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

Amph

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs3662659	snp	A/G	0.489796	0.070696	intron-variant	Amph	Mm_Celera	13:19048994	TGTGAAAATGTAACG[A/G]TACTTTATAACGATG	218038
rs3677044	snp	G/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19049114	ATATAATAAATTTAT[G/T]GCACATTTTCTTAGT	218038
rs3677588	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19049163	AAAGAGTTCTTTGCA[A/G]CCTCTATCACAGAGT	218038
rs3677592	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19049167	AGTTCTTTGCAACCT[C/T]TATCACAGAGTGTAG	218038
rs3691273	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19108103	CCTTCGAATAGAGTC[A/G]TTGATACAGCCAGTG	218038
rs3706716	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19108321	TACTGTTTTCTTGCG[A/G]TCACTTCTGGAGTTT	218038
rs4136930	snp	C/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19049204	TATGCATTGTTCTCT[C/G]TGTATTAAAGGCAGA	218038
rs6153182	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19044834	GAACTGGAGCTGAGC[C/T]CCCCACAGGCGTTAA	218038
rs6153704	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19044931	ATGCCACAGGATGTC[A/G]TAAGGCANATTTCTA	218038
rs6153717	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19044939	GGATGTCNTAAGGCA[A/G]ATTTCTAGAAGGCAA	218038
rs6153847	snp	A/G	0.32	0.24	intron-variant	Amph	Mm_Celera	13:19045020	ATATTAGGACACTTC[A/G]ACATCAACTACCAAA	218038
rs6166953	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19045086	TCAGATGGCTTCTTA[C/T]TTGTCTTCTNAAAAT	218038
rs6166971	snp	A/C	0.5	0	intron-variant	Amph	Mm_Celera	13:19045096	TCTTANTTGTCTTCT[A/C]AAAATGCTTCCTTTG	218038
rs6167514	snp	C/T	0.415225	0.187619	intron-variant	Amph	Mm_Celera	13:19045197	AAAAACTCTACTACA[C/T]TTCTGTCCATTGGAG	218038
rs6168069	snp	C/T	0.415225	0.187619	intron-variant	Amph	Mm_Celera	13:19045307	TATAACATCCTTGCA[C/T]TGCATATAATACAGT	218038
rs6168598	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19045364	TTATGAATTCTACTA[A/G]ACTGTCAGATGTTTT	218038
rs6289293	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19102624	TTTACATATCTAAAG[C/T]GGGGTCAATATTGCA	218038
rs6289882	snp	A/C	0.32	0.24	intron-variant	Amph	Mm_Celera	13:19102739	CTATTACTAACAACT[A/C]GNATTAAGCTGGACG	218038
rs6289884	snp	A/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19102741	ATTACTAACAACTNG[A/T]ATTAAGCTGGACGTG	218038
rs6289933	snp	A/G	0.484429	0.0868505	intron-variant	Amph	Mm_Celera	13:19102768	CGTGGGGGATGAAAT[A/G]ACAGTGACATTAAGC	218038
rs6289977	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19102801	CAGGATGCCTCTGGG[C/T]TAAAGAANCTTGNGT	218038
rs6289991	snp	C/T	0.244898	0.249948	intron-variant	Amph	Mm_Celera	13:19102809	CTCTGGGNTAAAGAA[C/T]CTTGNGTTTTAGGAA	218038
rs6290388	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19102814	GGNTAAAGAANCTTG[A/G]GTTTTAGGAACCCTG	218038
rs6291498	snp	A/G	0.5	0	intron-variant	Amph	GRCm38.p3	13:19103038	TACCGGGGGTGTGGG[A/G]AAACTCATGGGAGGT	218038
rs6328590	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19132091	TTACTCGAACAGTCC[C/T]GCGCTTCCATGCATA	218038
rs6328634	snp	A/G	0.493827	0.0552116	intron-variant	Amph	GRCm38.p3	13:19132109	GCTTCCATGCATACT[A/G]NAACATCACCTCCAA	218038
