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

Eml1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs3674805	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108426732	CACACCAAAAAGTAT[C/T]CATAGTAACCATTAG	68519
rs3683974	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108516767	ATTTACAAGTAAAAT[A/G]AGAGAATTTGAAGCT	68519
rs3683977	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108516769	TTACAAGTAAAATAA[A/G]AGAATTTGAAGCTAC	68519
rs3683995	snp	C/T	0.5	0	intron-variant	Eml1	Mm_Celera	12:108516784	GAGAATTTGAAGCTA[C/T]CCAACACTTCCTGTT	68519
rs3685901	snp	C/T	0.5	0	intron-variant	Eml1	Mm_Celera	12:108517122	ACCAGCGTGGGGATA[C/T]CACTCCATCCCCAGC	68519
rs3685943	snp	C/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108517142	CCATCCCCAGCTATG[C/G]AGGATGGAGGATTTC	68519
rs3693681	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521188	TGCACAGTAAGTTCA[A/G]GGCTAGCCTGGACTA	68519
rs3707852	snp	A/C	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521261	CCCAAAAAAGCCAAA[A/C]ACCAATTGAATGAAA	68519
rs3709227	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521495	CCCGTTAATATGGAC[A/G]CGTGTGAGTTTCCCA	68519
rs3709266	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521519	TTTCCCAGTGTGGTG[A/G]CCTCCTGCTTCAGTT	68519
rs3709283	snp	G/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521534	ACCTCCTGCTTCAGT[G/T]CGGTGTTCTGTGGCA	68519
rs3709399	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108426355	GCCCTAGCATGTACA[C/T]GTGTGCTCAGGCCAG	68519
rs3709760	snp	C/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521557	CTGTGGCATGATTAA[C/G]CTTGAGAGGAAAGAG	68519
rs3709797	snp	A/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521574	TTGAGAGGAAAGAGC[A/T]CATGAGACGGTCCTT	68519
rs3709814	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521582	AAAGAGCTCATGAGA[C/T]GGTCCTTCGGGGGTG	68519
rs3719674	snp	A/G	0.5	0	upstream-variant-2KB	Eml1	Mm_Celera	12:108370181	ATGTCAAGCCTGCTC[A/G]CTCAGTCCCTGCTTG	68519
rs4136848	snp	C/G	0.429688	0.173817	intron-variant	Eml1	GRCm38.p3	12:108431525	AACTGAGAAAGACCC[C/G]GGATCTCTGCTCCAG	68519
rs4136915	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108521607	GGGGTGCCGTTGTGA[C/T]GGTGGGATCTCAGAG	68519
rs4139205	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108516868	AACCTCTAGAATCCA[A/G]CATGCTTCGTGCACA	68519
rs4229553	snp	C/T	0.21875	0.248039	utr-variant-3-prime, nc-transcript-variant, intron-variant	Eml1, Gm16596	Mm_Celera	12:108539302	CTGGGGACTGTATCT[C/T]GGATCTTTAAATAGA	68519
rs4229554	snp	C/G	0.21875	0.248039	utr-variant-3-prime, intron-variant	Eml1, Gm16596	Mm_Celera	12:108539377	GTAAACTCGTTTAAG[C/G]GAGTGAGTGAGTTGA	68519
rs4229555	snp	C/T	0.21875	0.248039	utr-variant-3-prime, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108539408	GTTACCTGAACTCTG[C/T]AGCACTGGTTGTTCA	68519
rs4229556	snp	C/T	0.21875	0.248039	utr-variant-3-prime, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108539424	AGCACTGGTTGTTCA[C/T]AGTGATGAAGGACAG	68519
rs4229557	snp	A/G	0.48	0.0979796	utr-variant-3-prime, nc-transcript-variant	Eml1, Gm16596	GRCm38.p3	12:108539438	ATAGTGATGAAGGAC[A/G]GCACTGCAGACATCT	68519
rs4229558	snp	A/G	0.21875	0.248039	utr-variant-3-prime, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108539439	TAGTGATGAAGGACA[A/G]CACTGCAGACATCTC	68519
rs4229559	snp	A/C	0.375	0.216506	utr-variant-3-prime, nc-transcript-variant	Eml1, Gm16596	GRCm38.p3	12:108539445	TGAAGGACAGCACTG[A/C]AGACATCTCCCTTGC	68519
rs4229560	snp	A/G	0.277778	0.248452	downstream-variant-500B, intron-variant	Eml1, Gm16596	Mm_Celera	12:108539582	TTCTTATTGACCTAC[A/G]TTTCTGAAAGTATGT	68519
rs4229561	snp	A/T	0.252401	0.249988	downstream-variant-500B, intron-variant	Eml1, Gm16596	Mm_Celera	12:108539583	TCTTATTGACCTACG[A/T]TTCTGAAAGTATGTG	68519
rs4229562	snp	A/G	0.375	0.216506	downstream-variant-500B, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539598	TTTCTGAAAGTATGT[A/G]AATTAAAGAATTTAA	68519
rs4229563	snp	C/T	0.21875	0.248039	downstream-variant-500B, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539601	CTGAAAGTATGTGAA[C/T]TAAAGAATTTAAAAT	68519
rs4229564	snp	C/G	0.30839	0.243086	downstream-variant-500B, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539627	AAAATTAGATGGGGT[C/G]CACACTACATCCTGT	68519
rs4229565	snp	A/G	0.21875	0.248039	downstream-variant-500B, intron-variant	Eml1, Gm16596	Mm_Celera	12:108539631	TTAGATGGGGTCCAC[A/G]CTACATCCTGTTCCC	68519
rs4229566	snp	A/G	0.4992	0.019984	downstream-variant-500B, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539683	GGATCCCTTGCACAC[A/G]GAGTTCTGTTCTGCA	68519
rs6153877	snp	C/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108534200	TTATCAATTTAGGGC[C/T]CAATGGTTAAGAGCA	68519
rs6153878	snp	A/G	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108534203	TCAATTTAGGGCCCA[A/G]TGGTTAAGAGCACTA	68519
rs6153945	snp	C/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108534243	ACAAAGGATCTGGGC[C/T]CAATTCCCAGCACCC	68519
rs6239767	snp	A/C	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533097	GGTTTATTTATGTTG[A/C]GTTCCTGCTTTTCCA	68519
rs6239832	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533147	GTTATTTATGGGATA[A/G]CCTTCTTTCCTGGTA	68519
rs6239861	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108506449	GGAGCGCCCCGAGGC[A/G]TGTCACTGACACCTT	68519
rs6239906	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533196	AACCCCCCCACTCCC[C/T]GCCTGAGCCCNGTCT	68519
rs6240304	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533207	TCCCNGCCTGAGCCC[C/T]GTCTCAGACATTTGA	68519
rs6240371	snp	C/T	0.492188	0.0620098	intron-variant	Eml1	GRCm38.p3	12:108533247	TCAGCTCGCAGACGC[C/T]TCCCAGTTCCCCACG	68519
rs6240406	snp	C/T	0.459184	0.136902	intron-variant	Eml1	GRCm38.p3	12:108533274	CACGTGCATTCTCTG[C/T]TCTCANCTTTGTATT	68519
rs6240423	snp	A/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533280	CATTCTCTGNTCTCA[A/T]CTTTGTATTGATTCT	68519
rs6240517	snp	C/T	0.46281	0.131194	intron-variant	Eml1	GRCm38.p3	12:108506620	GGGTGTATCCTTTAC[C/T]GGCCAACCAGACTGT	68519
rs6240887	snp	C/T	0.459184	0.136902	intron-variant	Eml1	GRCm38.p3	12:108533345	AACAGATGAAGTTAG[C/T]GCAGGGACACGTCCT	68519
rs6241375	snp	A/G	0.426035	0.177515	intron-variant	Eml1	GRCm38.p3	12:108533407	CAGAGGCAGCAGGGT[A/G]GATGTTCTTCCCAGC	68519
rs6241420	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533437	CACCCCAGCTTCTGT[A/G]GTATCCNTCCCCCAG	68519
rs6241424	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533444	GCTTCTGTNGTATCC[C/T]TCCCCCAGAAAATAT	68519
rs6243578	snp	A/G	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108533873	ATGCTGGCAGTTTTT[A/G]GACTAGTCTCCAGGC	68519
rs6244188	snp	A/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108533973	GTCTAGCATTTCAGC[A/T]CCAGCACTACCACCC	68519
rs6244638	snp	C/G	0.396694	0.202437	intron-variant	Eml1	GRCm38.p3	12:108534007	AGCCCAGACTTCCTT[C/G]ACACAGGAGGCTCCA	68519
rs6244699	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108534043	GTGGACCCCCCAGGA[A/G]GATATGGGAAAGCCT	68519
rs13474898	snp	A/G			utr-variant-3-prime, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108538797	TACTACAGAACCCCC[A/G]AGCTGCTGTGGGTCC	68519
rs13474899	snp	A/G	0.486111	0.0821678	utr-variant-3-prime, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539171	CTGACTCTCGTGCAC[A/G]GACAGCATGCAGCAT	68519
rs13481641	snp	C/T	0.491278	0.0654592	intron-variant	Eml1	GRCm38.p3	12:108371681	AGTGGGTGCAGGGTG[C/T]ATGACCTTTGACACC	68519
rs29124775	snp	C/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108433004	TATGCTCTTCCCAGT[C/T]TGGTTCTCTGGGTCT	68519
rs29125627	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108373516	GAGATGAAGTCCAGC[A/G]GGCAGATGACATGCC	68519
rs29125630	snp	A/C	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108461322	GTTTTAAAACAGTTC[A/C]GACAGTATTCTGGAA	68519
rs29126227	snp	C/T	0.188366	0.242283	intron-variant	Eml1	Mm_Celera	12:108389430	GGAGAATGCTTTGTG[C/T]ACTCAGGAACACCTT	68519
rs29126556	snp	A/T	0.345679	0.230967	intron-variant	Eml1	Mm_Celera	12:108510113	TTATGTTTAAACTTT[A/T]GGAAGATTGTAGAAG	68519
rs29126641	snp	C/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108435092	GGTATGTCTTGGTAA[C/G]AGAAAACCAGTGAAG	68519
rs29127529	snp	G/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108433103	GTCTTACTGTGAGAC[G/T]CGAGATCCTGTACAC	68519
rs29128166	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108515693	CGCATGCGCACAGAT[C/T]AGACCTTTTTTTTTT	68519
rs29128195	snp	C/G	0.444444	0.157135	upstream-variant-2KB	Eml1	Mm_Celera	12:108369434	ACCTGGCATAGGACA[C/G]GACATGGGCCAGGCC	68519
rs29128306	snp	A/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108509431	CAGATTATCTGAGGG[A/T]AAAAGCTTCAGGAAG	68519
rs29128751	snp	C/T	0.32	0.24	intron-variant	Eml1	GRCm38.p3	12:108372769	TGACAAGAGACCCTG[C/T]GCAAGCTCTTGGAAT	68519
rs29128933	snp	A/C	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108513318	TAACAAACCCAGGAA[A/C]CCACTATGTGCTGGG	68519
rs29129879	snp	A/G	0.415225	0.187619	intron-variant	Eml1	GRCm38.p3	12:108389345	CAGATAAGTTACAGG[A/G]ACTGTTTTACATGAG	68519
rs29131598	snp	C/T	0.5	0	intron-variant	Eml1	Mm_Celera	12:108528333	CAAGAAAGGAGGCCC[C/T]CTTTCTCAGCTAGAG	68519
rs29131651	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108374893	AGACCTCGGAGGACA[A/G]ACCTGACAGCTGTCT	68519
rs29131881	snp	G/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108382326	CCAGGCATGTGCCTG[G/T]GACCCCAACATTGTG	68519
rs29132320	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108470672	CCTGACTACAATCAC[C/T]GGAGAGGACAGCTTC	68519
rs29133349	snp	A/G	0.375	0.216506	intron-variant	Eml1, Gm33385	Mm_Celera	12:108407769	TAGTTAACTTGGTTG[A/G]ACAGAAACTTCAGAC	68519
rs29133944	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108506006	AGAAGGGCAACAGAT[C/T]TCTTGGAGTATTGTG	68519
rs29134853	snp	C/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108502672	ACTTCTCAGGAAAGA[C/T]GCCCTTTGCCTGTAG	68519
rs29136747	snp	C/T	0.5	0	intron-variant	Eml1	Mm_Celera	12:108515732	TTTGGTTTTTTGAGA[C/T]AGGGTTTCTCAGTAT	68519
rs29136871	snp	A/G	0.48	0.0979796	intron-variant	Eml1	Mm_Celera	12:108371901	GATGTGTGTAGGATT[A/G]GCTACCTGAAATAGT	68519
rs29137688	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108532038	AGAGTCTGGAACTCA[C/T]TAACCTTCTTCTGAC	68519
rs29138318	snp	C/T	0.465374	0.126941	intron-variant	Eml1	GRCm38.p3	12:108396515	AGGGAATAGGGCATC[C/T]GAGATGCTGAAGTCT	68519
rs29138546	snp	C/T	0.32	0.24	intron-variant	Eml1	GRCm38.p3	12:108526105	TCCCTCTCTGGAGTT[C/T]GGTGGCAAAGACATC	68519
rs29138815	snp	A/C/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108437615	AACATTCGGCCACTG[A/C/T]GGCTTTTATCTTGTG	68519
rs29139004	snp	G/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108387438	TGGGGTTGGAGCCCA[G/T]AGAACCCAGAAGAAG	68519
rs29139323	snp	C/T	0.260355	0.249785	intron-variant	Eml1	Mm_Celera	12:108447868	TTGGAGGCTTCTCAT[C/T]ACCAGGTGCCCTGCG	68519
rs29139647	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108531057	ATGTATGTATGTGTG[A/G]TTTATGAGTGTATAA	68519
rs29140024	snp	A/G	0.49827	0.0293608	intron-variant	Eml1	GRCm38.p3	12:108530962	CCCAGCCCTTTTGAT[A/G]AGTTTATTCTTCTAG	68519
rs29141037	snp	A/G	0.387812	0.208586	intron-variant	Eml1	Mm_Celera	12:108420736	AACTCACACTTTCCC[A/G]TGTCTGTGCCCCATC	68519
rs29141754	snp	C/T	0.484429	0.0868505	intron-variant, nc-transcript-variant	Eml1, Gm16596	GRCm38.p3	12:108537139	AGCTGTTAGAAGAGA[C/T]GCAGGGCTTCTCAGG	68519
rs29142954	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108512584	AATACTGGCCTTCCA[A/G]AGGACTCGGGATCGA	68519
rs29143185	snp	A/G	0.475309	0.108333	intron-variant	Eml1	GRCm38.p3	12:108428529	GTGCTCTCTCAAAGG[A/G]CAACCCAATATAACC	68519
rs29143692	snp	A/C	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108431555	GCCCCACACATGCAC[A/C]GACACAGACACGTAC	68519
rs29143792	snp	C/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108432987	AGGTGCCCTGCCTGA[C/T]TTATGCTCTTCCCAG	68519
rs29144148	snp	C/T	0.260355	0.249785	intron-variant	Eml1	Mm_Celera	12:108503895	TCACTTTGAACTCCA[C/T]CATTCCCGCTTCCCT	68519
rs29145047	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108391442	GCTGGGCTGCGGCCC[A/G]TGTTAAATGAAGAAA	68519
rs29146868	snp	C/T	0.375	0.216506	intron-variant	Eml1, Gm33385	Mm_Celera	12:108407160	TTTTATACTTCTTGG[C/T]TGAGATGTGTTATCT	68519
rs29147133	snp	C/G	0.401235	0.199068	intron-variant	Eml1	Mm_Celera	12:108376546	CTCTCCTCCACTTCT[C/G]TATTCTCTCATTCAT	68519
rs29147196	snp	A/G	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108472225	AGTAGTATGGGGTAA[A/G]TATTTTTGCTTACCG	68519
rs29147218	snp	C/G/T	0.444444	0.157135	utr-variant-3-prime, nc-transcript-variant, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539255	CGAGAAGGCCTTACC[C/G/T]GTGGTGTGACAGATT	68519
rs29149162	snp	G/T	0.5	0	missense	Eml1	GRCm38.p3	12:108471939	AGTGCCTCCCTCCCG[G/T]CACCCTCCGGGGCCA	68519
rs29149683	snp	C/T	0.375	0.216506	upstream-variant-2KB	Eml1	Mm_Celera	12:108369232	AGGGTTGGTAGAGTT[C/T]AGGAGCAGGAGCAGT	68519
rs29149706	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108515784	CACTTTGTAGACCAG[A/G]CAGGCCTCGAACTCA	68519
rs29149916	snp	A/C			intron-variant	Eml1	GRCm38.p3	12:108500863	TCTGCAAGAAACTGG[A/C]CCAACAGAGTGGGCT	68519
rs29150047	snp	C/T	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108530298	TTTCTCTCATGTTTA[C/T]GACAGGTGGTTTGTG	68519
rs29150415	snp	C/T	0.465374	0.126941	intron-variant	Eml1	GRCm38.p3	12:108375253	AGGTCAGAGAGAGCC[C/T]GAGTCTAGGGGTGCA	68519
rs29150809	snp	A/G	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108461305	ATTAAAAGTAGAACA[A/G]AGTTTTAAAACAGTT	68519
rs29151566	snp	A/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108433095	GCCGGCACGTCTTAC[A/T]GTGAGACGCGAGATC	68519
rs29151609	snp	G/T	0.444444	0.157135	intron-variant	Eml1, Gm33385	Mm_Celera	12:108406958	ATGTGTTTGTTTAAT[G/T]TAATGCTTCAACTTT	68519
rs29153393	snp	C/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108459350	CCTCATGATTTGGGA[C/T]GAGTGCTTGTCATTT	68519
rs29153465	snp	C/G	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108525977	TGTCAGCGCTCCTGA[C/G]AGCAGGGTCTTAATG	68519
rs29154128	snp	C/G	0.459184	0.136902	intron-variant	Eml1	Mm_Celera	12:108394856	GCCCAGCACACACAT[C/G]GCCACAAAACCACAC	68519
rs29155418	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108399483	GAGGCAGCCTGGAGC[A/G]GGGCAAGGAGCCCTG	68519
rs29155431	snp	C/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108509755	TACAGAGAAACCCTG[C/T]CTCGAAAAATGAAAA	68519
rs29156751	snp	C/T	0.297521	0.245442	intron-variant	Eml1	Mm_Celera	12:108446764	TGCAGAGCTGGGATC[C/T]AAGTGTCTCTGAGAC	68519
rs29157633	snp	A/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108508562	AAAAAGTCTTCATTT[A/T]AAAAAAAATGTTCAT	68519
rs29158060	snp	A/G	0.444444	0.157135	intron-variant	Eml1, Gm33385	Mm_Celera	12:108403696	CAAGGAACTCAATTG[A/G]TAACTTTAAAAAAAA	68519
rs29158579	snp	A/G	0.359862	0.224567	intron-variant	Eml1	Mm_Celera	12:108398993	GTTCAGATGCTAAGC[A/G]TATGGCTTCCTGGAT	68519
rs29158889	snp	A/C	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108371436	GCACCCGGCCCCCCA[A/C]GGGCTGCAGGCAGCA	68519
rs29159829	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108525986	TCCTGAGAGCAGGGT[C/T]TTAATGGACCAAAGT	68519
rs29160143	snp	G/T	0.375	0.216506	intron-variant	Eml1, Gm33385	Mm_Celera	12:108407486	ATAGAGAGAGTCAGA[G/T]AGATACAGAAAGACA	68519
rs29160268	snp	A/G	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108508570	TTCATTTTAAAAAAA[A/G]TGTTCATACCAGACC	68519
rs29160410	snp	A/G	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108372607	ATTTCAGGAAGGCTA[A/G]GACAATATTTAGGCT	68519
rs29163075	snp	G/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108433109	CTGTGAGACGCGAGA[G/T]CCTGTACACATTTAG	68519
