690754	AAAGAGCTTTGGGGG[-/T]TTTTTTATTTTGTTT	67118
rs217970723	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674904	ACCTAGTCTGTCATA[A/G]TTAGGCATTTACATG	67118
rs218025670	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13684569	GCTCTTGTTGTCGTG[A/G]CCGCTGTGGGTAGCA	67118
rs218027443	snp	C/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673836	TAAGTCCTTTTAATT[C/G]ATGACAAGACCATAA	67118
rs218089976	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13683814	TACTAGACGCTGTAC[A/G]TGTATTAACTTATAG	67118
rs218114667	in-del	-/A			intron-variant	Bfar	Mm_Celera	16:13688931	TAAATGGAAGGTGAG[-/A]AAAAAAACCTGGCAC	67118
rs218367145	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13681105	TGCCTCCCAAGTGCT[A/G]GGACTAAAGGGTCTG	67118
rs218392011	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13691723	CGGGGCCTAGCAAAC[A/T]CAGAAGTGGATGCTC	67118
rs218419406	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13692166	AAAGCAAGTCACTTT[A/G]TTTCTAAAACCAGGT	67118
rs218421145	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13680556	GTGAGATAGGGTCTT[A/G]CTATGTAATTCTGCC	67118
rs218491987	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13702868	AGGTCTGTCCCATGA[A/G]TCAAATTTAGGAAAG	67118
rs218575628	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13701873	CCTGTCTTGAAAAAC[C/T]AAAGAGAAAGAAAAA	67118
rs218727500	in-del	-/AAAGCCGTATTCTAGGA			intron-variant	Bfar	Mm_Celera	16:13693721	TGTCAGGACACAGGT[-/AAAGCCGTATTCTAGGA]AAGAGAGCCAAGGAA	67118
rs218852006	in-del	-/C			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672950	TGTACTCTGTCCAGG[-/C]CTGTTCACACACACA	67118
rs218979263	in-del	-/TGTTTGTT			intron-variant	Bfar	GRCm38.p3	16:13696725	TGCCTAAGCTAATAC[-/TGTTTGTT]TGTTTGTTTGTTTGT	67118
rs219040946	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13679712	AAAAAAAGATTTTTA[C/T]TTATATGTATGTGTG	67118
rs219099269	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13690005	ATAAATAAAATCTTT[A/T]AAAAAAATAAGTAAC	67118
rs219151587	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13688414	TCTCCATCCCTGTTA[C/T]GGAATTCTTAAGAGC	67118
rs219154868	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13688222	TCTTGGGGGTCCTTC[A/G]TTTTTTTAAAAATTT	67118
rs219193184	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13689669	GCATGGTGGTGCAGG[C/T]CTTTAATCCCAGGAC	67118
rs219205108	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13699122	AGGAAATACCAATGA[C/G]GATGGTCCCTTTAAA	67118
rs219207591	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13687224	TTGGCTGTTTCCTTA[A/G]TGGTAGCACATAGAT	67118
rs219238920	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13698794	AGGGGTGTGTCCAAA[C/T]GTAAAGCTCATTCAT	67118
rs219260607	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13698319	TGAATGTGACATTGG[C/T]GCATATGTGTATACA	67118
rs219264998	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13699810	GCTGCTTCCTGGCTT[C/G]TTCTCTATGGCTTGC	67118
rs219423315	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13686080	TTTTGTTTGATTTGG[A/T]TTTGGTTTCTTTTTA	67118
rs219476103	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13684797	TCTTGGCTTCTAGGA[C/G]CTCAAAGCAGGAGGA	67118
rs219481200	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13697065	TAGCCAGCTTCTTGG[C/G]TTTTGAGATGTTCTT	67118
rs219523295	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13696372	ACAATTTTGGTGGTG[C/G]TGCTGCTGCTGCTAT	67118
rs219836077	in-del	-/AATA			intron-variant	Bfar	Mm_Celera	16:13679685	TCACATACATAAAAT[-/AATA]AATAAATCTTTAAAA	67118
rs219869805	in-del	-/GTTTA			intron-variant	Bfar	Mm_Celera	16:13683914	GGGGCCTGTGTTCTT[-/GTTTA]CTTGTTTGTTTGTTT	67118
rs220092718	snp	A/G/T			intron-variant	Bfar	GRCm38.p3	16:13694414	CTCAAAGGAACTTAC[A/G/T]GTTCTCCTACCTCCT	67118
rs220116180	in-del	-/AG			intron-variant	Bfar	Mm_Celera	16:13695014	GACAGAAGGAGAAAC[-/AG]AGAGAGATTTGTGTC	67118
rs220209571	in-del	-/GC			intron-variant	Bfar	Mm_Celera	16:13700312	TTCTGGGGTGGGGGG[-/GC]GTTATTTGAGAGATT	67118
rs220211493	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13693106	TTCTGCAAATAGCTG[C/G]TTTTTCCTAGGGCTC	67118
rs220321515	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13703277	AAGTATAATTATGCC[A/G]AGTCCTGCCATCATA	67118
rs220437937	in-del	-/GGT			intron-variant	Bfar	Mm_Celera	16:13692624	TGATGGGGAAGTGGG[-/GGT]GGCTAGAAAACAACT	67118
rs220470711	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13693274	GAATATAATGTTTAC[A/G]TATGCTGTGTTTGTC	67118
rs220501463	snp	A/G			utr-variant-5-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13672076	ACCAGGACTAGTGGC[A/G]AGGTGAGCTTCGGCA	67118
rs220501923	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13701982	GCAGAGTGTTTCCTC[A/G]GTTGTGAGAACAGGT	67118
rs220808355	snp	A/T			utr-variant-3-prime	Bfar	Mm_Celera	16:13703085	TCTGTGAGCATGGAG[A/T]TGAATGGAATGCCCA	67118
rs220950410	snp	C/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671432	CTGAGAAACAGGAAC[C/T]TTTTCTTTCTTTGGT	67118
rs220961885	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13700839	ACTTGAACATATAAG[A/T]CCTCAAAGCCTGACC	67118
rs221289473	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13702516	CTATGACCAATAGAA[A/G]TGAAAGTCTTGGTCA	67118
rs221295182	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13698186	TTCATTTTGCCCTGT[C/T]ATTCATAATTCAGGC	67118
rs221392342	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13697194	GCAAGACTGGAGCTT[C/T]TTACAGTATACCCCA	67118
rs221403733	snp	A/G			intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678603	ATTAGATCATGTGTT[A/G]CTTGGTAACCCCTAT	67118
rs221672716	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676281	GGGTAGAAAACCATT[A/G]TTCTAGTACCTTAAT	67118
rs221734969	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13675079	GTAGCTCAGTAGTAT[A/G]GTGTTTATCTGTTGT	67118
rs221738144	snp	C/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672252	GCCTCCTCACCCCGG[C/T]CTGGACGCGTCCCAG	67118
rs221778188	snp	A/G			upstream-variant-2KB	Bfar, 3110001I22Rik	GRCm38.p3	16:13671485	ACTGTCTTGGAATTC[A/G]CTCCGTAGACTAGAC	67118
rs222565375	snp	A/T			utr-variant-3-prime	Bfar	Mm_Celera	16:13703120	GCCGAGTCTTCTTAG[A/T]TGACTGAGCACTGCT	67118
rs222627762	snp	A/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13675243	CACCCTTCGATAGCT[A/T]CCCACCATTTCACAG	67118
rs222631759	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13702678	TCTACAACAGCCAGG[A/G]CTACATAGAGGAACC	67118
rs222687545	in-del	-/CATT			intron-variant	Bfar	Mm_Celera	16:13688394	TCTTAACTGCTGAGC[-/CATT]CATTTCTCCATCCCT	67118
rs222746030	snp	C/T			intron-variant, synonymous-codon	Bfar, 3110001I22Rik	Mm_Celera	16:13677335	GAAGAACTCCCCACA[C/T]AGCAGATCTGGATCC	67118
rs222811502	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13687056	AGTCTGGAACTCACA[A/G]AGTTCTGCCCTTGGA	67118
rs222874625	snp	C/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670382	AGACCTCTGGAAGAG[C/T]TCCCAGTGTTCTTAG	67118
rs222876063	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13686189	GCCCTGGAACTGGAG[C/T]TCTGGTTGTAAGCCA	67118
rs222898932	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13683731	TAGAATACCTGCCTA[C/G]TGTGGACAAAGCAGT	67118
rs222942592	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13680455	TTGTACAGCAAGCAC[C/T]TAACAGCTGAGTGTT	67118
rs222995069	in-del	-/A			intron-variant	Bfar	Mm_Celera	16:13701851	GCCAGGGCTACATAG[-/A]AAAAAACCTGTCTTG	67118
rs223006626	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13679764	TGTACCACATGTATA[C/T]GGTGCCTGTTAGAAG	67118
rs223135086	in-del	-/C			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670750	CGAACTCACAGAGAT[-/C]CTGCCTCTGCTTCCT	67118
rs223143027	snp	A/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672373	AGAGCCACTCGACCC[A/T]GGGGTGGTGACAGAG	67118
rs223226527	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13682441	ATCCCTAGTCCCTAT[A/G]TTTTGTTTTCTGTCT	67118
rs223299505	in-del	-/TCTCCTG			intron-variant	Bfar	Mm_Celera	16:13682250	ACTGAACCGCACAGA[-/TCTCCTG]TCTTTGGTTCCTTGG	67118
rs223423217	snp	A/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671404	GGGTTGCAAACAGTT[A/T]ATTAAATCAGAACTG	67118
rs223794917	snp	C/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670582	TGAAAAGAACACTCT[C/T]ATTTATTCCTTTAGA	67118
rs223834727	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13680471	TAACAGCTGAGTGTT[C/T]TCCTTAACCCAGGTT	67118
rs223839795	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13690274	CATAACTGAACATGG[C/T]GGCACACAGCTAACC	67118
rs224028831	in-del	-/AGAG			utr-variant-3-prime	Bfar	Mm_Celera	16:13703437	GACAGACGGACAGAC[-/AGAG]AGAATGTATGGGTGA	67118
rs224117425	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13679995	GAAATAGTCTTTAAA[A/G]ACATTCCTCAAATTT	67118
rs224127364	snp	C/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672526	ACTCCAAAGTGACAC[C/T]GAGGCTGACCTAGAA	67118
rs224189530	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690519	TGTTCAGTTTATATA[A/G]GTATATAAATATAGT	67118
rs224190835	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13682685	CTGGAAGCCAGTATT[C/T]GTCTAGCAGCCTTCA	67118
rs224252189	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13681867	AAAAGCTGACCATTC[C/G]AAAGCTAGTTAGCCT	67118
rs224252997	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13689652	AAGTAACATTTGGCC[A/G]GGCATGGTGGTGCAG	67118
rs224315682	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13680871	AAAGAGCTTGCTCTC[C/T]TTTCCTCCTATATAA	67118
rs224323971	snp	A/G			intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678563	ATAATCCCAGCATCA[A/G]AATGAATATTTTAAA	67118
rs224379100	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13688235	TCGTTTTTTTAAAAA[A/T]TTATTTATTTATTCA	67118
rs224380484	in-del	-/T			intron-variant	Bfar	Mm_Celera	16:13697683	GAATAATATTGAAAA[-/T]TTTTTTTTTAAGCTT	67118
rs224421155	snp	A/G			intron-variant, missense	Bfar, 3110001I22Rik	Mm_Celera	16:13677583	GGCTTGATGAAAAGG[A/G]ACGTCCTAAAGCTGC	67118
rs224495616	in-del	-/TTCTTTCTTTCTTTCTTTCTTTCTCTTCTTTCTCTTTCTC			intron-variant	Bfar	Mm_Celera	16:13688042	TTCTCTTTCTCTTCT[lengthTooLong]TTCTTTCTTTCTTTC	67118
rs224500556	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13687151	GCTGCCATTTATGAG[A/G]CCTCAGATTTAGTAC	67118