rs6328635	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19132110	CTTCCATGCATACTN[C/T]AACATCACCTCCAAG	218038
rs13481715	snp	C/T	0.393491	0.20472	missense	Amph	GRCm38.p3	13:19139173	TCTCTACCCACCAGG[C/T]CATCCCTTCTGTTGT	218038
rs29224605	snp	A/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19103402	ATCTACAAAGTTCCA[A/T]TTATTCTACATTCCT	218038
rs29224801	snp	A/G	0.375	0.216506	missense	Amph	GRCm38.p3	13:19139370	GCATCTGCAGGTGCT[A/G]TGGATGCCTCGCTGT	218038
rs29224802	snp	A/C	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19114655	GGGTCCTCCTTAACT[A/C]ATGATCTCTGCAGTG	218038
rs29225257	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19077161	GACTAGCACCTTTAT[A/G]AGTACCGAGATGGAT	218038
rs29225595	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19053078	GTTGAAGAGTCAAGA[C/T]AGGGGAGAATTAACA	218038
rs29226659	snp	A/G	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19134176	AGCCCACATAGAGAC[A/G]TATAGGAAATGATCA	218038
rs29226918	snp	A/G	0.5	0	intron-variant	Amph	GRCm38.p3	13:19138849	CTCCTGTTGCCCTGC[A/G]GCAATCAAAGTCAGT	218038
rs29227502	snp	A/G	0.487535	0.077957	intron-variant	Amph	GRCm38.p3	13:19103385	TGAATAAGAAAAAGC[A/G]TATCTACAAAGTTCC	218038
rs29227505	snp	A/C	0.408163	0.193609	intron-variant	Amph	GRCm38.p3	13:19138021	CAAAGTTTAAGATTC[A/C]GCACTGTGTTTATAT	218038
rs29227921	snp	C/G	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19137968	GGCTGGAAATGAAAA[C/G]GGACAGGGTAAGCCA	218038
rs29228135	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19069290	AAGTGTTTAATTTTA[C/T]CTCTGATTTTTTGTT	218038
rs29229489	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19139092	AGAGAAAGTGGGTGG[C/T]TGGGAGAAGACACTG	218038
rs29231183	snp	A/C/T	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19140204	GGCAGGTCCTCACCG[A/C/T]GTGACCTTCTGCTTT	218038
rs29232935	snp	A/G	0.497778	0.0332592	intron-variant	Amph	Mm_Celera	13:19096107	GGTAACCATGTTTCT[A/G]CTCCAGTTTGCACCC	218038
rs29233957	snp	C/T	0.415225	0.187619	intron-variant	Amph	GRCm38.p3	13:19114677	TCTGCAGTGCTCACA[C/T]AAGCTCTCAGAGCCT	218038
rs29233977	snp	A/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19106679	CCTTAACTATAGATA[A/G]CCCAGAATTTTCTGT	218038
rs29235057	snp	A/T	0.49827	0.0293608	intron-variant	Amph	Mm_Celera	13:19118073	CTGAAGAATGTTGTC[A/T]CTGGACAATGTGAGA	218038
rs29235173	snp	C/G/T	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19067656	TGATTGTTTTATGCC[C/G/T]CCCCTGTGAAGACTA	218038
rs29235361	snp	A/C	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19052979	AACTACTAACACGGG[A/C]TTGGCAACACAAATG	218038
rs29235365	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19138875	TCAGTATGTGCCAGG[C/T]CACATGGGCGGTCAT	218038
rs29236439	snp	A/G	0.475309	0.108333	intron-variant	Amph	Mm_Celera	13:19084008	AATGACACTGTTAAC[A/G]TTTCCTGAGACCCAG	218038
rs29236649	snp	A/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19140203	AGGCAGGTCCTCACC[A/G]CGTGACCTTCTGCTT	218038
rs29237058	snp	A/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19134580	GTACCAATTACTAAT[A/G]ATTTGTGCTGCTCAG	218038
rs29240458	snp	A/C	0.5	0	intron-variant	Amph	Mm_Celera	13:19135552	ATATGAATGACAGTT[A/C]ATCATGTATCCAACG	218038