rs29163174	snp	A/C	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108391353	AGACAGCCTCTACAC[A/C]CATCTGTGAAGGATC	68519
rs29163266	snp	C/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108461249	TCTCCTCCAGGGGAT[C/G]CAACACCCTTTGCTG	68519
rs29163972	snp	A/G	0.492188	0.0620098	intron-variant	Eml1	GRCm38.p3	12:108374894	GACCTCGGAGGACAA[A/G]CCTGACAGCTGTCTC	68519
rs29164444	snp	C/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108382254	CTCAGTAGGGATGAG[C/T]GCTTGGTCTTCAAGT	68519
rs29164930	snp	A/G	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108527951	ACTGAGTCCTTCCCA[A/G]TTGAAACCTGGAGGA	68519
rs29164966	snp	C/T	0.456747	0.140554	intron-variant	Eml1	Mm_Celera	12:108391168	TGCAAGCAGAGTCTC[C/T]AAGAGGGAATTCCCC	68519
rs29165012	snp	A/C	0.375	0.216506	upstream-variant-2KB	Eml1	GRCm38.p3	12:108370568	GTAGCGGTGTGTTCT[A/C]TCAATCACACGTTTC	68519
rs29165098	snp	C/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108429117	TTGCATTTCTATTTA[C/T]GTGGTGTGTGTGTGT	68519
rs29166521	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108375702	GGAGGAGATGCCCAA[A/G]TACTCTGCTATTCTG	68519
rs29167289	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108435068	AACTTATGTGAAGGT[A/G]TTTATGGTGGTATGT	68519
rs29167574	snp	A/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108532021	GGGAGAAGAGAAGGG[A/T]GAGAGTCTGGAACTC	68519
rs29167938	snp	C/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108528031	CCCATCTGCTTCCAG[C/T]TCCAGAGGCTCTAGA	68519
rs29169190	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108440982	ACTGTCTTTTGGATC[A/G]GGTTCACCATCTCCT	68519
rs29169929	snp	C/G/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108508697	GCCTCAAGCACAGCC[C/G/T]GAGAGCATTTGCCTA	68519
rs29170886	snp	C/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108532708	AGAAAAATCCTGTCT[C/T]AAAAATAAAATAAAA	68519
rs29171154	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108526894	GCACTGAGGGTAGGC[A/G]CTCCTACAGCAGAGG	68519
rs29171795	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108514545	TTTCAGTTTTCCTGC[A/G]TGGCACCTGGGAGGG	68519
rs29171995	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108472057	CTCTTTGGGGGTCTA[A/G]AAGGAGCACCCCTTT	68519
rs29172194	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108391216	GCGTCTGAGCCTGGC[C/T]AACTCCTCTTATGCT	68519
rs29173425	snp	A/G	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108531007	TTTTTTTTAGTGTTC[A/G]TGTGTGCACCGTGGT	68519
rs29174375	snp	C/T	0.260355	0.249785	intron-variant	Eml1	Mm_Celera	12:108447277	TTCTGGTTTCTTTTC[C/T]GCCATCTTTGTTAAA	68519
rs29174695	snp	A/G/T	0.473373	0.11227	intron-variant	Eml1	GRCm38.p3	12:108385963	CCCTCTGGACTGTTC[A/G/T]CCTGTGCAATGTTGG	68519
rs29175622	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108509677	CGGGAGGCAGAGGCA[A/G]GCAGATTTCTGAGTT	68519
rs29175805	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108470826	GAATGCTCTGAGAGG[A/G]TAGAGCTGAGAGAAG	68519
rs29175927	snp	C/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108432609	AGGGAGCTGGAACAG[C/T]ACCTGGGCTTGCGGC	68519
rs29176887	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108374966	AGAGGACCCAGGAGT[A/G]ACTCTGGGACATAGA	68519
rs29178084	snp	A/T	0.484429	0.0868505	intron-variant, utr-variant-3-prime	Eml1, Gm33385	GRCm38.p3	12:108400807	AAACACAAACACTTA[A/T]TTGTTTAAGAAAAAA	68519
rs29178357	snp	A/G	0.465374	0.126941	upstream-variant-2KB, intron-variant	Eml1	Mm_Celera	12:108422185	CCCCGGAGAGGTCTG[A/G]AAGTTTTCTTGATAA	68519
rs29179200	snp	C/T	0.465374	0.126941	intron-variant	Eml1	Mm_Celera	12:108415130	GCCCACTGTGGTGAG[C/T]GAGGCTCTGATGTTA	68519
rs29179751	snp	A/G	0.375	0.216506	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108407484	AGATAGAGAGAGTCA[A/G]AGAGATACAGAAAGA	68519
rs29180420	snp	A/G	0.375	0.216506	utr-variant-3-prime, intron-variant	Eml1, Gm16596	Mm_Celera	12:108538895	CACAAACTGCACCCC[A/G]TCTCTGTCCATGCAC	68519
rs29180454	snp	A/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108395884	TGAGACTGAACAGTT[A/T]GTCTGTCTCCAGGCT	68519
rs29180482	snp	G/T	0.5	0	intron-variant	Eml1	Mm_Celera	12:108465678	TGACTTTTTCACGGT[G/T]ACCTAACACCTCGCT	68519
rs29180727	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108472246	TTGCTTACCGTTCTT[C/T]ATAAAAACAACTAGG	68519
rs29181144	snp	C/T	0.495868	0.0452663	intron-variant	Eml1	Mm_Celera	12:108530225	GGTTTAAATGCCCCG[C/T]GGCAAACAGACTTCT	68519
rs29181553	snp	A/G	0.188366	0.242283	intron-variant	Eml1	Mm_Celera	12:108420381	TGTGCTACAGAGGTC[A/G]GAGGACAACCTGGAG	68519
rs29181836	snp	C/T	0.415225	0.187619	intron-variant	Eml1	Mm_Celera	12:108508519	GCAGACAGTAAAAGC[C/T]GTTTGGCTCAATAGC	68519
rs29182361	snp	A/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108459572	AAGGGTGAGTACTTT[A/T]ACACGGAGACAGGCC	68519
rs29182428	snp	A/G	0.197531	0.244432	intron-variant	Eml1	Mm_Celera	12:108375779	GGAAAGGGCCATTTT[A/G]GCTTCACCGTAGGGC	68519
rs29183088	snp	A/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108530589	GTCCTCTCTCTGTTT[A/T]TCCAGACAGGGTTTC	68519
rs29183592	snp	C/T	0.465374	0.126941	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108403461	TGTAGCAAGTGTTGC[C/T]ATGAGCCAAGACTCA	68519
rs29184970	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108501103	CCAGGGAGCTCACTT[C/T]CCCACTACAGCTCTT	68519
rs29186147	snp	C/T	0.32	0.24	intron-variant	Eml1	GRCm38.p3	12:108530713	GGGATTATAGGCGTG[C/T]AGCCTTACACTCCAC	68519
rs29186284	snp	G/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108501025	CAGTCCTGGGACGAA[G/T]TCTCTGGGACTGTGC	68519
rs29186333	snp	C/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108372069	GGTTTGCGAAAATTA[C/T]GATAATGTACAGAAG	68519
rs29187708	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108375703	GAGGAGATGCCCAAA[C/T]ACTCTGCTATTCTGC	68519
rs29187810	snp	G/T	0.375	0.216506	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108402017	GTTCTGTGGCGTGTT[G/T]TGTGTGTGTGTGTGT	68519
rs29187860	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108437424	ACAAGATCTCACCCA[A/G]GGAACTGGGAGGTTG	68519
rs29188013	snp	C/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108399198	CTGTCCTGAGCGTCC[C/T]GAGTGTCCTTTTCTC	68519
rs29188175	snp	C/T	0.345679	0.230967	intron-variant	Eml1	Mm_Celera	12:108511625	TTGAGAGCCTTCTCC[C/T]GACATCTCCATGGTT	68519
rs29189958	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	Eml1	Mm_Celera	12:108422566	AGAGGAAGGGGAATG[A/G]GATAATCTCTTTCTG	68519
rs29190429	snp	C/T	0.375	0.216506	intron-variant, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108536535	GCTGCCACGGAGGTG[C/T]CGGGACTCGAACCTT	68519
rs29190587	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108472402	CACCTGTGTTATCGT[C/T]AGAGAGATCACAGTT	68519
rs29191387	snp	C/T	0.197531	0.244432	intron-variant	Eml1	Mm_Celera	12:108399056	CTACACGAGAGCTGC[C/T]AGCCGAGAGCCCAGT	68519
rs29192273	snp	C/T	0.197531	0.244432	synonymous-codon, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108537371	TGGGACAGACATCAA[C/T]GCCGTCTGCCGGGCT	68519
rs29192310	snp	A/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108530881	TAGTTCAGAGGTTCC[A/T]GGGACTAGGGAGACG	68519
rs29193513	snp	A/T	0.197531	0.244432	intron-variant	Eml1	Mm_Celera	12:108466410	TTTGGGGTGCTTCCT[A/T]TATCTGAGAAGTTAT	68519
rs29193576	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108501070	CCCGTCACAGTTGAG[C/T]AGGACGGTGGGCGGT	68519
rs29193835	snp	A/G	0.197531	0.244432	intron-variant	Eml1	Mm_Celera	12:108395960	ATTGCTTTGGGAGAA[A/G]AGACTCAGCATCCCC	68519
rs29194020	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108505413	GCGTATCTTTAAGTT[C/T]GAGGCCAGCCTGGTC	68519
rs29194437	snp	A/G	0.375	0.216506	intron-variant, synonymous-codon	Eml1, Gm33385	Mm_Celera	12:108401431	CAGGGAAGGCTTCCT[A/G]AAGGGGACACTGGAT	68519
rs29195219	snp	C/T	0.5	0	intron-variant	Eml1	Mm_Celera	12:108434793	ACCTCATATCATACA[C/T]ACTTATATACATGCA	68519
rs29195618	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108437817	TTGCTTTCCTGTTCT[C/T]AAATGCGTGCTGATT	68519
rs29195627	snp	C/G	0.32	0.24	intron-variant	Eml1	GRCm38.p3	12:108385917	AGCCTCTGGCAGCTT[C/G]AGTCGGGCTTCCTGT	68519
rs29196246	snp	A/G	0.375	0.216506	intron-variant, downstream-variant-500B	Eml1, Gm33385	Mm_Celera	12:108400282	CTCAATAGGAATAGA[A/G]CAGGTGGGCTGTCAC	68519
rs29196423	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108517163	GGAGGATTTCCAACA[C/T]GTAGGATTTCTCCAG	68519
rs29196565	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108391702	TGATAGCCCATCACT[C/T]CCTCTGGGGCTGCTG	68519
rs29196731	snp	C/T	0.498615	0.0262793	intron-variant	Eml1	GRCm38.p3	12:108375105	ACTCATGAGCTGGGC[C/T]CACAACAGCAAGAGG	68519
rs29198322	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108530537	TCACTGTGCAGCTGT[A/G]GTTTAACTTTGTATA	68519
rs29198630	snp	C/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108513752	CCTGGCCTGACATTC[C/T]GTCTTCTAACATTGC	68519
rs29199668	snp	A/G	0.359862	0.224567	intron-variant	Eml1	Mm_Celera	12:108399047	TTAGGAGGACTACAC[A/G]AGAGCTGCCAGCCGA	68519
rs29200054	snp	A/G	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108420623	GGCCTTGAACTCAGA[A/G]ACTCAATGGCCTCTG	68519
rs29200447	snp	A/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108397363	CAAAGGGCTCCTTCC[A/T]TCTTCCTTCCTTCAC	68519
rs29200649	snp	A/G	0.345679	0.230967	intron-variant	Eml1	Mm_Celera	12:108441149	TGTCCTTCTGCAGGC[A/G]CTTGGTTTGCTCTTC	68519
rs29201650	snp	C/T	0.375	0.216506	upstream-variant-2KB	Eml1	Mm_Celera	12:108369182	CACAACAGGGCTAAG[C/T]GCAGGAAGGACCAGG	68519
rs29202262	snp	G/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108437822	TTCCTGTTCTCAAAT[G/T]CGTGCTGATTCCTCA	68519
rs29203398	snp	C/T	0.415225	0.187619	intron-variant	Eml1	Mm_Celera	12:108515442	TACCCTTGTGAAAGG[C/T]TTTTTAAGGTTAGGA	68519
rs29204736	snp	C/T	0.188366	0.242283	intron-variant	Eml1	Mm_Celera	12:108417373	CTAACATGGTATGGC[C/T]GGGTATCGTAGATGC	68519
rs29206702	snp	A/G	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108525132	AATGTACACAGATAT[A/G]TAATGCGTTTTAAAT	68519
rs29209150	snp	A/C	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108372771	ACAAGAGACCCTGCG[A/C]AAGCTCTTGGAATCG	68519
rs29209423	snp	A/G	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108525983	CGCTCCTGAGAGCAG[A/G]GTCTTAATGGACCAA	68519
rs29210153	snp	A/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108397370	CTCCTTCCTTCTTCC[A/T]TCCTTCACTGCCACA	68519
rs29211974	snp	G/T	0.444444	0.157135	upstream-variant-2KB, intron-variant	Eml1	GRCm38.p3	12:108421817	CCCTCCAGGCTTCTT[G/T]TCTAGACCCTTTCCC	68519
rs29212054	snp	C/T	0.197531	0.244432	intron-variant	Eml1	Mm_Celera	12:108395678	GGGTCCTACTTACTA[C/T]GAGATTCATATGTTT	68519
rs29212392	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108372234	GCTCTGGCCCATAGA[A/G]TCTTTATCCTAAAAC	68519
rs29212780	snp	G/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108445567	AATTACCAGCCCTGT[G/T]GATTCTGTGTTTCTC	68519
rs29213451	snp	A/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108511985	ACATTTCTAGCCACC[A/T]GGCTTCCAGCCTTTC	68519
rs29213527	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108453898	CCCATATGCTAATAC[A/G]TGGGCTTTGTAATGC	68519
rs29213644	snp	A/G	0.188366	0.242283	intron-variant	Eml1	Mm_Celera	12:108397664	TAAGAGAACTTGAAA[A/G]CAACCTGGCCATCTT	68519
rs29213991	snp	C/T	0.415225	0.187619	intron-variant	Eml1	GRCm38.p3	12:108399391	ACGGTCTGGAGGATG[C/T]TTCCAGGCAGAGTTT	68519
rs29214190	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108419551	AAAAATCTCTACTTT[C/T]AATTCTTCTAACCAT	68519
rs29214810	snp	A/G	0.359862	0.224567	intron-variant	Eml1	Mm_Celera	12:108531093	TAGGATCTTTCTCAT[A/G]TGATGTTAGATCATC	68519
rs29214883	snp	C/T	0.188366	0.242283	intron-variant	Eml1	Mm_Celera	12:108375124	AACAGCAAGAGGAGG[C/T]GTCATGTCCAAGTTG	68519
rs29215119	snp	C/T	0.345679	0.230967	intron-variant	Eml1	Mm_Celera	12:108512128	TAATCCTAAAACAGC[C/T]GTGGGCCTGGCCAGG	68519
rs29215327	snp	C/T	0.444444	0.157135	intron-variant	Eml1, Gm33385	Mm_Celera	12:108404709	GAACACACACATGCA[C/T]GTGCAAATATACACA	68519
rs29218676	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108394855	GGCCCAGCACACACA[C/T]GGCCACAAAACCACA	68519
rs29218782	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108518255	ATACGTGAGCACATA[C/T]ATACATGCAGACAAA	68519
rs29219501	snp	A/G	0.465374	0.126941	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108401788	TTCCCAGAAAGGTAG[A/G]ATTCCTGAGGGCAGA	68519
rs29220801	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108501844	ACATATATATATATA[C/T]ATATATATATATATA	68519
rs29221350	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108534323	CCCTCTTCTGGCCAC[C/T]TCAGCCACTGTATGT	68519
rs29483712	snp	A/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108530552	AGTTTAACTTTGTAT[A/T]ACAAATCCCCCGCCC	68519
rs29484316	snp	A/G	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108532581	ATAACTGGGCTAGGC[A/G]TTGGTGGCGCACGCC	68519
rs29485390	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108504628	TGTCTGGGTTAGATA[C/T]CATCGATTCTGGATT	68519
rs29485572	snp	A/G	0.375	0.216506	upstream-variant-2KB	Eml1	Mm_Celera	12:108369848	CTGCTGGGGACTGCC[A/G]CTTCTTCCTTTGTAC	68519
rs29486546	snp	A/G	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108395371	CAAGCACAAGGGAGG[A/G]CCCATGCTAGGATCC	68519
rs29488305	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108459342	TGTCAAAACCTCATG[A/G]TTTGGGATGAGTGCT	68519
rs29488817	snp	C/T	0.498615	0.0262793	intron-variant	Eml1	GRCm38.p3	12:108375444	CTCGAGTTATCTCTA[C/T]GTACCTTGACCCTGC	68519
rs29489201	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108373287	CTCTGTTCTTCTTAA[C/T]GCAGTAAGAGTAAAA	68519
rs29489652	snp	A/G	0.484429	0.0868505	intron-variant	Eml1	GRCm38.p3	12:108509815	CTGGCATGCCTATGG[A/G]TCATAGTATAGCTTA	68519
rs29490177	snp	A/G	0.18	0.24	upstream-variant-2KB, intron-variant	Eml1	Mm_Celera	12:108421502	GGTCTCCCAGTTCTT[A/G]TCACTACAACTGCCA	68519
rs29490225	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108391658	CTCTGCTTTTCCTTT[C/T]CTGATGGGGACGGTC	68519
rs29491188	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108461390	GTTAATGATATTGAT[A/G]ATCAAGCTTAGTTAT	68519
rs29492311	snp	A/G	0.444444	0.157135	upstream-variant-2KB	Eml1	GRCm38.p3	12:108369498	AGTTTTTCCTGGCCC[A/G]TGGGCCAGTGCTGGG	68519
rs30526340	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108479881	TCTGTTCCTCTGTTC[A/G]TTTTGCTAGAGGTGT	68519
rs30534903	snp	A/C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108485972	ATAGTTCTGTCCACA[A/C/T]CACAGGGTGAGTCGC	68519
rs30566564	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108485184	GAAAAGATGGGTAAT[C/T]GACAGGAGCCCAGCG	68519
rs30570992	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108477640	GGTTTCATAGTGTGC[A/G]TGTCTTTTGCCTTCT	68519
rs30579087	snp	A/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108491894	ACTAATCCACTAAGA[A/T]TTTTTTTTTAACTTT	68519
rs30582099	snp	A/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108497013	GAGTTCTGAGTTTAG[A/T]TTCCCAAAACTCATA	68519
rs30588496	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108482392	AAACCTGCCCTGATG[C/T]ACACGCACCACACAG	68519
rs30622905	snp	C/G	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108490372	GGTGGATACTCTGGG[C/G]CACCTATTGGGATAG	68519
rs30626596	snp	C/T	0.5	0	intron-variant	Eml1	Mm_Celera	12:108486224	CAAGGTTGACCTTGG[C/T]TAAGGTTAAGGATTA	68519
rs30643028	snp	C/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108493117	TCTCTTCTCGGGGAC[C/T]GCCCAAGTTTTGTTT	68519
rs30666200	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108495957	TAAGCCAGGGTGGGG[C/T]AGGAGTGTGGACTGT	68519
rs30668263	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108476308	TTTGCTTGATCGTTT[A/G]CTTTGACACTAACAG	68519
