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

Chaf1b

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs4220205	snp	C/T	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93888158	AAGGTGAGCTGTATA[C/T]GTATCTCATTAACAT	110749
rs4220206	snp	A/G	0.5	0	intron-variant	Chaf1b	Mm_Celera	16:93889466	AGGAAGTAGAATGGA[A/G]CCCAAAGCCCATCCC	110749
rs4220207	snp	A/G	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93895595	CTATGTCTTCATCTG[A/G]AGGCTACTAGCAGAA	110749
rs4220208	snp	C/T	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93899856	CCTGCCATCGGGTGC[C/T]TCTCCCTGCAGATCC	110749
rs4220209	snp	C/T	0.46281	0.131194	intron-variant	Chaf1b	Mm_Celera	16:93905590	CCTAGCTGTAGTCAG[C/T]GTCTCACTGGGCCAC	110749
rs6323022	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93890944	tgaggagacaccatg[C/T]ccaaggcacctctta	110749
rs6323161	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891023	ctgttatcatcatgg[C/T]gggaagcntggcagc	110749
rs6323571	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891031	atcatggngggaagc[A/C]tggcagcgtacaggc	110749
rs6323607	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891050	cagcgtacaggcaga[C/T]atggtgctggagagg	110749
rs6323655	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891078	agggagctgagagtt[C/T]tacctctggatcctc	110749
rs6323717	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891112	cagcagggagtgaac[C/T]tagacacacttcctc	110749
rs6324161	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891139	cctccaacgagacca[C/T]gcctactttaacatg	110749
rs13463333	snp	G/T	0.5	0	synonymous-codon	Chaf1b	Mm_Celera	16:93887198	GGATGAGGAGGAGGC[G/T]CAGCTGAATAAGGAG	110749
rs13463334	snp	A/G			synonymous-codon, utr-variant-5-prime	Chaf1b	Mm_Celera	16:93892785	GTCGTTCTTCCGAAG[A/G]CTCAGCTTTACTCCA	110749
rs32577585	snp	A/G	0.444444	0.157135	intron-variant	Chaf1b	Mm_Celera	16:93890416	TGCACGTGCACACAT[A/G]CATACATAGTTAAGG	110749
rs32623814	snp	C/T	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93889043	CTTTGATAGGCCTGA[C/T]CTTGCTTTTGTTTGG	110749
rs32626099	snp	C/T	0.375	0.216506	upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883622	GTAGGTAGGACGTCT[C/T]GCATCTCGGGTTAGC	110749
rs32650214	snp	A/G	0.444444	0.157135	intron-variant	Chaf1b	Mm_Celera	16:93899763	TTGAGCTCATTGCAT[A/G]TGTGCTGGTCAGAGG	110749
rs32692974	snp	C/T	0.444444	0.157135	intron-variant	Chaf1b	Mm_Celera	16:93890387	GGCTAGCCTGGGCTA[C/T]GAGATGAGATGTGTG	110749
rs32815045	snp	A/G	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93888591	TACTTTTCTATTGCT[A/G]TGATAAGTCACCATC	110749
rs32927394	snp	A/G	0.375	0.216506	intron-variant	Chaf1b	GRCm38.p3	16:93897273	TTCTCACCAGAGACT[A/G]TGAAAGCTAGAAGAT	110749
rs32944815	snp	A/G	0.444444	0.157135	intron-variant	Chaf1b	Mm_Celera	16:93899008	AGCCTTTCAGCGGGG[A/G]GGCTTCTAGGCCACG	110749
rs32965016	snp	A/G	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93888706	TGTTGGAGGAAGTGT[A/G]TCACTGTGGGGGTGG	110749
rs45755726	snp	C/T	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93893299	AAGGTGTGTAAGGCT[C/T]TGGGGTCAACCCTTA	110749
rs45854472	snp	A/T			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906596	CCAGGCACAGCACAC[A/T]CTTCAGGGCAACCAG	110749
rs45860696	snp	C/T	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93902835	TGGTCGCAACTGTTC[C/T]GAGGCTTCCCGTTGG	110749
rs46007323	snp	A/T	0.444444	0.157135	intron-variant	Chaf1b	Mm_Celera	16:93890529	CTCAGGCCTCGCCCA[A/T]CCATCCTTCAGTTTC	110749
rs46030149	snp	C/T	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93902894	ACTTACTCCAGAGCT[C/T]ACTCCTCGTCTGGCC	110749
rs46150905	snp	G/T	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93893188	AATGTATCCTATACC[G/T]CGGCCCTCTCACTTG	110749
rs46158181	snp	A/T	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93895371	AGGCTTTTTGTTGTT[A/T]TGTGGCTTTTGGGGA	110749
rs46222996	snp	A/G	0.142012	0.225474	intron-variant	Chaf1b	Mm_Celera	16:93894072	AGTAGGGTCCTCTCT[A/G]GCAGTTCCAGAATCG	110749
rs46531190	snp	C/T	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93886518	AGACCATTGCTCCGT[C/T]AGGCTGACATGGCTG	110749
rs46682108	snp	A/G	0.231111	0.249285	synonymous-codon	Chaf1b	Mm_Celera	16:93905960	GAGACCCAGGCTTGA[A/G]GAACGTGAAGGAGAT	110749
rs46756019	snp	A/G	0.260355	0.249785	intron-variant	Chaf1b	Mm_Celera	16:93900805	ACAGTCTGTCGTGCC[A/G]GTCCCCTGTCTAACA	110749
rs46830996	snp	A/C	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93894098	AATCGTCACATGTTA[A/C]GATGGCGTGTGTAGG	110749
rs46966661	snp	A/T	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93893267	ACTTAGATGAAGCTC[A/T]TTAGTCAGGTGTGTC	110749
rs47090767	snp	A/G	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93893892	CGTAGCACTGCAGAG[A/G]CTGACTTTTATGGAC	110749
rs47150383	snp	A/C	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93899484	TGGCGCGCAGAAGTC[A/C]TTGATTACTGGTCTG	110749
rs47238196	snp	C/G	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93892948	AACCGACTACTGCAT[C/G]CCATTTGTTCTGAGT	110749
rs47259276	snp	A/C	0.277778	0.248452	synonymous-codon	Chaf1b	Mm_Celera	16:93905024	AATAAATTTAACACC[A/C]TTGAAAACAGACACT	110749
rs47274567	snp	C/T	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93893951	TGCAGTTCTCTAGTC[C/T]TACAACAAATGCATT	110749
rs47275317	snp	A/G	0.493827	0.0552116	intron-variant	Chaf1b	Mm_Celera	16:93899145	AGTGTATCGGGGACC[A/G]GAAATCTGGTCCCCG	110749
rs47423866	snp	C/T	0.124444	0.216185	synonymous-codon, utr-variant-5-prime	Chaf1b	Mm_Celera	16:93892758	CCGGATGTTTCACGA[C/T]GACAGCATGAAGTCG	110749
rs47445888	snp	A/G	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93893543	TGATAACGCCATCCA[A/G]TCCTATGCCTCACAG	110749
rs47573211	snp	G/T	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93893165	GCGCCACCTGGTGCC[G/T]TTGATACAATGTATC	110749
rs47599950	snp	A/G	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93895296	CTCATTGTCCAGAAT[A/G]CAACTTTCTCATCTA	110749
rs47743664	snp	G/T			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906468	TTGTCTAGAGTTGTG[G/T]ATCTGGTGGCAGCAC	110749
rs47751454	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891259	TGAGGGCTCTGATAT[C/T]GCTCCTAATTTCTCG	110749
rs47764205	snp	C/T	0.277778	0.248452	intron-variant	Chaf1b	Mm_Celera	16:93898750	AAATAACTATTCTGT[C/T]TGTTGAATATCAACA	110749
rs47854157	snp	C/T	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93894534	AAGCTCCTGGCTTGG[C/T]GTCGTCACTCAGGTG	110749
rs47856349	snp	A/G	0.260355	0.249785	intron-variant	Chaf1b	GRCm38.p3	16:93904945	TTGAACCTTGGCTTC[A/G]TACCTAAACGGCTCC	110749
rs48003120	snp	C/T	0.375	0.216506	downstream-variant-500B	Chaf1b	Mm_Celera	16:93906349	AAATTCAAGTGAGAG[C/T]ATGCAGTGCTTCCAA	110749
rs48139339	snp	A/T	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93895912	ATCCCTCCATCTTCC[A/T]TTTGTGTGTCTGTTT	110749
rs48271425	snp	A/T	0.260355	0.249785	intron-variant	Chaf1b	Mm_Celera	16:93894049	GGATAGCTGTACGAT[A/T]AAGTAAGAGTAGGGT	110749
rs48335103	snp	C/T	0.142012	0.225474	intron-variant	Chaf1b	Mm_Celera	16:93894086	TAGCAGTTCCAGAAT[C/T]GTCACATGTTAAGAT	110749
rs48367003	snp	C/T	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93899229	ATGACATCAGTAAGT[C/T]GACAGAGCTCTAAAA	110749
rs48539904	snp	C/T	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93899912	CTTCATGGTTTACCG[C/T]AAACTGGCTTTTAGT	110749
rs48634014	snp	A/G	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93894854	CTTTTTGCCTCTGAC[A/G]AGCATCTGTGCCTGT	110749
rs48976386	snp	A/G			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906296	TTGGTAGAGAGGAGG[A/G]CTAGGAGAAGACAGG	110749
rs49006166	snp	C/T	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93893107	TGTAAAACTTCCATA[C/T]GGTAAAGGTGTAGCA	110749
rs49061553	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93899806	CCTCAGTGCTTCCAC[A/G]TGTGGGTCCTGTGAA	110749
rs49078370	snp	A/G	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93894389	CTTAAAGGCTGGCTC[A/G]GAGAGAGGACAGCCA	110749
rs49088394	snp	A/C	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93893844	GACTGGTTTTCTGCT[A/C]GTAAATATTACAGAG	110749
rs49115530	snp	A/G	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93904717	CAAATTTAAAACGGG[A/G]TTGAGTGTGGTTTGG	110749
rs49236241	snp	A/C	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93894622	GTGCTTGTCTCTGTC[A/C]CAGATGCCCTGTCAG	110749
rs49283852	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891611	GGTTCGTAAGTAACA[C/T]GAACGTGTTTTGCAA	110749
rs49364355	snp	C/G	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93902980	ATGTGAGACCAAGCC[C/G]GGTGGAACCATGCTA	110749
rs49473439	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93896215	CACGCCCAGGATCAC[A/T]GGATCACAGGATCAC	110749
rs49738361	snp	G/T	0.132653	0.220748	intron-variant	Chaf1b	Mm_Celera	16:93901494	TCCCGTGATTCCGTG[G/T]GCTAGGTGGGCTGCT	110749
rs49890927	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93896283	TCCCAGAGGCAACTT[G/T]ACTTCCAGGAGCTCT	110749
rs49904238	snp	C/G	0.132653	0.220748	intron-variant	Chaf1b	Mm_Celera	16:93904883	ACACTGAAGGCCATG[C/G]GTGATATGCTCTGCA	110749
rs49973450	snp	G/T	0.391111	0.206368	intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892618	ACTTGCCCGACCTGC[G/T]GGCCAACTGATGAGG	110749
rs50011492	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891607	GACAGGTTCGTAAGT[A/G]ACATGAACGTGTTTT	110749
rs50057015	snp	C/T	0.5	0	intron-variant	Chaf1b	Mm_Celera	16:93886331	AGAGTGTTGATCTGT[C/T]CAGCCATCTCATCTC	110749
rs50059813	snp	A/G	0.375	0.216506	intron-variant	Chaf1b	Mm_Celera	16:93890110	GAGCAGGCCTCTGGA[A/G]GAACAATAGAGAAAT	110749
rs50201505	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93899701	GAATTCTGTATTTTT[A/T]TTTTATTTTATTATT	110749
rs50215802	snp	A/G	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93893132	GTAGCAGACTAAGTC[A/G]GTAGACACATGGTGG	110749
rs50384652	snp	A/C	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93893430	AACTTAGATGTTGCT[A/C]TTCTGTTCAGGTTGA	110749
rs50448695	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93899765	GAGCTCATTGCATAT[A/G]TGCTGGTCAGAGGAA	110749
rs50464734	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93904811	GTGTGGTGAACATTG[A/T]CTGTGGCTGTGATGC	110749
rs50618759	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891682	TTTGGCTTTTTTGTT[C/T]GGATCTGCTATTCTG	110749
rs50733452	snp	C/T	0.32	0.24	intron-variant	Chaf1b	Mm_Celera	16:93899431	GATAGTGTTCCTAAA[C/T]GAAACCATTTTCCTG	110749
rs50744051	snp	A/G	0.336735	0.234472	intron-variant	Chaf1b	Mm_Celera	16:93901851	AGCCCTGCATCGGGA[A/G]GTTTTCTGACACGGT	110749
rs50946690	snp	A/G	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93899208	ACCTTTAAATCCTGA[A/G]TATAAATGACATCAG	110749
rs50958601	snp	A/G	0.391111	0.206368	intron-variant, utr-variant-5-prime	Chaf1b	Mm_Celera	16:93892845	GCCTGACGGCATGTG[A/G]CATAGGGGTGTGATG	110749
rs51030621	snp	A/C/G			intron-variant	Chaf1b	GRCm38.p3	16:93904751	CGCATTCAGCAAGGT[A/C/G]TGTACTGGACTCCTC	110749
rs51043672	snp	A/G	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93900713	TGAAGTTGAGAGGAA[A/G]GTACATAGATCAAGA	110749
rs51122935	snp	C/G	0.408163	0.193609	intron-variant	Chaf1b	Mm_Celera	16:93900207	AACAGACACGGGTGT[C/G]GAGGATAGACCTCTG	110749
rs51196038	snp	A/C/T			intron-variant	Chaf1b	Mm_Celera	16:93899387	AACACACACACACAC[A/C/T]TACTCCTACAAAAAA	110749
rs51234037	snp	C/G	0.142012	0.225474	intron-variant	Chaf1b	Mm_Celera	16:93902043	CCGGAGGGTAGCACT[C/G]AGAAGGAACCTGTGT	110749
rs51243797	snp	A/G	0.124444	0.216185	intron-variant	Chaf1b	Mm_Celera	16:93899491	CAGAAGTCCTTGATT[A/G]CTGGTCTGGCCTCAT	110749
rs51400260	snp	A/G	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93895263	GTAGTGTCCCATGAT[A/G]CATAGTGTGTCTTTT	110749
rs51414044	snp	C/T	0.391111	0.206368	intron-variant	Chaf1b	Mm_Celera	16:93899530	GTGTAAATGTAAGAA[C/T]TGATTTTTTTACCCC	110749
rs51430194	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93899780	GTGCTGGTCAGAGGA[A/C]AACTTACAGCCCTCA	110749
rs51883938	snp	C/T	0.244898	0.249948	intron-variant	Chaf1b	Mm_Celera	16:93903202	GGGCCAAGTAGCGGC[C/T]GCCTTTGTCCTTCTG	110749
rs51988881	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93887706	AATACTCCACCCTAT[C/T]CCCTCAGTTTCCTAG	110749
rs52029908	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93896238	TGTGACCAAGCTCCT[A/G]GGATCCTGGGATCCT	110749
rs52410750	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93904706	AAGCCAAACTCCAAA[A/T]ATAAAACGGGATTGA	110749