rs29240701	snp	A/G	0.465374	0.126941	intron-variant	Amph	Mm_Celera	13:19085652	GACATTTGAACCCTC[A/G]GCTCCAGTTTCAAAC	218038
rs29241095	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19100050	TTACCAACTAGTTTG[C/T]TGATGTACATACATG	218038
rs29241106	snp	A/G	0.497041	0.0383476	intron-variant	Amph	Mm_Celera	13:19101277	GGGTCATTTTGCTTT[A/G]TTTTCCTTATTGAAG	218038
rs29242021	snp	C/T	0.290657	0.246672	intron-variant	Amph	Mm_Celera	13:19121255	TTTTTTTTAATGGCC[C/T]ATTTTCTTTCAATTT	218038
rs29243069	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19067699	CCCAGAAACACTATG[C/T]AAACTTCCAAAAGAA	218038
rs29243077	snp	A/C	0.444444	0.157135	intron-variant	Amph, Gm31887	Mm_Celera	13:19146794	CAGTATTTCTAGCTG[A/C]TTCCAAATATTTGGA	218038
rs29243519	snp	C/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19121447	TTTTTTTATGGCTTC[C/T]CCCTTTTCTCAGAAA	218038
rs29243820	snp	A/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19097508	AAAATGCGTGAAATC[A/G]GGGTCACAGGGTTAC	218038
rs29244042	snp	C/T	0.415225	0.187619	intron-variant	Amph	GRCm38.p3	13:19123218	ATTCTCATCACTGAG[C/T]GTTTTCAGAATATGT	218038
rs29244260	snp	A/G	0.387812	0.208586	intron-variant	Amph	Mm_Celera	13:19110681	GTTGAATATTTTACT[A/G]CACATAATAAATGAT	218038
rs29245326	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19134783	AGGTGTAGTTCTGTT[C/T]AAGACAGATGAAAAG	218038
rs29245821	snp	C/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19097919	TGACTCCTGGTTCCA[C/G]TAACCCTCAAGTTTT	218038
rs29245958	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19100028	AAGCACAGGGCATTG[C/T]ATAGAATTACCAACT	218038
rs29247186	snp	A/G	0.495868	0.0452663	intron-variant	Amph	GRCm38.p3	13:19132939	ATTACAAAGTCTCCT[A/G]CAGCTTCCACCTTGG	218038
rs29248051	snp	G/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19078722	CTCACCAAAGAATGG[G/T]GAAGATGACAATGAC	218038
rs29248423	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19079749	CTGTGTGCTGGACTC[C/T]GTGCTAAGCACTTTA	218038
rs29248685	snp	C/T	0.49827	0.0293608	downstream-variant-500B, intron-variant	Amph, Gm31887	GRCm38.p3	13:19154111	GCACATGGCGGAATC[C/T]TGGACCTGCTGAATT	218038
rs29249718	snp	A/C	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19069271	TTTTGCCAAAAGATA[A/C]AAAAAGTGTTTAATT	218038
rs29250399	snp	A/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19052822	AAGAGTAACAACAAG[A/T]AGACACAGATCACCA	218038
rs29250807	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19138778	TTATAGAAGCTTATC[C/T]CAGTTTTCAAGGAAA	218038
rs29251637	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19079908	CAATTATATTAAAAT[A/G]TAAATCTCTCTCTCT	218038
rs29251812	snp	A/C	0.497778	0.0332592	intron-variant	Amph	Mm_Celera	13:19117233	TAGAAGCTACACATG[A/C]CTAAGACATGTTTAC	218038
rs29492531	snp	G/T	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19097301	TGCCTCTGACAAGAA[G/T]CCCGAGGACCAGAGA	218038
rs29493212	snp	A/C	0.429688	0.173817	intron-variant	Amph	GRCm38.p3	13:19117350	CTAACCTCAACTTTG[A/C]ATTCCTTTTATTATT	218038
rs29493258	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19053064	CCCCATGTTGTTCTG[C/T]TGAAGAGTCAAGACA	218038