rs30674790	snp	C/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108483174	AAGCCGCTTTCTCTT[C/T]AGACTTAGAAGTTTG	68519
rs30725480	snp	A/G/T	0.625	0.125	intron-variant	Eml1	GRCm38.p3	12:108484289	GGTAGAGAGGGCGTG[A/G/T]ACTGGAGCCACTAAC	68519
rs30730784	snp	C/T	0.32	0.24	intron-variant	Eml1	GRCm38.p3	12:108482796	TATAAGGACAAAGAG[C/T]CCCCTTGGGCCCCAG	68519
rs30779028	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108486514	TCATTCATATGGGCT[C/T]TCCCTACACTCTTGT	68519
rs30781721	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108485979	TGTCCACAACACAGG[A/G]TGAGTCGCACACTTG	68519
rs30816104	snp	A/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108492492	TCCCAGCAGAAAAAA[A/T]TTTTTTTTTCTTCTC	68519
rs30857831	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108492682	ACAATCCTGCCTCAG[C/T]GTTCCAAGTGCTGAG	68519
rs30862461	snp	C/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108477700	CTGACGTTGTAATAA[C/G]TAGAAGTGGTCTCTC	68519
rs30877484	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108482015	AACCATGCCGTTCCC[A/G]TAGCTCAAGAAGTCA	68519
rs30914816	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108492733	TATTCTATGCCAACA[A/G]GGGTTTTCTCAACCA	68519
rs30924645	snp	A/G	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108476221	ATTCACCGCTTATTA[A/G]ATGTGTGACTTGCAG	68519
rs30932032	snp	A/C/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108496727	CCAGCTCCCTGTGGG[A/C/T]GGGGCCACCTCTGGA	68519
rs30950316	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108494890	TGTGTGTGTGCGTGC[A/G]CACGCGCACGCTCAC	68519
rs30967665	snp	A/G	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108484515	TTGACTTTGGTTAGC[A/G]TTTGCCATAGCGGGA	68519
rs31021884	snp	G/T	0.5	0	intron-variant	Eml1	Mm_Celera	12:108487926	CCAGAGATGCCTCCA[G/T]ACATTGCTAAGTGTC	68519
rs33844105	snp	C/T	0.18	0.24	upstream-variant-2KB, intron-variant	Eml1	Mm_Celera	12:108421697	TAACAAGTGCTGACT[C/T]TGGCTGTCCAGGTCA	68519
rs33844463	snp	C/G	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108520374	ACACAGACACACACA[C/G]ACACACACACACACA	68519
rs33846152	snp	C/T	0.277778	0.248452	intron-variant	Eml1	Mm_Celera	12:108437194	GCCAGGTGGCTCTAG[C/T]GCTCAAATGAGGAGA	68519
rs33846682	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108531211	CAGGGACGGTCAGGC[C/T]GACTCTCTTGTTTTG	68519
rs33846748	snp	C/G	0.486111	0.0821678	intron-variant	Eml1	GRCm38.p3	12:108504126	GGTGGATATAGAAGA[C/G]GAGGTCAGCTAAAAG	68519
rs33846970	snp	C/T	0.35503	0.226867	intron-variant	Eml1	GRCm38.p3	12:108503396	ACGGGCTTCGACATG[C/T]GGCTGTGATTTGGAT	68519
rs33847754	snp	A/G	0.345679	0.230967	intron-variant	Eml1	Mm_Celera	12:108438298	AGTGCAGGCTAAGCC[A/G]TGTTCTCAGCACACA	68519
rs33864364	snp	G/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108483956	AAATGTCTATACACA[G/T]AAAATTAAAATAAAT	68519
rs33865890	snp	A/T	0.5	0	intron-variant	Eml1	Mm_Celera	12:108487927	CAGAGATGCCTCCAG[A/T]CATTGCTAAGTGTCC	68519
rs33866985	snp	G/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108482584	GGTTGTGAGCCACCA[G/T]GTGGTTGCTGAAATT	68519
rs36241330	snp	A/G	0.473373	0.11227	intron-variant	Eml1	GRCm38.p3	12:108432214	GACAATCCAGACCTG[A/G]GAAAGCCGCAGGAAG	68519
rs36247860	snp	C/T	0.46281	0.131194	intron-variant	Eml1	GRCm38.p3	12:108458126	TCTGCCAAAGCTCCT[C/T]GTGCAGGTATTGACA	68519
rs36254681	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108490256	GCCACTGTGAGTGTT[C/T]GCTTGGAGCCAAACC	68519
rs36256452	snp	C/G	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108457890	TATGGATACCTGTTG[C/G]TCAGTCTCTCTGTGA	68519
rs36258128	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	Mm_Celera	12:108498561	AGACCCACAAGTTCT[C/T]TCATCAAGACTTGGA	68519
rs36258172	snp	A/T	0.42	0.183303	intron-variant	Eml1	GRCm38.p3	12:108531855	AGGAGCGTTGGTATG[A/T]AGTGTCAGTTACTAT	68519
rs36261648	snp	A/C/T	0.396694	0.202437	intron-variant	Eml1	GRCm38.p3	12:108504428	CTATAAAGTCAAGCT[A/C/T]CGTTAAACCCAGAGT	68519
rs36265225	snp	A/G	0.197531	0.244432	intron-variant	Eml1	GRCm38.p3	12:108451848	ATAATGGTAGATGTG[A/G]TACTGTTTTTATGAG	68519
rs36271432	snp	C/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108440294	CCAGGGTTTTTTCTA[C/T]ATTGCTTATCAGCAC	68519
rs36287261	snp	A/G	0.48	0.0979796	downstream-variant-500B, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539916	AGTGGCTCATTTGGC[A/G]TCATCAGAACTGAAT	68519
rs36291892	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108494920	CCTGCATGGACATGT[A/G]TGCGAGCCAAAGGTT	68519
rs36292220	snp	A/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108464428	GAGGGCAGTGGCTCA[A/T]CTTTCGCCAGAGTTG	68519
rs36296247	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108504537	AGCTGCTGAAGCACG[A/G]TGATTCTCCCAATTT	68519
rs36298799	snp	A/G	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108430254	GACTGGGGAGTCTTC[A/G]CTTCAGTCAGCACAA	68519
rs36302006	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108428742	GGCCTTCTTTTCTTG[C/T]TAATGACCAGGGCCA	68519
rs36303997	snp	A/C/T	0.493827	0.0552116	intron-variant	Eml1	GRCm38.p3	12:108458508	TCTTGTGTCCCTTTT[A/C/T]CTGTTAGGTCTCAGA	68519
rs36315819	snp	C/G	0.132653	0.220748	intron-variant, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108536752	CCTACCGCCTAAAAC[C/G]TTCACTTCTTTCAAA	68519
rs36316246	snp	C/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108534451	GATTTTATAAACTTT[C/T]ACCAGCCTCTATAAT	68519
rs36316409	snp	G/T	0.18	0.24	intron-variant	Eml1	Mm_Celera	12:108429948	ACGGCTCCAAGCCTC[G/T]CGCGTTCTGAAGGCG	68519
rs36318575	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108465228	TCACTGGAGTCAGGA[A/G]AGGGCTGTCTAACAT	68519
rs36319521	snp	C/T	0.497041	0.0383476	synonymous-codon	Eml1	GRCm38.p3	12:108515139	GAAGCCAAAGTTTGT[C/T]CTCTGCGTGACGTTT	68519
rs36321435	snp	A/G	0.32	0.24	intron-variant	Eml1	GRCm38.p3	12:108514326	GAACAGTTTTGTTAA[A/G]CATCCTAAGAGGCCT	68519
rs36322921	snp	A/G	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108492035	CAACCTTAGAATTAA[A/G]ATACTATGTGTCCAT	68519
rs36327435	snp	A/C	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108456086	CAGGACAGCCTTGGG[A/C]GGAGCCAGCAGGGTA	68519
rs36341088	snp	A/C	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108509384	TGTTGTCTTTGGGCT[A/C]CCTAATTCTGCTCTC	68519
rs36342603	snp	C/T	0.132653	0.220748	intron-variant	Eml1	Mm_Celera	12:108492464	TACACCTCTTCAGCC[C/T]GCCTCTTCTATTTCC	68519
rs36344065	snp	G/T	0.244898	0.249948	intron-variant	Eml1	Mm_Celera	12:108431490	GTGAGAGGTCCTGTC[G/T]CAAAAAGAAAGTGGG	68519
rs36348455	snp	C/G	0.124444	0.216185	synonymous-codon	Eml1	Mm_Celera	12:108463657	CGTGGTTCGGAGGCT[C/G]AACATCACGGAGGAG	68519
rs36350674	snp	A/C	0.486111	0.0821678	intron-variant	Eml1	GRCm38.p3	12:108509901	TTCCTAATTAACACA[A/C]CCAAAAATGACTTGT	68519
rs36351807	snp	A/G	0.35503	0.226867	intron-variant	Eml1	Mm_Celera	12:108429862	GAAAAGAGAAATAAC[A/G]CCTGCTGTAGGAGTT	68519
rs36353564	snp	A/G	0.142012	0.225474	intron-variant	Eml1	Mm_Celera	12:108533677	GGCTGAGGGCTGTGT[A/G]CAGGAGTCTGCACAT	68519
rs36361089	snp	A/G	0.486111	0.0821678	intron-variant	Eml1	GRCm38.p3	12:108531301	GTCTGGCTTGGTCTC[A/G]GCATAAGAAGTGTTG	68519
rs36361605	snp	C/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108428546	AACCCAATATAACCT[C/G]TACCGCACTCACTGC	68519
rs36368784	snp	C/T	0.46281	0.131194	intron-variant	Eml1	GRCm38.p3	12:108457377	AGCTGGCCATGAACT[C/T]AAGTCAATTTGGAGT	68519
rs36377622	snp	C/T	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108463868	GTGGGTCTTTGTAGA[C/T]GCTCCCTAAATGCTC	68519
rs36385584	snp	C/T	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108510652	CATACATGATCAACA[C/T]GAAAATATACCAATC	68519
rs36392052	snp	C/T	0.345679	0.230967	intron-variant	Eml1	Mm_Celera	12:108435903	CTATTAACCTTCCGA[C/T]TTTCCTTAGCCTAGA	68519
rs36396421	snp	A/G	0.459184	0.136902	intron-variant	Eml1	GRCm38.p3	12:108432236	CGCAGGAAGCTCAGA[A/G]TGAAGAGTAGAGATA	68519
rs36400585	snp	C/T	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108492897	CCCAAGCCTCCATCC[C/T]GGCTCTGCCACTTTG	68519
rs36402946	snp	C/T	0.396694	0.202437	intron-variant	Eml1	GRCm38.p3	12:108529064	TAAGTGGAAGGACAG[C/T]GGAGCAGCTCCCTGG	68519
rs36411102	snp	A/G	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108439946	GCAGCGGTTCAGCGT[A/G]TAACATTTTCTGGTG	68519
rs36411863	snp	C/T	0.493827	0.0552116	intron-variant	Eml1	Mm_Celera	12:108458502	AGAATGTCTTGTGTC[C/T]CTTTTCCTGTTAGGT	68519
rs36414820	snp	C/T	0.46281	0.131194	intron-variant	Eml1	GRCm38.p3	12:108456147	CACTGTTCCAGGATT[C/T]GTGCCCTGGTTGTTC	68519
rs36416753	snp	C/T	0.197531	0.244432	intron-variant	Eml1	Mm_Celera	12:108531918	GAGTGTGATGAGGCG[C/T]GTGCCTCCTGTGTTC	68519
rs36416927	snp	A/G	0.486111	0.0821678	intron-variant	Eml1	GRCm38.p3	12:108453702	GTCCAACACTGCATG[A/G]CTCATTCAGGGTGAC	68519
rs36417769	snp	C/T	0.5	0	intron-variant, nc-transcript-variant	Eml1, Gm16596	GRCm38.p3	12:108536940	GCCTCTAATATACAA[C/T]GCTCTCAACCAAAAG	68519
rs36419772	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108427760	AGGGCAAAGTGGGGC[A/G]TGCTTTTAATCCCAG	68519
rs36420730	snp	A/G	0.473373	0.11227	intron-variant	Eml1	GRCm38.p3	12:108427962	CCTTCTTTTTGCGTT[A/G]CTTTTTAACTCGATA	68519
rs36421338	snp	G/T	0.48	0.0979796	intron-variant	Eml1	Mm_Celera	12:108442407	CACCAGTCTTTCTGC[G/T]CTCACAGAACGGCAC	68519
rs36421978	snp	A/G	0.46281	0.131194	intron-variant	Eml1	GRCm38.p3	12:108504192	TCAGTAAGCAAGTAG[A/G]CAAAGGCAGGATGGA	68519
rs36422530	snp	A/G	0.486111	0.0821678	intron-variant	Eml1	GRCm38.p3	12:108530248	AGACTTCTGCTGTTG[A/G]AACAGCCTTGCATCT	68519
rs36432852	snp	A/G	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108518356	ACTTCTTACATTATG[A/G]TACATGGGGCAGGCC	68519
rs36434519	snp	G/T	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108465747	AAAGACACTGAGAAA[G/T]GAAAGGAAATCAGGA	68519
rs36439192	snp	A/G	0.142012	0.225474	intron-variant	Eml1	Mm_Celera	12:108534191	TTTATAAAGTTATCA[A/G]TTTAGGGCCCAATGG	68519
rs36444370	snp	A/G	0.495868	0.0452663	intron-variant	Eml1	GRCm38.p3	12:108455744	TGAACCTTTATGACG[A/G]ACAAAATTTGATCAA	68519
rs36445174	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108491455	GTTTGTCATGTTCCC[C/T]GAGTGTCCTCACTTC	68519
rs36448247	snp	A/C	0.497778	0.0332592	intron-variant	Eml1	Mm_Celera	12:108464080	GCATGGCGGCCCCTC[A/C]CTCCGTCTGGGTGTA	68519
rs36456207	snp	C/G	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108428366	ACCAATCCAGTCTGA[C/G]ATGATATCAACTCCT	68519
rs36457615	snp	A/G	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108531203	AGTGTGAACAGGGAC[A/G]GTCAGGCCGACTCTC	68519
rs36463201	snp	A/G	0.46281	0.131194	intron-variant	Eml1	GRCm38.p3	12:108463374	GGGAGGAAGAAAGAA[A/G]CGTCCACAAAGTGAA	68519
rs36472831	snp	C/T	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108431344	ATTCAAACAAGAGGA[C/T]GAGGATTTGGATCCT	68519
rs36472832	snp	C/T	0.277778	0.248452	intron-variant	Eml1	GRCm38.p3	12:108440701	GGACTCAAAGCTAGG[C/T]TGGAAATAGTCAAGT	68519
rs36473548	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108505833	GGATGCTCTGAACTT[A/G]AGTGAGAAGCTCAAA	68519
rs36480597	snp	C/T	0.336735	0.234472	intron-variant	Eml1	Mm_Celera	12:108490427	GGGCACTGCTTGGCC[C/T]AGATCGCCACATCGT	68519
rs36481950	snp	C/T	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108491957	TTCTAAGTTTATGAG[C/T]ACAGTTGACATTAGA	68519
rs36482874	snp	A/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108501162	TCTGTTGTGTGTCTA[A/T]ACTTCATTTTTATTC	68519
rs36493399	snp	G/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108436344	CACAAGCACGTGAAC[G/T]AGACCACACGCACTA	68519
rs36497628	snp	C/T	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108510358	ACAGCATTTGAGAAC[C/T]ATTGGGTCCTCACCA	68519
rs36500914	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108531155	CTAGAGGCCTTTATA[C/T]CTCTTTCACTGCATA	68519
rs36502582	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108463199	CAGAGGGTTCTGCAA[C/T]GTTGAGGACTTGATG	68519
rs36504837	snp	A/T	0.493827	0.0552116	intron-variant	Eml1	GRCm38.p3	12:108457358	CATGAGCAGAAGAGG[A/T]TGTAGCTGGCCATGA	68519
rs36505698	snp	C/T	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108492451	TTGGCCCTGACAGTA[C/T]ACCTCTTCAGCCCGC	68519
rs36511197	snp	G/T	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108428111	AGTGGTGGGACCACA[G/T]GGACCAGCCTGTGCC	68519
rs36511274	snp	A/G	0.132653	0.220748	missense	Eml1	Mm_Celera	12:108530341	ACAAAGGACTTGGTC[A/G]CCGTCCACACGGATG	68519
rs36513650	snp	A/G	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108510907	CATCCACGAGTGACT[A/G]TCATGTTTTATCAAA	68519
rs36515214	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108516861	TCACTAGAACCTCTA[A/G]AATCCAACATGCTTC	68519
rs36522367	snp	A/G	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108535799	ACCTACCCATAGGCT[A/G]CCAGTGAGAGTCACT	68519
rs36546661	snp	A/T	0.297521	0.245442	intron-variant	Eml1	Mm_Celera	12:108503317	ATACAGGCAGGAGCC[A/T]CCACGCATGACAGCA	68519
rs36547454	snp	A/G	0.495868	0.0452663	intron-variant	Eml1	GRCm38.p3	12:108453961	GAGGATGTGTGGTTA[A/G]ATGGCTGGATCGCTC	68519
rs36561314	snp	C/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108430341	TTCCTAAGAGCATAG[C/T]ATTTATTACTTATTT	68519
rs36566838	snp	C/G	0.42	0.183303	intron-variant	Eml1	GRCm38.p3	12:108460042	CTTGTCAACCACACT[C/G]TGTCTTGAGGTTGTC	68519
rs36569109	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108495879	GAAGATGCTGTATTC[A/G]TGGGCCTTTCTGCTC	68519
rs36574783	snp	A/G	0.495868	0.0452663	intron-variant	Eml1	GRCm38.p3	12:108514307	GAGACTCAGTGCCCC[A/G]CTCGAACAGTTTTGT	68519
rs36574839	snp	A/T	0.244898	0.249948	intron-variant	Eml1	GRCm38.p3	12:108488525	TGAGTCAAGCCTACA[A/T]CTGAGCGCCAGGCCT	68519
rs36584863	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108463399	AGTGAACCGTCTCAC[A/G]TGATTCTGCCAACAA	68519
rs36600798	snp	A/G	0.426035	0.177515	intron-variant	Eml1	Mm_Celera	12:108534635	TGGTGTCACATTTGC[A/G]TCTGTCCTGTTTCTG	68519
rs36602756	snp	A/G	0.260355	0.249785	intron-variant	Eml1	Mm_Celera	12:108516802	AACACTTCCTGTTTG[A/G]AACATTGCTTTAATA	68519
rs36610462	snp	C/T	0.408163	0.193609	intron-variant	Eml1	Mm_Celera	12:108459410	AGGGTTTATCATTGG[C/T]TCTGCCACTGCCACA	68519
rs36615714	snp	C/T	0.48	0.0979796	intron-variant	Eml1	Mm_Celera	12:108436377	TCACGCGCACTAGCT[C/T]ACACGCCACGCTCTA	68519
rs36617482	snp	C/T	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108530819	AGGACCACTCTGCTA[C/T]CTTCATGGCCCTCCA	68519
rs36621052	snp	A/C	0.459184	0.136902	intron-variant	Eml1	GRCm38.p3	12:108454094	CGCAGAAATGAAAAA[A/C]TCTGGCTGCTCACTT	68519
rs36639441	snp	A/G	0.297521	0.245442	intron-variant	Eml1	GRCm38.p3	12:108532157	AGACAGCGTGGAGCT[A/G]TGCTTTGTGGGTGGT	68519
rs36642712	snp	G/T	0.459184	0.136902	intron-variant	Eml1	GRCm38.p3	12:108493825	GATTGATTCACCTTC[G/T]CGGGACTTGTTGACA	68519
rs36648125	snp	C/G	0.408163	0.193609	intron-variant	Eml1	Mm_Celera	12:108459921	AGGGACAGAGCCTGT[C/G]TGGTGTCAGCAAGGC	68519
rs36649249	snp	C/T	0.493827	0.0552116	intron-variant	Eml1	GRCm38.p3	12:108454971	GTTCCATAGAAAGGT[C/T]GTTGAGTTGCCCTGA	68519
rs36650245	snp	C/T	0.142012	0.225474	intron-variant	Eml1	Mm_Celera	12:108513788	GAGATGTATGTTGTT[C/T]ACCCCTTGTGCCAGG	68519
rs36651214	snp	A/G	0.396694	0.202437	intron-variant	Eml1	GRCm38.p3	12:108490646	TTCGAGCTCTAGGGA[A/G]TCACCTTAGGTGGCT	68519
rs36656696	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108513303	TGGCTTTTATTCATA[C/T]AACAAACCCAGGAAA	68519
rs36661537	snp	C/T	0.497041	0.0383476	intron-variant	Eml1	Mm_Celera	12:108515567	CACTATTCTGATCCA[C/T]ATAGCATTTGACAAA	68519
rs36662711	snp	G/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108490433	TGCTTGGCCCAGATC[G/T]CCACATCGTCATTCC	68519
rs36664359	snp	C/T	0.497041	0.0383476	intron-variant	Eml1	Mm_Celera	12:108515480	ATAAAGTTAATCACT[C/T]TGCTGTGAGAGCTGT	68519