rs108462872	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93897254	TATCAGAATTACACC[A/T]GACTTCTCACCAGAG	110749
rs108553745	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93897281	AGAGACTGTGAAAGC[C/T]AGAAGATCCTGGGCC	110749
rs211700311	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93885527	TCCTTAAACCTGACA[C/G]GAATCTCCTGTCTAA	110749
rs211877819	in-del	-/A			intron-variant	Chaf1b	Mm_Celera	16:93901808	TCTGTGGCGCCAGAT[-/A]ACCTCCTGGCATGTA	110749
rs211884383	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892705	GGGTTAGAGGCTTTC[A/G]GGTGATTTCAAGCTC	110749
rs211886706	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93900674	TGGCCCCGAATTTAT[C/T]TTTTATGTTGGGAAA	110749
rs211955492	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93884194	CCTCCCTTGCTGCTC[C/T]CCGGGATGATAGCCA	110749
rs212249998	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93899938	TTAGTGACGTGACAT[C/T]TCCTCCCCCGGCGGA	110749
rs212364118	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892326	ATGTGTGATATTCAC[A/G]TTTGGGCACATGTGT	110749
rs212464507	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93904565	ACTCGGGAGGCCAAG[A/G]CAGGCGGATTTCTGA	110749
rs212489297	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93899472	GTACTTAGTTCCTGG[C/T]GCGCAGAAGTCCTTG	110749
rs212527711	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93896585	AAAAGGACATAAATA[A/C]ACTCCTTTAAAGAAA	110749
rs212669867	in-del	-/C			intron-variant	Chaf1b	Mm_Celera	16:93904672	AAACAAACAAACAAA[-/C]AAAACACTGGCTGTT	110749
rs212725558	snp	C/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883307	ATATCCACTGCCTGG[C/G]ACACTCTTATTTGGT	110749
rs212845507	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93889433	CAAAATGTGTGGGTT[A/C]AAGAGTGAAGGGACA	110749
rs212845541	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93898113	CCTCATAGTACCTTT[C/T]CCAGAATTGACCATA	110749
rs212907532	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93889961	TTGTTGTACTTGGAG[A/G]TGAATTCAGGTCTAA	110749
rs212988470	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93904216	TGTTTTTTTAATATT[A/C]TATTTCTTTGAGGGG	110749
rs213030208	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93895006	CATCAGAACTGCTCT[G/T]TGTGGTGGGTGGGGT	110749
rs213042760	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882507	CCTACTCCAACAAAG[C/T]CACACCTTCTAATAG	110749
rs213057838	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93888411	TTGGAAACTGTTTTG[A/G]CAGAGGCTGAAATCC	110749
rs213093607	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93895651	AGGGTCTTAAGTCCA[C/T]ACCCACAGTGATACA	110749
rs213292707	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93899169	GTCCCCGTGTTCTCC[A/G]TGATGGAGCAGACAC	110749
rs213313833	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93888949	TTGTCCTTTATAAGA[C/G]TTGCCTCGGTCATGG	110749
rs213485263	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93905439	TTGTGAACTGCCATG[A/G]ATTGAACTCAGGACC	110749
rs213527366	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93884000	CTGATACCCGGCTTC[A/C]GCGCTTCTGACCTGG	110749
rs213646361	snp	A/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883500	AGAACCGCTGCTGTT[A/G]GCTAAGCGTGCAATC	110749
rs213850355	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93889252	GAATGTGACTGCTTT[C/T]TGCCCTTGTTTCAAG	110749
rs213987396	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93898552	AGAGGAGTAGACAGC[A/G]GGAAATAATCAAACC	110749
rs214294348	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93888996	TAAAGCCCTAACTAA[A/G]ACAGAAGTTGGTACC	110749
rs214494546	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93893864	ATATTACAGAGTGAC[C/T]AAAGCAGGGGGCCGT	110749
rs214648774	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93896453	GGAGGCAAGCATAAG[A/G]ACAGAAGCAACAGAA	110749
rs214691683	in-del	-/T			intron-variant	Chaf1b	Mm_Celera	16:93905637	TAATGTGTGTGTGTG[-/T]TGTTTTTTTTAAAGA	110749
rs214718997	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93902869	GGACGTCCCTGTTCC[A/G]TGCACTGGCACTTAC	110749
rs214783593	in-del	-/T			intron-variant	Chaf1b	Mm_Celera	16:93902379	GTTTTGGTTTTGTTG[-/T]TTTTTTGGTTGTTTC	110749
rs214806978	snp	A/C			synonymous-codon	Chaf1b	Mm_Celera	16:93887126	TTACCTCACAGATGC[A/C]GTCATTCTGTTGTGG	110749
rs214827302	in-del	-/CA			intron-variant	Chaf1b	Mm_Celera	16:93903114	TCAGTCTCCCATCTC[-/CA]CACACAGGAAAAATC	110749
rs214841581	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903561	CTGTAGACCAGGCTA[A/G]CCTCGAACTCAGACT	110749
rs214945500	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93895697	CCATACCTTCTAATA[A/G]TGCTACTTCCTGGGC	110749
rs215010365	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93901760	GTAAGCCTACAGGAC[A/G]GGAAGTGCCCCCCTT	110749
rs215012500	in-del	-/TA			intron-variant	Chaf1b	Mm_Celera	16:93887559	AGACAATAAAAACAT[-/TA]TAAAAATAGATTTTT	110749
rs215141902	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93904162	GCCTCCTTGAGTGCC[A/G]GGGCTAAAGATGTGC	110749
rs215170701	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93903539	CTAGGCTGTTCTGGA[A/C]CTCACTCTGTAGACC	110749
rs215186983	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93902168	CTATCTGATAATCTT[A/G]CATATCAGGTATTTA	110749
rs215329322	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93902201	ATTGCGATTTTTTTC[C/T]TTTTTTTTTTTAAAG	110749
rs215398270	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93902787	TGTGCAGGTCAAGTC[C/T]TCAGCACTTCCAGGC	110749
rs215559168	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93889917	CAAAACGGGCCTGAA[A/G]TTAAATGGATAGAAT	110749
rs215675150	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93895840	TTTTAGTTGGTGCTG[A/G]TGATTAAGCCAGAGT	110749
rs215721694	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93886592	TCCAGGCCACTGAGC[C/T]GTAGGTGCTTCATGA	110749
rs215889436	in-del	-/GAGA			intron-variant	Chaf1b	Mm_Celera	16:93889754	GTTGGGAAAATGGAG[-/GAGA]GAGTCTTTTCTCTCA	110749
rs215956131	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93889301	GGTGAAGAGACTCGT[C/T]AGATTAATTGCATTG	110749
rs215972448	snp	A/G			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906432	TGGCTGCCTTGCTTG[A/G]CCCTCCGTCTGAGCC	110749
rs216182781	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93896482	AACCCAATTCTCTCA[A/C]CATAGCAAGTCCTGG	110749
rs216199470	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93885688	TGTGAGATCTGAGCT[G/T]ATTGTATCTATTCCC	110749
rs216210284	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93894648	GTCAGGGTTACCACA[C/T]GAGGGGAGGATGTTT	110749
rs216233795	in-del	-/TTA			intron-variant	Chaf1b	Mm_Celera	16:93885504	TGGTAAGTATTGTCC[-/TTA]TTATTAATCCTTAAA	110749
rs216270766	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93888330	TCTGACCTGCTGAGC[C/T]CCAAACCAAGTGGTT	110749
rs216538175	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93902845	TGTTCTGAGGCTTCC[C/T]GTTGGTAAGGACGTC	110749
rs216673019	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93902275	ACACACCAGAAGAGG[C/G]CATCAGATGGTTGTG	110749
rs216707562	snp	C/T			synonymous-codon	Chaf1b	Mm_Celera	16:93901048	GAGCATAAGGACTCC[C/T]GACACAGCCAAGAAA	110749
rs216906764	in-del	-/AAAA			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882897	GAAACCCTGTCTTGG[-/AAAA]AAAAAAAAACAAAAA	110749
rs216990438	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93901698	TGGTCTCTGTAACCC[C/G]AGGCCCCCATAGTAT	110749
rs217039664	snp	G/T			synonymous-codon, utr-variant-5-prime	Chaf1b	Mm_Celera	16:93892773	CGACAGCATGAAGTC[G/T]TTCTTCCGAAGACTC	110749
rs217180910	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93899252	CTCTAAAATCATCAG[C/T]TGGTGTTCACACCTG	110749
rs217430863	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93900827	TGTCTAACAAAGCCT[A/G]TGGTTGGTGCCAGCT	110749
rs217587322	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93899958	CCCCCGGCGGAGAGA[A/G]TTTGGGGAGACTGGT	110749
rs217633832	snp	A/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882399	TGCAGGCAGAGCTGA[A/G]GGTTCCACATCTTGA	110749
rs217660425	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93905544	GTCTGTCTCTTGACA[C/T]GAGAACCAGCTGTGT	110749
rs217884042	in-del	-/TT			intron-variant	Chaf1b	Mm_Celera	16:93895069	TTGGCTCAGGTTTTG[-/TT]TTTTTTGTTTGTTTG	110749
rs218193652	snp	A/C			intron-variant	Chaf1b	GRCm38.p3	16:93897411	CCACAAAGGATAATA[A/C]ATAGATGGAAAATAC	110749
rs218339971	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93889108	AGTGGGGCTTAATGG[A/G]CCATCCTAGTAGGAA	110749
rs218360244	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93886698	TGCAGACCCTTGCCT[C/T]TCTTCCTCCTGACCA	110749
rs218361450	snp	A/G			synonymous-codon, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891507	CTTTGTAGGGCAGAA[A/G]ATTTCCATTTTCAAC	110749
rs218449295	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93895446	CCATGACCAAGGCAA[A/G]TCTTATACAACAAGG	110749
rs218473180	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93898905	GCTGGATGCCTCCTC[C/T]GAGCCTCCTCCCTCC	110749
rs218475100	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93887004	TCTTGGATATGAGTG[A/G]CTCCTCATGGCCAGA	110749
rs218498391	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93896048	ACAAACCTTACACCC[C/T]GAGTCCTACAACACC	110749
rs218528768	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93890719	CTTTGAAGCGCAGAT[A/C]GTTTCCCAGCTAGCT	110749
rs218546413	snp	C/T			intron-variant, utr-variant-5-prime	Chaf1b	Mm_Celera	16:93892876	GCACCACAGGGACGG[C/T]TCTGTTCACTTCAGC	110749
rs218642610	snp	G/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883604	ATGTGACACTGACGC[G/T]TGGTAGGTAGGACGT	110749
rs218665239	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891952	AGCAGTGCATGCTCA[C/T]AGCCACTGGTGCATC	110749
rs218759475	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93884117	CCACCGGGACCGGGA[C/T]TCGCGCGCCTTCCGC	110749
rs218773751	in-del	-/CAGAGAGTCTTCTG			intron-variant	Chaf1b	Mm_Celera	16:93887932	GGCTGGCCTTGAACT[-/CAGAGAGTCTTCTG]CTTCTGCCTCCTTAG	110749
rs218863441	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891326	TGCCTTGAGTGCTGC[A/G]GGGGTGGGGGTGGGG	110749
rs219107461	snp	G/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882653	TCATGATCCACCATG[G/T]GGGTTCTGGAAACTG	110749
rs219161145	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93889138	ATATGGAAGACAGTG[A/G]TGCTGAGGGTGATTT	110749
rs219224971	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93889599	AGATGCCCTCAGGTG[G/T]GTTAGGGAGGGCAGC	110749
rs219479184	in-del	-/AA			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906303	GAGGAGGGCTAGGAG[-/AA]AAGACAGGGGCCATC	110749
rs219949600	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93893616	TGAATCTGTCAGCTA[A/C]ACGTGGTAGCATTTT	110749
rs220050573	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93886114	TTCTGCGCCCTAATG[C/T]CCAAAATATGTGGGG	110749
rs220081343	snp	G/T			missense	Chaf1b	Mm_Celera	16:93906000	CTGGCCCCTGATGAC[G/T]CTTCCAAGACTGTCT	110749
rs220108483	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93886811	ACGGGATCTGTTTTG[A/C]CCTGCTGGTGAAGAA	110749
rs220117590	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93888585	CTTGGTTACTTTTCT[A/G]TTGCTGTGATAAGTC	110749
rs220174556	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892523	ACCCTCCGAGCCATT[C/T]AGCAGCCCAGCATAA	110749
rs220188349	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93900279	CCATTTCCATGAATG[A/G]ACTTTTATTAAAATG	110749
rs220221273	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93884925	GTGCTGGGAATAAAG[G/T]CGTGGGCCACCACGG	110749
rs220227406	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93892973	CTGAGTCATGGTCTC[A/G]CGTAGCTCAGGCTGG	110749
rs220293645	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93887475	TTCCAGCCCCCAAGT[A/G]ACTCTTCTTTACAGC	110749
rs220332076	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904440	GGCTATTTTTGGTGT[C/T]CAGTTAATTCTCTTG	110749
rs220377926	snp	A/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883092	TGAGGCTGGCCTCAA[A/T]CTTGCTGTGTAGTTA	110749
rs220395708	snp	A/G			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906555	ATTTGTGTTTCACTC[A/G]TTCAGAGTCAGGTAC	110749
rs220475534	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93904817	TGAACATTGACTGTG[A/G]CTGTGATGCGGCCTC	110749