rs29493726	snp	G/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19108836	ATAGAGGCTCAGGTG[G/T]GGGGGGGTGGTGTAA	218038
rs29494576	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19136393	TGATCCCCTCTGATC[C/T]CCTCATCCCCTAGTG	218038
rs29495440	snp	A/G	0.432133	0.171253	intron-variant	Amph	Mm_Celera	13:19120639	CCCAGGTAAGGAGAC[A/G]GTTTTTCTTATGAGA	218038
rs29496962	snp	A/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19095981	TGTGCTCCGCTGTGT[A/G]TAAATGTGTTGTGTG	218038
rs29509132	snp	A/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19108607	TCTTTGCCCCATAGG[A/G]CCCATGAACTATTGA	218038
rs29511162	snp	C/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19120403	CATCTTCCCCCCCCC[C/T]TTTTTTTTTGTCAGC	218038
rs29511691	snp	C/G	0.456747	0.140554	intron-variant	Amph	Mm_Celera	13:19097649	TTTCAGAGTTCTTAC[C/G]TTTGGCTCCCAGTTT	218038
rs29513181	snp	C/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19085689	CTTTGGACAATAAAG[C/T]GATCATTATATGTTC	218038
rs29513753	snp	A/G	0.32	0.24	intron-variant	Amph	GRCm38.p3	13:19100075	TACATGGATACTGTA[A/G]TACTGTGTATTACTC	218038
rs29514085	snp	C/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19071107	CTTGAAACACAGGCC[C/T]TTTTCTAGATATGAG	218038
rs29515066	snp	C/T	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19134128	AGGAGAGCTACGATG[C/T]ATAGTATATCTTGTG	218038
rs29515169	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19103226	CCTTTGGCTTTTCTA[A/G]CCCCATCCCCACCTT	218038
rs29528489	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19079926	AATCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT	218038
rs29528501	snp	A/G	0.49827	0.0293608	intron-variant	Amph	GRCm38.p3	13:19112253	CTTTCATTCTGTGTC[A/G]CAGCTACTTACCTGC	218038
rs29528837	snp	C/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19073551	TAACATTGGAGAAAG[C/T]GGAGAAATCATTAGA	218038
rs29529353	snp	A/G	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19128858	TGACCACAGTGACCT[A/G]AGGAAGAAAAGGATT	218038
rs29533260	snp	C/G	0.359862	0.224567	intron-variant	Amph	Mm_Celera	13:19123329	CATAGCATGTTACTG[C/G]CCCATTAACATCTGT	218038
rs29535216	snp	A/G	0.5	0	intron-variant	Amph	GRCm38.p3	13:19138896	GGGCGGTCATGAACA[A/G]CCATGGCAAACCCTC	218038
rs29546050	snp	C/T	0.484429	0.0868505	intron-variant	Amph	Mm_Celera	13:19078860	TTTGACACAGCACTT[C/T]ACTCCTAAGATGATA	218038
rs29547259	snp	A/T	0.32	0.24	intron-variant	Amph	GRCm38.p3	13:19117797	GCATGGAGGCATTTC[A/T]TGTCCTCTATGCTTG	218038
rs29548671	snp	C/T	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19139876	TGGGAAGAAAGATTT[C/T]CTGGCCAGGGACTAA	218038
rs29550226	snp	C/G	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19138212	TTTAGCCTACTCAAG[C/G]CTGGGGGAAGGGCAC	218038
rs29551283	snp	C/T	0.497778	0.0332592	downstream-variant-500B, intron-variant	Amph, Gm31887	GRCm38.p3	13:19154170	AGGAACACACACCCA[C/T]TGTTGTCTCTTCCCT	218038
rs29551594	snp	G/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19141351	AGGACACTGTCAGTA[G/T]CTCTGCTCTGGCTGC	218038
rs29553926	snp	C/T	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19138449	ACAGAGACAGTGTGC[C/T]GCTATGCCTGGTTTG	218038