rs36669674	snp	A/G	0.142012	0.225474	intron-variant, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108536919	AAGGAGCTGGTGTGT[A/G]CTCAGGCCTCTAATA	68519
rs36670505	snp	C/T	0.345679	0.230967	intron-variant	Eml1	GRCm38.p3	12:108501959	TGTAGTGTGGAGCTG[C/T]GGAGCTCTGAGAGGA	68519
rs36671695	snp	A/G	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108503989	CGGCAACTTGGGTGA[A/G]AGGTTAGAGTAGGCA	68519
rs36674783	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108528972	AATACTCTCCTTGGA[A/G]CAGACACAATGTAAA	68519
rs36680736	snp	A/G	0.244898	0.249948	intron-variant	Eml1	Mm_Celera	12:108433256	CTCTCATACAGAAGC[A/G]CGCTAGCTGGACACT	68519
rs36680804	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108464500	TAAGACACCCTGAGG[C/T]TGTAGTATGTTAAAG	68519
rs36683810	snp	A/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108463431	CCATCGTCTTAGGTC[A/G]GCAGAGTGTATCACG	68519
rs36687227	snp	C/G	0.244898	0.249948	intron-variant	Eml1	Mm_Celera	12:108438636	GATATGCTTTCTGTG[C/G]CTTAGCGGAGGCGAA	68519
rs36691026	snp	A/C	0.132653	0.220748	intron-variant	Eml1	Mm_Celera	12:108492297	CTGGGCAGGCCATGG[A/C]TTTGTCCTTTGGCTG	68519
rs36693217	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108494685	GACACTCCAGTAGCC[C/T]TTGATGCCTCTCCCA	68519
rs36695464	snp	C/T	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108427061	TCGTCATATATTAAG[C/T]ATGCACAATAATGGG	68519
rs36711461	snp	C/T	0.495868	0.0452663	intron-variant	Eml1	GRCm38.p3	12:108428923	TTAGGTCTTGCTGTT[C/T]TGGAACTCACTGTGT	68519
rs36712415	snp	G/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108506142	TTTCCTCTGGAAAAC[G/T]AATTGAAAGGGACAT	68519
rs36729367	snp	C/T	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108490849	GAAGAAAACACTCAA[C/T]GGCATGCTTAATGCT	68519
rs36729551	snp	C/G/T	0.493827	0.0552116	intron-variant	Eml1	GRCm38.p3	12:108455332	TCAGAAGCAGACCAA[C/G/T]GTTCCTTTCTGTTCT	68519
rs36734985	snp	A/G	0.165289	0.235211	intron-variant	Eml1	Mm_Celera	12:108502649	AGTCAGTGAGGGTTA[A/G]AGCAGGGACTTCTCA	68519
rs36736501	snp	C/G	0.336735	0.234472	intron-variant	Eml1	Mm_Celera	12:108534577	TCCATGAATTGGTCT[C/G]ACACTGCCCCAGCCT	68519
rs36747422	snp	G/T	0.165289	0.235211	intron-variant	Eml1	Mm_Celera	12:108506762	TTCCCATGATTGTGG[G/T]TCCCGTTCGAATGCG	68519
rs36751750	snp	A/C	0.165289	0.235211	intron-variant	Eml1	Mm_Celera	12:108503067	ATATATGTCATGTCA[A/C]GATACATACAATATC	68519
rs36754233	snp	C/G	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108511276	TCCATTTTTGGCATC[C/G]TGATTGAATCCTTAC	68519
rs36755431	snp	A/G	0.260355	0.249785	intron-variant	Eml1	Mm_Celera	12:108517467	TCAAGGATGTCAGGT[A/G]TCTGCTTTGTCACTC	68519
rs36755485	snp	C/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108466378	ATCTTGTCCTTGATG[C/G]TGCTTCCACCTCAGT	68519
rs36757446	snp	G/T	0.408163	0.193609	intron-variant	Eml1	GRCm38.p3	12:108490357	GTCCCCACTGGTACT[G/T]GTGGATACTCTGGGG	68519
rs36762875	snp	C/T	0.48	0.0979796	intron-variant	Eml1	Mm_Celera	12:108438753	CCATTACACCTACCA[C/T]GCTCTGCTCATCGAC	68519
rs36763805	snp	C/T	0.408163	0.193609	intron-variant	Eml1	Mm_Celera	12:108430797	TATTTATTCAGAACT[C/T]TACCTTTCTTTAAAA	68519
rs36766408	snp	A/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108528504	CTGTGAGCCAATTAC[A/G]TACACTCTCTGACTG	68519
rs36776828	snp	A/G	0.165289	0.235211	intron-variant	Eml1	GRCm38.p3	12:108495216	TCCTGTCTGGCTCCA[A/G]CATCCCGTTCCTATG	68519
rs36785925	snp	A/G	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108518424	TGGGAAAGTCATTTC[A/G]TTTAATCCCTGTCCC	68519
rs36789154	snp	G/T	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108508350	AATTATCCCCAAAAT[G/T]CTGGGGCACCATTAG	68519
rs36791191	snp	A/G	0.260355	0.249785	intron-variant	Eml1	Mm_Celera	12:108534622	AGTGATGTCACCCTG[A/G]TGTCACATTTGCGTC	68519
rs36792680	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108428077	ATAAGAACACTGAAC[C/T]TCCTGTCCCTACATC	68519
rs36802442	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108515339	CCACTAAACTCCCGG[C/T]TACATAGGTGTGTTT	68519
rs36803236	snp	C/T	0.231111	0.249285	intron-variant, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108536579	TCAGTCTTGTCCATC[C/T]GTTCTGTTCCCACCT	68519
rs36806329	snp	C/T	0.444444	0.157135	downstream-variant-500B, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539994	TTCAGGCCACTGTCA[C/T]TTGGCCCTGGGCATT	68519
rs36815409	snp	A/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108427357	AAACTTCTGTCTGTC[A/G]GCTCACCAGGAGTTC	68519
rs36817691	snp	C/T	0.21875	0.248039	intron-variant	Eml1	Mm_Celera	12:108531388	AACCTTGTGTGGTTG[C/T]GCACATCTGTAGTCC	68519
rs36820906	snp	C/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108449375	TATATGATCCTGTAA[C/T]GACACGCCACTTGAG	68519
rs36829510	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108494777	TCAGATTCCTGGAGA[C/T]CTGAGCATCCCGTGG	68519
rs36829522	snp	A/G	0.459184	0.136902	intron-variant	Eml1	GRCm38.p3	12:108529485	GGGACTCACCCACAA[A/G]TATACATACCATCTT	68519
rs36841321	snp	A/G	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108494118	ACTTTACCTCACCCT[A/G]CAAGGCTCAGCTGAA	68519
rs36846730	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108508819	AGGTACTGAGGTCCA[C/T]TGGGCACTGAGTGTC	68519
rs36850576	snp	A/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108463466	AGCGGTGTCCCCGCG[A/T]GTGCTGGATCTGGTT	68519
rs36858927	snp	G/T	0.132653	0.220748	intron-variant	Eml1	Mm_Celera	12:108535448	GATGTTACTTAGGAC[G/T]CACACTGCTGTTTGC	68519
rs36860570	snp	A/C	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108490695	TGTGCCTGCCTCCTG[A/C]GTTCCTGTGTAGCCA	68519
rs36871191	snp	A/G	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108428375	GTCTGACATGATATC[A/G]ACTCCTTCTCTGGTC	68519
rs36872255	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108516429	CTTTTGATTCTGCCC[C/T]AGATAATGGTGGCGT	68519
rs36882986	snp	A/C	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108535634	GGGAGGAAGTTACAC[A/C]TGCCAGGGCTGTTGC	68519
rs36883959	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	Mm_Celera	12:108464012	GCCCACTGGTATATC[C/T]CATCTCTTCCTGTGT	68519
rs36898046	snp	C/T	0.277778	0.248452	intron-variant	Eml1	Mm_Celera	12:108516325	AAGATTTTAAGTCCT[C/T]CCTAGGAATGTATTA	68519
rs36899324	snp	A/G	0.277778	0.248452	intron-variant	Eml1	Mm_Celera	12:108438649	TGGCTTAGCGGAGGC[A/G]AAGCTGTTAGGTCAG	68519
rs36906319	snp	C/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108429307	CCTTTACCAACTGAG[C/T]CATCTCAGCAGCCCC	68519
rs36915341	snp	C/T	0.244898	0.249948	intron-variant	Eml1	Mm_Celera	12:108490779	GCCCTGGCTGTTCCT[C/T]GGGGATTTTGTGACA	68519
rs36923068	snp	C/T	0.260355	0.249785	synonymous-codon	Eml1	Mm_Celera	12:108516533	TTGTATGCTGAGAGA[C/T]GGGACGCTGGTGTCC	68519
rs36924707	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108436396	CGCCACGCTCTAGGA[A/G]CCTTTGCCCGGCCTA	68519
rs36927069	snp	G/T	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108518686	AGATTTGGACCCTGT[G/T]TCAGTTTGTTTAGTT	68519
rs36927458	snp	G/T	0.46281	0.131194	intron-variant	Eml1	GRCm38.p3	12:108506817	GCCATGGAAACAATC[G/T]TTGTACAGATGGATG	68519
rs36933594	snp	A/G	0.497041	0.0383476	utr-variant-3-prime, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108538457	AAGGTTTACATGGCA[A/G]CAGAAGGGACTGGTG	68519
rs36939796	snp	A/T	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108463005	CTCCATCTGCATAGC[A/T]AGCGCTGTGTGGTCA	68519
rs36939859	snp	C/T	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108515278	TGACTAAGACATTGG[C/T]GGTGGGGTTTATAGA	68519
rs36944122	snp	C/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108441056	CTGGTCCTGCTCATA[C/T]GGCGGGTTGGACAGT	68519
rs36949282	snp	G/T	0.426035	0.177515	intron-variant	Eml1	GRCm38.p3	12:108432007	TACTGTGCTCATCAG[G/T]AGTAAAATGTCAACA	68519
rs36960074	snp	C/G	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108441397	ATGCTTGTCAATCTC[C/G]ACCTTCTCTTCAGAA	68519
rs36960786	snp	G/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108463856	TGTGATGCTGAGGTG[G/T]GTCTTTGTAGACGCT	68519
rs36962220	snp	A/C	0.473373	0.11227	intron-variant	Eml1	GRCm38.p3	12:108513992	CAAACTGACTTAGGT[A/C]GTTGATGCAGAAGCA	68519
rs36964940	snp	C/T	0.473373	0.11227	intron-variant	Eml1	GRCm38.p3	12:108494568	CACTTTGTCCTGTCT[C/T]GCTCAGTCCTGAAGT	68519
rs36967942	snp	C/T	0.345679	0.230967	intron-variant	Eml1	Mm_Celera	12:108459624	AACAAGGACAAAATC[C/T]CTATTATTCCTTGAC	68519
rs36972070	snp	A/G	0.18	0.24	intron-variant	Eml1	Mm_Celera	12:108448781	ATAAACAATATAATA[A/G]CCTCCAACAGTCCAG	68519
rs36983754	snp	C/T	0.124444	0.216185	intron-variant, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108537484	GGCCTTGGCCATTCA[C/T]CACCTTTCTTACAGG	68519
rs36983882	snp	A/G	0.297521	0.245442	intron-variant	Eml1	GRCm38.p3	12:108529472	TTGTACACACGTAGG[A/G]ACTCACCCACAAGTA	68519
rs36998198	snp	C/G	0.142012	0.225474	intron-variant	Eml1	Mm_Celera	12:108528931	AGGTCAAAGGACTCG[C/G]TTCCTTACGGAGATG	68519
rs37005049	snp	G/T	0.21875	0.248039	intron-variant	Eml1	Mm_Celera	12:108451617	GATGACGTGTATTTT[G/T]GGTCCTGAGTTAACT	68519
rs37011686	snp	A/G	0.493827	0.0552116	intron-variant	Eml1	GRCm38.p3	12:108432207	CAGGAAGGACAATCC[A/G]GACCTGGGAAAGCCG	68519
rs37024275	snp	A/G	0.260355	0.249785	intron-variant	Eml1	Mm_Celera	12:108510947	GCCTCTTAAGTCCCT[A/G]TTTGTACAGCTTTGT	68519
rs37025454	snp	G/T	0.46281	0.131194	intron-variant	Eml1	GRCm38.p3	12:108535729	TCCTTCTTGGGTCCC[G/T]CCTGACACAAGTGCA	68519
rs37027499	snp	A/G	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108502623	CCTGCCCCTTGTCAG[A/G]CCCACATGGAAGTCA	68519
rs37029805	snp	C/G	0.46875	0.121031	intron-variant	Eml1	GRCm38.p3	12:108505502	AAAAAGTCTTATTTA[C/G]CATTCTTGTTGCATC	68519
rs37036393	snp	A/C	0.459184	0.136902	intron-variant	Eml1	Mm_Celera	12:108430717	TGAGATCCTACCTTA[A/C]CACCTCCATTCCCAC	68519
rs37037806	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108529047	CTGAGGTTGGCGAAG[A/G]GTAAGTGGAAGGACA	68519
rs37039328	snp	A/G	0.48	0.0979796	downstream-variant-500B, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539777	AACAACCTAGGCTTA[A/G]TAACCCAATCCAATT	68519
rs37044140	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108465484	AGACGTTCATGACCC[A/G]CTCAACTTTCCACAA	68519
rs37057311	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108443892	TGCACAGTTAATAGT[A/G]GCGTGTTTCAAGATG	68519
rs37058820	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108441763	CTTGTCTATAATGCC[A/G]AGGGTTTGCTTTGGT	68519
rs37068172	snp	A/C	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108493844	GACTTGTTGACAGCA[A/C]GGAAACAGGCTGACC	68519
rs37069990	snp	A/G	0.277778	0.248452	intron-variant	Eml1	Mm_Celera	12:108488470	TTTATTACCCACGGG[A/G]CAACTCTACCCAAGG	68519
rs37075653	snp	A/G	0.486111	0.0821678	intron-variant	Eml1	GRCm38.p3	12:108431810	TTGTGTTCTCAGCTC[A/G]GTCTTTGCCTGTTTG	68519
rs37093195	snp	A/G	0.297521	0.245442	intron-variant	Eml1	Mm_Celera	12:108431124	CTGGACAGATGGTGT[A/G]CTTTGCTCTGTACAC	68519
rs37095561	snp	G/T	0.21875	0.248039	intron-variant	Eml1	Mm_Celera	12:108493107	CCTATGTGTCTCTCT[G/T]CTCAGGGACTGCCCA	68519
rs37097043	snp	A/G	0.489796	0.070696	intron-variant	Eml1	Mm_Celera	12:108466601	TTATTCCTTTCCCAC[A/G]ATCTGTGGTGTGTGT	68519
rs37098741	snp	A/G	0.165289	0.235211	intron-variant	Eml1	Mm_Celera	12:108454357	TGGTAACTGACAAAC[A/G]GACACTTGACATTTG	68519
rs37111348	snp	C/T	0.495868	0.0452663	intron-variant	Eml1	GRCm38.p3	12:108458482	GTGTATACCACTTTC[C/T]ATGCAGAATGTCTTG	68519
rs37114690	snp	G/T	0.46281	0.131194	intron-variant	Eml1	GRCm38.p3	12:108531457	CTCAAGCCCAGCTTG[G/T]TTTACATAGGGAGTT	68519
rs37115171	snp	A/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108462961	CGTCTGGTGTTGCTA[A/T]GGACATCCTCCCCTT	68519
rs37119198	snp	A/G	0.486111	0.0821678	intron-variant	Eml1	GRCm38.p3	12:108465313	CCCTCTATGGAAAGG[A/G]ACCCATCCCTTGTCC	68519
rs37125982	snp	C/T	0.473373	0.11227	intron-variant	Eml1	GRCm38.p3	12:108530519	AGACAGCGAACCTTT[C/T]CGTCACTGTGCAGCT	68519
rs37126261	snp	C/T	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108534797	ATGTGGCCAGTTCGT[C/T]GCAGCAGCATAGCGT	68519
rs37126557	snp	C/G	0.165289	0.235211	intron-variant	Eml1	Mm_Celera	12:108492291	TTAGAGCTGGGCAGG[C/G]CATGGATTTGTCCTT	68519
rs37127301	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108466499	AAGCACTTAACATTT[C/T]ATGAGGCAGAAGGAT	68519
rs37137411	snp	G/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108492855	GAGGATGAAAGACGG[G/T]TAAAATGTTGGATCC	68519
rs37139335	snp	A/T	0.408163	0.193609	intron-variant	Eml1	Mm_Celera	12:108430704	ACAGCCTCAGCTGTG[A/T]GATCCTACCTTACCA	68519
rs37140280	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108531869	GAAGTGTCAGTTACT[A/G]TGATGTCATTAGTAC	68519
rs37147113	snp	A/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108528283	ACAGCAGGAGCCTCC[A/G]CTTTTGAAATGGGCA	68519
rs37153784	snp	A/G	0.495868	0.0452663	intron-variant	Eml1	GRCm38.p3	12:108516312	CTGAGAGCATCAAAA[A/G]ATTTTAAGTCCTCCC	68519
rs37156136	snp	C/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108511485	GCGATGATGGATCTG[C/T]TGACTGCACTGTGGT	68519
rs37166193	snp	A/G	0.277778	0.248452	intron-variant	Eml1	GRCm38.p3	12:108441325	AAAGCGGGTTCTCGG[A/G]CCACTTCCGGATTCC	68519
rs37170349	snp	A/C	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108494937	GCGAGCCAAAGGTTA[A/C]TATCAGTTGTCTTCT	68519
rs37182732	snp	G/T	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108429543	TGACTTAGAAGGATA[G/T]GGTAGGGTCCCTGGT	68519
rs37182858	snp	A/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108463316	AGTGCCAGTCTAGAC[A/G]TTAAACGTGGCAAGC	68519
rs37187672	snp	G/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108488914	CAGAAATACAAACCA[G/T]TTTCCATTCAGGTTT	68519
rs37188559	snp	C/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108429362	TGATGTCGGTAATAC[C/T]GGTGGCTGTCTCTTA	68519
rs37192227	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108493111	TGTGTCTCTCTTCTC[A/G]GGGACTGCCCAAGTT	68519
rs37205693	snp	A/G	0.46281	0.131194	intron-variant	Eml1	GRCm38.p3	12:108530939	GTGTGAGTCTCGAGG[A/G]TCTGTCTCCCAGCCC	68519
rs37208153	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108434232	CTGGCTCCAGTGCTT[A/G]GGCCATACTGAATAG	68519
rs37210240	snp	C/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108492074	TCTGGCAGTGAGTTG[C/G]GTTTGTAGAGTAAGA	68519
rs37210281	snp	C/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108467192	CACATAATGGCAAAA[C/T]GTTTTACATACAACC	68519
rs37212168	snp	C/T	0.408163	0.193609	intron-variant	Eml1	Mm_Celera	12:108432943	CTTAGGGCTCCTCCA[C/T]CTACTGTGCCTTGGC	68519
rs37213637	snp	C/T	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108494037	CATCACTCTGAGATG[C/T]CACCCAGCTGTGGTC	68519
rs37217618	snp	C/T	0.32	0.24	intron-variant	Eml1	GRCm38.p3	12:108454161	ACTTGTGACGAGGAG[C/T]TCTGGTGTCTCGGTG	68519
rs37217823	snp	C/T	0.244898	0.249948	intron-variant	Eml1	Mm_Celera	12:108510611	GTCTTATCAAAGAAT[C/T]GATCAGTTCCTGAAA	68519
rs37218952	snp	C/T	0.32	0.24	intron-variant	Eml1	GRCm38.p3	12:108443545	ACCAAATTCCTGCAG[C/T]GGTTGTGCTCTCCAC	68519
rs37226168	snp	C/G	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108492569	CCCAAGAGAGGACTT[C/G]AAGGTCCCCTATAGT	68519
rs37226702	snp	A/G	0.497041	0.0383476	intron-variant	Eml1	Mm_Celera	12:108518596	ATGAAACCGTGCTTG[A/G]AAATAACCAGGCAGT	68519
rs37227261	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108440831	GAGCTTGGCCAGCGC[A/G]GAGCCAGTCTTCTTT	68519
rs37231613	snp	A/C	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108528726	TCTGGAAATGTTGGC[A/C]CGGAACCCGTATAAC	68519
rs37233131	snp	G/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108503878	CAGAGTGACTTTCCG[G/T]TTCACTTTGAACTCC	68519
rs37234895	snp	C/G	0.345679	0.230967	intron-variant	Eml1	Mm_Celera	12:108529071	AAGGACAGCGGAGCA[C/G]CTCCCTGGCTGAGGA	68519