rs225018960	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13683922	GTGTTCTTCTTGTTT[G/T]TTTGTTTGTTTTATT	67118
rs225072607	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13694549	AGAACTAATTCCAGG[A/G]ATACACAGAGAAATA	67118
rs225129352	in-del	-/C			downstream-variant-500B	Bfar	Mm_Celera	16:13703965	CCTCCCAATATCCCA[-/C]CCCCCACCTGAGGCC	67118
rs225156991	in-del	-/AG			intron-variant	Bfar	Mm_Celera	16:13684948	GAGAGAGAGAGAGAA[-/AG]AGAGAGAGAGAGAGT	67118
rs225186483	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13684635	ATAGGTGCCCTTTGC[C/T]CCTACCTTTTGTGAG	67118
rs225256131	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13696360	ATGAAAATGTGTACA[A/G]TTTTGGTGGTGCTGC	67118
rs225338010	in-del	-/GTTCTTTAACG			intron-variant	Bfar	Mm_Celera	16:13682411	CTTAACATTATACAT[-/GTTCTTTAACG]GTTCCACAGCACTAA	67118
rs225400621	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13686432	CACTGTAGCTGTCTT[A/C]AGACACACCAGAAGA	67118
rs225469850	snp	A/G			synonymous-codon	Bfar	Mm_Celera	16:13685309	CTGCCGGCACTGCCT[A/G]GCTTTATGGTGGATG	67118
rs225504348	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13684058	ACTCCTGCCACAAAT[A/T]TTTAGCCAAAATTGA	67118
rs225535433	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13696842	CAAGCTGGCCTCGAA[A/C]ACAGAAATCCGACTG	67118
rs225567249	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13694822	AAAATGGTAGGTAGG[G/T]TTTAGGTCTAGTGAG	67118
rs225596392	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13692296	TGCTCTTGGCATTCA[C/T]CAACACAGCGTTTAA	67118
rs225632657	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13693683	GGATTTTCTCTTTGA[G/T]CATGGAGAAACAATA	67118
rs225764024	snp	A/T			utr-variant-3-prime	Bfar	Mm_Celera	16:13703494	GACAGAAGGAGAGAG[A/T]CAGAGAGACTTGGTA	67118
rs225833519	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13682289	GTGGGCTTGGCAAGC[C/T]CACACCACCCTTGCC	67118
rs225937350	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13692784	CATAATCTGTGGGAG[A/G]TGTCCTGCCTGAGTG	67118
rs226043802	in-del	-/AAA			intron-variant	Bfar	Mm_Celera	16:13701722	AAAGTTTGTCTTAGG[-/AAA]AAAAAAAAAAAAGTG	67118
rs226190702	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690168	ACCCTGTCTCGAGGG[A/G]AAAATAATAATAATA	67118
rs226265143	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13700443	GTTTTACCAACACTT[A/G]GGAGAATAACTTCCA	67118
rs226607708	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13691392	AGCCTTCCAAGTCAG[C/T]AGTATTGCAGATGTG	67118
rs226660143	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690673	GAGAAGTAGAGGCCG[A/G]CCATGAACACATGGA	67118
rs226664536	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13702743	AAAGAAAAGAAAAAA[A/G]AAAGAAATCAAAACA	67118
rs226721881	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13701371	ACAAGGCAGGCATCT[C/T]CAGAGCAAGTCAGAC	67118
rs226725199	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13688552	CTCCTAGATTGTCTG[C/T]CATGTACCCTTTCCA	67118
rs226761919	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13698598	TGCGTGGACAGCGTG[C/T]ATCCTTAACCACTAA	67118
rs226809317	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13699198	ATCAGGCAGTCTACA[A/G]TGACTCCAACCTCAG	67118
rs226824963	in-del	-/GC			intron-variant	Bfar	Mm_Celera	16:13680515	TGCTGTTGCACTGTT[-/GC]ACGGAGGCATTTGGG	67118
rs226925141	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13697960	TTCTCTGAATCTAGT[C/T]GGTCTTTTGAGAGTA	67118
rs227061342	in-del	-/CT			intron-variant	Bfar	Mm_Celera	16:13688245	AAAATTTATTTATTT[-/CT]ATTCATGCATGTGAG	67118
rs227062561	in-del	-/C			intron-variant	Bfar	Mm_Celera	16:13701062	TCACAGGCTGGCCTT[-/C]CCTGTGCTACTCAGC	67118
rs227456739	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13697146	GATTCACCATCTTCT[C/T]CCACATATTAGAGAT	67118
rs227472178	in-del	-/AGGAAGGAAGGAAGG			intron-variant	Bfar	Mm_Celera	16:13694611	GGAAGGAAGGAAGGA[-/AGGAAGGAAGGAAGG]AAGGAAGAAAACAGT	67118
rs227607414	snp	A/C			utr-variant-5-prime, upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671878	TGCGCATGCGCCCGC[A/C]TGCCCCTAGAGCAGC	67118
rs227796400	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13696568	GGATCTGTGTGCACA[C/T]ATGCAGCTGCCAAGG	67118
rs227845247	in-del	-/A			intron-variant	Bfar	Mm_Celera	16:13692075	AATAAATACCTAATT[-/A]AAAAAAAAAAAAGCA	67118
rs227849753	snp	C/T			utr-variant-3-prime	Bfar	Mm_Celera	16:13703374	ATGTGAGCTCATCAG[C/T]CTTGGCCTGGCTGAA	67118
rs227959525	snp	G/T			utr-variant-3-prime	Bfar	Mm_Celera	16:13702827	CCTCACTAACTGACA[G/T]ACTCCCAAACCAGGC	67118
rs228116170	snp	C/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672622	GTGTGTGTTTTAGAA[C/G]AGAGACGCTGTGTCT	67118
rs228118797	snp	A/G			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670993	TTAAAATTTTGAAAG[A/G]TCAAATCAATGATTG	67118
rs228125575	in-del	-/TG			intron-variant	Bfar	Mm_Celera	16:13692849	GGGAGGTGTCCTGCC[-/TG]TGAGTGCTGCATAAA	67118
rs228200723	snp	A/G			upstream-variant-2KB	Bfar, Parn	Mm_Celera	16:13669876	ATGCTGACCTTCAGA[A/G]ACTTCTGTTAGAGAC	67118
rs228201148	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13680597	TGGCCTAGAACTCTT[A/C]CATTGACCAGGCAAG	67118
rs228282449	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13680121	TTCAGGTTCCATCCA[G/T]CTTCACTAGGCCTGG	67118
rs228444371	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13703319	AGCTAAAGGATGACC[A/G]TTATGCCCGTGTAGA	67118
rs228715044	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13699753	GTTTGTAGTTCATCC[C/T]GGGAAGTCAGAGCAG	67118
rs228798227	in-del	-/AT			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671564	TCATAGATTGAAAAC[-/AT]AGTACCATTGAGTTC	67118
rs228833990	snp	G/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670694	GTACAACAGTGCCCT[G/T]GCAGTCTTAAGAGGA	67118
rs228911965	snp	A/C			intron-variant, utr-variant-3-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13678047	ATGCTTCATATGTGG[A/C]GTTTTTGTGATGAAA	67118
rs228944588	in-del	-/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676691	GAATTGGTATGCATA[-/G]GTATGGATCCTCTTG	67118
rs229221418	snp	C/T			intron-variant, synonymous-codon	Bfar, 3110001I22Rik	Mm_Celera	16:13677728	AAACAAAAAAGATCA[C/T]ACAGAATTCATTGAT	67118
rs229250003	in-del	-/CCCTGTC			intron-variant	Bfar	Mm_Celera	16:13692762	ACAAGCCTCTCGGGT[-/CCCTGTC]CATAATCTGTGGGAG	67118
rs229405240	in-del	-/ATAAAG			utr-variant-3-prime	Bfar	Mm_Celera	16:13702927	AGTTGGACATACAAA[-/ATAAAG]ATAAAGACCTAGAAT	67118
rs229443194	snp	A/G			intron-variant	Bfar, 3110001I22Rik	GRCm38.p3	16:13674302	GAGCTAAGATTTAAC[A/G]TGATCATTCTGCCTC	67118
rs229443301	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13684857	TATGATCTCCACGCA[C/T]ACCTACCCCTTAAAA	67118
rs229453195	in-del	-/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673818	ATGCCAGTTAAAAAA[-/T]TTTAAGTCCTTTTAA	67118
rs229497912	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13684160	TGGCTGTGAATTACA[C/T]ATTAGTCCCAGTGTT	67118
rs229560684	in-del	-/TCTA			intron-variant	Bfar	Mm_Celera	16:13700956	ACTCAAACACATGAC[-/TCTA]TCTATGGTGGGCATA	67118
rs229609824	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13682186	TGGAATTAAAGGTGT[C/T]CACTTAATTTTTTGA	67118
rs229692249	snp	A/G			intron-variant, utr-variant-5-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13676891	GTACCAGCATCCTGG[A/G]ACCTGGAACCATCAA	67118
rs230028654	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13680340	AGCCTGAGTCCTTTG[A/G]AAGAGCACCTGATAA	67118
rs230083022	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13679738	GTGTGTTTTGTCTGC[A/G]TGGGTATCTCTGTAC	67118
rs230086277	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690754	AAAAGAGCTTTGGGG[A/G]TTTTTTATTTTGTTT	67118
rs230189135	in-del	-/AG			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673982	ACTTTCATTCCTGGC[-/AG]GGCATAATTTTAGAT	67118
rs230215054	snp	C/T			intron-variant	Bfar, 3110001I22Rik	GRCm38.p3	16:13672996	CCTTTTCCCCCTTTC[C/T]CTCTGGCAGTATAAA	67118
rs230298860	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13682910	TCAGTTCAAATCTCA[C/G]CAACCACATGGTGGC	67118
rs230365084	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674075	ATTCAAAACAGGATG[A/G]CATTACCTTAGTCAT	67118
rs230373903	in-del	-/TTATTTATTTATTTATTTATTTAT			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670229	TACAAAGGTTGTGTC[-/TTATTTATTTATTTATTTATTTAT]TTATTTATTTATTTA	67118
rs230439979	in-del	-/GT			intron-variant	Bfar	Mm_Celera	16:13689473	TTGATTTCATTTGTA[-/GT]TATTTTGAATAGTGC	67118
rs230622604	snp	A/G			intron-variant, utr-variant-3-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13678309	AGGATTCGAGTTGTG[A/G]TTTTTATTGGCTTTT	67118
rs230690240	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13687860	AAAGGGGCAGAACAA[A/G]ACTTGAGAAACCATG	67118
rs230747597	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13687001	AGTCAGTCTCATTGT[G/T]TCACCCAGGCAACCT	67118
rs230782603	in-del	-/C			intron-variant	Bfar	Mm_Celera	16:13687918	TCTTTCTTTCTTTCT[-/C]TTCTTTCTTTCTTTC	67118
rs230824370	snp	A/G			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671073	GTCTCCTCCTAAATC[A/G]GGTTTTGAGAGAGCA	67118
rs230860756	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13697070	AGCTTCTTGGGTTTT[A/G]AGATGTTCTTTTTCT	67118
rs230879954	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13680664	ATTTAAGACATGAAC[C/T]GTAAGGCCTGGCAAA	67118
rs231004354	snp	C/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671646	CATTTTACCCCAAAT[C/T]CCGACTCTATAAATA	67118
rs231074048	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13681796	GTGTGCAAGACCTAA[A/G]CTATCATTTTCTCAA	67118
rs231401207	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13679179	ATTGTGAATGTTCTC[C/T]GTGGAACATTCTAAG	67118
rs231456447	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13689417	AAACTCCTTGTATAG[A/G]TAGATCAGATTGTCA	67118
rs231496277	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13683747	TGTGGACAAAGCAGT[A/G]CAAAACCAAAACAAA	67118
rs231496398	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13696110	GGACTACACGCCTTC[C/T]TCACCATGCTTGACG	67118
rs231589687	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13694314	TAACACAAAGGAGGA[C/T]GGTTTGTTAATAATA	67118
rs231749721	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13692608	TTTTTGTTTGTTTGT[A/C]TTGATGGGGAAGTGG	67118