rs220542560	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93902472	CTGGAACTCAGAAAT[A/C]TGCCTGCCTCTGCCT	110749
rs220554830	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93902960	CTCAGCAGTTGTTTC[A/T]GTCTATGTGAGACCA	110749
rs220805299	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883641	TCTCGGGTTAGCACG[C/T]CAAAGCTGGACGAGC	110749
rs220903617	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93886225	TTTGAGGGGGCAATA[A/G]GCTGTCTCCTATAAG	110749
rs220959234	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93886847	ATTTACTAGCCCTGT[A/T]CAAATTCTTCGTGTT	110749
rs221039106	in-del	-/GTA			intron-variant	Chaf1b	Mm_Celera	16:93904945	TTGAACCTTGGCTTC[-/GTA]CCTAAACGGCTCCTC	110749
rs221182814	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93903745	GATGGTTGTGAGCCA[C/T]CATGTGATCAGCGGG	110749
rs221252039	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93888730	GGGGTGGGCTTTGAG[A/G]TCCTATGTTCAGGTT	110749
rs221277288	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93887383	GGGTAGCAGATTCCT[C/T]GGAACCGCAGTCACA	110749
rs221376361	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903083	CAGAGCCGCCTGAGT[A/G]TTTACAAGACCCTGT	110749
rs221384385	in-del	-/T			intron-variant	Chaf1b	Mm_Celera	16:93902589	AGATACATTGTTTCA[-/T]TTTTTTCCAGACAGT	110749
rs221555876	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93905795	GAAGAGCAGTCAGTG[C/T]TCTTAACCGCCGAGC	110749
rs221884063	in-del	-/C			intron-variant	Chaf1b	Mm_Celera	16:93903488	AGAATAGGAATGCAT[-/C]TTTTTTTTTTCCGAG	110749
rs222053067	in-del	-/CAAA			intron-variant	Chaf1b	Mm_Celera	16:93900787	TCTGAAGTGCTTGTT[-/CAAA]CAGTCTGTCGTGCCA	110749
rs222091490	snp	A/G			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906477	GTTGTGGATCTGGTG[A/G]CAGCACCTTTGGATC	110749
rs222092164	snp	A/G			utr-variant-5-prime	Chaf1b	Mm_Celera	16:93884480	GCCTCCCTTTGCCTG[A/G]CGGAAACTCTGGAGG	110749
rs222101356	snp	A/T			missense	Chaf1b	Mm_Celera	16:93900062	CCGAGCTGGTGAACC[A/T]GCCCTACCGTATGGT	110749
rs222258580	snp	A/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883713	CCCAACAGGAGCCAC[A/G]AGCCGCGACAGCCCC	110749
rs222316102	in-del	-/T			intron-variant	Chaf1b	Mm_Celera	16:93904008	GGGTTTTGTTTGGGA[-/T]TTTTTTTGTTATTGG	110749
rs222332178	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93897206	ATTAAAAGCAGTAAA[A/G]GAAAAAGGTCAAGTA	110749
rs222438493	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93896155	CGCTAACTCCGAAGC[C/T]AGTCCCACAACACCC	110749
rs222530519	in-del	-/CTTGGATGCTGCCCAC			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906279	GACAGACTTTACACT[-/CTTGGATGCTGCCCAC]CTTGGTAGAGAGGAG	110749
rs222534827	in-del	-/GCTTACGTGGG			intron-variant	Chaf1b	Mm_Celera	16:93889489	CCCATCCCCTGGTTA[-/GCTTACGTGGG]GCTTACGTGGGCCCC	110749
rs222568952	in-del	-/AA			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882995	GAGACAAGAATCTTT[-/AA]AAAATATGTGACATT	110749
rs222583391	snp	C/T			synonymous-codon	Chaf1b	Mm_Celera	16:93905940	GAGGAGCCTCCTGAA[C/T]TGAAGAGACCCAGGC	110749
rs222638195	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93901894	GAAATAATCAGCTTA[A/T]AAGGAGGAAAGCCTT	110749
rs222638748	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903755	AGCCACCATGTGATC[A/G]GCGGGAATTGAACTC	110749
rs222653995	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93893486	AGCTGAGCAGAAGGT[A/G]GGTGTTGCCGCTTGG	110749
rs222658341	in-del	-/ACACACAC			intron-variant	Chaf1b	Mm_Celera	16:93899372	GCTAAAGAATGAGAA[-/ACACACAC]ACACACACACACACA	110749
rs222707682	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93902328	ATTGAACTCAGGACC[A/T]CTTAACCACTGAGCA	110749
rs222810410	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904292	TTTTGTTTTGTTTTT[C/T]CGAGACGGGGTTTCT	110749
rs223097174	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93894178	GGTCCTGAGTTTAAT[C/T]CTCAGCAACCACATG	110749
rs223136934	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93901968	TCTCATTGCCCTGGC[C/T]AGAGCCAGTATTACA	110749
rs223332011	snp	A/G			synonymous-codon	Chaf1b	Mm_Celera	16:93901192	ACAGTCTCCAGCTCC[A/G]TCGGCCATCAAGGAC	110749
rs223359564	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891847	TGTGCCTGGTGCTCT[C/T]GGAGGCCAGAAGAGG	110749
rs223548068	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903864	GTGCACATACACGAA[A/G]GTACCTTTGGAGGCC	110749
rs223681547	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93898686	AGACAGTATCCAAAC[C/T]AATAAAATCGGAAAT	110749
rs223772611	in-del	-/GC			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93890860	TCCAGGGTCTAAGCT[-/GC]GAGTGAGGGATTCTC	110749
rs223803399	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904412	GGGATTAAAGGTGTG[C/T]GCCACCACGCCTGGC	110749
rs223989494	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93894354	CAGGAGGCTGCAGCG[C/T]GGGCTAAGTCTCCTG	110749
rs224147938	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93888637	AAAAGGAAGTACGAG[A/G]TGGTTTGAGTGTGCT	110749
rs224231151	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93889065	TTTGTTTGGAAGAAC[A/G]TGGATTTGGAAGCAG	110749
rs224261342	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93889236	CTGATATTTTGGTGA[A/C]GAATGTGACTGCTTT	110749
rs224380027	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93893413	GAACTGAACTGTGTG[A/G]CAACTTAGATGTTGC	110749
rs224382203	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93895663	CCATACCCACAGTGA[C/T]ACACCTACTCCAACA	110749
rs224391382	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93896383	AGAATCACAGGAAAG[C/T]CAGGCACTAGTGAGA	110749
rs224559086	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93889860	TGTGAATTTTGGGGC[C/T]AGTCTGTAGTTCTAT	110749
rs224669296	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93894498	TGTCTCTCTTCTCCA[G/T]CACAGGATTTTACAA	110749
rs224716782	in-del	-/C			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892315	ATGCATATGTATGTG[-/C]TGATATTCACGTTTG	110749
rs224812730	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93902144	AGGCCAGGACCCCAC[A/G]GGGGTTACCTATCTG	110749
rs224817338	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93892999	GCTGGTGCTGAACTC[C/G]GGTAGCTGAAGGTGA	110749
rs224828346	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93902544	GCAAAATAGCAGTTG[C/T]GAAGTAGCAACAAAA	110749
rs224951261	snp	C/T			missense	Chaf1b	Mm_Celera	16:93901317	AACCCCGCAGGGTCA[C/T]CCTGAACACGCTGCA	110749
rs225181933	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904530	AGCCGGGCATGGTGG[C/T]GCACGCCTTTAATCC	110749
rs225559837	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93888872	TGCCTGAATGCTGCC[G/T]TGCTCCTGCCTTGAT	110749
rs225601732	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93886872	CGTGTTTTTCTAGGA[A/T]CTCGTGTAGCCCAGG	110749
rs225715445	snp	C/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892408	AGGAACATGCACACA[C/G]GTGTTACAGTGTGCT	110749
rs225716767	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93888159	AGGTGAGCTGTATAC[A/G]TATCTCATTAACATT	110749
rs225794769	snp	A/C			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892450	GGAGTCAGTTCCCTT[A/C]GTGCACTGTATGGGT	110749
rs226165376	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93884755	GTTCTGAGGCCTGGG[A/G]AAAGCAAGGAATGCT	110749
rs226211646	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93886388	TGTAGCTAGGCTTCC[A/G]GGTAGCTTTGAGTGA	110749
rs226234188	snp	C/T			utr-variant-5-prime	Chaf1b	Mm_Celera	16:93883938	GCGCGCGGGAAGCTG[C/T]GGGCTGTGGCGGCCC	110749
rs226351010	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892711	GAGGCTTTCAGGTGA[C/T]TTCAAGCTCTGTTAC	110749
rs226362274	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93893081	GTGTGCAGCCCAGGC[C/T]TGGCTGGGAATGTAA	110749
rs226400248	snp	C/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891744	GGTGCCCTGTGCAGA[C/G]CTGGCACCAGTGAAT	110749
rs226498690	snp	G/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882710	AGTGCTCTTACATGC[G/T]GAGTCCTCTCCAGCT	110749
rs226513067	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93886926	CCTTGCACTTCAGAT[C/T]CACCTGCCTCAGACT	110749
rs226622292	in-del	-/GGTTTT			intron-variant	Chaf1b	Mm_Celera	16:93904259	TTGAGGTATTTTGGG[-/GGTTTT]GTTTGTTTGTTTGTT	110749
rs226705053	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93885930	GGCTTCGGGAATGTT[C/T]AGAATTTGTGCCTGT	110749
rs226762094	in-del	-/TGTGTGTGTG			intron-variant	Chaf1b	Mm_Celera	16:93904049	GGGGGAGGGTAGGGA[-/TGTGTGTGTG]TGTGTGTGTGTGTGT	110749
rs226859838	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882076	AGCTGACTTCAGATG[C/T]ACCAGCAGAGGGCAT	110749
rs227113894	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93902008	GTGTGTGTGGTAAAG[A/G]AAGCTGTTTACCCCG	110749
rs227192668	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93901641	ACTCCTGGTGACATT[A/G]GAATCTTCCTGAGAC	110749
rs227327927	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93905369	TTTTAAATGCTGGTG[C/T]TCGTGTATGTCTGTA	110749
rs227349663	in-del	-/TTGTTTGTC			intron-variant	Chaf1b	Mm_Celera	16:93904273	GGTTTGTTTGTTTGT[-/TTGTTTGTC]TTGTTTTGTTTTGTT	110749
rs227367158	in-del	-/TTG			intron-variant	Chaf1b	Mm_Celera	16:93895366	CCACTAGGCTTTTTG[-/TTG]TTATGTGGCTTTTGG	110749
rs227425521	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93885191	AACTGGAAGAGGGGA[A/C]TAGCAGGTAAGGGGA	110749
rs227454000	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93889674	GTGGGTTAGCAGTGC[C/T]GATGGACGGTGGGTG	110749
rs227554916	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93884034	GGGCTGCAGCTCCTC[A/G]CCGGGGCCGTGAGTT	110749
rs227645801	in-del	-/T			intron-variant	Chaf1b	Mm_Celera	16:93905639	ATGTGTGTGTGTGTG[-/T]TTTTTTTTAAAGATT	110749
rs227869647	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93905452	TGAATTGAACTCAGG[A/T]CCTTTGGAAGAACAG	110749
rs227885273	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93903892	GCCAGGAAAGAGTGT[C/T]GGTTCCCTAGAGCTG	110749
rs227889255	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93904598	TCGAGGCCAGCCTGG[G/T]CTACAGAGTGAGTTC	110749
rs227919415	snp	C/T			utr-variant-3-prime	Chaf1b	Mm_Celera	16:93906034	CCTGCTATGCACCTG[C/T]GTGCAGAGGAGGCAA	110749
rs227947435	snp	A/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883308	TATCCACTGCCTGGG[A/T]CACTCTTATTTGGTT	110749
rs228120749	snp	A/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882239	GAGTTTTGCCTGTAT[A/G]TATGTGTCTTAGGAT	110749
rs228151138	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93899735	TGCAGGCGTGTGTGT[C/T]GGGACTGTGCTTTTG	110749
rs228216718	snp	G/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882131	AGCCACCATGTGGTT[G/T]CTGGGATTTGAACTC	110749
rs228304567	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883150	TCCCATTTCCACCTT[C/T]AGAGTGTTGGGATTA	110749
rs228349380	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892648	GCTTCTCCTTGGACT[A/G]CCTTGTTGGCGTGCC	110749
rs228399393	in-del	-/AT			intron-variant	Chaf1b	Mm_Celera	16:93903119	CTCCCATCTCCACAC[-/AT]AGGAAAAATCCATGA	110749
rs228416780	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93899821	ATGTGGGTCCTGTGA[A/T]TCAAAGTCATGTTGG	110749
rs228423700	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93900652	CGTACCAGCTGAGCC[C/G]TCTCACTGGCCCCGA	110749
rs228522694	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93893041	TGATCCTCTTATCCC[A/T]GTTTCCTGAATGCTG	110749
rs228525442	in-del	-/CT			intron-variant	Chaf1b	Mm_Celera	16:93902914	CTCGTCTGGCCGTGA[-/CT]CTCTCATCCCTGCCC	110749
rs228944978	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93887851	TTTGAACTTTTTTCC[C/T]CCCCCTATTTTTCAA	110749
rs229107286	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93887008	GGATATGAGTGACTC[C/T]TCATGGCCAGAGAGT	110749
rs229122560	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93903403	CTGGGCCTGCTATGT[A/T]CTTCCAACTATTGAT	110749
rs229149205	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93899079	CAGGATCACGGTGTC[C/T]CGCCACCTGCTGCCC	110749
rs229212270	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93904561	AAGCACTCGGGAGGC[A/C]AAGACAGGCGGATTT	110749
rs229228555	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93905163	CTTTAGGTCAGCTCT[C/G]GGAAGGCCAGACTGT	110749
rs229230442	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93898017	CAGAGACAATAAAAC[G/T]AACACATTATGAACC	110749
rs229345261	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93902824	ACTTAGCCTTTTGGT[C/T]GCAACTGTTCTGAGG	110749