rs37236129	snp	C/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108429632	AGGATGCCTAATTGC[C/T]GCACGGGCCCTCCAC	68519
rs37238564	snp	A/C	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108463062	AAGATGGATTCAGAC[A/C]GACCTGCTGTGGTTT	68519
rs37241626	snp	C/T	0.408163	0.193609	intron-variant	Eml1	Mm_Celera	12:108437690	TGACTTGTCCATGTT[C/T]CCAGTACCCATAGTG	68519
rs37242013	snp	G/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108499275	TGTTGCAAGCTAGGA[G/T]CCACATTTGAGAGAA	68519
rs37254199	snp	A/G	0.408163	0.193609	intron-variant	Eml1	Mm_Celera	12:108438428	GAGTGAGGACGACAC[A/G]CTTACTTTCAGCTAG	68519
rs37254923	snp	C/T	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108531901	GTGCTATTGGCCTTA[C/T]AGAGTGTGATGAGGC	68519
rs37259712	snp	C/T	0.46281	0.131194	intron-variant	Eml1	Mm_Celera	12:108530534	TCGTCACTGTGCAGC[C/T]GTGGTTTAACTTTGT	68519
rs37264670	snp	C/T	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108463018	GCTAGCGCTGTGTGG[C/T]CATGGTTTGGGGAGG	68519
rs37270685	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108501798	ATATTTGCTCTTAAA[C/T]GGGATTACAATCTTA	68519
rs37272213	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108462840	AAGGATTTCTTTACC[A/G]GACAGATTTGACCAC	68519
rs37276114	snp	C/T	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108492825	CATTGAGCAAATATA[C/T]CTATTCCTCTTAATG	68519
rs37279046	snp	A/T	0.408163	0.193609	intron-variant	Eml1	Mm_Celera	12:108431346	TCAAACAAGAGGACG[A/T]GGATTTGGATCCTCA	68519
rs37290854	snp	A/G	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108440041	AGGGGACCGGCTTTC[A/G]TTGTATTGGCACGAA	68519
rs37294522	snp	C/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108429018	CGTGAGGAGCTGCTT[C/T]CAACTACAAATTTGT	68519
rs37296860	snp	C/T	0.46875	0.121031	intron-variant	Eml1	GRCm38.p3	12:108502720	TCCTGCGCTTCTCCC[C/T]GAGGGAAAGTCTCCC	68519
rs37296932	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108431152	CACCCTTTGTAGAGG[A/G]TACTGCCTCTGGAGT	68519
rs37307254	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108498478	ACATTCCCTTATGGG[C/T]GGCCTCTGTTCTACC	68519
rs37308228	snp	A/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108464051	TATACCAAAGCACAC[A/G]AAAGTCATGTGATGC	68519
rs37311390	snp	C/T	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108498613	ATGTATACAGTATTA[C/T]GCTTTATTATGGCAT	68519
rs37313487	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108431127	GACAGATGGTGTACT[C/T]TGCTCTGTACACCCT	68519
rs37317048	snp	G/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108465192	GCTCTTTCTCTCCTT[G/T]TTTCCTGGAAGCTTG	68519
rs37341371	snp	G/T	0.132653	0.220748	missense	Eml1	Mm_Celera	12:108534901	CACTTGGACTGGTCC[G/T]TGAACTCACAATTCC	68519
rs37344297	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108462820	GACACCCATAGCTGT[C/T]ACATAAGGATTTCTT	68519
rs37357364	snp	A/G	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108494189	AGACAGCCTGTGTCT[A/G]CGGTTGTCCATAGCC	68519
rs37382294	snp	A/G	0.244898	0.249948	intron-variant	Eml1	Mm_Celera	12:108492528	GAGTTGCTTTATTTC[A/G]CAAGTTACCTGTTTC	68519
rs37385588	snp	A/G	0.18	0.24	missense	Eml1	Mm_Celera	12:108506554	ACCAAGTGGATTCGT[A/G]CAGTTTGGAAGCAAA	68519
rs37387200	snp	G/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108510074	TTGGGGTGAGTCTGT[G/T]AGAAGCTAGGCAGTG	68519
rs37396139	snp	A/G	0.497778	0.0332592	synonymous-codon	Eml1	GRCm38.p3	12:108463666	GAGGCTGAACATCAC[A/G]GAGGAGCAACAGGCT	68519
rs37401528	snp	G/T	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108514066	CTCACAGGGCTGCGG[G/T]ACATGCAGAGTCCTG	68519
rs37410816	snp	A/G	0.5	0	intron-variant	Eml1, Gm16596	GRCm38.p3	12:108537907	CCTACTTGATTTCAG[A/G]CCTATCATGTGCTGT	68519
rs37422628	snp	C/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108448763	TGCGACTTCTTATTT[C/T]CCATAAACAATATAA	68519
rs37431259	snp	C/T	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108492376	CTAGGTACTACTAAC[C/T]TAGTGATGACCTTTC	68519
rs37439581	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108436893	CACAATTTTCTGACA[C/T]GAACGCCTGATTGGG	68519
rs37441440	snp	A/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108528539	TCTAGTCTCTGAGAT[A/G]TGTTGATACCACCAA	68519
rs37449272	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108498201	GCCCTTTAGGTCAAC[C/T]ATAGCAGTCTCTGGG	68519
rs37455117	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108464153	TAGCTGGCCGGTTTG[C/T]TCGGTTTCTTTTAGT	68519
rs37463092	snp	A/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108530531	TTTTCGTCACTGTGC[A/T]GCTGTGGTTTAACTT	68519
rs37470310	snp	G/T	0.132653	0.220748	missense	Eml1	Mm_Celera	12:108511917	GCTGTCACCTGCATC[G/T]CATTCTCAAAGTCTG	68519
rs37471621	snp	G/T	0.165289	0.235211	intron-variant	Eml1	Mm_Celera	12:108502666	GCAGGGACTTCTCAG[G/T]AAAGACGCCCTTTGC	68519
rs37478139	snp	C/T	0.132653	0.220748	intron-variant, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108536817	AATGCGTTGCTACAG[C/T]CGGAGCAATTGGGAG	68519
rs37487655	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108511611	TCAAAGTTTAAAACT[C/T]GAGAGCCTTCTCCCG	68519
rs37488635	snp	G/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108529414	GCACCCTCTGCTGGT[G/T]TCCTCTGGCACTGCA	68519
rs37491568	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108498182	ACCAAGCTTCCAGCT[A/G]GTGGCCCTTTAGGTC	68519
rs37506151	snp	A/G	0.459184	0.136902	intron-variant	Eml1	GRCm38.p3	12:108529390	ACTCTTGTCTTTCTG[A/G]GAGATCTGGCACCCT	68519
rs37510757	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108530085	TCCCACTTCCCATGC[A/G]CATACAAGTCCCAGA	68519
rs37517384	snp	C/T	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108457760	TCTGTTCTTCTCTCA[C/T]CTGCATATGGACCTC	68519
rs37532070	snp	A/G	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108530020	CAGCTCTCTGCTGCA[A/G]CTCCTATATGCCCTC	68519
rs37533542	snp	A/G	0.408163	0.193609	intron-variant	Eml1	GRCm38.p3	12:108533925	TGGTAGGACAGCTAC[A/G]GGAAGGGCTCTGTCA	68519
rs37533961	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108465708	TGTGTGCCGCTTTCA[C/T]GAGTGGAAATCGTCA	68519
rs37546342	snp	A/T	0.459184	0.136902	downstream-variant-500B, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539750	AAAGGAATTGGCTTA[A/T]TTTCTTGCTTTAACA	68519
rs37554527	snp	A/G	0.495868	0.0452663	utr-variant-3-prime, intron-variant	Eml1, Gm16596	Mm_Celera	12:108539483	AGCCTGCTGTGGAAG[A/G]AAACAACGTGACTCA	68519
rs37561227	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108529565	AAGATAAACATCACC[A/G]TCGTCGATCTGCTGA	68519
rs37571010	snp	A/T	0.197531	0.244432	intron-variant	Eml1	GRCm38.p3	12:108443814	ATCCTAAGGGACATA[A/T]TCTGGGTGACTGTCC	68519
rs37579714	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108441261	TGATCTTAAATGGAA[C/T]CCAGCTCATGGCCCT	68519
rs37583847	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108493929	AAGGGTTTGGACGTG[C/T]AGCTCACTGAGAAAG	68519
rs37588240	snp	A/G	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108503413	GCTGTGATTTGGATT[A/G]TCATTCCTCATTGCC	68519
rs37592180	snp	G/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108511121	CCACACTTGCAAAGA[G/T]CGATAACAGAAGCCA	68519
rs37609801	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108462886	TCAAAGAGTGGGACC[A/G]TGTTTCCCCAGTCTG	68519
rs37612116	snp	A/C	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108528935	CAAAGGACTCGGTTC[A/C]TTACGGAGATGACAT	68519
rs37619811	snp	A/G	0.473373	0.11227	synonymous-codon	Eml1	GRCm38.p3	12:108513067	GAGACTGGCCGACGT[A/G]AAGGTTCGCATGAGC	68519
rs37634865	snp	A/G	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108493077	GACTATTGTTGCTCC[A/G]TTCCAAGGTCACAGC	68519
rs37635636	snp	G/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108428142	ACTCTGGCCAGCCCT[G/T]GCATGTTTATTTTTT	68519
rs37641640	snp	G/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108459420	ATTGGCTCTGCCACT[G/T]CCACACCATGGCCTT	68519
rs37644841	snp	C/T	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108501525	GGACATATAGTTGGT[C/T]CTGTCCCTTCTGTTG	68519
rs37657288	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108489786	TGTGTGGTAAATTGA[A/G]TCCATGGTCCACTGA	68519
rs37658130	snp	C/T	0.497041	0.0383476	intron-variant	Eml1	Mm_Celera	12:108518875	ATTTGTGAAGACCAG[C/T]TCTCTACCGACATCA	68519
rs37659420	snp	C/T	0.495868	0.0452663	intron-variant	Eml1	Mm_Celera	12:108459689	ACCTAAGCAAATAAA[C/T]AGGATGAAACACTGT	68519
rs37660531	snp	A/G	0.42	0.183303	intron-variant	Eml1	Mm_Celera	12:108427324	AATAGGAAGGAAATA[A/G]GAGTTGTAGGTCCAT	68519
rs37663987	snp	C/T	0.459184	0.136902	intron-variant, nc-transcript-variant	Eml1, Gm16596	GRCm38.p3	12:108536818	ATGCGTTGCTACAGT[C/T]GGAGCAATTGGGAGT	68519
rs37664384	snp	C/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108463151	CAAACTTCTGGTCAA[C/G]TAGCACCAGTGGATA	68519
rs37667484	snp	A/G	0.21875	0.248039	intron-variant	Eml1	Mm_Celera	12:108502721	CCTGCGCTTCTCCCC[A/G]AGGGAAAGTCTCCCC	68519
rs37667712	snp	C/T	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108493694	AAGAGAAGAACGAGG[C/T]GCTTGGACAATGTCT	68519
rs37669047	snp	A/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108461317	ACAGAGTTTTAAAAC[A/T]GTTCAGACAGTATTC	68519
rs37683939	snp	A/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108530125	CAGTGCTAACTTCTG[A/G]AGAGCTTCGAGCGTT	68519
rs37690501	snp	C/T	0.142012	0.225474	intron-variant	Eml1	Mm_Celera	12:108535082	ATGAGGATTTGGCCT[C/T]ACAGCCTCTTGGAGT	68519
rs37736343	snp	A/G	0.21875	0.248039	intron-variant	Eml1	Mm_Celera	12:108451394	CCTATAGCAGACTGA[A/G]CTCTGGAGCAGGGGA	68519
rs37752743	snp	C/G	0.345679	0.230967	intron-variant	Eml1	GRCm38.p3	12:108501770	CACTTGACTAGCCAG[C/G]TGCCCCTAACCTATA	68519
rs37781328	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108503756	CAACAGACACGCACT[A/G]TCGGCACCCACAGCA	68519
rs37786092	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108507686	TTTCCACCATGGAGG[A/G]AGGCTGCAGCAGCCT	68519
rs37786303	snp	C/T	0.473373	0.11227	intron-variant	Eml1	GRCm38.p3	12:108463315	AAGTGCCAGTCTAGA[C/T]GTTAAACGTGGCAAG	68519
rs37790590	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108455278	TCAGCGTGGTGACAA[A/G]TGTGGGTTCCAGAAG	68519
rs37791227	snp	G/T	0.473373	0.11227	intron-variant	Eml1	GRCm38.p3	12:108427938	GGTTTGTGCCACCTA[G/T]ACCTGCTTCCTTCTT	68519
rs37817089	snp	G/T	0.5	0	intron-variant	Eml1	Mm_Celera	12:108439184	GGGTATGCTGAGCCA[G/T]CACTCTGTGTTCCAG	68519
rs37823059	snp	G/T	0.132653	0.220748	intron-variant	Eml1	Mm_Celera	12:108533315	GAGGTTGTCAGTGCA[G/T]AGGGCTGCGGTCATA	68519
rs37825759	snp	C/T	0.426035	0.177515	downstream-variant-500B, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539764	AATTTCTTGCTTTAA[C/T]AACCTAGGCTTAGTA	68519
rs37832886	snp	C/G	0.18	0.24	intron-variant	Eml1	Mm_Celera	12:108506766	CATGATTGTGGTTCC[C/G]GTTCGAATGCGTACC	68519
rs37835038	snp	A/C	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108532427	ATATGTAATCATCGC[A/C]GGTATACACTTGGCT	68519
rs37841368	snp	C/T	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108496311	CAGAGTTTAGAAAGT[C/T]TTGCCAACAGCAAAT	68519
rs37852485	snp	C/T	0.375	0.216506	intron-variant	Eml1	Mm_Celera	12:108455479	TTGTAAAACTACCAT[C/T]AAGGAGACTATGGTG	68519
rs37877167	snp	C/T	0.473373	0.11227	intron-variant	Eml1	GRCm38.p3	12:108516281	TAGGACGATCCAGTT[C/T]ATGCATGCTAGGACT	68519
rs37880803	snp	C/T	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108432074	TGACCACAAAACAGC[C/T]TGTGCTAAGCCCACT	68519
rs37886546	snp	G/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108514807	CTGGCTTTGCTAAGG[G/T]AGACAGGACCCTGTC	68519
rs37887993	snp	C/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108437663	CTGGCTCCTGAGTGC[C/T]GTCAGCTGGCCTGAC	68519
rs37907201	snp	A/C	0.277778	0.248452	intron-variant	Eml1	Mm_Celera	12:108487725	TCCTGAAGCTGAGTT[A/C]CTATAGGGGCTCAGA	68519
rs37923763	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108497266	GTGAGAAACGCCTCC[A/G]CAAGCTCATCTGAAC	68519
rs37928574	snp	G/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108462692	TCTCATTCACACCTC[G/T]GCAGGGAAGTTGGTG	68519
rs37928773	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108490949	CAGCCATTTCTTCCT[C/T]GTGTGTAACATGAAG	68519
rs37934616	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108498120	ATTAATGATCACGGT[A/G]CCCCATGACCTGATC	68519
rs37941755	snp	A/C	0.495868	0.0452663	intron-variant	Eml1	Mm_Celera	12:108529109	GAGGAGGGACTGAGT[A/C]TGTTGTAGCTCCAGG	68519
rs37945079	snp	A/G	0.244898	0.249948	intron-variant	Eml1	GRCm38.p3	12:108457503	TGTGTGTGTGTGTGT[A/G]CAGCATCTCCATCAC	68519
rs37978592	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108493035	ATCCTCCACACCAGG[C/T]TGGCCTGCAGGTGCC	68519
rs37997785	snp	A/T	0.35503	0.226867	intron-variant	Eml1	GRCm38.p3	12:108493096	CAAGGTCACAGCCTA[A/T]GTGTCTCTCTTCTCA	68519
rs37999119	snp	A/T	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108465736	TCATTGGTTTGAAAG[A/T]CACTGAGAAATGAAA	68519
rs38013638	snp	A/C	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108488706	AGTATAGCAATGTCT[A/C]AGAAATTAGCCCAGG	68519
rs38014549	snp	C/T	0.132653	0.220748	intron-variant	Eml1, Gm16596	Mm_Celera	12:108537983	CACAAAGCTGACACA[C/T]AGAGAAGAAGAGCTT	68519
rs38032243	snp	C/T	0.277778	0.248452	intron-variant	Eml1	GRCm38.p3	12:108440789	TCTTCCCGCACAGGC[C/T]TTAGGTAGCTCTTCT	68519
rs38038528	snp	C/T	0.244898	0.249948	intron-variant	Eml1	GRCm38.p3	12:108440726	TCAAGTCGGCTGCCA[C/T]TGAACCGTGGCATCT	68519
rs38044302	snp	C/T	0.277778	0.248452	intron-variant	Eml1	Mm_Celera	12:108441178	TCCAGCCGCTGCAGT[C/T]TTCTGTACTCCCTTT	68519
rs38045064	snp	G/T	0.426035	0.177515	intron-variant	Eml1	GRCm38.p3	12:108432307	ACAAACTTTCAGCTG[G/T]CCTTTTCTTTCTTAT	68519
rs38064870	snp	G/T	0.132653	0.220748	intron-variant	Eml1	Mm_Celera	12:108530837	TCATGGCCCTCCAAG[G/T]TACATGCCATTAGTG	68519
rs38080662	snp	C/T	0.493827	0.0552116	intron-variant	Eml1	GRCm38.p3	12:108455145	ACCCTAGACTGCTGA[C/T]GCCTCTCTCTAGCCT	68519
rs38084108	snp	A/T	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108503361	TCCTAAGTTCAGTGC[A/T]CCTCCGAACATTCAC	68519
rs38108238	snp	A/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108530806	ATTACCGCTTGGAAG[A/G]ACCACTCTGCTACCT	68519
rs38116969	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108503950	TGCCTTTTAAGCCTG[C/T]CTTTGTGGTCACCAA	68519
rs38121631	snp	A/C/T	0.486111	0.0821678	intron-variant	Eml1	GRCm38.p3	12:108430460	CCCACATGGCAGTTC[A/C/T]TGACTGTCTGTAACT	68519
rs38121701	snp	A/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108462733	GTAGTCAGTGAGGAG[A/G]AAGATTCTAAAAACG	68519
rs38146143	snp	A/G	0.152778	0.230321	intron-variant	Eml1	Mm_Celera	12:108513810	TGTGCCAGGTTAGAA[A/G]CAGCCAGGGGCAGAG	68519
rs38151693	snp	C/G	0.165289	0.235211	intron-variant	Eml1	GRCm38.p3	12:108530445	GTTTTGTACAAGAAA[C/G]AGGTTGACAAAGCTC	68519
rs38152003	snp	C/T	0.459184	0.136902	downstream-variant-500B, intron-variant	Eml1, Gm16596	GRCm38.p3	12:108539699	GAGTTCTGTTCTGCA[C/T]ACAGTGTGGAAGCCT	68519
rs38169246	snp	G/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108516630	GTAAGCCACAGCGTG[G/T]ACCCTGCACCTGTTA	68519
rs38179055	snp	G/T	0.46281	0.131194	intron-variant	Eml1	GRCm38.p3	12:108535659	TGTTGCCCACTTGCT[G/T]AGGAGTCTGGGAAAG	68519
rs38182219	snp	C/G	0.142012	0.225474	intron-variant	Eml1	Mm_Celera	12:108430386	GGAGGCTGGAGAGAT[C/G]ACTCAACGGTTAAGA	68519
rs38187790	snp	A/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108531763	CTTCACATTCCTCTA[A/G]TAGGATACTGTTGGC	68519
rs38198417	snp	A/G	0.132653	0.220748	intron-variant, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108537022	ACTTACAGTGGAAAG[A/G]CATCAGTTTATAAGC	68519
rs38199975	snp	A/G	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108528201	ataatgttatggctt[A/G]ggtcatcacaacatg	68519