rs231804470	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13692109	TGACAGTAGGAATCT[A/G]TAATGGATTGGAGGC	67118
rs231863750	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13703023	AAGAGACAGTGCTGC[A/G]TAGCTGTGTTGTTTC	67118
rs231869290	snp	A/G			intron-variant, utr-variant-3-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13678113	GGTCAGCTTAAAATC[A/G]TCTTCAGAAATGTTT	67118
rs231887383	snp	A/C			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676731	TAAAGTTTTATAAAT[A/C]TATAAGAGGTGTGCA	67118
rs231913139	snp	A/C			utr-variant-3-prime	Bfar	Mm_Celera	16:13702276	GCAGCAAGGCCCGAG[A/C]GAGCCCGTGAATCTA	67118
rs231942322	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13687602	GGTGTGGCAGTAAGT[C/T]TGGCTGTTTAATCTG	67118
rs231947068	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13686239	CAAACTCAGGTCCTC[C/T]GCAAGAGCAGCAACA	67118
rs232117419	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13695276	TGTGTAGACATGCCT[A/G]GAACTCAGCATCTTC	67118
rs232353927	in-del	-/A			intron-variant	Bfar	Mm_Celera	16:13683040	TATAATAATAAATTT[-/A]TTAAAAAATGTGTTG	67118
rs232508174	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13675815	ACTTGATTCGAATTC[A/G]TGGAGTCCAGATTTG	67118
rs232541468	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13681975	CATTAAAATGGAGGA[C/T]CGAGGGGCTGGAGAG	67118
rs232590992	snp	G/T			utr-variant-5-prime	Bfar	Mm_Celera	16:13685080	TTATGATGCATTGCA[G/T]CAGTGTCCTGAGTCT	67118
rs232594331	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13692581	TGGGAGTACAAGGTA[A/T]CTCGTGGGGGGTTTT	67118
rs232714544	in-del	-/ATTG			intron-variant	Bfar	Mm_Celera	16:13697874	GATGTGACTACTGCC[-/ATTG]ATTGGCCAGTTATTT	67118
rs232830129	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13697675	GCCAGAGTGAATAAT[A/C]TTGAAAATTTTTTTT	67118
rs232881861	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13696990	TGCCACATGCCCTCA[A/G]AGGCCAGAAGAAGGA	67118
rs233087488	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690636	AGTAGAGGCAGAGTG[A/G]CAGGTAGAGAAAGAG	67118
rs233118224	in-del	-/AC			intron-variant	Bfar	Mm_Celera	16:13697809	AGTTAGCCGACTACA[-/AC]AGGATTTGGATCTGC	67118
rs233144734	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13700035	TTATTAAATTATTTT[A/G]TAAATATATATGTTT	67118
rs233170531	in-del	-/TTTA			intron-variant	Bfar	Mm_Celera	16:13697692	GAAAATTTTTTTTTT[-/TTTA]AAGCTTTGATTTTGT	67118
rs233198117	snp	G/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674570	TTACTACTATGTCAT[G/T]CATATTCTTTACTGA	67118
rs233229993	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13682861	TGGAGAATGGCTCAG[C/T]AGGTAGGAGCTCTGA	67118
rs233230494	snp	C/G			synonymous-codon	Bfar	Mm_Celera	16:13699022	CAATGCCGTGCTGCT[C/G]TCTGTTCTGGAGTTG	67118
rs233254981	snp	C/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673458	TGGACTTCTGATTTC[C/T]CTGGCTTTCTGAATT	67118
rs233588831	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13687359	CTATATCTTGTCAAA[C/T]ACCTGTTCTGTGATT	67118
rs233642550	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13698562	TTTATGAAGTACAGA[A/G]GATCCAAACTCCAGT	67118
rs233905813	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13702873	TGTCCCATGAGTCAA[A/G]TTTAGGAAAGCAAGG	67118
rs233954723	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13691264	TTAGGGGTTTATAAT[C/T]CTTATTAAATTGAAT	67118
rs233958872	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13701891	AGAGAAAGAAAAAAG[G/T]GGCGACAAAGCAGGT	67118
rs234161610	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13696408	TTTGTTTATGATTTT[C/T]CCAGGGTAGAGTTGA	67118
rs234182560	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13699867	ACCTTTGCAGAAATG[A/T]CAAGGCCTATAGTAT	67118
rs234274247	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13679533	GTGTCTGAAGACAGC[A/T]ACAGTGTAGTTATTA	67118
rs234275270	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13693991	ATCCTCATTCTTCAG[C/T]TTATTCACAATATAT	67118
rs234341683	snp	C/T			intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678534	ATTCTAGGCATCTGA[C/T]CCACCACTGAGCTAT	67118
rs234421599	in-del	-/AACAAGGCCACACTTATTCC			intron-variant	Bfar	Mm_Celera	16:13700876	TGGCACACTTCCTAA[-/AACAAGGCCACACTTATTCC]AACAAGGCCACACCT	67118
rs234485285	snp	G/T			utr-variant-3-prime	Bfar	Mm_Celera	16:13703110	TGCCCACCAGGCCGA[G/T]TCTTCTTAGATGACT	67118
rs234675609	snp	A/G			downstream-variant-500B	Bfar	Mm_Celera	16:13704040	AGTAATGCCCAGGAA[A/G]AGAGGAGATTGGGCA	67118
rs234712274	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13686630	CCTCTGATGGAATTG[A/T]ATTCATGTGCTACCA	67118
rs234780497	snp	C/G			upstream-variant-2KB	Bfar, 3110001I22Rik, Parn	Mm_Celera	16:13670156	GGGGAAGTATGGTGG[C/G]ACACACCTGCAATCC	67118
rs234782697	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13697552	GTGTTGTACAAAGCT[A/G]GAGAAAGTAGACCAG	67118
rs234882127	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671979	TGATCGTAGTCGGCC[C/T]CTAGGCCCAGGTTAT	67118
rs234966782	snp	A/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671171	GGTGGCGCATGCCTT[A/T]AATCCCAGCACTTGG	67118
rs235025658	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13700322	GGGGGGGTTATTTGA[A/G]AGATTTTATTAATTG	67118
rs235452321	snp	C/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673353	TACACAGAAATCCAC[C/T]TGCCCGTGGGGATTA	67118
rs235499239	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13682982	GTCTGAAGTCAGCTA[C/T]AGTGTACTTATGTAT	67118
rs235504524	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672172	GAACCCGCTCCCGGA[A/G]CTGCGCTGGCGGGGA	67118
rs235524977	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13697900	TATTTCTCCATGTCA[A/T]GTGTCGTTCTCCAAC	67118
rs235556446	snp	C/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671455	TCTTTGGTTAAGTTT[C/T]ACTATGTAGCTTTGA	67118
rs235612470	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13681135	GCGCTACATCTGCCC[A/G]GCTTAGAAATATTTT	67118
rs235666811	snp	A/C/T			intron-variant	Bfar	Mm_Celera	16:13680558	GAGATAGGGTCTTAC[A/C/T]ATGTAATTCTGCCAG	67118
rs235680128	in-del	-/TTC			intron-variant	Bfar	Mm_Celera	16:13683910	TCACTGGGGCCTGTG[-/TTC]TTCTTGTTTGTTTGT	67118
rs235722201	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13694894	GCCACCATTGTTGAC[G/T]TTTGGTCTGTGCATA	67118
rs235762105	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690532	TAGGTATATAAATAT[A/G]GTGTTGGGTTTTGGG	67118
rs235861984	snp	A/C			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676035	AAAGTCTTGATTCTA[A/C]GATAGATTTACTTCC	67118
rs235887243	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13692698	CAGACATTGAAACTA[A/C]AAGCACAGCTAATCT	67118
rs235965031	in-del	-/ACTG			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671051	GGTACACCTAGGCTA[-/ACTG]ACTGTCTCCTCCTAA	67118
rs236111704	in-del	-/C			intron-variant	Bfar	Mm_Celera	16:13689746	CTACAAAAGTAAGTT[-/C]CCAGGACAGCCAGGG	67118
rs236147049	snp	C/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676226	ATGGTTGGGGGTCAC[C/G]ACACATGAGGAACTG	67118
rs236213677	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13685511	AGCTTGGAACCAAAA[A/G]CCAGATTCCTTTCTT	67118
rs236275762	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13684599	AATGGCGAGTCTTAG[A/G]AATGTACCCTACTAC	67118
rs236558642	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13681058	CACTCTGTAGACCAG[G/T]CTGGCCTAGACCTCA	67118
rs236609942	snp	A/C			intron-variant	Bfar	GRCm38.p3	16:13701653	GGCAGAAAGATGAGA[A/C]GTTTAAGATCATTCT	67118
rs236783553	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13686107	TTTATTTGTATGTAT[G/T]ATTTTTATCTGCATG	67118
rs236846240	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13684800	TGGCTTCTAGGAGCT[C/T]AAAGCAGGAGGATCT	67118
rs236916946	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13696405	TGGTTTGTTTATGAT[G/T]TTTCCAGGGTAGAGT	67118
rs236948722	in-del	-/A			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672506	TGAGGATAACGGAAC[-/A]TCAGACTCCAAAGTG	67118
rs236975119	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13694865	AGAAAATAAGATAGC[A/C]AGTAATAGAAGAGGC	67118
rs237110781	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13679562	TAATAGTAATAAATA[A/C]ATTTTTGGGCCAGAG	67118
rs237230719	snp	A/G			intron-variant, synonymous-codon	Bfar, 3110001I22Rik	Mm_Celera	16:13677266	CCATTACTCAGAACA[A/G]CAGTCTCCCCATAAA	67118
rs237618590	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13688417	CCATCCCTGTTATGG[A/G]ATTCTTAAGAGCACA	67118
rs237680580	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13687243	TAGCACATAGATTGT[A/T]GTGAATTTTTTGTTT	67118
rs237687218	snp	C/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674747	GATTACAGGCCTGTG[C/T]TGTCGGGTCCAGTTT	67118
rs237721947	snp	A/G			intron-variant, synonymous-codon	Bfar, 3110001I22Rik	Mm_Celera	16:13677083	CCGTCCAGGATCAGT[A/G]TACAGAAGAGACAAG	67118
rs237784812	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13686917	TTGTCATCTAACCCC[C/T]ACATGTGCGTGACCA	67118
rs238030508	in-del	-/A			intron-variant	Bfar	Mm_Celera	16:13690004	ATAAATAAAATCTTT[-/A]AAAAAAAATAAGTAA	67118
rs238135829	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690292	CACACAGCTAACCCA[A/G]CACTTGGAAGATGGA	67118
rs238194954	in-del	-/TGTGTGTG			intron-variant	Bfar	Mm_Celera	16:13700156	CTCATTGTTCTAATT[-/TGTGTGTG]TGTGTGTGTGTGTGT	67118
rs238199359	in-del	-/TCTA			intron-variant	Bfar	Mm_Celera	16:13689542	GTATTCTGAGAACTC[-/TCTA]TGAGGAATGGCCACA	67118
rs238201731	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13700520	TCTCTTAGTGGCAGG[G/T]GACAAGAGCCAACCT	67118
rs238263606	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13699502	TAGGTTTCTAATGCC[A/G]TGCTAAAACACTGTG	67118
rs238279819	in-del	-/T			intron-variant, utr-variant-3-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13678049	GCTTCATATGTGGCG[-/T]TTTTGTGATGAAATA	67118
rs238327434	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13684469	CTTTAGCCCTCATAG[C/T]GGGTCTCATGCAGGA	67118
rs238396394	snp	A/C			utr-variant-5-prime	Bfar, 3110001I22Rik	GRCm38.p3	16:13672052	GCAGGTGGCGGTGAC[A/C]GAGTGGGTACCAGGA	67118
rs238488279	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13682096	TGGGATCTGATGCCC[C/T]CTTCTTACTGTATAG	67118