rs29556969	snp	C/T	0.456747	0.140554	utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19151653	CTAAGCAAAGTGCAG[C/T]GAGGTGACCCTTTTT	218038
rs29564455	snp	C/G	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19068095	AAGTTTTCTGCCTCT[C/G]GCCTCTGTGCCCAGT	218038
rs29564684	snp	A/C/G	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19099379	GTGGAATGCATGCCC[A/C/G]TGTGGCATGGTGGGA	218038
rs29566357	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19052621	TGTGCTCACAAATTG[A/G]TAATCTAGTTCTTAC	218038
rs29569992	snp	C/T	0.255	0.24995	intron-variant	Amph	Mm_Celera	13:19066564	CCCATAACAGCCCTG[C/T]GATTATGGAGGAGTG	218038
rs29571492	snp	C/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19089996	GTCACCAACCCCGGC[C/G]GGCTTACAGCTGTGA	218038
rs29572300	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19127999	GATTCTGATGGGACT[A/G]CAGGAAGGACTAGAG	218038
rs29584695	snp	C/T	0.345679	0.230967	intron-variant	Amph	Mm_Celera	13:19139813	TGTCTAAAGGCACTA[C/T]GGGCCTTCTGTGAAA	218038
rs29584980	snp	A/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19128675	TTAGCTGGTGAACAT[A/G]ATTGAAACATTCTTG	218038
rs29587830	snp	A/T	0.475309	0.108333	intron-variant	Amph	Mm_Celera	13:19084060	GTAACTGAGGAGGTA[A/T]AGCATGAGAGCGAAT	218038
rs29588379	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19134523	ATTCCATAAAATTAT[C/T]ATATTTTCTTCTAAA	218038
rs29588435	snp	C/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19048279	CAAGAGACTCTAACA[C/G]ATATGCTAGATATGG	218038
rs29589684	snp	C/G/T	0.432133	0.171253	intron-variant	Amph	GRCm38.p3	13:19103655	TGCATTGTGTGAACA[C/G/T]ATTTCTGTAGCTACA	218038
rs29630146	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19117573	TCTGGACATACTGCC[C/T]GTGACTCGTAGTCCA	218038
rs29632668	snp	A/G	0.5	0	intron-variant	Amph	GRCm38.p3	13:19100484	CTTAGAAGAGGTGGA[A/G]CTTCTCATTAAACAA	218038
rs29637634	snp	A/G	0.465374	0.126941	intron-variant	Amph	Mm_Celera	13:19084612	CTTGATTTCCATGCA[A/G]TGATTCCATTCCCTT	218038
rs29637758	snp	A/G	0.429688	0.173817	downstream-variant-500B, intron-variant	Amph, Gm31887	GRCm38.p3	13:19154063	CCTATAACTTTTGCA[A/G]AGCGATTCTACAAGG	218038
rs29638206	snp	A/T	0.49827	0.0293608	downstream-variant-500B, intron-variant	Amph, Gm31887	GRCm38.p3	13:19154290	TCAACTCATTTTGTG[A/T]ACATTAGCACCAATG	218038
rs29660698	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19018345	CACAAGAAGCTTCGC[C/T]TCCCCTACTGTTTAC	218038
rs29678727	snp	G/T	0.265928	0.249492	intron-variant	Amph	Mm_Celera	13:19007917	TTTGACTTGTCCTAC[G/T]TAGTTTTCTTGCTGG	218038
rs29684070	snp	A/G	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19138434	CTGGGTCCACAGGCA[A/G]CAGAGACAGTGTGCC	218038
rs29713609	snp	C/T	0.345679	0.230967	intron-variant	Amph	Mm_Celera	13:19077081	TGACTTGTAAGTGCA[C/T]AGGGGTTTGCCTGCT	218038
rs29719907	snp	C/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19095974	GCAGAAATGTGCTCC[C/G]CTGTGTGTAAATGTG	218038
rs29720989	snp	A/C	0.49827	0.0293608	intron-variant	Amph	GRCm38.p3	13:19138097	ATTGAGTTGCAAAAC[A/C]CGCTCAGCAGGTGGT	218038
rs29728301	snp	C/T	0.475309	0.108333	intron-variant	Amph	Mm_Celera	13:19071503	AGCTCAAGCAGTGCC[C/T]GAGGAGTGCTCAAGT	218038
rs29730203	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19099115	ACTTTTTTTGGGGGG[A/G]GGGGCTGATATCTAC	218038