rs38240060	snp	C/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108431797	GACATGGAAGGCTTT[C/G]TGTTCTCAGCTCGGT	68519
rs38253964	snp	C/G	0.260355	0.249785	intron-variant	Eml1	Mm_Celera	12:108516835	GGCAGTCTTGTGGCC[C/G]GTTGGGTTTATCACT	68519
rs38261163	snp	A/C	0.42	0.183303	intron-variant	Eml1	GRCm38.p3	12:108457205	TTTTTCACTAAGGAA[A/C]GCTCCTGTCTGAAAT	68519
rs38284230	snp	A/G	0.32	0.24	intron-variant	Eml1	GRCm38.p3	12:108435346	ACCACTTGTACTTTC[A/G]GAAGTTTCTGAACAT	68519
rs38294406	snp	C/T	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108510730	CCTTGACTGTGGGTG[C/T]CTGCCAGTCATTTCT	68519
rs38311817	snp	A/G	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108513842	ACCAGCCGGGATTAA[A/G]AACATAGAATTGAAT	68519
rs38326690	snp	A/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108460646	CTCCAAAATATGAAT[A/T]CTTACTTGCACAAAA	68519
rs38330801	snp	A/G	0.489796	0.070696	intron-variant	Eml1	Mm_Celera	12:108436660	GTTTAGAGAGCTGAC[A/G]AGGGGCGCATGTTTG	68519
rs38361097	snp	A/C	0.408163	0.193609	intron-variant	Eml1	Mm_Celera	12:108436038	GCTCTGTTTCTCGTT[A/C]CAAGGGAAAACTCTG	68519
rs38373946	snp	A/G	0.497041	0.0383476	synonymous-codon	Eml1	GRCm38.p3	12:108516569	AGGGAAGGACCGGCG[A/G]CTCATTTCCTGGAAC	68519
rs38381052	snp	A/G	0.132653	0.220748	intron-variant	Eml1	Mm_Celera	12:108491147	CCAGCCAGGCCACTA[A/G]CAGTACACTGATCGA	68519
rs38386101	snp	A/G/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108440423	CTGTCTGCAACTGCC[A/G/T]GGCCATTGGGAGGTT	68519
rs38405274	snp	C/T	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108492997	CAGGTGTTCCGAGGA[C/T]TGAGTACCTTCTTCT	68519
rs38414556	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108460620	ACTGTATCTTGTTTC[C/T]ATCTCTCTAGCTCCA	68519
rs38419143	snp	G/T	0.152778	0.230321	intron-variant	Eml1	Mm_Celera	12:108444897	GCCATACAGCTTTGA[G/T]GTGTCCCATGCTTTC	68519
rs38543480	snp	A/G	0.486111	0.0821678	intron-variant	Eml1	Mm_Celera	12:108531691	AAGACAAAAGGTGGA[A/G]AAGGTGTGTTTGTTC	68519
rs38553951	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108460078	GCTGACAGCAGTCTA[A/G]GTGATCTCACAGGGC	68519
rs38577822	snp	A/G	0.46875	0.121031	intron-variant	Eml1	Mm_Celera	12:108531015	AGTGTTCGTGTGTGC[A/G]CCGTGGTGCCTGGGC	68519
rs38600613	snp	A/T	0.489796	0.070696	intron-variant	Eml1	Mm_Celera	12:108526336	CGGTTGAAGAACTTT[A/T]GCTTTGCTCTGACTC	68519
rs38602582	snp	C/T	0.197531	0.244432	intron-variant	Eml1	Mm_Celera	12:108449614	GAGGTAACAGGCTTG[C/T]TCCTGGTTGTTATTA	68519
rs38603605	snp	C/T	0.132653	0.220748	intron-variant, nc-transcript-variant	Eml1, Gm16596	Mm_Celera	12:108536787	ATCTTAGGAATACAT[C/T]CATAAATAGCTCACA	68519
rs38627561	snp	A/T	0.132653	0.220748	intron-variant	Eml1	Mm_Celera	12:108430079	GAGGGCAGGTTCTAG[A/T]ATTGGGGAAATGGTC	68519
rs38637782	snp	A/C	0.486111	0.0821678	intron-variant, downstream-variant-500B	Eml1, Gm16596	GRCm38.p3	12:108536067	GACTGAAAGGCAGAC[A/C]CTCCTGAGACCCAGA	68519
rs38644952	snp	C/T	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108530783	TGTCAGGGTGAGTCT[C/T]CCACCTCATTACCGC	68519
rs38705084	snp	A/T	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108514908	GCAGCTTTGGGCTTC[A/T]TTCCCCAGCCATTGA	68519
rs38705937	snp	G/T	0.345679	0.230967	missense	Eml1	Mm_Celera	12:108502406	AAACCCAAGGAGCCC[G/T]CATTCAGTCCAGGTA	68519
rs38718222	snp	A/G	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108493759	ACTTGGACCTACTAT[A/G]TGTGTGGCATGATGC	68519
rs38728584	snp	C/T	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108494107	TGTTTGAACAGACTT[C/T]ACCTCACCCTACAAG	68519
rs38796007	snp	A/G	0.197531	0.244432	intron-variant	Eml1	Mm_Celera	12:108506407	CTGTGTGCCCTACAA[A/G]CTAACCAGACTGTGG	68519
rs38833031	snp	C/T	0.197531	0.244432	intron-variant	Eml1	Mm_Celera	12:108449271	AGAGACACCTGTTGA[C/T]GCCTTCACTTCTCAT	68519
rs38834802	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108430837	GAGTGGAAAACCATA[C/T]GTTTGCCGTGTTCTC	68519
rs38841576	snp	A/G	0.473373	0.11227	intron-variant	Eml1	GRCm38.p3	12:108528358	CTAGAGAGGCTTTCA[A/G]CACTGGGGAAAGTTC	68519
rs38844338	snp	C/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108457848	GAACCGGATGTTGCT[C/T]TGATGTCTGTGTTCC	68519
rs38914234	snp	C/T	0.277778	0.248452	intron-variant	Eml1	Mm_Celera	12:108430457	GCACCCACATGGCAG[C/T]TCCTGACTGTCTGTA	68519
rs38934546	snp	G/T	0.408163	0.193609	intron-variant	Eml1	GRCm38.p3	12:108501703	CTCTGCTCATTTTAA[G/T]TAAGTTCCTTAAATG	68519
rs38945573	snp	C/T	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108463381	AGAAAGAAACGTCCA[C/T]AAAGTGAACCGTCTC	68519
rs38955406	snp	C/T	0.486111	0.0821678	intron-variant	Eml1	GRCm38.p3	12:108528382	AAAGTTCCCAGATCC[C/T]GGGCCTCATGTTCAG	68519
rs39012302	snp	C/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108463412	ACGTGATTCTGCCAA[C/G]AAACCATCGTCTTAG	68519
rs39118913	snp	A/C	0.32	0.24	intron-variant	Eml1	GRCm38.p3	12:108441823	ATCCAGAATCCTGAG[A/C]ATGCATGTGCAGGCC	68519
rs39130514	snp	C/G	0.5	0	intron-variant	Eml1	Mm_Celera	12:108432706	GACTTGGATGTGAAT[C/G]CGAGGTGCTGAGCAG	68519
rs39153212	snp	C/T	0.297521	0.245442	intron-variant	Eml1	GRCm38.p3	12:108529423	GCTGGTTTCCTCTGG[C/T]ACTGCACTTGAGTAC	68519
rs39159793	snp	G/T	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108432664	AGATGGACGAGCAGA[G/T]AACAGGGTCACTGTT	68519
rs39270904	snp	C/T	0.493827	0.0552116	intron-variant	Eml1	GRCm38.p3	12:108453596	ATGTCCCCAGCTCTT[C/T]GTCAGCTCTTAGTCA	68519
rs39286222	snp	A/G	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108427142	CACTTCTGTGTGGAC[A/G]TACATCCTTATTTTC	68519
rs39290126	snp	C/T	0.21875	0.248039	intron-variant	Eml1	GRCm38.p3	12:108448394	CACCTGAGAATCTTG[C/T]GAGAAAAGCCAGTTC	68519
rs39380152	snp	A/G	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108430161	GCTCTTATGACCATC[A/G]ATGATGGAAACCTCC	68519
rs39406212	snp	A/T	0.495868	0.0452663	intron-variant	Eml1	GRCm38.p3	12:108453943	GCAAGCTGTTCACAG[A/T]AAGAGGATGTGTGGT	68519
rs39478689	snp	A/G	0.21875	0.248039	intron-variant	Eml1	Mm_Celera	12:108452443	TACTGTTTAGTTGGT[A/G]GCTGAGCCTTAGCTG	68519
rs39602800	snp	G/T	0.277778	0.248452	intron-variant	Eml1	Mm_Celera	12:108460284	GAGTATCACCGGGGT[G/T]TATTTTAGATTTCAG	68519
rs39643845	snp	A/G	0.408163	0.193609	intron-variant	Eml1	Mm_Celera	12:108440379	GAGACATTCAAGTCC[A/G]AGAACTGGCAAGGTA	68519
rs39665674	snp	C/T	0.459184	0.136902	intron-variant	Eml1	GRCm38.p3	12:108429446	TGGATCTAGGAACTC[C/T]GGAGGAACCACCTGG	68519
rs39674975	snp	A/C	0.486111	0.0821678	intron-variant	Eml1, Gm16596	GRCm38.p3	12:108537835	TGAACATCTTTCAGC[A/C]AGAAGACCCTGTCTC	68519
rs39758230	snp	A/G	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108529951	CATTTCCGATACTTA[A/G]CACACCATCTCCTCA	68519
rs39780429	snp	A/T	0.459184	0.136902	intron-variant	Eml1	GRCm38.p3	12:108427343	TTGTAGGTCCATAGA[A/T]ACTTCTGTCTGTCGG	68519
rs40065812	snp	A/G	0.459184	0.136902	intron-variant	Eml1	GRCm38.p3	12:108492001	AGTGTCCCCATTCTG[A/G]CCTCCGATAGAGATG	68519
rs40342267	snp	C/T	0.152778	0.230321	intron-variant	Eml1	Mm_Celera	12:108454196	ACAGACTTGCTCCAC[C/T]TCGGCTTTCTCAAAA	68519
rs45633571	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108380605	TATCGCATGGCGATC[A/G]ATCGTATGCTGTCCT	68519
rs45669981	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108460588	CCTACTGTGTGTGCC[C/T]GGGCTCTGCTCTCTC	68519
rs45673954	snp	C/G			intron-variant	Eml1	GRCm38.p3	12:108443343	TGGTCCTGAGAAAGC[C/G]GGGTTGGGAAGGGTC	68519
rs45681816	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108379409	GCCTGCGAGGCAAGC[A/G]CATCTCTCCCATGAA	68519
rs45683660	snp	A/G	0.391111	0.206368	intron-variant	Eml1	Mm_Celera	12:108380486	CTAACTATGTAGCAC[A/G]TGCCAGCTATGCCAT	68519
rs45685002	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108433648	ACACCACACCCATAG[C/T]GAAACGCACTCGGCT	68519
rs45703510	snp	C/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108394298	TGGAGAGTCTGTGTG[C/G]TCCCCTAATGTCAGC	68519
rs45735401	snp	C/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108399121	CAACTGAAGAAACAG[C/T]CAGAGGAGTGCTTAG	68519
rs45738756	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108477979	GTAGAAGGGAACAGG[A/G]AGGCAAAATGATAGC	68519
rs45751380	snp	A/T			intron-variant	Eml1	GRCm38.p3	12:108373161	ATCCAGGAGGCTCAG[A/T]GGAATCTCCCTGTTG	68519
rs45774227	snp	A/G	0.297521	0.245442	intron-variant	Eml1	GRCm38.p3	12:108394864	CACACATGGCCACAA[A/G]ACCACACCCGTGCAT	68519
rs45777398	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108393989	CAGGATGTAAGATCA[C/T]AGAGTGGTTGGTCAT	68519
rs45785358	snp	A/C			intron-variant	Eml1	GRCm38.p3	12:108486909	CTAGAGCATACCTTC[A/C]ACTGTGGATGACAAC	68519
rs45794938	snp	C/G			intron-variant	Eml1	GRCm38.p3	12:108394946	CACACACTTATATGC[C/G]TATACACTGAAAATT	68519
rs45802492	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108389702	CACCCTCCCTGCAAA[A/G]TCAGGCCCTTAAGTA	68519
rs45808510	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108420759	GCCCCATCTTACTAT[A/G]GGGATGCCAGGACTG	68519
rs45812405	snp	A/G	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108387905	GGCAAGGATCTCACC[A/G]TCTCTGTCTGCAGAT	68519
rs45812406	snp	A/T	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108400029	AGAAACATGGGTGTT[A/T]GTGAGACCCTCAGGC	68519
rs45843771	snp	A/G	0.46875	0.121031	intron-variant	Eml1	Mm_Celera	12:108416263	CTGCGAAGAGCTAGC[A/G]TGGAAATGCTTGGCA	68519
rs45853186	snp	A/G	0.375	0.216506	intron-variant	Eml1	GRCm38.p3	12:108396711	AGGAAGAGATCAGCC[A/G]GTGCCTGTGTTAGGG	68519
rs45862448	snp	A/C			intron-variant	Eml1	Mm_Celera	12:108507624	GTATGAGCTTACGCT[A/C]CCCTAAAGAGCTAGT	68519
rs45863346	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108502345	CAAATATTATACACA[C/T]ATATAAATAAATAAA	68519
rs45886255	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108476543	TCATCCCTTGGCATG[C/T]GATTCCCAGTTTCCC	68519
rs45886632	snp	C/G			intron-variant	Eml1	Mm_Celera	12:108462263	CCATGGCATGTATGA[C/G]TGCACACACACACAC	68519
rs45887143	snp	A/G	0.497778	0.0332592	upstream-variant-2KB, intron-variant	Eml1	GRCm38.p3	12:108422113	CATCTTTGAGGACCA[A/G]AGTGACAGATCCCAT	68519
rs45903032	snp	A/G	0.391111	0.206368	intron-variant	Eml1	Mm_Celera	12:108384245	AGGTCCTTGCCAGGA[A/G]CACAACACAAAGATA	68519
rs45908780	snp	A/G	0.497778	0.0332592	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108404340	GAGGGGTTCTGTAAC[A/G]GAGCTTGCTATAGCT	68519
rs45914520	snp	A/G	0.459184	0.136902	intron-variant	Eml1	GRCm38.p3	12:108377311	GTTTGGGGACAACTG[A/G]CGCCCTCATTATCCT	68519
rs45945959	snp	C/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108396204	CAGTGACTCATTATG[C/T]GAGGAGCCTTCACAG	68519
rs45946353	snp	C/G	0.32	0.24	intron-variant	Eml1, Gm33385	Mm_Celera	12:108401503	AGGGAGCAGGCAGGA[C/G]TTGCCACATTAGTCA	68519
rs45961324	snp	A/G	0.32	0.24	intron-variant	Eml1, Gm33385	Mm_Celera	12:108404017	GTGTTTGCAGGGAGC[A/G]CACAGGTCAGCCTCT	68519
rs45974213	snp	G/T	0.408163	0.193609	upstream-variant-2KB, intron-variant	Eml1, Gm33385	GRCm38.p3	12:108410297	AGGAAACATGTTTCC[G/T]TTCCTGACACATTTA	68519
rs45975030	snp	C/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108414294	CCTATTCGATGGAGA[C/G]CTGCACCTCTTCTCC	68519
rs45980008	snp	C/T	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108385268	GCTCTCCACTCTGTG[C/T]CCCTATATCCTCTGA	68519
rs45997540	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108449241	TACAGGGCCACCTTG[C/T]CTGGCAGCTGACAGA	68519
rs46014020	snp	A/T			intron-variant	Eml1	GRCm38.p3	12:108507306	CACAAAACCAGCCAA[A/T]ACAAGCTGGGGTGGT	68519
rs46018950	snp	A/C			intron-variant	Eml1	Mm_Celera	12:108448333	AGGAAATGCTCTTAA[A/C]TCCTGAGCTGTAGCC	68519
rs46022551	snp	C/T	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108387250	AGATTGACGTTGGCA[C/T]TTGAGTTCTGCCACC	68519
rs46027543	snp	A/C	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108399060	ACGAGAGCTGCCAGC[A/C]GAGAGCCCAGTGTAT	68519
rs46042148	snp	G/T			intron-variant	Eml1	GRCm38.p3	12:108448023	CTAGGGCTGAAGTGG[G/T]ACAAATGGTGGATGC	68519
rs46048091	snp	C/T	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108381701	GGAGACATTAGCTGT[C/T]GATGGTCAAGAGTCT	68519
rs46048471	snp	A/G	0.497778	0.0332592	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108401673	AGGGAGGGTGGATAC[A/G]CCTTGGAGAATTAAG	68519
rs46049818	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108384423	CTCTATCCTGTCCAG[A/G]ACTGGAATGATGTTG	68519
rs46050372	snp	C/G			intron-variant	Eml1	Mm_Celera	12:108458286	TCAGAGTCACCGCTC[C/G]AAGGACAGAACCCAG	68519
rs46053907	snp	C/T	0.124444	0.216185	upstream-variant-2KB, intron-variant	Eml1	Mm_Celera	12:108421338	GAAGTTCTGTGCTGG[C/T]GGCTTCCTGAGGCCA	68519
rs46060034	snp	A/G	0.495868	0.0452663	intron-variant	Eml1	GRCm38.p3	12:108417756	AGGCAGGAAGCCACA[A/G]TGTAATGCTCCCTAT	68519
rs46070225	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108376478	GGGATTTGAACTCAG[A/G]ACCTTTAGAAGATCA	68519
rs46071945	snp	A/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108397496	TCATGTCAGTCTTAC[A/T]AAGCAGTCTGTTTGG	68519
rs46072997	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108435737	AAGGAAGGGACAGAC[C/T]GTGGCTCAGGGTGCC	68519
rs46073670	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108459284	TAGCTGATCCCTCTT[C/T]CCAGTTCTTCCTCCC	68519
rs46077259	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108472679	GACAAGAGCTACCCC[A/G]CAGGCCAGCCAGACT	68519
rs46093859	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108461861	TGAAGCAGATACAGA[A/G]CCCATCGACTGTCAC	68519
rs46104879	snp	A/G	0.32	0.24	intron-variant, downstream-variant-500B	Eml1, Gm33385	Mm_Celera	12:108400221	CAATTTGGCTTCTTT[A/G]CTGTCTGGTTTCAGT	68519
rs46112871	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108436207	TAAATGGTTCCCTCC[A/G]GGACCCTTTTGAGAA	68519
rs46120820	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108417016	CTCGTCCACATTTGG[A/G]AGTGTATTGTGTATG	68519
rs46124816	snp	A/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Eml1, Gm33385	GRCm38.p3	12:108412506	ATACATTCTGTTAGC[A/T]GGCTGTGTTCTTAAT	68519
rs46126106	snp	A/G	0.497041	0.0383476	intron-variant	Eml1	GRCm38.p3	12:108390466	AGAAATGCCCTTGTA[A/G]TAATAATAATAAAAA	68519
rs46143072	snp	C/T	0.396694	0.202437	intron-variant	Eml1	GRCm38.p3	12:108389386	ATTGGCCTCTAAGTC[C/T]GCATTTGCGGCCTCT	68519
rs46144704	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108433750	GTCAGTGCCGTGGGG[A/G]GGAACAGAGTATGCA	68519
rs46145895	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108436131	CCGTTCTACTTGGTC[A/G]CTGTGACTTTAAACA	68519
rs46150418	snp	A/G	0.497778	0.0332592	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108405917	TGTGTAGAAGAGGCC[A/G]TGGGCTTCGATCCTT	68519
rs46154127	snp	A/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108378321	CTCTTGGGTGTCACT[A/G]ACGGCACTGAAAGCC	68519
rs46155105	snp	A/G			intron-variant	Eml1, Gm33385	Mm_Celera	12:108406502	GCACCCCTCCCCCCC[A/G]GTCTCCTTTCTAATC	68519
rs46161371	snp	A/T	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108381330	GGTGAGGCTCTCAGG[A/T]TTAGACAGCTACGTG	68519
rs46161394	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108458675	GTAGTGTGTGTGTGT[A/G]TGTGTACATGGAGGT	68519
rs46165592	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108481588	GCCACCAATAGCAAA[C/T]CAGTGGTGGGGGAGG	68519
rs46166029	snp	C/T	0.32	0.24	intron-variant, upstream-variant-2KB	Eml1, Gm33385	Mm_Celera	12:108412106	TCTAACTCCCAAGCA[C/T]CCAGAGGGTCTAGTC	68519
rs46167695	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	Mm_Celera	12:108415340	ATGTTTACAGGCCCA[A/G]GATTTCTCAATGTGA	68519
rs46169348	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108463987	CCTTTCTGGAGGTTC[C/T]ACCCAGAAAGCCCAC	68519
rs46183782	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108502193	AACAGCTCTGGGTTC[C/T]GTGAGAGACCCTGCC	68519