rs238512168	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13692785	ATAATCTGTGGGAGG[C/T]GTCCTGCCTGAGTGC	67118
rs238744878	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13682553	AGCTGTTTGGGTAGT[A/G]TGATGGTTTGTATAT	67118
rs238881022	in-del	-/G			intron-variant, utr-variant-3-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13678012	AAGTCTATCTTGATT[-/G]TCATTCCAGAATTGT	67118
rs238881385	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13692338	ACTAAGCAAGCCTGT[A/G]TACCTGTGCAGAAAG	67118
rs238984624	snp	A/G			upstream-variant-2KB	Bfar, Parn	Mm_Celera	16:13669991	TGAACCTTGTGTGAT[A/G]AACCTCAGCGTAATA	67118
rs238999290	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13680461	AGCAAGCACCTAACA[A/G]CTGAGTGTTCTCCTT	67118
rs239043471	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13680267	CATGTGAGAGTATCA[A/G]ACCCCCAGACCTGGG	67118
rs239262694	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13688370	GGACCTCTGGAAGAG[C/T]AGTCAGCGCTCTTAA	67118
rs239283874	in-del	-/TTGAC			intron-variant, utr-variant-3-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13678322	GGTTTTTATTGGCTT[-/TTGAC]TTGTTTTCTTAGGCT	67118
rs239326818	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13696367	TGTGTACAATTTTGG[A/T]GGTGCTGCTGCTGCT	67118
rs239388936	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13694783	GGTAGGTCCCCACCT[A/G]TTAGCCAGCCAGCCA	67118
rs239582002	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13688229	GGTCCTTCGTTTTTT[A/T]AAAAATTTATTTATT	67118
rs239729571	snp	A/C			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672269	TGGACGCGTCCCAGC[A/C]GGGCTGCGGACCGTA	67118
rs239792299	snp	C/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671513	GACTGGCTTCGAACT[C/T]ACAAAGATCATCCTG	67118
rs240051939	in-del	-/GTGTGT			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672597	TGTGCTGATGAGAGC[-/GTGTGT]GTGTGTGTGTGTTTT	67118
rs240145095	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13697297	GCTGGCCACAACATA[C/T]ATAACATGGTCCCAT	67118
rs240178775	in-del	-/GGG			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673260	CTTTGTTTGTTTATT[-/GGG]GGGGGGGGTGCATTT	67118
rs240198856	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13696854	GAACACAGAAATCCG[A/C]CTGCCTCTGCCTCCC	67118
rs240528664	in-del	-/G			intron-variant	Bfar	Mm_Celera	16:13679593	CGAGTGGGGTTAACC[-/G]GAACAAGCGTAGGTC	67118
rs240537819	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13700450	CAACACTTGGGAGAA[G/T]AACTTCCAGATTAAT	67118
rs240622401	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13683339	GAGCAGTAAATAAGA[C/T]ATCTTTGTGACTTAT	67118
rs240823961	snp	C/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670836	TGCCTACTCCTTGCC[C/T]CGTTTGGGGATTACA	67118
rs240995484	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676666	TTAGGTTACAGAATG[A/G]CTTGTCTTAAGAATT	67118
rs241095821	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13700855	CCTCAAAGCCTGACC[C/T]CACAGTGGCACACTT	67118
rs241226112	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13703138	ACTGAGCACTGCTTG[A/G]TGTTGTGTTTTGAAT	67118
rs241276154	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13702717	AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAAGA	67118
rs241308229	in-del	-/GA			intron-variant	Bfar	Mm_Celera	16:13690163	GTGAAACCCTGTCTC[-/GA]GGGGAAAATAATAAT	67118
rs241399243	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13681011	GGTTTTCCGAGACAA[G/T]GTTTCTCTGTAGTTC	67118
rs241479023	snp	C/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670411	AGCCATCTCACCAGC[C/T]CAGGGCTGTGTCTTA	67118
rs241485821	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13691983	GAACGCCAGGGCCAA[A/G]AAGTAGGAGTGGAGG	67118
rs241600697	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13679889	GCTGTAACCACTGAG[C/T]CATCTCTTCAGACTC	67118
rs241662448	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13679066	GCCTCAGTTAGTCTG[A/G]GCACATTAATGTTTA	67118
rs241789465	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13698323	TGTGACATTGGTGCA[C/T]ATGTGTATACACACA	67118
rs241798291	in-del	-/AA			utr-variant-3-prime	Bfar	Mm_Celera	16:13702702	AGGAACCATGTCTCT[-/AA]AAAAAAAAAAAAAGA	67118
rs242012804	in-del	-/ATAAAT			utr-variant-3-prime	Bfar	Mm_Celera	16:13702933	ACATACAAAATAAAG[-/ATAAAT]ACCTAGAATCCAGTC	67118
rs242118061	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13689730	TTTGAGGCCACCGTG[A/G]TCTACAAAAGTAAGT	67118
rs242143653	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13680024	TTTAGGTATAATTTC[A/G]ATCATGATAACTGAG	67118
rs242198912	snp	A/C/T			intron-variant	Bfar	Mm_Celera	16:13679413	GGAGAGATGGCTAAG[A/C/T]GGTTAAGAGCACTGA	67118
rs242241086	in-del	-/CAAAAC			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674120	TGAAGAAAAAAAAAA[-/CAAAAC]AAAACACTCAAGGAG	67118
rs242258686	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13689667	AGGCATGGTGGTGCA[C/G]GCCTTTAATCCCAGG	67118
rs242261180	in-del	-/G			intron-variant	Bfar	Mm_Celera	16:13697937	GGAACTCGTTTTGCT[-/G]GGACGACTTCTCTGA	67118
rs242364620	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13698014	TATCTGTGTACTATA[C/T]TGTACATACTATCAA	67118
rs242508772	in-del	-/AC			intron-variant	Bfar	Mm_Celera	16:13690374	CTCAAAAAAAAAAAA[-/AC]CAAACAACTTATTAC	67118
rs242658575	snp	C/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673940	AAGACCTTAATTTAC[C/G]TCAAAGTTAGATGAG	67118
rs242714822	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13683845	ATTCTGCAAATGTCA[C/T]GGGAGTAGACTCTAG	67118
rs242732695	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672528	TCCAAAGTGACACCG[A/G]GGCTGACCTAGAACT	67118
rs242795078	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13682704	TAGCAGCCTTCAGAT[A/G]AAGATGTAGAACTCT	67118
rs242815759	in-del	-/AAAA			intron-variant	Bfar	Mm_Celera	16:13690362	ATCACACCCTGTCTC[-/AAAA]AAAAAAAAACCAAAC	67118
rs242843855	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673582	TGTGCCACCATGCCC[A/G]GTTTATACACTGCTG	67118
rs242988167	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13696249	CCTGCCTCTGCCTCG[A/C]AAGTGCTGGGAAGAA	67118
rs243089050	in-del	-/GGCCTAGT			intron-variant	Bfar	Mm_Celera	16:13683565	ACAGTGCCTGAGGCA[-/GGCCTAGT]TCTTACTTAGATGGC	67118
rs243278397	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13684082	AAATTGAAGCAAGTT[A/T]TTATTAAATACTGGC	67118
rs243336476	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13682950	CCCATAATGAGATCT[G/T]ATGCCCTCTTCTGTA	67118
rs243450611	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13692621	GTCTTGATGGGGAAG[G/T]GGGGGCTAGAAAACA	67118
rs243749057	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13679987	CTGAATTTGAAATAG[A/T]CTTTAAAAACATTCC	67118
rs243774561	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13691034	TTTTTAAAATTTTAT[C/T]TATTTTTATATGTAT	67118
rs243854070	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13702569	AAAAGGCTAATATAG[A/G]CTGGGTGTGGTAGTG	67118
rs243894480	in-del	-/TGTT			intron-variant	Bfar	GRCm38.p3	16:13696726	TGCCTAAGCTAATAC[-/TGTT]TGTTTGTTTGTTTGT	67118
rs243920558	snp	C/T			intron-variant, utr-variant-5-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13676893	ACCAGCATCCTGGAA[C/T]CTGGAACCATCAATT	67118
rs243979221	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13686459	AAGAAGGCATCAGAT[C/T]CCATTACAGATGGTC	67118
rs244033616	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13685439	TGGTGTGCAGTGTGG[C/T]TTCTCTGTGGGAACT	67118
rs244342117	in-del	-/CA			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672955	TCTGTCCAGGCTGTT[-/CA]CACACACACACACAC	67118
rs244403271	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13689504	CTGCTAAAATCATTC[C/T]TGCACAGGGTTTTGT	67118
rs244407290	snp	C/T			intron-variant, missense	Bfar, 3110001I22Rik	Mm_Celera	16:13677585	CTTGATGAAAAGGGA[C/T]GTCCTAAAGCTGCAA	67118
rs244435140	in-del	-/AAAG			intron-variant	Bfar	Mm_Celera	16:13689815	AAAAACAAAAAAAAA[-/AAAG]AAAGAAAGAAAGTAA	67118
rs244457536	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13687676	GATATCACTTAAACA[C/G]TTGATGGTGTAACCA	67118
rs244489343	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13687155	CCATTTATGAGACCT[C/T]AGATTTAGTACCCAG	67118
rs244515394	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13698606	CAGCGTGCATCCTTA[A/G]CCACTAAGCCATTTT	67118
rs244567521	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13697756	TAAGAGATTAGGTGG[A/C]TAGCCCTCGAGATTT	67118
rs245071280	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13691560	TGTGGTTGCTGGGAA[A/T]TGAACTCAGGACCTC	67118
rs245122657	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13690686	CGGCCATGAACACAT[G/T]GAGAAAGGCGGGAAG	67118
rs245125992	snp	A/C			utr-variant-3-prime	Bfar	Mm_Celera	16:13702813	GTCAGTAGCCCTAAC[A/C]TCACTAACTGACATA	67118
rs245131956	snp	A/C			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13675244	ACCCTTCGATAGCTT[A/C]CCACCATTTCACAGA	67118
rs245191183	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13701376	GCAGGCATCTCCAGA[G/T]CAAGTCAGACTGTTT	67118
rs245203896	snp	C/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13675123	GAGTTCTACCTCCAG[C/T]CCTGCCAGAAAAATC	67118
rs245291416	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13684716	AGAGTTCTGTCTAGC[A/G]TATATGAAGCCCTGG	67118
rs245466104	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13693561	CTGCCAAGAGTATAG[A/G]GGAGGCGCTGGAGAG	67118
rs245579808	snp	C/T			utr-variant-3-prime	Bfar	Mm_Celera	16:13703413	GCATCCAACGTGAGA[C/T]CGACAGACGGACAGA	67118
rs245625289	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13702904	ATAGGTTTTGTCATA[A/G]ATATGGATAGTTGGA	67118
rs245760084	snp	A/C			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672413	GTTTCCACTTACTTG[A/C]GGGCTATGGGCGCCC	67118
rs245833679	snp	A/C			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671001	TTGAAAGATCAAATC[A/C]ATGATTGTCCAATTA	67118
rs245886095	snp	A/T			upstream-variant-2KB	Bfar, Parn	Mm_Celera	16:13669877	TGCTGACCTTCAGAA[A/T]CTTCTGTTAGAGACT	67118
rs245968793	in-del	-/TTTTG			intron-variant	Bfar	Mm_Celera	16:13690565	TTATTTTGTTTTTGT[-/TTTTG]TTTTTTAGTATAGAA	67118
rs246049622	snp	A/T			utr-variant-3-prime	Bfar	Mm_Celera	16:13703287	ATGCCGAGTCCTGCC[A/T]TCATAAGTATGGAGT	67118