rs229400260	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903334	CATTCTCTAGGTCGG[A/G]GGTGTGCGGGGTTTG	110749
rs229456142	in-del	-/A			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882699	CAAAGCAGCCAGTGC[-/A]TCTTACATGCTGAGT	110749
rs229554458	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93896324	GGATCTCAGGATCAC[A/T]GGATCACAGAGACAG	110749
rs229686165	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93889447	TCAAGAGTGAAGGGA[C/T]ACCAGGAAGTAGAAT	110749
rs229686213	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93898117	ATAGTACCTTTTCCA[A/G]AATTGACCATATAAT	110749
rs229773106	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93897176	AACACCAAATGCACT[A/G]AACAGAGAAAGAATA	110749
rs230028871	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93888454	GACCTTCATCATTTC[A/G]TTCTGCCAGGGTCAG	110749
rs230042035	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93888956	TTATAAGACTTGCCT[C/T]GGTCATGGTGTCTGT	110749
rs230091704	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93896461	GCATAAGGACAGAAG[C/T]AACAGAACCCAATTC	110749
rs230156146	in-del	-/GCACC			intron-variant	Chaf1b	Mm_Celera	16:93893314	TGGGGTCAACCCTTA[-/GCACC]GCACCACAGATAGAC	110749
rs230190445	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903984	CTAAGCCATCACTCA[A/G]CCCATCATGGGGTTT	110749
rs230217516	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93902177	AATCTTGCATATCAG[A/G]TATTTAACATTGCGA	110749
rs230330434	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93902729	GCCGCGCCGCTGCCA[C/T]GCTGGCCTGCTCATT	110749
rs230500641	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93895517	CAGAGGTTCAGTCCA[A/T]TATCATCAAGGCAGG	110749
rs230515241	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93895171	GTAGACCAGGCTCAG[G/T]TTTGTGTATATAATG	110749
rs230657875	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93894591	CAGAGAGTGGGACCA[C/T]ACAGAGGGAGCATTT	110749
rs230819585	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93901699	GGTCTCTGTAACCCC[A/T]GGCCCCCATAGTATT	110749
rs230822695	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93892937	AGCCTTGTACCAACC[A/G]ACTACTGCATGCCAT	110749
rs230896760	snp	A/G			synonymous-codon	Chaf1b	Mm_Celera	16:93901096	CCAGGGATCTTCGCC[A/G]GGATCCAGATCAGTC	110749
rs230902941	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93901530	AGCCTGGGGCTTTTC[C/G]TAGCCTTGTCTCCCA	110749
rs231043625	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93893189	ATGTATCCTATACCT[C/G]GGCCCTCTCACTTGG	110749
rs231183011	in-del	-/GAGA			intron-variant	Chaf1b	Mm_Celera	16:93901583	CACACTCTGCCCTTT[-/GAGA]GAGATATCCATGTCT	110749
rs231331474	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93887830	TTCCAATGTGTGGTT[A/C]TAGACTTTGAACTTT	110749
rs231458031	in-del	-/CGG			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891379	CCCCTGAGTCTGACT[-/CGG]CTTCTCTGAGGTTGC	110749
rs231478734	in-del	-/TG			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892237	CATGGGTGTGTGTTT[-/TG]TGTGTGTGTGTGTGT	110749
rs231515542	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93886813	GGGATCTGTTTTGCC[C/G]TGCTGGTGAAGAAGG	110749
rs231612572	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93889020	TGGTACCAGGGTCTC[A/G]GATATGGCTTTGATA	110749
rs231752140	snp	A/G			synonymous-codon	Chaf1b	Mm_Celera	16:93887165	TGACAGCAAGGAGCC[A/G]GAGCAGATCGCCTTT	110749
rs231848420	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93893758	AAATTAAAACCAAAC[A/C]AATAAAATCAGTCAA	110749
rs231872562	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93886971	TACAGGCATGCACCA[C/T]GCACCACCTAGCCAT	110749
rs232269511	in-del	-/T			intron-variant	Chaf1b	Mm_Celera	16:93904202	TTGGCTCAAGATGTG[-/T]TTTTTTTAATATTCT	110749
rs232282448	in-del	-/AG			intron-variant	Chaf1b	Mm_Celera	16:93897333	CAAAATTCTAAAGAC[-/AG]AGAAAACAAGATATT	110749
rs232337820	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891918	TCAGTGCTGGGAACA[A/G]ACTGGGCTTCCCTAC	110749
rs232513014	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93884222	CCAGTACTCCGGTAC[C/G]GGTCTCTGGGACCCC	110749
rs232514230	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93885562	GACATTTGAGCTGGG[G/T]TGACATGGACCAGTG	110749
rs232538004	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93897663	GCTGCATACAGTAAA[C/T]GCACCTCAGTGACTA	110749
rs232550645	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93889889	ATATGGTCTAGAAGC[C/T]GCCCCTTACCAGCAA	110749
rs232590582	in-del	-/GT			intron-variant	Chaf1b	Mm_Celera	16:93899726	TTATTATGTGCAGGC[-/GT]GTGTGTGTTGGGACT	110749
rs232901009	snp	A/T			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906442	GCTTGACCCTCCGTC[A/T]GAGCCTGCCCTTGTC	110749
rs233054972	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93900424	CTGAACCCAGGGTCT[C/T]GTGCACACTAGGTAA	110749
rs233068745	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892609	AATCACGGCACTTGC[C/T]CGACCTGCTGGCCAA	110749
rs233077390	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93885353	TGTATGCTTTGCTGT[C/T]GACAGATCTGGAAGT	110749
rs233104716	in-del	-/T			intron-variant	Chaf1b	Mm_Celera	16:93899550	TTTTTACCCCTTTTG[-/T]TTTTTTGAGATGGTT	110749
rs233148300	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93900857	TTCCTGGCTAGCCAT[A/G]GGAGGGTAAAGTGTG	110749
rs233148736	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93890901	TCATCCCTCCCACCC[C/T]CGTCCTACCTTCTCA	110749
rs233235147	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892340	CGTTTGGGCACATGT[A/G]TGAGTGTGTGTGCAA	110749
rs233285268	snp	G/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883212	CATCGCTAAGAGAGG[G/T]CGAAGGCATTGCTGT	110749
rs233314774	snp	G/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882658	ATCCACCATGTGGGT[G/T]CTGGAAACTGAACCC	110749
rs233350321	snp	C/T			synonymous-codon, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891576	TTTGGGTCAATATAT[C/T]GCGACCCTGAGCTGT	110749
rs233402182	snp	C/T			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906185	TCCCATGGGTCTCTG[C/T]GTATTATGCTAGGCA	110749
rs233550445	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883536	CCTGCGTCTCTAGTC[C/T]CGCTTTTCTTTCTAG	110749
rs233815661	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93902212	TTTCTTTTTTTTTTT[A/T]AAAGAGTTATTGATT	110749
rs233911418	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93901863	GGAAGTTTTCTGACA[C/T]GGTGACTAAATGCCT	110749
rs233991082	in-del	-/TT			intron-variant, upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93892234	TTTCATGGGTGTGTG[-/TT]TTGTGTGTGTGTGTG	110749
rs234101861	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93886294	CCTCGAAGACCGAAA[C/G]CTCCCTTTAGTCGGC	110749
rs234130923	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883781	CGGAAGCCAAGGTGC[C/T]GGGAGATTGCTGGCC	110749
rs234236103	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93889184	GGCTCTAGATGTCTC[A/C]GAGGAGAAGAACTTT	110749
rs234293435	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93885805	ATATATCTGAAAATA[G/T]TTCTTTCTCCATTTG	110749
rs234377159	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904235	TTCTTTGAGGGGTGG[C/T]GAGGTATTTTTGAGG	110749
rs234651124	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882553	AAACCATATACAAGC[C/T]ATCACAGTATGTATG	110749
rs234881510	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93889948	TTCAAGTTGATGCTT[C/G]TTGTACTTGGAGGTG	110749
rs234882962	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93895872	TTGCACGATAAGCCA[A/G]TATCCTGCCAACTGA	110749
rs234884770	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904189	GTGCACCACCGCCTT[C/T]GGCTCAAGATGTGTT	110749
rs234945975	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93889281	AGAGTCTTACCTGAG[A/G]CTAAGGTGAAGAGAC	110749
rs234976042	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903566	GACCAGGCTAACCTC[A/G]AACTCAGACTCTGCC	110749
rs235054447	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904293	TTTGTTTTGTTTTTC[C/T]GAGACGGGGTTTCTC	110749
rs235083911	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93895560	TCCAGGCAGACATGG[G/T]GCAGGAGGAGCTGAG	110749
rs235100554	in-del	-/G			intron-variant	Chaf1b	Mm_Celera	16:93905639	AATGTGTGTGTGTGT[-/G]TTTTTTTTAAAGATT	110749
rs235114779	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904719	AATTTAAAACGGGAT[C/T]GAGTGTGGTTTGGGT	110749
rs235167434	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93896578	GAATTTAAAAAGGAC[A/G]TAAATAAACTCCTTT	110749
rs235353399	snp	C/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892273	GTGTGTGTGCCCACA[C/G]GAGTATGCCTTTGGC	110749
rs235408307	in-del	-/AA			intron-variant	Chaf1b	Mm_Celera	16:93898809	GACAAACAAAAAAAC[-/AA]AAATCCTTACACCCT	110749
rs235451628	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93902850	TGAGGCTTCCCGTTG[G/T]TAAGGACGTCCCTGT	110749
rs235650314	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93896068	CCTACAACACCCAAA[C/G]GACGCTCCACTCCCA	110749
rs235650358	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93888749	TATGTTCAGGTTCTG[C/T]CCAGTGCAGAAGAGA	110749
rs235700652	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93889129	CTAGTAGGAATATGG[A/G]AGACAGTGGTGCTGA	110749
rs235725310	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93888880	TGCTGCCGTGCTCCT[A/G]CCTTGATGATAATGA	110749
rs235780103	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93886098	AAGAGGAATAGTTGC[A/G]TTCTGCGCCCTAATG	110749
rs235865248	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93899279	CCTGTTATCCCTGCA[C/T]TTGGGAGGCTGGCCT	110749
rs235897056	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904808	TGGGTGTGGTGAACA[C/T]TGACTGTGGCTGTGA	110749
rs235967411	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93905558	ACGAGAACCAGCTGT[A/G]TAGATCCATTATTCC	110749
rs235967748	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93898696	CAAACCAATAAAATC[A/G]GAAATGAAAGGGGAG	110749
rs236143914	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93903545	TGTTCTGGACCTCAC[A/T]CTGTAGACCAGGCTA	110749
rs236192521	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93895451	ACCAAGGCAAGTCTT[A/T]TACAACAAGGCAAGT	110749
rs236205186	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93895771	TCAGACTTATTGTCA[C/T]GTATCAGAGAATGAC	110749
rs236282110	in-del	-/C			upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93882937	CAAAAACAAAAAAAA[-/C]CTTAACTTTCATATG	110749
rs236391588	in-del	-/CA			intron-variant	Chaf1b	Mm_Celera	16:93904133	GACTGACCTTGAACT[-/CA]CAGAGAGGCCTCTGC	110749
rs236637162	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903751	TGTGAGCCACCATGT[A/G]ATCAGCGGGAATTGA	110749
rs236830900	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891816	TTTGCCTGCATGTAT[A/G]TCTTTGTACCAGGTG	110749
rs236895209	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892466	GTGCACTGTATGGGT[C/T]CTGGGAACTCAGATC	110749
rs236912240	snp	G/T			synonymous-codon	Chaf1b	Mm_Celera	16:93901195	GTCTCCAGCTCCGTC[G/T]GCCATCAAGGACAGT	110749
rs237113038	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93905591	CTAGCTGTAGTCAGC[G/T]TCTCACTGGGCCACT	110749
rs237195595	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93902303	GTGAGCCACCATGTG[A/G]TTGCTGGGAATTGAA	110749
rs237363309	in-del	-/G			intron-variant	Chaf1b	Mm_Celera	16:93893362	TATAGATTACATCCA[-/G]GGACAGGTTCTGATA	110749
rs237540463	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93886796	GTGTGGTGATTCTAG[A/G]CGGGATCTGTTTTGC	110749
rs237646424	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93886593	CCAGGCCACTGAGCT[C/G]TAGGTGCTTCATGAA	110749
rs237708404	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93892974	TGAGTCATGGTCTCG[C/T]GTAGCTCAGGCTGGT	110749
rs237716088	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93884944	GGGCCACCACGGCCC[A/G]GCTATTTGCTACATT	110749
rs237723174	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93901523	CTGTCAGAGCCTGGG[A/G]CTTTTCCTAGCCTTG	110749
rs237781991	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93886142	GGGTGTGAGTGTCTG[G/T]GTACATGCATTCATT	110749
rs237787568	snp	A/C/G			intron-variant	Chaf1b	Mm_Celera	16:93893066	ATGCTGGGATCACAG[A/C/G]TGTGCAGCCCAGGCC	110749
rs237788627	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93901917	AAAGCCTTACTTTGG[A/C]TTACAGGTTCCAAAG	110749