rs46195044	snp	G/T			intron-variant	Eml1	Mm_Celera	12:108471756	GCTTTTAGAATTGAA[G/T]TCATCTGTGCAGGTT	68519
rs46198714	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108378289	TTGCTTTCGAGGTTG[A/G]CACTCATGAGAATGG	68519
rs46253029	snp	A/G	0.391111	0.206368	intron-variant	Eml1	Mm_Celera	12:108398714	AGCTTTGATGGTCAC[A/G]AAGTCCAGCACCCAG	68519
rs46272626	snp	A/G	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108386033	CAGAGTCAGGACATC[A/G]TCTTACCTCTGTGCA	68519
rs46274801	snp	C/T			intron-variant	Eml1, Gm33385	Mm_Celera	12:108406494	CCCACCCCGCACCCC[C/T]CCCCCCCAGTCTCCT	68519
rs46275316	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108500664	TTTGCCATTCTATCA[A/G]GGAGGGCAAACTTTA	68519
rs46280371	snp	A/G	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108417157	CTCCAGGAGAGGAGG[A/G]TACCGACGTCAGAGA	68519
rs46286412	snp	A/C	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108385301	AGGCAGGTCAGGAGC[A/C]ATAGGCAGGCGCTGT	68519
rs46289550	snp	C/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108386096	TGATGGCTCTGGCTA[C/G]CACACCCGGCCATGT	68519
rs46311931	snp	G/T			intron-variant	Eml1	Mm_Celera	12:108430821	TTTAAAAACACATGT[G/T]GAGTGGAAAACCATA	68519
rs46344406	snp	G/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108414732	TGACCTCTACCCACA[G/T]GTTTGGACTCTGTGT	68519
rs46352162	snp	A/T	0.32	0.24	intron-variant, upstream-variant-2KB	Eml1, Gm33385	Mm_Celera	12:108413602	GTTTAAAAAAGATTT[A/T]TCTACTTTATTGAAT	68519
rs46357765	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108399159	CATGTCCTTACTGGC[C/T]ATGATGGAGGCTCAG	68519
rs46375052	snp	A/G	0.42	0.183303	intron-variant	Eml1	Mm_Celera	12:108415807	TGTCTTGGTTGGTGC[A/G]TCTCTGACTCCTGAC	68519
rs46378615	snp	G/T			intron-variant	Eml1	Mm_Celera	12:108462921	AATCTGGGCCTGTGC[G/T]CTGCATCTGAAGCTC	68519
rs46381022	snp	A/T	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108379618	ATTTGGATTGCTTGG[A/T]TCTTCACTATGAAGC	68519
rs46385391	snp	A/G	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108378591	AGCATGTCACATGAC[A/G]TACATGAAGGCAGAG	68519
rs46391034	snp	C/T	0.497778	0.0332592	intron-variant, upstream-variant-2KB	Eml1, Gm33385	GRCm38.p3	12:108412359	CTGACACACAACAGG[C/T]ATGGTAAGTTCCAGG	68519
rs46398639	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108492942	AAATCACTAGATTGG[A/G]GAATAGGGACTCTTC	68519
rs46399340	snp	C/T	0.426035	0.177515	intron-variant	Eml1	GRCm38.p3	12:108416808	CACCATCAATATCAA[C/T]AATAAAGTCAATGAG	68519
rs46399463	snp	G/T			intron-variant	Eml1	Mm_Celera	12:108529571	AACATCACCGTCGTC[G/T]ATCTGCTGACAGATG	68519
rs46403512	snp	A/G	0.391111	0.206368	intron-variant	Eml1	Mm_Celera	12:108384864	CCAGGGTGAAGGATC[A/G]TGGGAGTGGGAGGTA	68519
rs46411391	snp	C/G	0.489796	0.070696	intron-variant, downstream-variant-500B	Eml1, Gm33385	GRCm38.p3	12:108400263	ACCTCGTGACCCACA[C/G]TGCCTCAATAGGAAT	68519
rs46414831	snp	C/G	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108398818	GTGGGACAGAGAGGA[C/G]TTTATATAAATCAGC	68519
rs46439057	snp	A/G	0.391111	0.206368	intron-variant, synonymous-codon	Eml1, Gm33385	GRCm38.p3	12:108401047	CTGTGTTGACTAGGA[A/G]CCAAAAGAGGGGGAT	68519
rs46445071	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108430884	CATCCTTCTTTATTC[C/T]GCTAGCTTTTTGGAA	68519
rs46472271	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108374947	GACACTGTGAAAGGG[A/G]CAAAGAGGACCCAGG	68519
rs46481004	snp	A/G	0.391111	0.206368	intron-variant	Eml1	Mm_Celera	12:108387982	AGGGAGCTGTGCATG[A/G]GGACCACCAAGCTGG	68519
rs46498192	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	Mm_Celera	12:108380775	ATGATGATTACATTG[A/G]TAGATGAATGGATAA	68519
rs46531653	snp	A/C			intron-variant	Eml1	GRCm38.p3	12:108500129	CGCTCTTCGAAAATC[A/C]AAATCTTTATACAAA	68519
rs46532163	snp	A/G	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108378356	CATGCTCAGTTTGCT[A/G]TGGAAAACACAAACG	68519
rs46547102	snp	A/C	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108375802	CGTAGGGCCTCAGCA[A/C]ATGGTCACTTGGAAT	68519
rs46548516	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108390319	GCTGGCTTCCATACA[C/T]GTATAGGCATATACA	68519
rs46566712	snp	C/T	0.497778	0.0332592	upstream-variant-2KB, intron-variant	Eml1	GRCm38.p3	12:108421754	CCATCCACCGATGCC[C/T]GAGTCTTTCTTTTGT	68519
rs46569681	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108462258	ATGTGCCATGGCATG[C/T]ATGAGTGCACACACA	68519
rs46580245	snp	C/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108381804	AAGAGACAGTGCGGC[C/G]CGTGAGGCTTGGAAC	68519
rs46584193	snp	A/C	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108393590	CCCAAGGAACCTGTG[A/C]GCATGTGTGGGTCCT	68519
rs46590968	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108462371	GGTTTTTATTGCTAT[A/G]AGAAAACACCATGCT	68519
rs46608724	snp	A/T	0.497778	0.0332592	intron-variant, downstream-variant-500B	Eml1, Gm33385	GRCm38.p3	12:108400210	CCATGGTTCCACAAT[A/T]TGGCTTCTTTGCTGT	68519
rs46616253	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108374053	GCACTTAGCACCTTC[C/T]GGACATACAAAGTGA	68519
rs46625661	snp	C/G			intron-variant	Eml1	GRCm38.p3	12:108378339	GGCACTGAAAGCCCA[C/G]GCATGCTCAGTTTGC	68519
rs46627211	snp	A/T	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108387187	CTATATTCTGGGCCA[A/T]AAAGGTCACAGGTGG	68519
rs46630755	snp	G/T			intron-variant	Eml1	Mm_Celera	12:108449426	GCACAGTGTGCCTGC[G/T]TGTGATATATGTATT	68519
rs46634062	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108458231	CATGGCATCTGGCTC[A/G]AGACACGGAACACAC	68519
rs46641197	snp	A/C			upstream-variant-2KB	Eml1	Mm_Celera	12:108370513	GAGGGGACTCGGTTG[A/C]CTCTTAGTCACGCAT	68519
rs46645075	snp	A/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108417550	GATATTTCTGCACAC[A/T]TGGAAGCTTCAGGCA	68519
rs46676169	snp	A/G	0.244898	0.249948	intron-variant	Eml1, Gm33385	Mm_Celera	12:108402357	CATTGAGATACCCGA[A/G]TAATTATTGTATTAT	68519
rs46680185	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108390203	AGGCAGACATAGGAC[A/G]GTCACTGGAGCTTCC	68519
rs46688970	snp	A/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108387277	CACCTGGTGCCATGC[A/G]ATCTGTACTTCTCCT	68519
rs46701201	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108481838	TTGGCCAGACAAGGC[A/G]GCCCAGTTAGGAGAA	68519
rs46702105	snp	A/G	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108399225	TCTCCTACAGCATTG[A/G]TGTGACAGAAGCTTG	68519
rs46703339	snp	A/G	0.489796	0.070696	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108401554	GTCTGTGGCCAAGAT[A/G]CTGTGCTTGGAGAGC	68519
rs46711878	snp	C/T	0.48	0.0979796	intron-variant, utr-variant-5-prime	Eml1, Gm33385	Mm_Celera	12:108411658	GGTCTGCTCTGTCCA[C/T]GTGGGTCCCTCCCTG	68519
rs46717854	snp	C/T	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108381805	AGAGACAGTGCGGCG[C/T]GTGAGGCTTGGAACA	68519
rs46724857	snp	G/T	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108380445	AGGAAGAAATGACAA[G/T]GTGTCCAATAAGTGA	68519
rs46734405	snp	A/C	0.391111	0.206368	intron-variant	Eml1	Mm_Celera	12:108384839	GCTCTGTCCCAGCCT[A/C]AGTCTGTATCCAGGG	68519
rs46747607	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108417397	TAGATGCTAACACCG[A/G]CCTTTGAGGCAGGGA	68519
rs46777205	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108481602	ATCAGTGGTGGGGGA[A/G]GCGGCGGAGATATAG	68519
rs46777916	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108373154	GCAACAGATCCAGGA[A/G]GCTCAGTGGAATCTC	68519
rs46785141	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108481830	TGCAGGACTTGGCCA[A/G]ACAAGGCAGCCCAGT	68519
rs46795160	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108392511	ACTCAGCTTGGCATC[C/T]GCACGGTCACCACTG	68519
rs46809465	snp	C/G/T	0.48	0.0979796	intron-variant, utr-variant-5-prime	Eml1, Gm33385	GRCm38.p3	12:108411309	GATGACTGTGTTGTA[C/G/T]TCTGTATTTGTGTGT	68519
rs46810517	snp	A/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108398956	TATCTCATAAACTTT[A/T]AAAAATTATAGCATC	68519
rs46811567	snp	A/T			intron-variant	Eml1	Mm_Celera	12:108508569	CTTCATTTTAAAAAA[A/T]ATGTTCATACCAGAC	68519
rs46814763	snp	A/G	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108378183	GTCTAAATAAGCACC[A/G]GAAGTCTAAATAAGT	68519
rs46830164	snp	A/C/G			intron-variant	Eml1	GRCm38.p3	12:108436058	GGAAAACTCTGAAAA[A/C/G]TCCCTCTCCACAGGA	68519
rs46849570	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108506998	TATTCAGCTTACACT[C/T]CCACACTGCTGTTCA	68519
rs46870146	snp	A/C			intron-variant	Eml1	Mm_Celera	12:108481829	CTGCAGGACTTGGCC[A/C]GACAAGGCAGCCCAG	68519
rs46879578	snp	A/C	0.459184	0.136902	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108403501	CTGTGTACAGGCGGG[A/C]CGGGGTATCCACTTA	68519
rs46879655	snp	C/T	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108378658	TAGTAGTAGTAGTAG[C/T]AGTAATTATTTCCCT	68519
rs46881959	snp	C/T	0.345679	0.230967	intron-variant	Eml1	Mm_Celera	12:108416302	GTCATTAACAGCCGA[C/T]GATCCGTTCCCTCTC	68519
rs46882170	snp	C/T	0.497778	0.0332592	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108406002	CTACTGTTCTGGGAG[C/T]TTCACTCAGTTTGTC	68519
rs46884774	snp	C/T	0.497778	0.0332592	intron-variant, upstream-variant-2KB	Eml1, Gm33385	GRCm38.p3	12:108413503	TAAATGGAGGAAGTC[C/T]GAAGTCCTGTGAGAT	68519
rs46894282	snp	C/T	0.32	0.24	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108408332	ACACGTGCACGCATG[C/T]TCATGCAATGCCACT	68519
rs46932423	snp	A/C	0.391111	0.206368	intron-variant, synonymous-codon	Eml1, Gm33385	Mm_Celera	12:108401377	CCCTGGCTTGCGGAG[A/C]GTGTGGACAGGTGGA	68519
rs46933374	snp	G/T	0.391111	0.206368	intron-variant	Eml1	Mm_Celera	12:108380571	GGCAGGGACACAGAG[G/T]TTGACTGTACTTTGC	68519
rs46933718	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108507597	TCACTCTCCTGAATG[C/T]TGGGGTTATAGGTAT	68519
rs46933965	snp	A/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108376882	AGCAGTTACAGGTGG[A/T]AGTCCTGGATGGGTT	68519
rs46936506	snp	A/G	0.497778	0.0332592	upstream-variant-2KB, intron-variant	Eml1, Gm33385	GRCm38.p3	12:108409013	GCCCTGACTGCTGTT[A/G]CTAACCTCAGGGCCT	68519
rs46936748	snp	A/C			intron-variant	Eml1	Mm_Celera	12:108502356	CACACATATAAATAA[A/C]TAAATACTTTTTTTT	68519
rs46947714	snp	A/T			intron-variant	Eml1	Mm_Celera	12:108502543	ACAAACAGTCAGTCA[A/T]TGGGAGCTCAGATAA	68519
rs46971081	snp	A/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108396403	TAGACTTGAGGGGCG[A/T]GTTAAGTCAGGCCAG	68519
rs47018253	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108380550	GTTGGATCCACAGAT[A/G]CAGCAGGCAGGGACA	68519
rs47023366	snp	C/T	0.391111	0.206368	intron-variant	Eml1	Mm_Celera	12:108386168	GTACATATTTTTGTG[C/T]TCCACTAGCACTGTC	68519
rs47040534	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108502594	AGGCAGCAGGCATAG[C/T]GACTAGACCCCTACC	68519
rs47050269	snp	A/C	0.497778	0.0332592	intron-variant, upstream-variant-2KB	Eml1, Gm33385	GRCm38.p3	12:108413354	TGCAGGATTTCTGAG[A/C]ATGTGTGGGCTTTGT	68519
rs47054453	snp	A/T	0.493827	0.0552116	intron-variant	Eml1, Gm33385	Mm_Celera	12:108403096	AATATGCTCAGTACA[A/T]TTAAGGCAGTTCCCA	68519
rs47068757	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108518260	TGAGCACATACATAC[A/G]TGCAGACAAACATTC	68519
rs47099022	snp	C/T	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108378398	TAGTGGTACAAGGTC[C/T]TCATTCATGCCAAGT	68519
rs47107240	snp	C/G	0.396694	0.202437	intron-variant	Eml1	Mm_Celera	12:108417767	CACAGTGTAATGCTC[C/G]CTATTGATGCTAAGA	68519
rs47110159	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108374019	AAAATAGAGACATGC[C/T]CCATTTCTCATTGGG	68519
rs47111352	snp	C/T	0.408163	0.193609	intron-variant	Eml1	GRCm38.p3	12:108385065	GTGTCAAACCCAAGT[C/T]TGCACTAGGCCAGGG	68519
rs47122335	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108450718	TGAACCTGGGGTAGG[A/G]CACGAAGTCTAAAGC	68519
rs47156207	snp	A/G	0.142012	0.225474	intron-variant, upstream-variant-2KB	Eml1, Gm33385	Mm_Celera	12:108412298	GAGATGGGAAGTGGG[A/G]GCAAGCCCAAAGAAC	68519
rs47183734	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108389701	CCACCCTCCCTGCAA[A/G]GTCAGGCCCTTAAGT	68519
rs47184911	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108481668	TAAGACCCTGGGTTT[C/T]GTTTTGTTTTGTTTA	68519
rs47205395	snp	G/T			intron-variant	Eml1	Mm_Celera	12:108500328	TTCCTTCTGGTTTGC[G/T]GGCGACAACCTATGC	68519
rs47211241	snp	A/C			intron-variant	Eml1	GRCm38.p3	12:108508393	CTTAATTAACAGTTA[A/C]AGGTTAATTAATTTT	68519
rs47226422	snp	A/G/T			intron-variant	Eml1	GRCm38.p3	12:108507629	AGCTTACGCTCCCCT[A/G/T]AAGAGCTAGTGGTCA	68519
rs47252799	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108498843	GGGGGCTGGAGAGAT[A/G]GCTCAGTGGTTAAGA	68519
rs47260852	snp	A/T			intron-variant	Eml1	GRCm38.p3	12:108501316	TTCTGTTGATGGACA[A/T]ATGGCTGGTTCTAGC	68519
rs47284789	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108500542	ATCCTAGGGTGTATG[C/T]TCACTTTGATCGTTA	68519
rs47286659	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108435777	TGTGGGGCGCCTTTG[A/G]TTTAATCCTCAGTGC	68519
rs47300200	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108502155	GGGACCCTCTGGAGC[A/G]GCCGGCCAGCCACAC	68519
rs47302310	snp	A/C	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108389745	GCCCCCTTAGTAAAA[A/C]GACTAAGCCTGGGCC	68519
rs47308012	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108461891	CAATAACAGCCTGAC[A/G]TATGTGCTGATGTCC	68519
rs47312958	snp	C/G	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108396793	CTTTATGTGCACACC[C/G]ATGGCACACGATCGG	68519
rs47319606	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	Mm_Celera	12:108416527	GGGACTTCTCACTCT[A/G]TACTCACTTCCTGTC	68519
rs47356620	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108460745	TGGATCTCTGAGTTC[A/G]AGGCCAACCCGGTCT	68519
rs47385627	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Eml1, Gm33385	GRCm38.p3	12:108413150	ATGTAGAGGATCCTT[C/T]AAATAACACAGCGTC	68519
rs47385977	snp	C/G/T			intron-variant	Eml1	GRCm38.p3	12:108377430	AGCCACAAATAACTG[C/G/T]GTGCGTGTGCCCTCC	68519
rs47397089	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108416849	GCATCAATAAGGACA[C/T]GGTATCCTGGGTGCT	68519
rs47411584	snp	A/G	0.497778	0.0332592	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108402333	GGTCCAAGCCAATGT[A/G]CAGAGATGCATTGAG	68519
rs47412896	snp	A/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108377216	ACCTCCTGCTATCTC[A/T]CTGGGCAGTATTCCT	68519
rs47413609	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108448262	GAATCACAAGACATT[A/G]TGAGCCACCTGCTGT	68519
rs47427279	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108415610	CCAGCTGCAAATTGC[C/T]TTCCGTTTTCCAATT	68519
rs47484282	snp	A/C	0.345679	0.230967	intron-variant	Eml1	GRCm38.p3	12:108389801	GAGCCCCTGAGGTGC[A/C]GAGAGAGAGCCCACT	68519
rs47484908	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108483835	AAGGTTCAGTTACCA[A/G]CACCAACATGGTAGC	68519
rs47486806	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108507004	GCTTACACTCCCACA[C/T]TGCTGTTCATCACCA	68519
rs47490906	snp	C/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108380271	ACCCTTCCATAACCC[C/G]GAGGATACCGGGATC	68519
rs47524355	snp	A/G	0.124444	0.216185	intron-variant	Eml1, Gm33385	Mm_Celera	12:108410810	GACATGAGAGGCACA[A/G]TCTGCTCATTGTCTG	68519
rs47529589	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108506905	CTTAGTGAAAATCAT[C/T]AAAATTGGTGTCTTA	68519
rs47532482	snp	C/T	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108399556	TGATTTTCGGCATGG[C/T]GTTCTTCTTTTCCAC	68519
rs47538602	snp	C/T	0.497041	0.0383476	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108402354	ATGCATTGAGATACC[C/T]GAGTAATTATTGTAT	68519
rs47541440	snp	A/G	0.152778	0.230321	intron-variant	Eml1	Mm_Celera	12:108394321	ATGTCAGCGATCTTC[A/G]CTCTTAAGTGCCATT	68519
rs47567928	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108449263	GCTGACAGAGAGACA[C/T]CTGTTGACGCCTTCA	68519