rs246082855	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13682326	TCCATGGGTGCTGAG[A/G]CTCCAAACTCAGGCA	67118
rs246164807	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13696690	GTTTGGGAGCAGACG[C/T]CTTTATTCACTGAGT	67118
rs246194043	in-del	-/TTATTTATTTATTTAT			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670230	TACAAAGGTTGTGTC[-/TTATTTATTTATTTAT]TTATTTATTTATTTA	67118
rs246217255	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13695353	GCTGCTAGGACTACA[C/T]GCCTTCCTCACCATG	67118
rs246391285	snp	A/C			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670591	CACTCTCATTTATTC[A/C]TTTAGAGGTGGCTGA	67118
rs246465055	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13680497	AGGTTTGTTCTGTTG[C/T]TGCTGCTGTTGCACT	67118
rs246510457	snp	C/T			missense	Bfar	Mm_Celera	16:13692471	AAGAGTTTTCCAGGG[C/T]ACCTTATACCATAGA	67118
rs246587080	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672634	GAAGAGAGACGCTGT[A/G]TCTAACTGGGGACCT	67118
rs246643406	in-del	-/TAA			intron-variant	Bfar	Mm_Celera	16:13680193	TCAGCTTTGTAATTG[-/TAA]TAAGCTACACGTGCC	67118
rs246654315	snp	C/G			utr-variant-5-prime, upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671980	GATCGTAGTCGGCCC[C/G]TAGGCCCAGGTTATT	67118
rs246859123	in-del	-/A			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670484	GTTATCACAATGAAG[-/A]AAAAAAAGGTTTCTA	67118
rs246910155	snp	A/C			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13675774	CCCCACTTTGCAGCT[A/C]TTGTGTGATATAATA	67118
rs246969550	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674329	CCTCAAGTTTGTGCT[A/G]TAAGTGAAAATGTTC	67118
rs247005607	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13689223	TTTCTTCCTGGTCTA[C/T]CCTCACTTCTTCTCC	67118
rs247083489	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13683097	AGTAAAACCCTGAAC[A/G]GGTATGCTAGAGAAA	67118
rs247285984	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13686287	CTTCAGCTCCTCCTA[A/G]TTTTTGTTTGTTGGT	67118
rs247316547	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13701231	TGGTCACACAGACAT[A/G]CTACACTGCAGGAGT	67118
rs247379240	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13699877	AAATGACAAGGCCTA[C/T]AGTATGCCAGGTTAT	67118
rs247715199	snp	C/T			intron-variant, utr-variant-3-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13678063	GTTTTTGTGATGAAA[C/T]AACCTCAGTTAAACA	67118
rs247730069	in-del	-/GGGGCTACAG			intron-variant	Bfar	Mm_Celera	16:13698513	CCGCCCCTCAGTGCT[-/GGGGCTACAG]GGGTGTCAAGAACCA	67118
rs247742135	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13686199	TGGAGCTCTGGTTGT[A/G]AGCCATTGTATGGGT	67118
rs247771498	snp	A/G			intron-variant, utr-variant-5-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13677002	TCAAAGAACTGCTAG[A/G]ATTGTCTTGGTGAAC	67118
rs247841281	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13697147	ATTCACCATCTTCTT[A/C]CACATATTAGAGATG	67118
rs247855465	snp	A/G			intron-variant	Bfar, 3110001I22Rik	GRCm38.p3	16:13674038	CAGACATTGGGTTGC[A/G]GAAAAGGGAAAGACA	67118
rs247925133	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13683946	TTTTATTTGCATGTT[C/G]TGTTTTTTTGGGGTA	67118
rs248134255	snp	C/T			intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678478	ATGAGTTGAAGTTGA[C/T]GTATCTGTGAGGTAC	67118
rs248186038	snp	A/G			intron-variant, missense	Bfar, 3110001I22Rik	Mm_Celera	16:13677312	TCCAGAAAATCAGGT[A/G]TAGATCAGAAGAACT	67118
rs248239706	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13687012	TTGTGTCACCCAGGC[A/T]ACCTGGAACTGCCTA	67118
rs248290877	in-del	-/ACA			intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678829	AGGCAATCTGTTCAG[-/ACA]ACAAGTCAGGGTCTA	67118
rs248300575	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13686145	TACTTGTGCCTGCTG[C/T]CTGAGGAAGTTAGAA	67118
rs248350271	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13694434	TCCTACCTCCTCCTC[C/T]TGAGTGCTGGGATTG	67118
rs248462412	in-del	-/G			intron-variant	Bfar	Mm_Celera	16:13690009	TAAAATCTTTAAAAA[-/G]AAATAAGTAACATTT	67118
rs248653762	in-del	-/T			intron-variant	Bfar	Mm_Celera	16:13680990	TTTTGTTTGTTTTGG[-/T]TTTTTGGTTTTCCGA	67118
rs248738809	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13681473	GGCTTGAAGGGTGGG[A/G]GGTCATATTGAGATA	67118
rs248808357	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13692299	TCTTGGCATTCATCA[A/G]CACAGCGTTTAATGT	67118
rs248841761	snp	G/T			utr-variant-5-prime, upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671879	GCGCATGCGCCCGCA[G/T]GCCCCTAGAGCAGCC	67118
rs248906813	snp	A/G			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671110	GCTGGCTTATAGGAG[A/G]TAAGAGTTTAAAGAG	67118
rs248906876	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13681928	AGGCATCCCATTAAG[A/G]GCAAGACCTGAGAAC	67118
rs248962113	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13680872	AAGAGCTTGCTCTCC[C/T]TTCCTCCTATATAAC	67118
rs249185961	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13698783	TTGTTAGAGGTAGGG[C/G]TGTGTCCAAACGTAA	67118
rs249247502	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13682115	CTTACTGTATAGCTG[C/T]ATAGCTGTGGCTGGC	67118
rs249307403	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13681080	TAGACCTCAGAAATC[C/T]GCCTGCCTCTGCCTC	67118
rs249361829	in-del	-/ATTTGTAGTT			intron-variant	Bfar	Mm_Celera	16:13689466	ATCTGAGTTGATTTC[-/ATTTGTAGTT]ATTTTGAATAGTGCT	67118
rs249367877	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13692132	TTGGAGGCTTAAGAA[C/G]AAACATTCTGATGTG	67118
rs249424488	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13691027	TAAATATTTTTTAAA[A/T]TTTTATCTATTTTTA	67118
rs249695450	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13696843	AAGCTGGCCTCGAAC[A/C]CAGAAATCCGACTGC	67118
rs249918624	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13698585	ACTCCAGTCCTCATG[C/T]GTGGACAGCGTGCAT	67118
rs250048902	snp	C/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674076	TTCAAAACAGGATGG[C/T]ATTACCTTAGTCATT	67118
rs250232119	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13684565	CCAAGCTCTTGTTGT[C/T]GTGGCCGCTGTGGGT	67118
rs250296005	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13696126	TCACCATGCTTGACG[A/C]TTTTTAGTTCCTTTA	67118
rs250313612	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13683811	TTGTACTAGACGCTG[C/T]ACATGTATTAACTTA	67118
rs250374039	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13687090	CTACAATTAAGGACA[C/T]ATGCACCATACCTGG	67118
rs250383081	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13694356	ACTGCACTGGCCTTG[A/G]GTGGGGGTTGTTTTC	67118
rs250426057	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13686926	AACCCCCACATGTGC[A/G]TGACCAAACTCACAC	67118
rs250547803	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13697056	AATCACGTCTAGCCA[A/G]CTTCTTGGGTTTTGA	67118
rs250603769	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13696371	TACAATTTTGGTGGT[A/G]CTGCTGCTGCTGCTA	67118
rs250628567	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13696448	AACCGATGCTAGTCT[C/T]GAGCTACCTCCATTC	67118
rs250711351	in-del	-/C			intron-variant	Bfar	Mm_Celera	16:13684547	ACAGGTGTCTTAGCT[-/C]CCCCAAGCTCTTGTT	67118
rs250786588	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13680301	ACCGACTGCTGTGAG[C/T]TGTCGAGTGGGTGCT	67118
rs250836630	in-del	-/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676389	ATTCGATTGTTTTTG[-/T]TTTTTTTGAGACAGA	67118
rs251182049	in-del	-/TTTAT			intron-variant	Bfar	Mm_Celera	16:13698634	TTTTCTAGCCCCAAC[-/TTTAT]TTTAAGATGAACTAT	67118
rs251329875	snp	C/T			intron-variant, utr-variant-3-prime	Bfar, 3110001I22Rik	Mm_Celera	16:13678158	CATGATTCATACACT[C/T]ACCAGTGTGTGTCTT	67118
rs251458145	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13700041	AATTATTTTGTAAAT[A/G]TATATGTTTATTTGT	67118
rs251462457	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13688402	TGCTGAGCCATTTCT[C/T]CATCCCTGTTATGGA	67118
rs251470056	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13693294	CTGTGTTTGTCAGAT[A/G]TAGTTAGGTGTGTCC	67118
rs251512339	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13699108	GTAGATGGTTGGTAA[A/G]GAAATACCAATGACG	67118
rs251643691	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13701948	AGAGGACACATGCTA[A/G]GAGCTGGAGACTGGT	67118
rs251850016	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13675845	GGAGAGACAAATGTG[A/G]CTGGAATAGGATGTG	67118
rs251886087	in-del	-/C			intron-variant	Bfar	Mm_Celera	16:13690070	GTGTATGCCTTTAAT[-/C]CCCAGCATTCAGAAG	67118
rs251907152	snp	A/G			synonymous-codon	Bfar	Mm_Celera	16:13685177	GAGCATGAGAGAGCA[A/G]GAGGAAGAGCATCCT	67118
rs252020156	snp	A/C			intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678548	ATCCACCACTGAGCT[A/C]TAATCCCAGCATCAA	67118
rs252436897	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13682896	TCTTCCGAAAGGCCT[C/G]AGTTCAAATCTCAGC	67118
rs252588817	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13699771	GAAGTCAGAGCAGGA[A/G]CTAAAGCAGAGTTCA	67118
rs252613148	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13694227	AACTCTTAAATATGT[A/G]GTGGGAAATATTTGT	67118
rs252630974	in-del	-/GTGTGTGTGTGTGTGT			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672596	TGTGCTGATGAGAGC[-/GTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG	67118
rs252680431	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13693061	TAGATACATTGTTTC[A/T]CAGGCAAGAGGCAAG	67118
rs252822510	in-del	-/TA			intron-variant	Bfar	Mm_Celera	16:13684972	GAGAGAGTGAGAGAG[-/TA]AGAGAGAACAAACTT	67118
rs252822963	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13703175	ATCTGTACAATAAAT[A/G]CAGTATAGGCTGATC	67118
rs252844159	in-del	-/A			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674825	ATGATTCAAACATTG[-/A]AAAAAAAGAAATTCA	67118
rs252871068	snp	A/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673368	CTGCCCGTGGGGATT[A/T]AATGCCACCATGCCT	67118
rs252915349	snp	C/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672241	CAGGCTCTGGGGCCT[C/T]CTCACCCCGGCCTGG	67118
rs252955034	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13682288	AGTGGGCTTGGCAAG[C/T]TCACACCACCCTTGC	67118
rs252994991	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13681227	AATTGACTAGGTGGT[A/G]GTGACTTTGCTATAT	67118