rs237878300	in-del	-/CTGTCTGT			intron-variant	Chaf1b	Mm_Celera	16:93903302	CCTCTCCTACTCCAC[-/CTGTCTGT]CTTCCTTCTCATTCT	110749
rs237967091	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93887396	CTCGGAACCGCAGTC[A/T]CAGGTTCTGTGCTAC	110749
rs237999384	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93893511	GCTTGGGAACGTGGC[A/T]TGTTTAGAATGCAGC	110749
rs238001007	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93900015	TCAGCTTGTTTCCCC[C/G]CTTACAGAGAAAGCA	110749
rs238209120	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892409	GGAACATGCACACAC[A/G]TGTTACAGTGTGCTT	110749
rs238230534	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93901789	TTTTTCAGCTCAGCC[C/T]TGCTCTGTGGCGCCA	110749
rs238299729	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892547	AGCATAAAATATCTC[A/G]CCCTTTGAGATCTGG	110749
rs238321775	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93893281	CATTAGTCAGGTGTG[A/T]CCAAGGTGTGTAAGG	110749
rs238411135	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93898651	GATAAACCCTTAGCC[A/T]GACTAACCAGAGGGC	110749
rs238573563	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93886935	TCAGATCCACCTGCC[C/T]CAGACTCCCAAGGGC	110749
rs238793385	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93887555	TATAAGACAATAAAA[A/G]CATTATAAAAATAGA	110749
rs238849514	in-del	-/C			intron-variant	Chaf1b	Mm_Celera	16:93899041	TGGAATCTCTGCCCT[-/C]TCTGGGCCTCTCAGG	110749
rs238919484	in-del	-/G			intron-variant	Chaf1b	Mm_Celera	16:93895035	GTATGGCTGTCCTGT[-/G]GGGGGAAAAGTATGT	110749
rs239258996	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891459	TCCTGCAGCGTGCTT[C/T]CTGGAAATCTTGATA	110749
rs239267404	snp	C/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883620	TGGTAGGTAGGACGT[C/G]TTGCATCTCGGGTTA	110749
rs239373068	snp	A/G			synonymous-codon	Chaf1b	Mm_Celera	16:93905921	GGCTCCTGGGGAGCC[A/G]CCGGAGGAGCCTCCT	110749
rs239373675	snp	A/G			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906375	TCCAATGGCCACTGG[A/G]GGTCACTGTGCCCAC	110749
rs239413411	snp	A/G			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906513	GGGATGGGCTCAGAA[A/G]ACAAGATAACATCAG	110749
rs239458739	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93899943	GACGTGACATCTCCT[A/C]CCCCGGCGGAGAGAG	110749
rs239830758	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93889865	ATTTTGGGGCCAGTC[A/T]GTAGTTCTATATGGT	110749
rs239882235	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904534	GGGCATGGTGGTGCA[C/T]GCCTTTAATCCAAGC	110749
rs239946354	snp	A/G			missense	Chaf1b	Mm_Celera	16:93905059	CAAATCCACAGCCCA[A/G]TAGCGGGACCGCCCC	110749
rs240032650	snp	A/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883702	TCCCAGTCCCGCCCA[A/G]CAGGAGCCACGAGCC	110749
rs240046166	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93890773	CAGAGCTCTCTGACT[A/G]CAGTACCTCTCTTTC	110749
rs240121773	snp	A/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883139	CCTGATCATCTTCCC[A/G]TTTCCACCTTCAGAG	110749
rs240244311	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93900508	TTTATATGAATGCTT[C/T]TATCTAGTGTGTGTA	110749
rs240294762	snp	C/G/T			intron-variant	Chaf1b	Mm_Celera	16:93889354	TCAGTTTAGACTCTG[C/G/T]CCTGTGGCTCGCTCT	110749
rs240425144	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93888366	CTGCTACTACGAGGA[A/G]GAAGGAGGTACGAGG	110749
rs240459464	snp	C/G			synonymous-codon	Chaf1b	Mm_Celera	16:93901318	ACCCCGCAGGGTCAC[C/G]CTGAACACGCTGCAG	110749
rs240513596	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93894731	CCTCCCTCCCCTGCT[C/T]TGCAGCCGGATGTAT	110749
rs240615626	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891180	CTGGTAGTACCAACT[C/T]CCTTGGAGCATGTGG	110749
rs240623518	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883183	ATCATAACAACCATT[C/T]TAGGCGTCTGTCACA	110749
rs240631197	in-del	-/CAGTGCTCTTAACCTCGGAGC			intron-variant	Chaf1b	Mm_Celera	16:93903790	CTCTGGAAGAGCAGT[-/CAGTGCTCTTAACCTCGGAGC]CATCTCTCTAGCTCA	110749
rs240761381	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93899726	ATTATTATGTGCAGG[C/T]GTGTGTGTTGGGACT	110749
rs240839572	in-del	-/A			intron-variant	Chaf1b	Mm_Celera	16:93905491	ACACACTGATGCTAC[-/A]CTACCTCTTACCCTG	110749
rs240842826	snp	A/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883714	CCAACAGGAGCCACG[A/G]GCCGCGACAGCCCCG	110749
rs240906192	snp	A/G			missense	Chaf1b	Mm_Celera	16:93884571	TTCCAGCATGGGGCA[A/G]CCTGGAAGATCCACA	110749
rs241044991	in-del	-/T			intron-variant	Chaf1b	Mm_Celera	16:93899696	AGCTTGAATTCTGTA[-/T]TTTTTTTTTATTTTA	110749
rs241358963	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93895393	TTTTGGGGACAGGGT[C/T]ATTGTCTTAGTTAGG	110749
rs241495751	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93897236	AACATATAAAGGCAG[A/G]CCTATCAGAATTACA	110749
rs241512075	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903170	TAACCTCTGAGGGAG[A/G]TCATGCGTTCCTTTC	110749
rs241571736	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903760	CCATGTGATCAGCGG[A/G]AATTGAACTCGGGAC	110749
rs241656123	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93884152	CCGGGTTGGGCCGCC[C/G]GGACCCGCGCCCCTC	110749
rs241771234	in-del	-/TTCTGGACATGCC			intron-variant	Chaf1b	Mm_Celera	16:93886445	CTCCTTCACTGGCCT[-/TTCTGGACATGCC]AAAAGGATCGCGTTA	110749
rs241857568	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93902480	CAGAAATCTGCCTGC[C/T]TCTGCCTCTCAAGTG	110749
rs242057362	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903881	TACCTTTGGAGGCCA[A/G]GAAAGAGTGTCGGTT	110749
rs242118583	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93896343	TCACAGAGACAGCTG[A/G]ACTCTGAGGAGTTCT	110749
rs242118669	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93904413	GGATTAAAGGTGTGT[A/G]CCACCACGCCTGGCT	110749
rs242224704	in-del	-/T			intron-variant	Chaf1b	Mm_Celera	16:93899302	GCTGGCCTGGGATGC[-/T]TTGCCCTGCGTTTGA	110749
rs242303297	snp	A/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882420	CACATCTTGATCTGA[A/G]GGCTGCTAGGAGAAG	110749
rs242370998	in-del	-/C			intron-variant	Chaf1b	Mm_Celera	16:93902199	CATTGCGATTTTTTT[-/C]CTTTTTTTTTTTTAA	110749
rs242406836	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883892	CCCGGAACTCCGCCC[C/T]GAGGAGGCGTGACCG	110749
rs242415661	in-del	-/GC			intron-variant	Chaf1b	Mm_Celera	16:93904260	TGAGGTATTTTGGGG[-/GC]TTTGTTTGTTTGTTT	110749
rs242562524	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93887117	TATACTGATTTACCT[C/T]ACAGATGCCGTCATT	110749
rs242622512	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93888004	AGCTTTTCTCTTTTT[A/G]CAGTAATAATGTTAA	110749
rs242635847	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93893852	TTCTGCTAGTAAATA[C/T]TACAGAGTGACCAAA	110749
rs242725511	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93902398	TTTGGTTGTTTCAAG[A/G]CAGGGTTTCTCTGTG	110749
rs242790472	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93894234	ATCCAATGCCTTCTT[C/T]CGGTGTGTCTGAAGA	110749
rs243008516	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93889089	GAAGCAGTGGAATGC[C/T]TGTAGTGGGGCTTAA	110749
rs243207942	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93894062	ATTAAGTAAGAGTAG[A/G]GTCCTCTCTAGCAGT	110749
rs243284720	snp	A/G			synonymous-codon	Chaf1b	Mm_Celera	16:93887210	GGCGCAGCTGAATAA[A/G]GAGAACTGGACTGTG	110749
rs243417083	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93895667	ACCCACAGTGATACA[A/C]CTACTCCAACAGGGC	110749
rs243739316	snp	C/T			utr-variant-3-prime	Chaf1b	Mm_Celera	16:93906024	ACTGTCTGAGCCTGC[C/T]ATGCACCTGCGTGCA	110749
rs243745602	in-del	-/C			intron-variant	Chaf1b	Mm_Celera	16:93884905	TCGAACCCTCTGACT[-/C]CCAAGTGCTGGGAAT	110749
rs243749641	in-del	-/AA			upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93881908	AGAGACCTTGTCTCC[-/AA]AAAAAAAAAAAAAAG	110749
rs243824705	in-del	-/AG			intron-variant	Chaf1b	Mm_Celera	16:93887931	AGGCTGGCCTTGAAC[-/AG]TCTTCTGCCTCCTTA	110749
rs243917494	snp	C/T			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906416	CAGAGGGCTTGATGG[C/T]TGGCTGCCTTGCTTG	110749
rs243951472	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892659	GACTGCCTTGTTGGC[A/G]TGCCAGTTCTAAGTG	110749
rs244030690	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93900672	ACTGGCCCCGAATTT[A/G]TCTTTTATGTTGGGA	110749
rs244030794	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892278	TGTGCCCACACGAGT[A/G]TGCCTTTGGCATGTG	110749
rs244058592	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93899739	GGCGTGTGTGTTGGG[A/G]CTGTGCTTTTGAGCT	110749
rs244191050	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93897428	TAGATGGAAAATACC[A/T]ACACAAGGAGGGAAA	110749
rs244288654	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904441	GCTATTTTTGGTGTT[C/T]AGTTAATTCTCTTGA	110749
rs244429632	in-del	-/G			intron-variant	Chaf1b	Mm_Celera	16:93898238	TCCAGCAGAAACAAT[-/G]GAAAGCCCACATACA	110749
rs244435513	snp	A/C			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891853	TGGTGCTCTTGGAGG[A/C]CAGAAGAGGGCATTG	110749
rs244441193	snp	A/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883420	CCTGGAACTCTCTGT[A/T]GCTGAGGATAACCTT	110749
rs244445807	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93902666	CTCTGTAAACCTTAA[A/G]CTCAGCAGAGGTCTA	110749
rs244498066	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93883996	TTTGCTGATACCCGG[C/T]TTCCGCGCTTCTGAC	110749
rs244508970	snp	G/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892236	TCATGGGTGTGTGTT[G/T]TGTGTGTGTGTGTGT	110749
rs244762171	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93885578	TGACATGGACCAGTG[A/G]TCACAGCATGTTGGA	110749
rs245013600	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93886915	TCACCATGTAACCTT[A/G]CACTTCAGATCCACC	110749
rs245113912	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93893428	GCAACTTAGATGTTG[C/T]TATTCTGTTCAGGTT	110749
rs245146138	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93884772	AAGCAAGGAATGCTG[A/G]GAAGATTAGCTTTCT	110749
rs245427522	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93899065	TCTCAGGCCCCTCTC[A/G]GGATCACGGTGTCTC	110749
rs245472273	snp	A/C/T			upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93882937	caaaaacaaaaaAAA[A/C/T]CTTAACTTTCATATG	110749
rs245488075	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93897314	CCCAGGCTAATTTAC[A/C]CAGCAAAATTCTAAA	110749
rs245521480	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93890903	ATCCCTCCCACCCCC[A/G]TCCTACCTTCTCAGG	110749
rs245564607	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93893617	GAATCTGTCAGCTAC[A/C]CGTGGTAGCATTTTG	110749
rs245574072	in-del	-/TCCCA			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93890903	TCCCTCCCACCCCCG[-/TCCCA]TCCTACCTTCTCAGG	110749
rs245661200	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93901971	CATTGCCCTGGCTAG[A/T]GCCAGTATTACAGGG	110749
rs245695898	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903560	TCTGTAGACCAGGCT[A/G]ACCTCGAACTCAGAC	110749
rs245779666	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93889237	TGATATTTTGGTGAA[A/G]AATGTGACTGCTTTC	110749
rs245823825	in-del	-/CTGACC			intron-variant	Chaf1b	Mm_Celera	16:93904121	ATTCTCTAGACAAGA[-/CTGACC]TTGAACTCAGAGAGG	110749
rs245852544	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93896410	GAGATAAGCAAGGGC[A/G]GGTAGCACTAGAGAT	110749
rs245859645	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93888994	AGTAAAGCCCTAACT[A/G]AAACAGAAGTTGGTA	110749
rs245900724	in-del	-/TC			intron-variant	Chaf1b	Mm_Celera	16:93904453	TTCAGTTAATTCTCT[-/TC]TGAGTTCTTCTGAGC	110749
rs245933488	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93904150	AGAGAGGCCTCTGCC[A/T]CCTTGAGTGCCAGGG	110749
rs246002466	in-del	-/AAGG			intron-variant	Chaf1b	GRCm38.p3	16:93898295	AATGATAACTTGGTA[-/AAGG]AAGGAAGGAAGGAAG	110749
rs246038296	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882153	TTTGAACTCAGGACC[C/T]TCAGAAGATAGTGGC	110749
rs246212760	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93888875	CTGAATGCTGCCGTG[C/T]TCCTGCCTTGATGAT	110749
rs246218456	snp	G/T			utr-variant-3-prime	Chaf1b	Mm_Celera	16:93906065	GGCCAAAGCTCGAAG[G/T]CTGGTGATGGTGGCC	110749
rs246287726	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93888224	AGTGCCCATGAAATC[A/C]AGAACAGGCTGCCTG	110749
rs246395699	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93904197	CCGCCTTTGGCTCAA[A/G]ATGTGTTTTTTTAAT	110749