rs47567930	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Eml1, Gm33385	Mm_Celera	12:108412003	AACAATGCAGCTTCC[A/G]TGGGGACACGGCCCA	68519
rs47571754	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108453650	AGCCCCGCAGAAGAC[A/G]GTCATCACTCTTTCC	68519
rs47573951	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108502220	TGCCTGCATATGTGC[A/G]ACAGGCATGACCAGG	68519
rs47591449	snp	C/T	0.391111	0.206368	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108405478	AACGTGGGCTAGCTC[C/T]GGCTATGCCTGTCTT	68519
rs47593846	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108495247	ACCGCAGGAGGTTTG[C/T]CTTGCTGTCTTTTTT	68519
rs47618176	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108381644	AAAAATCAATTTCTG[A/G]AAGATTTGGTTCCAG	68519
rs47621109	snp	C/T	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108378044	ATCTACCTTGTGGCC[C/T]GTCAGCTTGACAGCA	68519
rs47626767	snp	C/T	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108392764	GAAAGAGCTGTAAAC[C/T]TAACCGGCTGCAATC	68519
rs47648114	snp	A/G	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108386761	AGTTTGGCCACCCGG[A/G]GACTTTGCTGCAGTG	68519
rs47650621	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	Mm_Celera	12:108417997	TTTTATATTTTAATA[C/T]CAGGCCTGGGAGTGG	68519
rs47662191	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108377147	CTGCCTTCTTCAGGG[A/G]CCCTTCCCCGAGATT	68519
rs47665028	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108499656	CATTAACCCTTTCCC[C/T]GCCATGTTGCTTTAC	68519
rs47668373	snp	A/G	0.391111	0.206368	intron-variant	Eml1	Mm_Celera	12:108381958	CACAGCAGAGTCGGG[A/G]TCCATGGTGAACATC	68519
rs47669202	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108435197	GAAGCCTTACTTATG[C/T]CTGAATTCTAAGATG	68519
rs47682151	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108414062	GGCCAACACACAGAC[A/G]TGTTTACACATCGAC	68519
rs47709023	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108397114	GACAACTGTCTTCCT[C/T]AGCAATCCAGCTTTG	68519
rs47712250	snp	A/C/T	0.396694	0.202437	intron-variant	Eml1	GRCm38.p3	12:108389779	GCTGACCTGAGGTGC[A/C/T]GAGAGAGAGCCCCTG	68519
rs47712448	snp	A/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108390397	AGATAGGTAGATGGA[A/T]AAAGGGCTTGAGTTT	68519
rs47713670	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108471760	TTAGAATTGAATTCA[C/T]CTGTGCAGGTTGGTT	68519
rs47751819	snp	A/G	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108388144	GAAGTTAGTGTCCCA[A/G]GGCTCAGTCCCGGGT	68519
rs47753748	snp	A/T			intron-variant	Eml1	GRCm38.p3	12:108373543	TGCCCAAGGTCATCG[A/T]CTGCTGTAGGGTCTA	68519
rs47786286	snp	A/G	0.497778	0.0332592	intron-variant, upstream-variant-2KB	Eml1, Gm33385	GRCm38.p3	12:108413558	AGGTACAAGCTCACT[A/G]TTGTCACATCTGTTG	68519
rs47786707	snp	A/C	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108376948	CTTTCGGCTTATAGT[A/C]TCCACAGTATGCAGG	68519
rs47798789	snp	A/T	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108396150	AGCCCAGTAGTGATG[A/T]TGAGGACTGGAGGCC	68519
rs47813702	snp	A/G	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108381692	AGAGCTAGGGGAGAC[A/G]TTAGCTGTTGATGGT	68519
rs47840938	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108460770	CGGTCTATAGAGTGA[A/G]TTTGAGAACAGTCAG	68519
rs47841049	snp	C/T	0.444444	0.157135	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108403840	GCTCTTCACCATTGA[C/T]ACTCTACTGGACAAC	68519
rs47852165	snp	A/C			intron-variant	Eml1	Mm_Celera	12:108481865	AGAACGGGATCCAGA[A/C]TCTGTTATTTTCAGT	68519
rs47877944	snp	A/G	0.48	0.0979796	intron-variant, utr-variant-5-prime	Eml1, Gm33385	Mm_Celera	12:108411640	TCTCTGCTAGTTAGG[A/G]ATGGTCTGCTCTGTC	68519
rs47885779	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108373658	TTGCCTTCAGCCACA[C/T]CCCTTCTTTTCAGAG	68519
rs47887862	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108535379	GGGCAGAGCGGAGGG[A/G]GTCGTGGGGGGGGGG	68519
rs47905580	snp	A/C	0.473373	0.11227	intron-variant	Eml1	GRCm38.p3	12:108384802	GTCCTGGAAGTGTAG[A/C]GAAGTTCTTAGAGGA	68519
rs47915122	snp	A/G	0.231111	0.249285	intron-variant	Eml1	GRCm38.p3	12:108382138	TTGAAACAAATTTCA[A/G]TGAAAACTTAACAGT	68519
rs47930791	snp	A/T			intron-variant	Eml1	Mm_Celera	12:108433583	CCTGTTGGGACGGCT[A/T]AGCAATAGCACTTAG	68519
rs47934257	snp	C/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108417835	CGTGGGTATAATATA[C/T]ATTTACTTACATTGT	68519
rs47956794	snp	C/T	0.497778	0.0332592	upstream-variant-2KB, intron-variant	Eml1	GRCm38.p3	12:108422000	CATCTGGAGCCCTTC[C/T]GTCTCCACCCACAAC	68519
rs47966775	snp	C/T	0.497778	0.0332592	intron-variant, upstream-variant-2KB	Eml1, Gm33385	GRCm38.p3	12:108413528	TGAGATTCATTGGTG[C/T]GGAGTCCCTAGGATA	68519
rs47967855	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108450521	GGAATTCCAGGGGAG[A/G]ACCCGCAGCTCAGCT	68519
rs47968242	snp	C/G	0.18	0.24	intron-variant	Eml1	Mm_Celera	12:108395332	TCCCTCTCCTCCGCC[C/G]CAGGAGCAGGAAGGA	68519
rs47968950	snp	A/G	0.244898	0.249948	intron-variant	Eml1	Mm_Celera	12:108378550	AGAAGTGATGGGCAT[A/G]GCTATGCTGGCATCT	68519
rs47985974	snp	C/G			intron-variant	Eml1	Mm_Celera	12:108372919	GCTTTAGGCCAGCCT[C/G]AGGTACACAGAGAGA	68519
rs47987205	snp	A/G	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108398200	TGGTATTTGTCAGAT[A/G]TCTGGGGCTTGACAG	68519
rs48008287	snp	A/C	0.48	0.0979796	intron-variant, utr-variant-5-prime	Eml1, Gm33385	Mm_Celera	12:108411543	AGTGGCTCAGCTGCT[A/C]CCCTGAGAGACTCTT	68519
rs48010320	snp	A/G	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108380281	AACCCCGAGGATACC[A/G]GGATCTAAGGATTCT	68519
rs48012724	snp	A/G	0.231111	0.249285	intron-variant	Eml1	Mm_Celera	12:108374597	GGCTCTGACATCCTC[A/G]CAGGGTCTCCTGATC	68519
rs48017290	snp	C/T	0.124444	0.216185	upstream-variant-2KB, intron-variant	Eml1	Mm_Celera	12:108422314	TCGGCTCAAGCATTC[C/T]TTTCTCTCTAGCTTT	68519
rs48033243	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108507758	TCTGCCACTCAAGGA[A/G]TAAAGTCGAGCTCTG	68519
rs48039108	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108535394	GGTCGTGGGGGGGGG[A/G]GGAGTGGGATGTGAG	68519
rs48053654	snp	A/G	0.489796	0.070696	intron-variant	Eml1	GRCm38.p3	12:108378340	GCACTGAAAGCCCAC[A/G]CATGCTCAGTTTGCT	68519
rs48072200	snp	A/G	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108377772	ATATGTATGTGTGGT[A/G]CTCAGGAGACAGCTT	68519
rs48077477	snp	C/T	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108394067	TGCTTTATTGGCCTT[C/T]CCAGATGAAGCCTAA	68519
rs48080267	snp	C/T	0.132653	0.220748	intron-variant	Eml1	Mm_Celera	12:108379486	GGTGTAAGGTGATGG[C/T]TTTCCGTTATTTCTG	68519
rs48081969	snp	G/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108415663	GCGAGCTCATTTGAT[G/T]GGATGCAAATTGCTA	68519
rs48082705	snp	A/T			intron-variant	Eml1	Mm_Celera	12:108377424	CAGGTTAGCCACAAA[A/T]AACTGCGTGCGTGTG	68519
rs48083354	snp	C/T	0.32	0.24	intron-variant	Eml1, Gm33385	Mm_Celera	12:108410890	AGGGAGGACCAGGCT[C/T]GGTGTCTGTCTTCTG	68519
rs48085287	snp	A/T	0.497778	0.0332592	intron-variant, downstream-variant-500B	Eml1, Gm33385	GRCm38.p3	12:108400121	AGAGCATCTGGGTCT[A/T]AGAGAGGTGAGGCAG	68519
rs48093158	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108430882	GTCATCCTTCTTTAT[C/T]CTGCTAGCTTTTTGG	68519
rs48101256	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108461609	TCTTTACTGGCTTGC[C/T]TCCCCTGGCTTGCTC	68519
rs48107968	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108458924	CTGCCTCCTGCTTGT[A/G]GATCAGATACAAACT	68519
rs48111262	snp	A/C	0.497778	0.0332592	intron-variant	Eml1	Mm_Celera	12:108375701	TGGAGGAGATGCCCA[A/C]ATACTCTGCTATTCT	68519
rs48117571	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108507384	TTCTGAGTTCGAGGC[C/T]AGCCTGGTCTACAAA	68519
rs48123653	snp	C/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108386023	AGGGCAATGCCAGAG[C/T]CAGGACATCGTCTTA	68519
rs48146458	snp	C/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108378370	TGTGGAAAACACAAA[C/T]GGCAGTGGTTCGTAG	68519
rs48151485	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108535681	CTGGGAAAGGCAGGG[A/G]GGAGAGGTAGCCAGT	68519
rs48153891	snp	C/T	0.48	0.0979796	intron-variant	Eml1	GRCm38.p3	12:108393220	CTCCCAGAGTTGGTG[C/T]AATGCCCTGTGCACA	68519
rs48164265	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108394407	ATTTACCGTATGGTA[C/T]GTGTGTGTGCGTACA	68519
rs48168998	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108435928	CCTAGAAAAACATAA[C/T]CATGGGAAGACACAT	68519
rs48191527	snp	C/T	0.142012	0.225474	intron-variant	Eml1	Mm_Celera	12:108376002	CTCTGGGCCCTGAGG[C/T]TCTAATTCAGGCTGC	68519
rs48195660	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108466856	TTGTATTTTAAATTA[C/T]GTCCAAGTGTATGTA	68519
rs48197122	snp	C/T	0.473373	0.11227	intron-variant	Eml1	GRCm38.p3	12:108394059	AGGGTGCCTGCTTTA[C/T]TGGCCTTTCCAGATG	68519
rs48218447	snp	A/G	0.473373	0.11227	intron-variant	Eml1	Mm_Celera	12:108384796	CTAACTGTCCTGGAA[A/G]TGTAGAGAAGTTCTT	68519
rs48230575	snp	C/T	0.444444	0.157135	intron-variant	Eml1	GRCm38.p3	12:108417628	TTCTTTTGGCAAGGG[C/T]ATCTAGGATTGAAAA	68519
rs48242231	snp	A/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108395099	GCGGCGAGGAGCACC[A/T]GATGGAACAGTCTGT	68519
rs48246231	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108389932	CTCTGTCCTCCCTAT[C/T]CCCAGGTTCTCTTCA	68519
rs48248392	snp	A/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108376906	ATGGGTTCTCTCATT[A/G]CTGTCCTTTATCATA	68519
rs48267791	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108443382	TCTCACTGAGTCCGT[C/T]GCTTCTCCTCCAGTC	68519
rs48275188	snp	C/T	0.497778	0.0332592	upstream-variant-2KB, intron-variant	Eml1	GRCm38.p3	12:108421424	CCATCGCTCCGATAC[C/T]AACACCTCGCCAACT	68519
rs48281647	snp	A/G	0.391111	0.206368	intron-variant	Eml1	Mm_Celera	12:108385382	GTGGCTAAGGCCACC[A/G]GATACATTTGCTGAA	68519
rs48290956	snp	C/T	0.444444	0.157135	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108404114	CCTGAAAAGGCTGCG[C/T]GTCCACTGGGAGTCC	68519
rs48290979	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108500060	TTTTCTATTAGGAAG[A/G]AAATTACCTCATAGC	68519
rs48298378	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108481706	TATTTATTCACTTTA[C/T]GTCTCAATATCAGCA	68519
rs48305748	snp	A/G	0.391111	0.206368	intron-variant	Eml1	Mm_Celera	12:108417810	TTCATTTTACAGAGC[A/G]TTTATCATGCGTGGG	68519
rs48325344	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108375876	ACAGGAAGCAGAGGG[A/G]TGGGGGTGGGGGAGG	68519
rs48364111	snp	C/G			intron-variant	Eml1	Mm_Celera	12:108444234	CATTGTGCTACCATA[C/G]CCAGACAGTTTTCTT	68519
rs48369448	snp	A/C	0.391111	0.206368	intron-variant	Eml1	Mm_Celera	12:108389105	TCTGTCCTGTGTGGT[A/C]ACTACAGTTTGGGCC	68519
rs48370992	snp	A/T			intron-variant	Eml1	GRCm38.p3	12:108500820	CATCTAGACAGCATT[A/T]TCTCAAGAATTTTCA	68519
rs48381111	snp	A/G	0.5	0	intron-variant	Eml1	GRCm38.p3	12:108384486	GTTACAGAGGGAGGC[A/G]GATGGAGCCAGGCTT	68519
rs48388442	snp	C/T	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108394585	CTGGCCCCTTTTGGA[C/T]CTTTTATGGAAACTC	68519
rs48410935	snp	A/G	0.336735	0.234472	intron-variant	Eml1	GRCm38.p3	12:108390524	TATTTTAAGAGTTAA[A/G]CCTAAATAAAGAGAT	68519
rs48423947	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108501012	GCAAAGAAGCAGTCA[A/G]TCCTGGGACGAATTC	68519
rs48437613	snp	C/T	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108420045	CCTTTAAGAGATTTT[C/T]TTTCCTTGAACATCT	68519
rs48441148	snp	C/T	0.391111	0.206368	intron-variant	Eml1	Mm_Celera	12:108388414	GTCAGAGATTAGGAC[C/T]GGTTTCTCTGAGCTC	68519
rs48451532	snp	C/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108378616	GCAGAGGGTGGGTGT[C/G]TGAGTGAGTAGTAGT	68519
rs48483303	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108507753	GATTGTCTGCCACTC[A/G]AGGAATAAAGTCGAG	68519
rs48497147	snp	G/T	0.497778	0.0332592	intron-variant, upstream-variant-2KB	Eml1, Gm33385	GRCm38.p3	12:108413456	ATCAGCAGCCCTACA[G/T]ATGGAAGGAAGGAGA	68519
rs48515642	snp	C/T	0.444444	0.157135	intron-variant	Eml1	Mm_Celera	12:108386677	ACAGACACTCCCCGG[C/T]GGAATGCCGACGGGC	68519
rs48516377	snp	C/T	0.497778	0.0332592	upstream-variant-2KB, intron-variant	Eml1, Gm33385	GRCm38.p3	12:108409067	CCAGAGTCTGATTTC[C/T]GATGGTGCCTGTGGA	68519
rs48533413	snp	C/T	0.497778	0.0332592	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108404204	TTGCATAATATTTTC[C/T]CATCACCATGGAGAC	68519
rs48534353	snp	A/G	0.124444	0.216185	intron-variant	Eml1	Mm_Celera	12:108393469	CACCTCTTGCTCTGC[A/G]CCCTGTCAGCTAGTC	68519
rs48549009	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108391266	TCTAGAGCCTCTGAC[C/T]TGGGGCTGCTCCTCC	68519
rs48549242	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108499929	GGGGGAAAATCAAAC[A/G]TTCACAGAGAGAGAG	68519
rs48549683	snp	A/G	0.444444	0.157135	intron-variant, utr-variant-5-prime	Eml1, Gm33385	GRCm38.p3	12:108411438	AAACATATCATGGCC[A/G]GCATACCAGGGGACT	68519
rs48555106	snp	A/G			intron-variant	Eml1	Mm_Celera	12:108502043	CGGGTAAGACACATC[A/G]TGTGGCTGAGAATGT	68519
rs48558581	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Eml1, Gm33385	GRCm38.p3	12:108411889	AAAATGGAAACCAGT[C/T]CAGTAACATAAAGAG	68519
rs48564186	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108431023	CTCATGGGACACTTC[C/T]TTCAGGGGGCTTTGT	68519
rs48566510	snp	C/T	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108384092	GCTCCTGACAATGAG[C/T]CACCTGCTCCCTGGG	68519
rs48573039	snp	G/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108399274	CCAGAAGCTGTCAGG[G/T]CAGGAGAGATGCCAG	68519
rs48595805	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108507383	TTTCTGAGTTCGAGG[C/T]TAGCCTGGTCTACAA	68519
rs48609360	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108462425	GTTTAATTGAGCTAG[C/T]AGTTCCAGAGGGTTA	68519
rs48609550	snp	A/G	0.32	0.24	intron-variant	Eml1	Mm_Celera	12:108398878	ACCTTGACTGCCAGC[A/G]TCTTCCTCTGTCTCA	68519
rs48613162	snp	C/G	0.391111	0.206368	intron-variant	Eml1	GRCm38.p3	12:108380887	AATCATGTTACTCAA[C/G]ATAATATTGAGTCTA	68519
rs48635868	snp	A/G			intron-variant	Eml1	GRCm38.p3	12:108394408	TTTACCGTATGGTAT[A/G]TGTGTGTGCGTACAC	68519
rs48662162	snp	C/G			intron-variant	Eml1	Mm_Celera	12:108481583	CAGATGCCACCAATA[C/G]CAAATCAGTGGTGGG	68519
rs48665304	snp	A/T	0.497778	0.0332592	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108408486	GTGATTGTTTTTCAG[A/T]CACAGGCGACTTCTG	68519
rs48665861	snp	A/T			intron-variant	Eml1	GRCm38.p3	12:108373429	ACCCAGACACCTTCC[A/T]AGTCCTGGGTGTTTT	68519
rs48682023	snp	C/T	0.497778	0.0332592	intron-variant	Eml1	GRCm38.p3	12:108420810	TAGTTTGCTCTGGCC[C/T]TGGGCATTCCACTCG	68519
rs48687084	snp	C/T	0.497778	0.0332592	intron-variant	Eml1, Gm33385	GRCm38.p3	12:108405848	CTCCAGGGAAGCCAG[C/T]CAGGGAGTAGAGGAG	68519
rs48704264	snp	C/T	0.497778	0.0332592	upstream-variant-2KB, intron-variant	Eml1	GRCm38.p3	12:108421979	TGGTAACAGTTGAAT[C/T]AGCAGCATCTGGAGC	68519
rs48711351	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108448505	GTACCCGGAAAATAG[C/T]CATGAGTCACATTTG	68519
rs48724963	snp	C/G			intron-variant	Eml1	GRCm38.p3	12:108374509	TGGCTGCTCTGGATA[C/G]TCTCGTTGGGGGAGG	68519
rs48730613	snp	C/T			intron-variant	Eml1	GRCm38.p3	12:108384334	CATCTGATAGAGCAG[C/T]TGGGGACTGCAGCTG	68519
rs48732037	snp	G/T			intron-variant	Eml1	GRCm38.p3	12:108462373	TTTTTATTGCTATGA[G/T]AAAACACCATGCTCA	68519
rs48752867	snp	A/C			intron-variant	Eml1	Mm_Celera	12:108459049	CTCAAACTATAAGCA[A/C]GCCTCCAATTAAATG	68519
rs48759382	snp	C/G			intron-variant	Eml1	GRCm38.p3	12:108518470	CCTGAGACCGGTGGG[C/G]GTGGGGCACCCACAT	68519
rs48770718	snp	C/T			intron-variant	Eml1	Mm_Celera	12:108494885	GTGTGTGTGTGTGTG[C/T]GTGCACACGCGCACG	68519

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