rs253065189	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13680622	GGCAAGCCTCAGATT[C/T]ACCTGCCTCTGCCTT	67118
rs253158643	in-del	-/A			intron-variant	Bfar	Mm_Celera	16:13683759	GTGCAAAACCAAAAC[-/A]AAAAATACTTTCGAT	67118
rs253191932	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13679545	AGCAACAGTGTAGTT[A/T]TTAATAGTAATAAAT	67118
rs253251100	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13689784	GAAATCCTGTCTCAA[A/G]AAAACAAAAAAACAA	67118
rs253398594	in-del	-/T			intron-variant	Bfar	Mm_Celera	16:13691066	TGTGTGTTTTTTGCC[-/T]CCATTTTTTGTCCCT	67118
rs253589398	snp	C/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676171	AACAATTCATAAACA[C/T]CAAAATTACAATTTA	67118
rs253677631	snp	C/T			synonymous-codon	Bfar	Mm_Celera	16:13697449	CCTACCCTTCATCCA[C/T]ACCATCTGCCCTCTG	67118
rs253799619	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13698810	GTAAAGCTCATTCAT[C/T]GACATTACTTGTATT	67118
rs253811427	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13697575	TAGACCAGCCTATCT[A/C]TGAGTTTTGCAGAGC	67118
rs253970164	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676618	CTGATGGAGATCTTA[A/G]TTCTATTGAGGGACA	67118
rs254082164	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13684847	CTGGACTATATATGA[C/T]CTCCACGCACACCTA	67118
rs254097752	in-del	-/G			intron-variant	Bfar	Mm_Celera	16:13692587	TACAAGGTATCTCGT[-/G]GGGGGTTTTTGTTTG	67118
rs254145370	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13684107	ACTGGCCAAGATGGT[A/G]GATACTAGCCATGTC	67118
rs254191881	snp	G/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676268	TGCAGCATCAGGAGG[G/T]TAGAAAACCATTGTT	67118
rs254275318	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13675054	TCAGTTCAATTGTGG[A/G]CTAGAGAATGTAGCT	67118
rs254330559	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13695042	TGTCCATCATTACCA[A/G]CAGGTTAGATAACTG	67118
rs254450777	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673212	TGGGAGCCCAGGTTG[A/G]CCTCGCTCTGAAGAC	67118
rs254825732	snp	C/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13703545	TCAGAGTGAAGATTT[C/G]ACTTAAACTTTGCAT	67118
rs254860221	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13692423	GTCATCTCCACCCTC[A/C]TCCCTTCAGGTTGCT	67118
rs255048713	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13701683	TTAGCTACATAGCAA[A/G]TTTAGGCTAAGCTTG	67118
rs255059203	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13680500	TTTGTTCTGTTGCTG[C/T]TGCTGTTGCACTGTT	67118
rs255173590	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13699172	GGGGGATGAGGTTGC[C/T]TAGCGCCCCCATCAG	67118
rs255190532	in-del	-/AA			intron-variant	Bfar	Mm_Celera	16:13701723	AAAGTTTGTCTTAGG[-/AA]AAAAAAAAAAGTGCC	67118
rs255206993	snp	C/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671092	TTTGAGAGAGCAGCC[C/T]CTGCTGGCTTATAGG	67118
rs255235989	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13689558	TGAGGAATGGCCACA[C/T]CCCAGGATCTGTCTG	67118
rs255241929	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13700545	CAACCTAATTGACTT[A/G]CTACAAAGGCTTTCA	67118
rs255264851	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13680830	TTAGCCTGGGCTACA[A/G]AGTGAGATCCTGTCT	67118
rs255317118	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13699685	CACAGAAACTCTTTT[A/T]TGAGGGGAAAAAAAA	67118
rs255418820	snp	A/G			upstream-variant-2KB	Bfar, 3110001I22Rik, Parn	Mm_Celera	16:13670182	AATCCAACCATCTGG[A/G]GAGTTCATTTGAATT	67118
rs255469606	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13680404	TTATTTACTTGTTTA[C/T]CTTTTAAATATGAGG	67118
rs255531244	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13679763	CTGTACCACATGTAT[A/G]CGGTGCCTGTTAGAA	67118
rs255694496	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13697139	GGCCTAAGATTCACC[A/G]TCTTCTTCCACATAT	67118
rs256016739	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674769	GTCCAGTTTAGTGGG[A/G]AAGGTTTTGGGCAAT	67118
rs256533755	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13694800	TAGCCAGCCAGCCAG[C/G]CTTGCCAAAATGGTA	67118
rs256604702	snp	G/T			intron-variant	Bfar	GRCm38.p3	16:13693630	CTCTCCAAAGGCTTG[G/T]AAGAGCCTTTATGGA	67118
rs256631811	snp	A/C			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676820	ACAGTTTATACTTAA[A/C]TTTTACTCACCAGCA	67118
rs256727788	snp	C/G			intron-variant	Bfar	Mm_Celera	16:13682666	AAACCCTTATTCTAG[C/G]TTCCTGGAAGCCAGT	67118
rs256785897	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13681839	CCAATATGGAAAAAC[G/T]TATCAGAACTTCAAA	67118
rs256819182	snp	C/T			utr-variant-3-prime	Bfar	Mm_Celera	16:13703080	CTCCTTCTGTGAGCA[C/T]GGAGTTGAATGGAAT	67118
rs256849668	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13692372	AAACTCAGTGTGTAA[A/G]CACGCGTTGTCTGCA	67118
rs257002023	snp	A/C			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671529	ACAAAGATCATCCTG[A/C]CAAGCATGGTCTCAC	67118
rs257062497	in-del	-/AT			intron-variant	Bfar	Mm_Celera	16:13694954	GTGAGCACACAAACC[-/AT]ACACACACAGAGAGA	67118
rs257212452	in-del	-/T			intron-variant	Bfar	Mm_Celera	16:13691069	TGTTTTTTGCCTCCA[-/T]TTTTTTGTCCCTGCA	67118
rs257282286	snp	A/G			intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678593	ACCAACTATTATTAG[A/G]TCATGTGTTACTTGG	67118
rs257537801	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13682019	TAAGAACACTAACTG[A/C]CCTTCCAGAGGTCCT	67118
rs257611126	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13692591	AGGTATCTCGTGGGG[G/T]GTTTTTGTTTGTTTG	67118
rs257802818	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676325	ACAGAGCTAGGTCAC[A/G]TGTATGATTCAAGAT	67118
rs257863459	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13686038	GGTTGGTTCTTCCGT[A/G]CTTCCATGCAGTAGG	67118
rs257939984	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13686365	TGTAGGGGTTGATTC[A/T]TTCCTTTGATTATTG	67118
rs257945282	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13698595	TCATGCGTGGACAGC[A/G]TGCATCCTTAACCAC	67118
rs257984321	in-del	-/GTT			intron-variant	Bfar	Mm_Celera	16:13690933	TGGTTTTAACAGTGA[-/GTT]GTTGTAGAAACAGGT	67118
rs258002904	snp	A/G			synonymous-codon	Bfar	Mm_Celera	16:13697344	GCAGGCTGTCAACCC[A/G]GGTAGATCCCTATTC	67118
rs258279066	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690640	GAGGCAGAGTGGCAG[A/G]TAGAGAAAGAGAAAG	67118
rs258319860	snp	A/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13676730	TTAAAGTTTTATAAA[A/T]CTATAAGAGGTGTGC	67118
rs258330355	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673479	TTTCTGAATTGAGTA[A/G]CAGGAAATGGAGAAG	67118
rs258352731	in-del	-/TG			intron-variant	Bfar	Mm_Celera	16:13687805	GCCCTCTTCCTGACC[-/TG]TTCAGTGGTGTCATG	67118
rs258383808	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13675804	AGGATTCTGTAACTT[A/G]ATTCGAATTCATGGA	67118
rs258389775	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13683561	CAAAACAGTGCCTGA[A/G]GCAGGCCTAGTTCTT	67118
rs258915859	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13681032	TCTGTAGTTCTGGCT[A/G]TCCTAGATCTCACTC	67118
rs258934142	snp	A/T			intron-variant, synonymous-codon	Bfar	Mm_Celera	16:13687571	ATTCTTCTCCGGTGT[A/T]CTCACAGCTTTAACT	67118
rs258977125	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13691988	CCAGGGCCAAGAAGT[A/G]GGAGTGGAGGGAGGG	67118
rs259023849	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13692305	CATTCATCAACACAG[C/T]GTTTAATGTTCAGCC	67118
rs259087636	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690257	GTTAATGTCATAATA[A/G]ACATAACTGAACATG	67118
rs259139554	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13702736	GAAAGAAAAAGAAAA[A/G]AAAAAAGAAAGAAAT	67118
rs259196974	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13696855	AACACAGAAATCCGA[C/T]TGCCTCTGCCTCCCA	67118
rs259428507	in-del	-/A			intron-variant	Bfar	Mm_Celera	16:13697512	CAAGCTTCTGGTAGG[-/A]AAAAACTAATTCTAC	67118
rs259448848	in-del	-/TAACTGGTGCTAATTTTCT			intron-variant	Bfar	Mm_Celera	16:13685928	CTATACAATTAGAGG[-/TAACTGGTGCTAATTTTCT]TAATATGTAAGTAAA	67118
rs259548005	snp	G/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671482	TTGACTGTCTTGGAA[G/T]TCACTCCGTAGACTA	67118
rs259611876	snp	C/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13670986	AGAGATGTTAAAATT[C/T]TGAAAGATCAAATCA	67118
rs259667413	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13687098	AAGGACACATGCACC[A/C]TACCTGGCAATATCA	67118
rs259670193	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13680573	TATGTAATTCTGCCA[A/G]TGCAGTTCTGGCCTA	67118
rs259732920	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13680066	TTTCTTTGAATATAT[A/G]TATGTGTGCACATGG	67118
rs259733949	snp	A/C			intron-variant	Bfar	Mm_Celera	16:13698145	CTTCCCATGTAGACG[A/C]GAAGAAATAGAACAG	67118
rs260212635	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13684602	GGCGAGTCTTAGGAA[C/T]GTACCCTACTACCAG	67118
rs260273110	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13696328	AGTTTATGAAGAATG[C/T]GTCTGGAGTTCCTCA	67118
rs260420754	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13691676	TCCTTCTAGTTTTCT[C/T]CTACATACACCCTTT	67118
rs260476506	snp	C/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13702845	TCCCAAACCAGGCTT[C/G]TTGGGCCAGGTCTGT	67118
rs260594375	snp	A/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673948	AATTTACCTCAAAGT[A/T]AGATGAGGATCAGAG	67118
rs260643743	snp	G/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672553	AGAACTTAGCTCTTC[G/T]CATTCCCATACACAC	67118
rs260688272	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13692777	CCCTGTCCATAATCT[A/G]TGGGAGGTGTCCTGC	67118
rs261011386	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13697906	TCCATGTCATGTGTC[A/G]TTCTCCAACCCTTGT	67118
rs261108116	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690800	TTTGAGACAGATTTA[A/G]CAATGTATTTCAGTC	67118
rs261342528	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13697549	TCAGTGTTGTACAAA[A/G]CTGGAGAAAGTAGAC	67118
rs261388273	in-del	-/C			intron-variant	Bfar	Mm_Celera	16:13682252	GAACCGCACAGATCT[-/C]CCTGTCTTTGGTTCC	67118
rs261539325	snp	C/T			intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678805	CCTCATCTTGCCCAA[C/T]ACAGCTTAAGGCAAT	67118
rs261587940	snp	A/G			intron-variant, synonymous-codon	Bfar, 3110001I22Rik	Mm_Celera	16:13677911	GCAGAATTTACATGA[A/G]CTAAGTGAGCGCTGT	67118