rs246417228	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93904562	AGCACTCGGGAGGCC[A/G]AGACAGGCGGATTTC	110749
rs246573782	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93899137	CTTGGCCTAGTGTAT[C/T]GGGGACCAGAAATCT	110749
rs246633636	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891034	ATGGCGGGAAGCCTG[A/G]CAGCGTACAGGCAGA	110749
rs246656111	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93898086	AAAGCAAAAGATTAT[A/T]CCTTCTCAGCACCTC	110749
rs246690728	snp	G/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882324	TAATTGGGGCTGGCT[G/T]ACAGGTTCAGAGTTT	110749
rs246702459	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93900370	TAGCACTGAACCTGG[C/G]TTCTTTTGTGTATCG	110749
rs246710090	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93896187	GAAAAAGCTTCACTG[C/T]CAGATGCTCTAACAC	110749
rs246779202	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93905523	CACATCCTCAGTGTC[A/G]CAGACGTCTGTCTCT	110749
rs246794583	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93889141	TGGAAGACAGTGGTG[C/T]TGAGGGTGATTTGAA	110749
rs246796316	in-del	-/A			intron-variant	Chaf1b	Mm_Celera	16:93893968	ACAACAAATGCATTG[-/A]AAATACCACTGTGTG	110749
rs246804959	snp	A/G			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906569	CGTTCAGAGTCAGGT[A/G]CTGTGGGTGAGCCAG	110749
rs247006752	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93898917	CTCTGAGCCTCCTCC[C/T]TCCTCAGCCTGTTCC	110749
rs247391609	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93905190	CTGTCTTTTTGGGAC[C/T]GTCCTTTGGACAAAC	110749
rs247526634	snp	C/T			synonymous-codon	Chaf1b	Mm_Celera	16:93901013	GAACTTGGCATACCT[C/T]TGAAAGAGAAGCCAG	110749
rs247685784	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93886281	CAAAGTCCCTTAGCC[G/T]CGAAGACCGAAACCT	110749
rs247744070	in-del	-/ACACAC			intron-variant	Chaf1b	Mm_Celera	16:93899373	GCTAAAGAATGAGAA[-/ACACAC]ACACACACACACTCC	110749
rs247769291	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93901660	TCTTCCTGAGACCCA[A/G]TTAAATGTGTCTTCT	110749
rs247798725	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93893011	CTCGGGTAGCTGAAG[A/G]TGATCCTCAACTTGT	110749
rs247846814	snp	A/C			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882082	CTTCAGATGTACCAG[A/C]AGAGGGCATCAGATC	110749
rs247874878	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93899577	GGTTTCTCTGTGTAA[C/G]AGCCCTGTCTTAGAA	110749
rs247980559	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93889737	AGGGAAGGGGGTGAA[A/G]GAGTTGGGAAAATGG	110749
rs248151982	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93903341	TAGGTCGGGGGTGTG[C/T]GGGGTTTGGGCTGGT	110749
rs248206983	in-del	-/T			intron-variant	Chaf1b	Mm_Celera	16:93889039	TGGCTTTGATAGGCC[-/T]TGATCTTGCTTTTGT	110749
rs248232860	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93893207	CCCTCTCACTTGGCA[A/G]GAAAACAAAACACAA	110749
rs248352992	snp	C/T			synonymous-codon	Chaf1b	Mm_Celera	16:93901129	AGGGACCCCCAGCAA[C/T]AGAACCCAAGACCCC	110749
rs248500031	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93886798	GTGGTGATTCTAGAC[C/G]GGATCTGTTTTGCCC	110749
rs248513881	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93886853	TAGCCCTGTACAAAT[A/T]CTTCGTGTTTTTCTA	110749
rs248585330	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93889641	AGGTTGAGGCATGTC[C/T]CCTGGGTCATGGGCA	110749
rs248780555	in-del	-/CTTTCTGGACATG			intron-variant	Chaf1b	Mm_Celera	16:93886443	CCCTCCTTCACTGGC[-/CTTTCTGGACATG]CTAAAAGGATCGCGT	110749
rs248786199	in-del	-/TTTAATTTTGTTCATTGTATCATGTAAAAATTTTGTATTTCTGGAGGTGCCATGTGATGTTTGG			intron-variant	Chaf1b	GRCm38.p3	16:93895173	GACCAGGCTCAGGTT[lengthTooLong]TGTGTATATAATGTA	110749
rs248813535	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93900225	GGATAGACCTCTGAG[C/T]CAGGGAATAGTTTGT	110749
rs249035253	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93903431	GATGAATTCATAATA[C/T]AACTCAAATATCATG	110749
rs249182267	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93902158	CAGGGGTTACCTATC[C/T]GATAATCTTGCATAT	110749
rs249210365	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93903322	TGTCTTCCTTCTCAT[C/T]CTCTAGGTCGGGGGT	110749
rs249475962	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93895173	AGACCAGGCTCAGGT[G/T]TGTGTATATAATGTA	110749
rs249481459	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93887432	AACAAAACCTGACTT[C/T]TCTGGAGGAGCCAGA	110749
rs249494110	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93888562	TTTCCTGGTCTATTA[A/G]CCCATGTCTTGGTTA	110749
rs249573726	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93895554	GCAGCATCCAGGCAG[A/G]CATGGTGCAGGAGGA	110749
rs249614585	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93894131	GCTGGAGAGATGGCT[C/T]AGTGGTTAAGAGCAC	110749
rs249819740	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93886315	TTTAGTCGGCTCATG[A/G]AGAGTGTTGATCTGT	110749
rs249850937	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882759	TAAAAACCCAACTTT[C/T]GCCGGGCAGTGGTGG	110749
rs249929295	in-del	-/CA			intron-variant	Chaf1b	Mm_Celera	16:93898246	AAACAATGGAAAGCC[-/CA]CATACACCTGGAAGC	110749
rs250178104	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93890348	GTGAGTTCCAAGCCA[G/T]CTTGGACTGTAGAGT	110749
rs250237646	in-del	-/AAC			upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93882935	AACAAAAACAAAAAA[-/AAC]CTTAACTTTCATATG	110749
rs250434618	snp	C/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882622	AGAAAAGGGTGTTGG[C/G]TTAACTGGAACTGTG	110749
rs250545041	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93890629	CTCTTTGTAACCAAG[G/T]CTGGCCTTGAACCCT	110749
rs250708705	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93890712	GCTCGCTCTTTGAAG[C/T]GCAGATCGTTTCCCA	110749
rs250724583	snp	G/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891481	ATCTTGATAATAACT[G/T]TCTCGTGCTTCTTTG	110749
rs250734217	in-del	-/TT			intron-variant	Chaf1b	Mm_Celera	16:93893898	ACTGCAGAGACTGAC[-/TT]TTATGGACTGTTGAT	110749
rs250846455	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93894430	GCTGGGAACAGATTT[C/G]GAGGCTCATGAGCTG	110749
rs250911821	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882709	CAGTGCTCTTACATG[C/T]TGAGTCCTCTCCAGC	110749
rs250959658	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93887849	ACTTTGAACTTTTTT[C/T]CCCCCCCTATTTTTC	110749
rs250970180	snp	A/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883566	GACCGTAAATTCCAG[A/G]CGGGAAGATCTGTCC	110749
rs250986178	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93901535	GGGGCTTTTCCTAGC[C/T]TTGTCTCCCAACTCT	110749
rs251004131	in-del	-/TGGTGGTAGGTTACTG			intron-variant	Chaf1b	Mm_Celera	16:93905205	GTCCTTTGGACAAAC[-/TGGTGGTAGGTTACTG]GTAGGAAAGTAACCC	110749
rs251120961	in-del	-/T			intron-variant	Chaf1b	Mm_Celera	16:93886300	AGACCGAAACCTCCC[-/T]TTAGTCGGCTCATGA	110749
rs251138913	snp	A/C			missense	Chaf1b	Mm_Celera	16:93905923	CTCCTGGGGAGCCAC[A/C]GGAGGAGCCTCCTGA	110749
rs251169719	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93898147	TTGGTCACAAAACAG[G/T]CCTCAACAGATACAA	110749
rs251321380	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904701	TTGGGAAGCCAAACT[C/T]CAAATTTAAAACGGG	110749
rs251450620	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883712	GCCCAACAGGAGCCA[C/T]GAGCCGCGACAGCCC	110749
rs251463823	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892386	TTAAGAGTGCAAGTA[C/T]GCATACAGGAACATG	110749
rs251475505	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93884382	TGTCTGAGCCGTCGG[C/T]GTCGCTAATGGCTTC	110749
rs251573926	in-del	-/G			intron-variant	Chaf1b	Mm_Celera	16:93901964	TTGTCTCATTGCCCT[-/G]GGCTAGAGCCAGTAT	110749
rs251649106	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93902930	TCTCTCATCCCTGCC[A/C]GAGGTTCCTCCAGCC	110749
rs251663780	in-del	-/AAC			intron-variant	Chaf1b	Mm_Celera	16:93904670	CCAAACAAACAAACA[-/AAC]AAAAAACACTGGCTG	110749
rs251786465	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93902399	TTGGTTGTTTCAAGA[C/T]AGGGTTTCTCTGTGT	110749
rs251916231	in-del	-/GTGA			intron-variant	Chaf1b	Mm_Celera	16:93886131	CAAAATATGTGGGGT[-/GTGA]GTGTCTGTGTACATG	110749
rs251991603	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93886825	GCCCTGCTGGTGAAG[A/T]AGGGAGATTTACTAG	110749
rs252050654	snp	G/T			missense	Chaf1b	Mm_Celera	16:93887186	GATCGCCTTTCAGGA[G/T]GAGGAGGAGGCGCAG	110749
rs252202295	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892617	CACTTGCCCGACCTG[C/T]TGGCCAACTGATGAG	110749
rs252263259	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93885201	GGGGAATAGCAGGTA[A/T]GGGGACTGATGGTGT	110749
rs252313068	in-del	-/T			intron-variant	Chaf1b	Mm_Celera	16:93896400	GGCACTAGTGAGATA[-/T]AGCAAGGGCGGGTAG	110749
rs252346400	in-del	-/AAAGGAAG			intron-variant	Chaf1b	GRCm38.p3	16:93898294	CAATGATAACTTGGT[-/AAAGGAAG]GAAGGAAGGAAGGAA	110749
rs252376659	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93896579	AATTTAAAAAGGACA[G/T]AAATAAACTCCTTTA	110749
rs252377261	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93903908	GGTTCCCTAGAGCTG[C/T]CTTCACAGTACTGGG	110749
rs252382928	in-del	-/CTCCAACCCACT			intron-variant	Chaf1b	Mm_Celera	16:93897965	AATAATAGTGGGAGA[-/CTCCAACCCACT]CTCAGCAATGGACAG	110749
rs252451972	in-del	-/G			intron-variant	Chaf1b	Mm_Celera	16:93894112	AAGATGGCGTGTGTA[-/G]GGGGCTGGAGAGATG	110749
rs252479700	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93903722	AGAGGGCATCAGATC[C/T]CATTACAGATGGTTG	110749
rs252479801	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93895397	GGGGACAGGGTTATT[A/G]TCTTAGTTAGGGTTT	110749
rs252509064	in-del	-/GC			intron-variant	Chaf1b	Mm_Celera	16:93898807	AAGACAAACAAAAAA[-/GC]ACAAATCCTTACACC	110749
rs252714230	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93901743	TTGTGTCCTCTTGGG[G/T]TGTAAGCCTACAGGA	110749
rs252826550	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93903066	GAACCACAAGTAAGT[C/T]CCAGAGCCGCCTGAG	110749
rs253022092	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93896469	ACAGAAGCAACAGAA[A/C]CCAATTCTCTCACCA	110749
rs253084360	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93889299	AAGGTGAAGAGACTC[A/G]TCAGATTAATTGCAT	110749
rs253130577	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93904727	ACGGGATTGAGTGTG[G/T]TTTGGGTCCGCATTC	110749
rs253219706	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93902756	CATTGTGATATTTTG[A/T]CAGGCGTGTACATTG	110749
rs253251931	snp	C/G			missense	Chaf1b	Mm_Celera	16:93900055	CCCAGCCCCGAGCTG[C/G]TGAACCTGCCCTACC	110749
rs253254929	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93904326	TGTAGCCCTGGCTGT[A/C]CTGGAACTCACTCTG	110749
rs253377513	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93899595	CCCTGTCTTAGAACT[A/C]GATCTGTAGACCAGG	110749
rs253460010	in-del	-/T			intron-variant	Chaf1b	Mm_Celera	16:93903488	TAGAATAGGAATGCA[-/T]TTTTTTTTTTCCGAG	110749
rs253653675	snp	G/T			synonymous-codon	Chaf1b	Mm_Celera	16:93885379	GAAGTTGGAGAGGGG[G/T]CCAGATGGGAAAGCC	110749
rs253743444	in-del	-/CT			intron-variant	Chaf1b	Mm_Celera	16:93904912	CAGGGAAATGAGTAG[-/CT]CTCTCTCTTTACAGC	110749
rs253793971	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93889954	TTGATGCTTGTTGTA[C/T]TTGGAGGTGAATTCA	110749
rs253837545	snp	A/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882446	AGAAGACTGGCTTCC[A/G]GGCAGCTAGGATGAG	110749
rs254026789	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93888892	CCTGCCTTGATGATA[A/C]TGAACTGAACCTCTG	110749
rs254079152	snp	A/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892500	AGGCTTGGTAACAAG[A/T]GCCTTTTACCCTCCG	110749
rs254360594	snp	A/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883226	GGCGAAGGCATTGCT[A/G]TTTTATTGACATTTT	110749
rs254442488	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93886982	ACCACGCACCACCTA[G/T]CCATATTCTTGGATA	110749
rs254475485	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93899728	TATTATGTGCAGGCG[G/T]GTGTGTTGGGACTGT	110749
rs254527022	snp	C/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891822	TGCATGTATGTCTTT[C/G]TACCAGGTGTGTGCC	110749
rs254644520	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93899144	TAGTGTATCGGGGAC[A/C]AGAAATCTGGTCCCC	110749
rs254943850	in-del	-/AG			intron-variant	Chaf1b	Mm_Celera	16:93888253	TGATCCCCTGGAGCC[-/AG]AGTTACAGGCAGTTG	110749
rs255020826	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93893774	AATAAAATCAGTCAA[C/T]CTCTCCACCCAAAAC	110749
rs255142674	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93902226	TTAAAGAGTTATTGA[C/T]TTATGTATATGAGTA	110749
rs255193055	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93902314	TGTGGTTGCTGGGAA[C/T]TGAACTCAGGACCAC	110749
rs255249860	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93884948	CACCACGGCCCGGCT[A/G]TTTGCTACATTGTTA	110749
rs255282943	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93901892	CTGAAATAATCAGCT[G/T]AAAAGGAGGAAAGCC	110749
rs255681974	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93893067	TGCTGGGATCACAGG[G/T]GTGCAGCCCAGGCCT	110749
rs255860034	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93905394	TCTGTATGAGGGTTT[C/T]AGATCCCCTGGAAAT	110749
rs255877533	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93899159	CAGAAATCTGGTCCC[C/T]GTGTTCTCCGTGATG	110749
rs255940149	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93884169	GACCCGCGCCCCTCC[C/T]CGTGAACTCCCTCCC	110749
rs256034992	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93886918	CCATGTAACCTTGCA[C/T]TTCAGATCCACCTGC	110749
rs256075467	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93889135	GGAATATGGAAGACA[G/T]TGGTGCTGAGGGTGA	110749
rs256174723	in-del	-/TTTGTG			intron-variant, upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93892235	TTCATGGGTGTGTGT[-/TTTGTG]TGTGTGTGTGTGTGT	110749
rs256201421	in-del	-/A			intron-variant	Chaf1b	Mm_Celera	16:93886080	TTAGTTTTGGTTTGG[-/A]AAAAGAGGAATAGTT	110749
rs256277965	in-del	-/CAAA			intron-variant	Chaf1b	Mm_Celera	16:93904657	AAAACCAAAACCAAC[-/CAAA]CAAACAAACAAAAAA	110749
rs256338489	in-del	-/GT			intron-variant	Chaf1b	Mm_Celera	16:93893814	CAAACTCCCAGATCA[-/GT]GCTTCTTGGCAGAGG	110749
rs256623070	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93895488	AACATGTAATTGGGG[A/C]TGGCTTACAGATTCA	110749
rs256635347	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93888777	AGACCTTCCTCCTGG[C/T]TGCCTGCAGAAGATA	110749
rs256692925	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93905585	TTCCTCCTAGCTGTA[C/G]TCAGCGTCTCACTGG	110749
rs256786382	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93894537	CTCCTGGCTTGGCGT[C/T]GTCACTCAGGTGGAG	110749
rs256806789	snp	A/G/T			intron-variant	Chaf1b	GRCm38.p3	16:93896360	CTCTGAGGAGTTCTG[A/G/T]CACAACCAGAATCAC	110749
rs256907258	snp	A/C			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891920	AGTGCTGGGAACAGA[A/C]TGGGCTTCCCTACAA	110749
rs256923555	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903342	AGGTCGGGGGTGTGC[A/G]GGGTTTGGGCTGGTG	110749
rs256966905	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93901846	AAGGAAGCCCTGCAT[C/T]GGGAAGTTTTCTGAC	110749
rs257042416	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93905106	CAGCCAGGTAAGGGA[A/G]GGTTTAGAGATGTAT	110749
rs257111188	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93899072	CCCCTCTCAGGATCA[C/T]GGTGTCTCGCCACCT	110749
rs257117670	in-del	-/GGGAA			intron-variant	Chaf1b	Mm_Celera	16:93901608	TGTCTGCTTCCCGGG[-/GGGAA]GGAAGGAAGCTTTGG	110749
rs257159733	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93889837	TATTGCTTAGTTTGA[A/G]TGAAGCCTGTGAATT	110749
rs257168717	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93884084	AGGCAGAAGGCAGTT[C/T]GTCCCAGACCACAGT	110749
rs257176915	in-del	-/AAAAAAC			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882904	TGTCTTGGAAAAAAA[-/AAAAAAC]AAAAACAAAAACAAA	110749
rs257188196	snp	C/T			utr-variant-3-prime	Chaf1b	Mm_Celera	16:93906032	AGCCTGCTATGCACC[C/T]GCGTGCAGAGGAGGC	110749
rs257239210	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904553	TTTAATCCAAGCACT[C/T]GGGAGGCCAAGACAG	110749
rs257419024	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93889890	TATGGTCTAGAAGCC[A/G]CCCCTTACCAGCAAA	110749
rs257473839	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93899950	CATCTCCTCCCCCGG[A/C]GGAGAGAGTTTGGGG	110749
rs257611613	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93889866	TTTTGGGGCCAGTCT[A/G]TAGTTCTATATGGTC	110749
rs257621465	snp	C/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882222	TTAAATTTTATGTGT[C/G]TGAGTTTTGCCTGTA	110749
rs257623479	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93890775	GAGCTCTCTGACTGC[A/G]GTACCTCTCTTTCCT	110749
rs257812370	in-del	-/TTTGTTTG			intron-variant	Chaf1b	Mm_Celera	16:93905345	CCACCTATTTATTTA[-/TTTGTTTG]TTTGTTTATTTTAAA	110749
rs257885370	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883149	TTCCCATTTCCACCT[C/T]CAGAGTGTTGGGATT	110749
rs258085912	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93903754	GAGCCACCATGTGAT[C/T]AGCGGGAATTGAACT	110749
rs258144185	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93896085	ACGCTCCACTCCCAG[A/G]CACTCTAGCATGGCC	110749
rs258150809	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93897824	TAAGGAAGGATACTT[C/T]ATACTGGTCAAAGGA	110749
rs258255541	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93886188	ATGCATGCATTCACA[C/T]ATTTGTTGTAAGTGG	110749
rs258439422	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93902183	GCATATCAGGTATTT[A/T]ACATTGCGATTTTTT	110749
rs258685098	in-del	-/AC			intron-variant	Chaf1b	Mm_Celera	16:93905136	TTCTTCTGGAAGCTA[-/AC]ACACACCTGACTTTA	110749
rs258882384	in-del	-/AAA			upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93881907	AGAGACCTTGTCTCC[-/AAA]AAAAAAAAAAAAAAA	110749
rs258923571	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93889642	GGTTGAGGCATGTCC[C/T]CTGGGTCATGGGCAC	110749
rs259103321	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93895334	ATTAGAAAGTACATT[A/C]GTATTATCTTATCTT	110749
rs259127051	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93903331	TCTCATTCTCTAGGT[C/T]GGGGGTGTGCGGGGT	110749
rs259189889	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903839	ATGTTGTGTGTGCAT[A/G]TTTGCATGTGTGCAC	110749
rs259281129	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93902497	CTGCCTCTCAAGTGC[C/T]GGGATTAAAGGCTAC	110749
rs259281262	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93893785	TCAATCTCTCCACCC[A/G]AAACCCAAATCCCTC	110749
rs259343207	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93894448	GGCTCATGAGCTGGC[A/G]GCTGGAGCCAGCCAC	110749
rs259408429	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93888599	TATTGCTGTGATAAG[C/T]CACCATCACCGAAGA	110749
rs259473124	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93902098	CTCAGTGACTTAACA[G/T]CATCCCCTAGACCAG	110749
rs259574603	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93889219	TGTGCCTAGAGACTG[C/T]TCTGATATTTTGGTG	110749
rs259582121	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93886942	CACCTGCCTCAGACT[C/T]CCAAGGGCCAGATTA	110749
rs259951591	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93889104	TTGTAGTGGGGCTTA[A/C]TGGACCATCCTAGTA	110749
rs260380383	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93887318	ATTTATGATTGTTTA[C/G]TTTATGACTGAGAGT	110749
rs260452334	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93893174	GGTGCCTTTGATACA[A/C]TGTATCCTATACCTC	110749
rs260502418	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93886680	AGCTCTGCAGGCACA[C/G]TCTGCAGACCCTTGC	110749
rs260896514	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93902868	AGGACGTCCCTGTTC[C/T]ATGCACTGGCACTTA	110749
rs260960886	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93886105	ATAGTTGCGTTCTGC[A/G]CCCTAATGCCCAAAA	110749
rs260975259	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93900611	CTCACATGGCACCCA[A/G]GAGTCAAGCTTAAAC	110749
rs261024677	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93901413	GCCCCAGCATAGCAA[A/G]TATTGAAGGTTCCAC	110749
rs261073828	snp	A/G			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906161	GCATGCCCTTGTTCA[A/G]TCACCCCTTCCCATG	110749
rs261082805	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93885845	GGCTGGTTGGGTGTG[C/G]TAGATCTGTCAGCAT	110749
rs261360926	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93901528	AGAGCCTGGGGCTTT[C/T]CCTAGCCTTGTCTCC	110749
rs261413213	snp	C/T			downstream-variant-500B	Chaf1b	Mm_Celera	16:93906530	CAAGATAACATCAGT[C/T]CCTGTGTGGATTTGT	110749
rs261505065	in-del	-/TGTGTGTGTGTG			intron-variant	Chaf1b	Mm_Celera	16:93904048	GGGGGAGGGTAGGGA[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT	110749
rs261557620	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93884839	TTGTTTCAAGACAGG[A/G]TTTCTCTGTGTAGCC	110749
rs261941982	snp	C/T			synonymous-codon	Chaf1b	Mm_Celera	16:93901297	GCAAAACATGAAAGC[C/T]CCCCAACCCCGCAGG	110749
rs261948199	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93892998	GGCTGGTGCTGAACT[C/T]GGGTAGCTGAAGGTG	110749
rs261953680	snp	A/G			missense	Chaf1b	Mm_Celera	16:93905965	CCAGGCTTGAGGAAC[A/G]TGAAGGAGATGCCCA	110749
rs261957995	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904424	GTGTGCCACCACGCC[C/T]GGCTATTTTTGGTGT	110749
rs261992657	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93889227	GAGACTGCTCTGATA[C/T]TTTGGTGAAGAATGT	110749
rs262056467	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93905747	GGTTGTGAGCCACCA[C/T]GTGGTTGCTGGGATT	110749
rs262091130	snp	A/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882851	AGCCTGGTCTACAGA[A/G]TGAGTTTCAGGACAG	110749
rs262137696	in-del	-/GG			intron-variant	Chaf1b	Mm_Celera	16:93893831	TTCTTGGCAGAGGAC[-/GG]TGGTTTTCTGCTAGT	110749
rs262210631	in-del	-/G			intron-variant	Chaf1b	Mm_Celera	16:93894395	GCTGGCTCGGAGAGA[-/G]GGACAGCCAAGGTCT	110749
rs262304447	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892590	TTGTCCTTCCTTGCC[C/T]CTGAATCACGGCACT	110749
rs262344070	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93897205	TATTAAAAGCAGTAA[A/G]GGAAAAAGGTCAAGT	110749
rs262372114	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93900402	TGTGCCCAGTTCACG[A/C]TTGGCACTGAACCCA	110749
rs262403054	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93898957	TAAGCTGACAACTCA[A/T]CCACAACCTGATCTT	110749
rs262614269	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93904243	GGGGTGGTGAGGTAT[C/T]TTTGAGGTATTTTGG	110749
rs262695542	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93903939	AACTGCACTTAGGCC[A/C]TCTGGCAGAGCAGCA	110749
rs262757670	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93890487	GCTGCTGTCTCCTCT[A/G]CTGAGGGCCTTTGTT	110749
rs262823471	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93902703	TCTGCACCCCCGCCA[C/T]CACAACCACCGCCGC	110749
rs262833232	in-del	-/AGTGGTAAG			intron-variant	Chaf1b	Mm_Celera	16:93898422	GGACACAATGAAAGC[-/AGTGGTAAG]AGGAAATTTCACTCA	110749
rs263058288	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93898674	CAGAGGGCACAGAGA[C/T]AGTATCCAAACCAAT	110749
rs263090383	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93897985	GCAATGGACAGATCA[C/T]GGAACCATAAACTAA	110749
rs263229525	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93895559	ATCCAGGCAGACATG[G/T]TGCAGGAGGAGCTGA	110749
rs263300914	in-del	-/GTCTAAGTTGAT			intron-variant	Chaf1b	Mm_Celera	16:93895743	CATCAGAGTCATGTA[-/GTCTAAGTTGAT]GTCAGACTTATTGTC	110749
rs263320831	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93895798	TGACCTGACAGTGGG[A/G]TCTAGGACATGTACC	110749
rs263369891	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93888879	ATGCTGCCGTGCTCC[C/T]GCCTTGATGATAATG	110749
rs263472022	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93893714	TTCAAGACCAGCCTG[A/G]TATGTGTGAGACCCT	110749
rs263714315	snp	A/T			intron-variant	Chaf1b	Mm_Celera	16:93889427	AAGATACAAAATGTG[A/T]GGGTTCAAGAGTGAA	110749
rs263777205	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93888378	GGAAGAAGGAGGTAC[C/G]AGGTTGGGGATGCTG	110749
rs263781636	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93901977	CCTGGCTAGAGCCAG[C/T]ATTACAGGGTGGTAG	110749
rs263925255	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93887850	CTTTGAACTTTTTTC[C/T]CCCCCCTATTTTTCA	110749
rs264146868	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93886858	CTGTACAAATTCTTC[G/T]TGTTTTTCTAGGATC	110749
rs264227218	in-del	-/G			intron-variant	Chaf1b	Mm_Celera	16:93887442	GACTTTTCTGGAGGA[-/G]CCAGAACCGTGATTA	110749
rs264267385	snp	C/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93892449	GGGAGTCAGTTCCCT[C/T]AGTGCACTGTATGGG	110749