rs261617307	in-del	-/T			intron-variant	Bfar	Mm_Celera	16:13685868	TATCATCCCCTACCC[-/T]AGAACACTTCTTTCT	67118
rs261636437	in-del	-/T			intron-variant	Bfar	Mm_Celera	16:13698764	AGCTATAACCAGGTG[-/T]TGATTGTTAGAGGTA	67118
rs261711055	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13694889	AAGAGGCCACCATTG[C/T]TGACTTTTGGTCTGT	67118
rs261750616	snp	A/G			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671422	TAAATCAGAACTGAG[A/G]AACAGGAACTTTTTC	67118
rs261884368	snp	A/C			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672436	GGGCGCCCGCCACGT[A/C]GGCTAAATCCGAGGC	67118
rs261894489	snp	C/T			utr-variant-3-prime	Bfar	Mm_Celera	16:13702282	AGGCCCGAGCGAGCC[C/T]GTGAATCTACCTGAC	67118
rs262097390	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13679674	GCTACAGTGTACTCA[C/T]ATACATAAAATAATA	67118
rs262125038	in-del	-/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674231	ATCCCCACTGTTATA[-/G]GGGATACAAAGAAAG	67118
rs262217610	in-del	-/T			intron-variant	Bfar	Mm_Celera	16:13680525	ACTGTTACGGAGGCA[-/T]TTGGGGGTGGAGGAT	67118
rs262382844	snp	C/T			intron-variant, synonymous-codon	Bfar, 3110001I22Rik	Mm_Celera	16:13677206	CCAACAGCATGAGTG[C/T]GGGGATGAGAAAGAT	67118
rs262401176	in-del	-/TGC			intron-variant	Bfar	Mm_Celera	16:13696369	GTACAATTTTGGTGG[-/TGC]TGCTGCTGCTGCTGC	67118
rs262530990	in-del	-/GGAGGAGACACCAAA			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13675594	ACCCTGGAAAGTCCC[-/GGAGGAGACACCAAA]GGAGGACTGTGTACT	67118
rs262683864	snp	C/T			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674580	GTCATTCATATTCTT[C/T]ACTGAATAAAACCAC	67118
rs262789079	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13682369	TGGAAAGCACTGTCT[C/T]CCCTTCCCCTTAATT	67118
rs262810977	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13674043	ATTGGGTTGCGGAAA[A/G]GGGAAAGACAAAATA	67118
rs262839384	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13683955	CATGTTCTGTTTTTT[G/T]GGGGTAAAAATTTTG	67118
rs262928269	in-del	-/TA			intron-variant	Bfar	Mm_Celera	16:13684838	GAGGCCAGCCTGGAC[-/TA]TATATGATCTCCACG	67118
rs263089776	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13680469	CCTAACAGCTGAGTG[C/T]TCTCCTTAACCCAGG	67118
rs263299863	in-del	-/C			intron-variant, downstream-variant-500B	Bfar, 3110001I22Rik	Mm_Celera	16:13678535	TTCTAGGCATCTGAT[-/C]CACCACTGAGCTATA	67118
rs263438121	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13688233	CTTCGTTTTTTTAAA[A/T]ATTTATTTATTTATT	67118
rs263461142	snp	A/T			intron-variant, synonymous-codon	Bfar	Mm_Celera	16:13687580	CGGTGTTCTCACAGC[A/T]TTAACTGGTGTGGCA	67118
rs263468883	in-del	-/TTCT			intron-variant	Bfar	Mm_Celera	16:13688039	TTCTTTCTCTTTCTC[-/TTCT]TTCTTTCTTTCTTTC	67118
rs263632790	in-del	-/AGA			intron-variant	Bfar	Mm_Celera	16:13691503	TTATTCAGACACACC[-/AGA]AGAAGACATCAGATC	67118
rs263692461	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13685576	ATTTTTTTAGGCAAG[A/G]TCTCACTACAACATG	67118
rs263788033	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13694503	AATCTAGAGGCAGGT[A/G]GATCTCTGAACTGAG	67118
rs263827683	snp	G/T			intron-variant	Bfar	Mm_Celera	16:13696511	ATGCCCAGTGTGTCT[G/T]ATTTATTTTTTATTT	67118
rs263967180	in-del	-/AT			intron-variant	Bfar	Mm_Celera	16:13701305	TCCAATTCAGACCAC[-/AT]AGGAAAATAGAGGAG	67118
rs264057071	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13682810	CTGTAAGCCAGCCCC[A/T]GTTAAATTTTGTCCT	67118
rs264108926	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13692278	AGTGGGCAGTAAGCA[A/G]ACTGCTCTTGGCATT	67118
rs264143028	snp	G/T			utr-variant-3-prime	Bfar	Mm_Celera	16:13703114	CACCAGGCCGAGTCT[G/T]CTTAGATGACTGAGC	67118
rs264362670	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13691138	CCTTCAGATTTCCTG[A/G]ACCTAGAATTACAGA	67118
rs264392058	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13702659	AGTGGTCTACAGAGT[A/G]AGTTCTACAACAGCC	67118
rs264459260	in-del	-/A			intron-variant	Bfar	Mm_Celera	16:13694581	GTCTCGGAAGGAAGG[-/A]AAGGAAGGAAGGAAG	67118
rs264480101	in-del	-/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13673261	CTTTGTTTGTTTATT[-/G]GGGGGGGTGCATTTT	67118
rs264522204	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13698463	TTTTCTGTAAGCTGG[C/T]AGCCAGTAAGCAAGC	67118
rs264724140	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13696406	GGTTTGTTTATGATT[A/T]TTCCAGGGTAGAGTT	67118
rs264847790	snp	G/T			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671852	GAAAAGGAAGGGGCG[G/T]GTCGCGTTGGTGCGC	67118
rs264913397	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13702819	AGCCCTAACCTCACT[A/G]ACTGACATACTCCCA	67118
rs265004435	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13679989	GAATTTGAAATAGTC[C/T]TTAAAAACATTCCTC	67118
rs265142228	snp	A/G			intron-variant, missense	Bfar, 3110001I22Rik	Mm_Celera	16:13677709	AGCCACAAGAACCTG[A/G]GTCAAACAAAAAAGA	67118
rs265287437	snp	A/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13675141	TGCCAGAAAAATCCA[A/G]GAAGTTCCAAAAAGC	67118
rs265305036	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13684737	GAAGCCCTGGGTTCA[A/G]TTCACAGTTTCACAG	67118
rs265339074	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13682903	AAAGGCCTCAGTTCA[A/T]ATCTCAGCAACCACA	67118
rs265391508	in-del	-/A			utr-variant-3-prime	Bfar	Mm_Celera	16:13702736	AAAGAAAAAGAAAAG[-/A]AAAAAAGAAAGAAAT	67118
rs265434071	snp	C/G			intron-variant	Bfar, 3110001I22Rik	Mm_Celera	16:13672337	AGGTCTCTAGTCCTC[C/G]CCCGCGTCGGGGTCT	67118
rs265485248	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13680663	AATTTAAGACATGAA[C/T]CGTAAGGCCTGGCAA	67118
rs265642711	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13689281	AAAATGGCTTTGCCT[A/G]TAGTTCTTGCATATT	67118
rs265783231	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13686207	TGGTTGTAAGCCATT[A/G]TATGGGTTCTAGGAA	67118
rs265799740	snp	C/T			intron-variant	Bfar	Mm_Celera	16:13697173	AGATGTGTACAACCA[C/T]GCCCAGCAAGACTGG	67118
rs265860027	in-del	-/TTTC			intron-variant	Bfar	Mm_Celera	16:13690995	CATTTTGTTTTCTGT[-/TTTC]TTTCTTTTATAGATA	67118
rs265869759	in-del	-/ACACA			intron-variant	Bfar	Mm_Celera	16:13694952	TGTGAGCACACAAAC[-/ACACA]CATACACACACAGAG	67118
rs265927396	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13683852	AAATGTCATGGGAGT[A/T]GACTCTAGTTCTGAG	67118
rs265975134	snp	A/T			synonymous-codon	Bfar	Mm_Celera	16:13692544	TGTGAGAGCCCTGGG[A/T]GTGAAGCCACCGCAG	67118
rs265985470	in-del	-/TT			intron-variant	Bfar	Mm_Celera	16:13699454	ATTTTCTTTGGTTTC[-/TT]TGTTTTATTTTGCTA	67118
rs265992061	snp	A/G			utr-variant-3-prime	Bfar	Mm_Celera	16:13703359	CTCAGCAGATGTAGA[A/G]TGTGAGCTCATCAGC	67118
rs266121609	snp	A/G			intron-variant	Bfar	Mm_Celera	16:13690622	GGAGTTAAGAGGGTA[A/G]TAGAGGCAGAGTGGC	67118
rs266137898	snp	A/T			intron-variant	Bfar	Mm_Celera	16:13700974	ATCTATGGTGGGCAT[A/T]TCTATTCAGACCAGC	67118
rs387319744	in-del	-/TTCTTTCTCTTTCTCTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTC			intron-variant	Bfar	Mm_Celera	16:13688024	CTTTCTTTCTTTCTC[lengthTooLong]TTTCTCTTCTTTCTC	67118
rs387356617	in-del	-/CAAA			upstream-variant-2KB	Bfar, 3110001I22Rik	Mm_Celera	16:13671286	ACCCTGTCTCGAAAA[-/CAAA]CAAACAAACAAACAA	67118
rs387702247	in-del	-/TTTG			intron-variant	Bfar	GRCm38.p3	16:13696728	CCTAAGCTAATACTG[-/TTTG]TTTGTTTGTTTGTTT	67118
rs578392388	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13691779	GGGCCCCCAATGGAG[A/G]AGCTAGAGAAAGTAA	67118
rs578399781	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13695533	GCTGCTAGGACTACA[C/T]GCCTTCCTCACCATG	67118
rs578486918	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13696073	GCTGCTAGGACTACA[C/T]GCCTTCCTCACCATG	67118
rs578514595	snp	C/G			intron-variant	Bfar	GRCm38.p3	16:13684901	AGACAGAGAGAGAGA[C/G]AGAGAGAGAGAGAGA	67118
rs578592547	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13687939	TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT	67118
rs578594458	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13696778	GTTTGTTTTTTGAGA[C/T]AGGGTTTCTCTGTGC	67118
rs578959776	snp	G/T			intron-variant	Bfar	GRCm38.p3	16:13686409	TTTTTTTTTTTTTAA[G/T]ATAAGCACACTGTAG	67118
rs579000343	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13696723	TCTTGCCTAAGCTAA[C/T]ACTGTTTGTTTGTTT	67118
rs579061747	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13695623	GCTGCTAGGACTACA[C/T]GCCTTCCTCACCATG	67118
rs579082821	snp	A/T			intron-variant	Bfar	GRCm38.p3	16:13691754	ACAGTCAGCTAATGG[A/T]TGGATCACAGGGCCC	67118
rs579112868	snp	G/T			intron-variant	Bfar, 3110001I22Rik	GRCm38.p3	16:13675617	CACCAAAGGAGGACT[G/T]TGTACTCTTCTGCCT	67118
rs579165026	snp	G/T			upstream-variant-2KB	Bfar, 3110001I22Rik	GRCm38.p3	16:13671554	TCTCACAACGTCATA[G/T]ATTGAAAACATAGTA	67118
rs579172700	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13695585	CTCACCATGCTGCTA[A/G]GACTACACGCCTTCC	67118
rs579337938	snp	A/C			intron-variant	Bfar	GRCm38.p3	16:13695369	GCCTTCCTCACCATG[A/C]TGCTAGGACTACACG	67118
rs579638320	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13698500	TGTCCTCACATCCCC[A/G]CCCCTCAGTGCTGGG	67118
rs579659430	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13687967	TCTCTTTCTCTTTCT[C/T]TTTCTCTTTCTCTTC	67118
rs579768809	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13692959	TGTGGGAGGTGTCCT[A/G]CCTGAGTGCTGCATA	67118
rs579837036	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13691907	AGAAGATGGCCTAGT[C/T]GGCCATCAGGGGAAA	67118
rs579885005	snp	A/T			intron-variant	Bfar	GRCm38.p3	16:13701847	GCCAGCCAGGGCTAC[A/T]TAGAAAAAAACCTGT	67118
rs579887779	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13695675	CTCACCATGCTGCTA[A/G]GACTACACGCCTTCC	67118
rs579895126	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13679665	ATCTGTACAGCTACA[A/G]TGTACTCACATACAT	67118
rs580288847	snp	A/T			intron-variant	Bfar	GRCm38.p3	16:13681581	TGTCACATAAAAAAA[A/T]TTATATATACACATA	67118
rs580338791	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13695713	GCTGCTAGGACTACA[C/T]GCCTTCCTCACCATG	67118
rs580353937	snp	G/T			intron-variant	Bfar	GRCm38.p3	16:13691815	GAGCTGAAGGGATCT[G/T]CAACCCTATAGGTGG	67118
rs580417168	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13691802	GAAAGTAACCAAGGA[A/G]CTGAAGGGATCTGCA	67118