rs264364791	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93886282	AAAGTCCCTTAGCCT[C/T]GAAGACCGAAACCTC	110749
rs264408405	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93884714	CAGCAACTCAAGTCG[G/T]GTTGCCACCTAGTCC	110749
rs264428262	snp	A/C			intron-variant	Chaf1b	Mm_Celera	16:93893022	GAAGGTGATCCTCAA[A/C]TTGTGATCCTCTTAT	110749
rs264458690	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93901962	TGATTGTCTCATTGC[C/T]CTGGCTAGAGCCAGT	110749
rs264463182	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891689	TTTTTGTTTGGATCT[A/G]CTATTCTGACAAGAC	110749
rs264464378	snp	A/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883739	GCCCCGCCCACGAGA[A/G]AGAAAAGAGCCCAGA	110749
rs264706515	snp	C/G			upstream-variant-2KB, utr-variant-5-prime	Chaf1b	Mm_Celera	16:93883899	CTCCGCCCCGAGGAG[C/G]CGTGACCGGAGGCGT	110749
rs264849518	snp	C/G			intron-variant	Chaf1b	Mm_Celera	16:93905334	GCATCCCTGATGCCA[C/G]CTATTTATTTATTTG	110749
rs264917901	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93903887	TGGAGGCCAGGAAAG[A/G]GTGTCGGTTCCCTAG	110749
rs264932160	snp	C/T			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93882118	ACGGGTGGTTGTGAG[C/T]CACCATGTGGTTGCT	110749
rs265074391	snp	G/T			intron-variant, upstream-variant-2KB	Chaf1b	Mm_Celera	16:93891896	CTGGAGTTACAGTTG[G/T]GAGCTGTCAGTGCTG	110749
rs265127169	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93897655	CATTTTTTGCTGCAT[A/G]CAGTAAATGCACCTC	110749
rs265257263	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93904516	AAAAGAAAACACTGA[A/G]CCGGGCATGGTGGTG	110749
rs265399040	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93903176	CTGAGGGAGGTCATG[C/T]GTTCCTTTCTGGGCC	110749
rs265412447	in-del	-/TC			intron-variant	Chaf1b	Mm_Celera	16:93884327	GTACACTGGTGGAAG[-/TC]TCTCTACCTGCGGGA	110749
rs265573755	snp	C/T			intron-variant	Chaf1b	Mm_Celera	16:93889181	CCTGGCTCTAGATGT[C/T]TCCGAGGAGAAGAAC	110749
rs265612293	snp	G/T			intron-variant	Chaf1b	Mm_Celera	16:93896225	ACCACTGGATCCCAG[G/T]ATCCCAGGATCCCAG	110749
rs265628716	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93894343	GACAGGTCCTGCAGG[A/G]GGCTGCAGCGTGGGC	110749
rs265775315	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93901606	CCATGTCTGCTTCCC[A/G]GGGGAAGGAAGCTTT	110749
rs265837869	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93888714	GAAGTGTGTCACTGT[A/G]GGGGTGGGCTTTGAG	110749
rs266142147	snp	A/G			intron-variant	Chaf1b	Mm_Celera	16:93885303	GTTGTTGTCTCCTGG[A/G]AGGGAGTTAGGAGGT	110749
rs266156450	snp	A/G			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93883198	CTAGGCGTCTGTCAC[A/G]TCGCTAAGAGAGGGC	110749
rs387072207	in-del	-/AA			upstream-variant-2KB	Chaf1b	Mm_Celera	16:93881922	CAAAAAAAAAAAAAA[-/AA]GCATAAATGTATGTG	110749
rs387433322	in-del	-/GA			intron-variant	Chaf1b	Mm_Celera	16:93897336	AATTCTAAAGACAGA[-/GA]AAACAAGATATTCCA	110749
rs387719732	in-del	-/GGAA			intron-variant	Chaf1b	Mm_Celera	16:93898325	GAAGGAAGGAAGGAA[-/GGAA]AAAAGAAAGAAAGGA	110749
rs578532268	snp	C/G			intron-variant	Chaf1b	GRCm38.p3	16:93904316	GGTTTCTCTATGTAG[C/G]CCTGGCTGTCCTGGA	110749
rs578584636	snp	G/T			intron-variant	Chaf1b	GRCm38.p3	16:93896282	GTCCCAGAGGCAGCT[G/T]GACTCCCAGGAGCTC	110749
rs578646111	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93904683	ACAAAAAAACACTGG[C/T]TGTTGGGAAGCCAAA	110749
rs578768667	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93886431	TGTATTTCCTGCTCC[C/T]TCCTTCACTGGCCTA	110749
rs578769669	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93898329	GAAGGAAGGAAGGAA[A/G]AAAGAAAGAAAGGAA	110749
rs579050274	snp	C/T			upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93883005	TCTTTAAAAAATATG[C/T]GACATTATTGAGAAG	110749
rs579180183	snp	A/G			upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93882924	ACAAAAACAAAAACA[A/G]AAACAAAAAAAACCT	110749
rs579252569	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93898628	TCTTTGAGAAAACCA[A/G]CAAGATAGATAAACC	110749
rs579295183	snp	A/T			intron-variant	Chaf1b	GRCm38.p3	16:93904430	CACCACGCCTGGCTA[A/T]TTTTGGTGTTCAGTT	110749
rs579345582	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93896267	CACCAGGATCTCAGG[A/G]TCCCAGAGGCAGCTT	110749
rs579437808	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93897124	CTCCAAATAGACTGG[A/G]CCAGAAAAGAAATTC	110749
rs579901608	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93903711	GACACACCAGAAGAG[A/G]GCATCAGATCTCATT	110749
rs579936041	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93897011	AGTGAAGATTCCCAA[C/T]TTAAAGGGCCAGTAA	110749
rs579979100	snp	G/T			intron-variant, upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93890989	TAATTGGGGCTGGCT[G/T]ACAGTTCAGAGGTTC	110749
rs580353975	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93902191	GGTATTTAACATTGC[A/G]ATTTTTTTCTTTTTT	110749
rs580401672	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93903799	GAGCAGTCATCTCTC[C/T]AGCTCAGGAATGCAT	110749
rs580402574	snp	A/C			intron-variant	Chaf1b	GRCm38.p3	16:93887425	ACCCGAGAACAAAAC[A/C]TGACTTTTCTGGAGG	110749
rs580476389	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93905666	GATTTATTTATTTAT[C/T]ATATGTAAGTACACT	110749
rs580530063	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93896836	CAACAGAATACAAGA[C/T]ATAGAAGAGAGAATC	110749
rs580731321	snp	A/C			upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93882904	TGTCTTGGAAAAAAA[A/C]AAAAACAAAAACAAA	110749
rs580942410	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93905713	ACACCAGAAGAGGGC[A/G]TCAGATCTCATTACG	110749
rs581001775	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93898322	AAGGAAGGAAGGAAG[A/G]AAGGAAAAAAGAAAG	110749
rs581118059	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93904310	AGACGGGGTTTCTCT[A/G]TGTAGCCCTGGCTGT	110749
rs581135342	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93895116	TGTTTGTTTGTTTTT[C/T]GAGACAGGGTTTCTC	110749
rs581232490	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93904042	TTTTTTAGGGGGAGG[A/G]TAGGGATGTGTGTGT	110749
rs581281867	snp	A/C			intron-variant	Chaf1b	GRCm38.p3	16:93896270	CAGGATCTCAGGGTC[A/C]CAGAGGCAGCTTGAC	110749
rs581531816	snp	A/T			intron-variant	Chaf1b	GRCm38.p3	16:93896249	ATCCCAGGAGCTTGG[A/T]CACACCAGGATCTCA	110749
rs581614116	snp	A/C			upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93882929	AACAAAAACAAAAAC[A/C]AAAAAAACCTTAACT	110749
rs581645242	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93898467	TCCAAAAAGAAACTG[A/G]AAAGAGCTTACACTA	110749
rs581693127	snp	A/C			intron-variant	Chaf1b	GRCm38.p3	16:93897943	AAAGCACACATCGCA[A/C]CCCACACAATAATAG	110749
rs581824246	snp	A/C			intron-variant	Chaf1b	GRCm38.p3	16:93886456	GGCCTAAAAGGATCG[A/C]GTTACACAGTGAACC	110749
rs582211712	snp	C/G			intron-variant	Chaf1b	GRCm38.p3	16:93884342	TCTCTCTACCTGCGG[C/G]AGCATTTTAGCTGAA	110749
rs582264589	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93904570	GGAGGCCAAGACAGG[C/T]GGATTTCTGAGTTCG	110749
rs582386500	snp	A/C			intron-variant	Chaf1b	GRCm38.p3	16:93896300	CTCCCAGGAGCTCTG[A/C]CACACCCAGGATCTC	110749
rs582445038	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93896863	AATCTCAGAGGGTGC[A/G]GAAGATACCATAGAA	110749
rs582520178	snp	G/T			intron-variant	Chaf1b	GRCm38.p3	16:93902926	TGACTCTCTCATCCC[G/T]GCCCGAGGTTCCTCC	110749
rs582747016	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93896391	AGGAAAGCCAGGCAC[C/T]AGTGAGATAAGCAAG	110749
rs582815219	snp	G/T			intron-variant	Chaf1b	GRCm38.p3	16:93903730	TCAGATCTCATTACA[G/T]ATGGTTGTGAGCCAC	110749
rs582843464	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93904339	GTCCTGGAACTCACT[C/T]TGTAGACCAGGCTGG	110749
rs582998325	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93899682	AGGTGTGTGCCACCA[A/G]CTTGAATTCTGTATT	110749
rs583120011	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93896246	AGGATCCCAGGAGCT[C/T]GGTCACACCAGGATC	110749
rs583179016	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93905488	TCTTACACACTGATG[C/T]TACCTACCTCTTACC	110749
rs583440589	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93905685	TGTAAGTACACTGTA[A/G]CTGTCTTCAGACACA	110749
rs583499941	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93905728	ATCAGATCTCATTAC[A/G]GGTGGTTGTGAGCCA	110749
rs583520388	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93897109	AAGAAGCCTACAGAA[C/T]TCCAAATAGACTGGA	110749
rs583792282	snp	A/G			intron-variant, upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93892227	ATCATTTTTTCATGG[A/G]TGTGTGTTTTGTGTG	110749
rs583894944	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93889492	ATCCCCTGGTTAGCT[C/T]ACGTGGGGCTTACGT	110749
rs583987060	snp	G/T			intron-variant	Chaf1b	GRCm38.p3	16:93904315	GGGTTTCTCTATGTA[G/T]CCCTGGCTGTCCTGG	110749
rs584188449	snp	A/T			intron-variant	Chaf1b	GRCm38.p3	16:93904033	TATTGGGGTTTTTTT[A/T]GGGGGAGGGTAGGGA	110749
rs584266522	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93898469	CAAAAAGAAACTGAA[A/G]AGAGCTTACACTAGC	110749
rs584339251	snp	A/C			upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93882923	AACAAAAACAAAAAC[A/C]AAAACAAAAAAAACC	110749
rs584427812	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93898326	AAGGAAGGAAGGAAG[A/G]AAAAAAGAAAGAAAG	110749
rs584908952	snp	G/T			intron-variant	Chaf1b	GRCm38.p3	16:93904043	TTTTTAGGGGGAGGG[G/T]AGGGATGTGTGTGTG	110749
rs584926630	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93898294	CAATGATAACTTGGT[A/G]AAGGAAGGAAGGAAG	110749
rs584960745	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93896276	CTCAGGGTCCCAGAG[A/G]CAGCTTGACTCCCAG	110749
rs584968851	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93896266	ACACCAGGATCTCAG[A/G]GTCCCAGAGGCAGCT	110749
rs585091513	snp	A/C			intron-variant	Chaf1b	GRCm38.p3	16:93904359	GACCAGGCTGGCCTC[A/C]AACTCAGAAATCCAC	110749
rs585295194	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93903124	CATCTCCACACAGGA[A/G]AAATCCATGAGAGCA	110749
rs585439376	snp	C/G			intron-variant	Chaf1b	GRCm38.p3	16:93896306	GGAGCTCTGACACAC[C/G]CAGGATCTCAGGATC	110749
rs585546110	snp	G/T			intron-variant	Chaf1b	GRCm38.p3	16:93904927	CTCTCTCTCTTTACA[G/T]CTTTGAACCTTGGCT	110749
rs585595295	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93886457	GCCTAAAAGGATCGC[A/G]TTACACAGTGAACCT	110749
rs585759117	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93886272	TCCCCATTACAAAGT[C/T]CCTTAGCCTCGAAGA	110749
rs585893146	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93896691	ACACAATCAAACAGG[C/T]GAAGGAAATGAACAA	110749
rs585976864	snp	A/C			intron-variant	Chaf1b	GRCm38.p3	16:93890698	CAGGTCTGGCTTCAG[A/C]TCGCTCTTTGAAGCG	110749
rs586017936	snp	A/T			intron-variant	Chaf1b	GRCm38.p3	16:93901795	AGCTCAGCCTTGCTC[A/T]GTGGCGCCAGATAAC	110749
rs586079220	snp	A/C			intron-variant	Chaf1b	GRCm38.p3	16:93904660	ACCAAAACCAACCAA[A/C]CAAACAAACAAAAAA	110749
rs586203090	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93896985	ACCTAAGGATAATAG[A/G]TATAGAAGAGAGTGA	110749
rs586377532	snp	G/T			intron-variant	Chaf1b	GRCm38.p3	16:93905489	CTTACACACTGATGC[G/T]ACCTACCTCTTACCC	110749
rs586392156	snp	G/T			intron-variant	Chaf1b	GRCm38.p3	16:93896247	GGATCCCAGGAGCTT[G/T]GTCACACCAGGATCT	110749
rs586463081	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93904299	TTGTTTTTCCGAGAC[A/G]GGGTTTCTCTATGTA	110749
rs586588297	snp	A/C			intron-variant	Chaf1b	GRCm38.p3	16:93897111	GAAGCCTACAGAACT[A/C]CAAATAGACTGGACC	110749
rs586739473	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93903731	CAGATCTCATTACAG[A/G]TGGTTGTGAGCCACC	110749
rs586791270	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93893350	AGTGAAAGCAAGGTA[C/T]AGATTACATCCAGGA	110749
rs586967444	snp	C/T			intron-variant	Chaf1b	GRCm38.p3	16:93897747	ATCCTAAGAAACAAG[C/T]TGGAGTAGCCATTCT	110749
rs586970407	snp	A/C			upstream-variant-2KB	Chaf1b	GRCm38.p3	16:93882310	ATAAGGACAACATTT[A/C]ATTGGGGCTGGCTGA	110749
rs587309094	snp	A/T			intron-variant	Chaf1b	GRCm38.p3	16:93905700	GCTGTCTTCAGACAC[A/T]CCAGAAGAGGGCATC	110749
rs587312774	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93904034	ATTGGGGTTTTTTTA[A/G]GGGGAGGGTAGGGAT	110749
rs587447004	snp	A/G			intron-variant	Chaf1b	GRCm38.p3	16:93898321	GAAGGAAGGAAGGAA[A/G]GAAGGAAAAAAGAAA	110749
rs864292039	snp	C/T			utr-variant-3-prime	Chaf1b	GRCm38.p3	16:93906070	AAGCTCGAAGGCTGG[C/T]GATGGTGGCCAAATA	110749