rs580451402	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13701276	ATGGCCAAGCTCAAG[A/G]TATAAAGCATATCTC	67118
rs580535414	snp	C/G			intron-variant	Bfar	GRCm38.p3	16:13688138	CTTTCTCTTCTTTCT[C/G]TCTTTCTTTCTCTCT	67118
rs580545925	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13692903	TGTGGGAGGTGTCCT[A/G]CCTGAGTGCTGCATA	67118
rs580683615	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13695555	CTCACCATGCTGCTA[A/G]GACTACACGCCTTCC	67118
rs580782244	snp	C/T			downstream-variant-500B	Bfar	GRCm38.p3	16:13703952	CTGTATATAGCCAGC[C/T]TCCCAATATCCCACC	67118
rs580865017	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13689871	TCAGCAGTTAAGAGC[A/G]CTGACTGCTCTTCCA	67118
rs580970212	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13695435	CTCACCATGCTGCTA[A/G]GACTACACGCCTTCC	67118
rs581056956	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13688192	TCTCTTTTTCTCTTT[C/T]TCTCTTTCTTTCTTT	67118
rs581166933	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13696054	TACACGCCTTCCTCA[C/T]CATGCTGCTAGGACT	67118
rs581357946	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13695765	CTCACCATGCTGCTA[A/G]GACTACACGCCTTCC	67118
rs581380879	snp	A/T			intron-variant	Bfar	GRCm38.p3	16:13691750	GCTCACAGTCAGCTA[A/T]TGGATGGATCACAGG	67118
rs581420523	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13682244	AGCTAGACTGAACCG[C/T]ACAGATCTCCTGTCT	67118
rs581461055	snp	G/T			intron-variant	Bfar	GRCm38.p3	16:13686303	TTTTTGTTTGTTGGT[G/T]GTGATGTGTGTGTGT	67118
rs581495257	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13691957	CAAACTTTATCTGCC[C/T]CAGTACAGGGGAACG	67118
rs581531238	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13695005	AAAGAGACAGACAGA[A/G]GGAGAAACAGAGAGA	67118
rs581547068	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13696095	CTCACCATGCTGCTA[A/G]GACTACACGCCTTCT	67118
rs581583605	snp	G/T			intron-variant	Bfar	GRCm38.p3	16:13691939	AGAGGCCCCTTGGTC[G/T]TGCAAACTTTATCTG	67118
rs581713410	snp	C/G			intron-variant	Bfar	GRCm38.p3	16:13691538	TACAAATGGTTGTGA[C/G]CCACCATGTGGTTGC	67118
rs581754205	snp	A/C/T			intron-variant	Bfar	GRCm38.p3	16:13691792	AGGAGCTAGAGAAAG[A/C/T]AACCAAGGAGCTGAA	67118
rs582108782	snp	C/T			missense	Bfar	GRCm38.p3	16:13692527	CTCACGGAGCTGGAG[C/T]GTGTGAGAGCCCTGG	67118
rs582161151	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13695645	CTCACCATGCTGCTA[A/G]GACTACACGCCTTCC	67118
rs582205280	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13691755	CAGTCAGCTAATGGA[C/T]GGATCACAGGGCCCC	67118
rs582238360	snp	A/G			intron-variant, utr-variant-3-prime	Bfar, 3110001I22Rik	GRCm38.p3	16:13678319	TTGTGGTTTTTATTG[A/G]CTTTTGTTTTCTTAG	67118
rs582318414	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13687957	TTTCTTTCTTTCTCT[C/T]TCTCTTTCTCTTTCT	67118
rs582320797	snp	A/T			intron-variant	Bfar	GRCm38.p3	16:13697697	ATTTTTTTTTTAAGC[A/T]TTGATTTTGTTACAA	67118
rs582378660	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13692945	CCCTGTCCATAATCT[A/G]TGGGAGGTGTCCTAC	67118
rs582412823	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13696774	GTTTGTTTGTTTTTT[A/G]AGACAGGGTTTCTCT	67118
rs582428722	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13687911	TTTCTCTTCTTTCTT[C/T]CTTTCTCTTCTTTCT	67118
rs582697329	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13695593	GCTGCTAGGACTACA[C/T]GCCTTCCTCACCATG	67118
rs582841651	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13692833	CCCTGTCCATAATCT[A/G]TGGGAGGTGTCCTGC	67118
rs582955491	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13691805	AGTAACCAAGGAGCT[A/G]AAGGGATCTGCAACC	67118
rs582979576	snp	A/C			intron-variant	Bfar	GRCm38.p3	16:13691932	GGGAAAGAGAGGCCC[A/C]TTGGTCTTGCAAACT	67118
rs583030230	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13695683	GCTGCTAGGACTACA[C/T]GCCTTCCTCACCATG	67118
rs583037059	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13680517	GCTGTTGCACTGTTA[C/T]GGAGGCATTTGGGGG	67118
rs583196353	snp	G/T			intron-variant	Bfar	GRCm38.p3	16:13691867	GTACCCCCAGAGCTC[G/T]TGTCTCTAGCTGCAT	67118
rs583272166	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13693001	CCCTGTCCATAATCT[A/G]TGGGAGGTGTCCTGC	67118
rs583427704	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13683089	TTCACAGCAGTAAAA[C/T]CCTGAACGGGTATGC	67118
rs583478730	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13688281	TGTCACTTCTTCAGA[C/T]ACACCAGAAGAGTGC	67118
rs583496537	snp	C/G			intron-variant	Bfar	GRCm38.p3	16:13684893	AAGGAGACAGACAGA[C/G]AGAGAGAGAGAGAGA	67118
rs583607795	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13688142	CTCTTCTTTCTGTCT[C/T]TCTTTCTCTCTCTTT	67118
rs583636444	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13701280	CCAAGCTCAAGGTAT[A/G]AAGCATATCTCCAAT	67118
rs583729968	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13687975	TCTTTCTCTTTCTCT[C/T]TCTCTTCTTTCTCTT	67118
rs583749870	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13695773	GCTGCTAGGACTACA[C/T]GCCTTCCTCACCATG	67118
rs583857366	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13695735	CTCACCATGCTGCTA[A/G]GACTACACGCCTTCC	67118
rs583949545	snp	G/T			intron-variant	Bfar	GRCm38.p3	16:13698748	GAGTTTGAAGGCAGC[G/T]AGCTATAACCAGGTG	67118
rs584029234	snp	G/T			intron-variant	Bfar	GRCm38.p3	16:13681620	TGTGTATATATATAT[G/T]TATATATATATAAAT	67118
rs584039062	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13694492	ATAACCCCTTTAATC[C/T]AGAGGCAGGTAGATC	67118
rs584184517	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13692758	CTTCACAAGCCTCTC[A/G]GGTCCCTGTCCATAA	67118
rs584247430	snp	C/T			downstream-variant-500B	Bfar	GRCm38.p3	16:13703963	CAGCCTCCCAATATC[C/T]CACCCCCACCTGAGG	67118
rs584259161	snp	C/G			intron-variant	Bfar	GRCm38.p3	16:13684897	AGACAGACAGAGAGA[C/G]AGAGAGAGAGAGAGA	67118
rs584261040	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13696065	CTCACCATGCTGCTA[A/G]GACTACACGCCTTCC	67118
rs584339553	snp	C/T			upstream-variant-2KB	Bfar, 3110001I22Rik	GRCm38.p3	16:13670471	TCTGTTATGTATCTG[C/T]TATCACAATGAAGAA	67118
rs584368129	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13695563	GCTGCTAGGACTACA[C/T]GCCTTCCTCACCATG	67118
rs584606718	snp	G/T			intron-variant	Bfar	GRCm38.p3	16:13692058	ATTGGAAATGTAAAT[G/T]AAATAAATACCTAAT	67118
rs584652255	snp	G/T			intron-variant	Bfar	GRCm38.p3	16:13691765	ATGGATGGATCACAG[G/T]GCCCCCAATGGAGGA	67118
rs584760310	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13695443	GCTGCTAGGACTACA[C/T]GCCTTCCTCACCATG	67118
rs584982017	snp	C/G			intron-variant	Bfar	GRCm38.p3	16:13696375	ATTTTGGTGGTGCTG[C/G]TGCTGCTGCTATGGT	67118
rs585083170	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13687963	TCTTTCTCTTTCTCT[C/T]TCTCTTTCTCTTTCT	67118
rs585167073	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13692791	TGTGGGAGGTGTCCT[A/G]CCTGAGTGCTGCATA	67118
rs585173814	snp	A/C			intron-variant	Bfar	GRCm38.p3	16:13691794	GAGCTAGAGAAAGTA[A/C]CCAAGGAGCTGAAGG	67118
rs585267186	snp	A/T			intron-variant	Bfar	GRCm38.p3	16:13686385	TTTGATTATTGGTTT[A/T]TGTTTTTGTTTTTTT	67118
rs585346474	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13691947	CTTGGTCTTGCAAAC[C/T]TTATCTGCCTCAGTA	67118
rs585480835	snp	G/T			intron-variant	Bfar	GRCm38.p3	16:13680975	AAGGTTAGAAACATT[G/T]TTTGTTTGTTTTGGT	67118
rs585492733	snp	G/T			intron-variant	Bfar	GRCm38.p3	16:13697802	GAGTAGTAGTTAGCC[G/T]ACTACAACAGGATTT	67118
rs585606469	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13695705	CTCACCATGCTGCTA[A/G]GACTACACGCCTTCC	67118
rs585747574	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13692953	ATAATCTGTGGGAGG[C/T]GTCCTACCTGAGTGC	67118
rs585846452	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13700150	TGCCTGGCTCATTGT[C/T]CTAATTTGTGTGTGT	67118
rs585964224	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13695615	CTCACCATGCTGCTA[A/G]GACTACACGCCTTCC	67118
rs585991813	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13695653	GCTGCTAGGACTACA[C/T]GCCTTCCTCACCATG	67118
rs586009186	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13679483	ACATGGTGGCTCACA[A/G]CCATCCGTAATGAGA	67118
rs586041397	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13691811	CAAGGAGCTGAAGGG[A/G]TCTGCAACCCTATAG	67118
rs586230842	snp	A/C			intron-variant	Bfar	GRCm38.p3	16:13689812	CAAAAAAACAAAAAA[A/C]AAAAAGAAAGAAAGA	67118
rs586474674	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13688081	TTTCTCTTTCTCTTC[C/T]TTCTCTTCTTTCTCT	67118
rs586498269	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13692841	ATAATCTGTGGGAGG[C/T]GTCCTGCCTGAGTGC	67118
rs586603800	snp	C/T			utr-variant-3-prime	Bfar	GRCm38.p3	16:13703429	CGACAGACGGACAGA[C/T]GGACAGACAGAATGT	67118
rs586773056	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13682243	CAGCTAGACTGAACC[A/G]CACAGATCTCCTGTC	67118
rs586779710	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13690573	GTTTTTGTTTTTTTA[A/G]TATAGAATAGAATTT	67118
rs586795098	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13684853	TATATATGATCTCCA[C/T]GCACACCTACCCCTT	67118
rs586808106	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13691900	ATATATCAGAAGATG[A/G]CCTAGTCGGCCATCA	67118
rs586821165	snp	A/T			intron-variant	Bfar	GRCm38.p3	16:13691937	AGAGAGGCCCCTTGG[A/T]CTTGCAAACTTTATC	67118
rs586824835	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13695795	CTCACCATGCTGCTA[A/G]GACTACACGCCTTCC	67118
rs586877935	snp	A/G			intron-variant	Bfar	GRCm38.p3	16:13695405	CTCACCATGCTGCTA[A/G]GACTACACGCCTTCC	67118
rs587215396	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13695743	GCTGCTAGGACTACA[C/T]GCCTTCCTCACCATG	67118
rs587274005	snp	C/T			intron-variant	Bfar	GRCm38.p3	16:13688172	TCTCTCTTTTTTTCT[C/T]TTTCTCTCTTTTTCT	67118
rs587275286	snp	G/T			intron-variant	Bfar	GRCm38.p3	16:13701288	AAGGTATAAAGCATA[G/T]CTCCAATTCAGACCA	67118
rs587311436	snp	A/C			intron-variant	Bfar	GRCm38.p3	16:13691952	TCTTGCAAACTTTAT[A/C]TGCCTCAGTACAGGG	67118
rs587456775	snp	A/C/T			intron-variant	Bfar	GRCm38.p3	16:13694955	TGAGCACACAAACCA[A/C/T]ACACACACAGAGAGA	67118
rs864290270	snp	C/T			intron-variant, synonymous-codon	Bfar, 3110001I22Rik	GRCm38.p3	16:13677974	TGATGCTGCTGCTTC[C/T]TAAGGACTGGTGCTC	67118