rs29730507	snp	C/T	0.265928	0.249492	intron-variant	Amph	Mm_Celera	13:19103272	ATTCATCTTTACCTT[C/T]CCTTGCTCCTAGGCT	218038
rs29730776	snp	C/T	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19134192	TATAGGAAATGATCA[C/T]GCATAAGCTAAAGAT	218038
rs29735049	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19098806	AGAGTCTCTTACCTG[C/T]CAGGTCTCTGGTGTA	218038
rs29735126	snp	A/G	0.432133	0.171253	intron-variant	Amph	Mm_Celera	13:19069026	CTAGTATGCCATAAA[A/G]GTCAAGTCTCCCACT	218038
rs29758714	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19052830	CAACAAGTAGACACA[A/G]ATCACCAGTCTGAGA	218038
rs29763562	snp	A/C	0.188366	0.242283	intron-variant	Amph	Mm_Celera	13:19066798	TTCTACTGAGACTTC[A/C]ATGGACCTCACTGCT	218038
rs29776265	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19136394	GATCCCCTCTGATCC[C/T]CTCATCCCCTAGTGT	218038
rs29777132	snp	A/C	0.5	0	missense	Amph	GRCm38.p3	13:19139349	GATTCTCAGGCAACT[A/C]TGCCTGCATCTGCAG	218038
rs29778639	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19077230	TATTTTTTCCAATAA[C/T]AAGGTTCTGGCAATG	218038
rs29783609	snp	A/G	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19097415	CTTAAAGAATGAGGT[A/G]AGGACAGAACCATGG	218038
rs29806330	snp	G/T	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19137950	TGTGTTACCTGGAAG[G/T]GGGGCTGGAAATGAA	218038
rs29819856	snp	A/C	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19117828	ATAGCGTCTTGGTAT[A/C]CTCAGACTCACATAC	218038
rs29821755	snp	A/G	0.401235	0.199068	intron-variant	Amph	Mm_Celera	13:19119535	ATATTCCAGATGGCC[A/G]CACAAGCACATTTGC	218038
rs29827742	snp	A/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18984695	GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG	218038
rs29856719	snp	A/C	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19015215	AAGTGATTGCACAGT[A/C]CAGTGACCAAAGCAC	218038
rs29858115	snp	A/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19078738	GAAGATGACAATGAC[A/T]CAGGGGTCATCCCGG	218038
rs29861173	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19093677	TCTCTCCCTCCCTCC[C/T]CTCTTCCTTTGCAAA	218038
rs29863865	snp	A/T	0.456747	0.140554	utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19151666	AGCGAGGTGACCCTT[A/T]TTAAAGGAACTCACT	218038
rs29867802	snp	C/T	0.487535	0.077957	intron-variant	Amph	Mm_Celera	13:19031855	CAGCTAAGAACTTAG[C/T]GGGTATTTGGCTGTT	218038
rs29872008	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19084306	GTTGGTGAGGTAAGA[A/G]CTGGATGGCAACTTC	218038
rs29875985	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19123717	GGAAATACGGTTAGA[C/T]TCATATCTAAAGCCA	218038
rs29877673	snp	A/C	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19134123	GCCAAAGGAGAGCTA[A/C]GATGCATAGTATATC	218038
rs29878185	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19077223	ATATTTATATTTTTT[C/T]CAATAACAAGGTTCT	218038
rs29879630	snp	A/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19142984	TTTCTATGCCACTAC[A/T]TTGCCCCTTCTTTTG	218038
rs29881503	snp	A/G	0.465374	0.126941	intron-variant	Amph	Mm_Celera	13:19084579	GTAACAGCTATTTGT[A/G]GCTGAGCCTTTTATC	218038
rs29902408	snp	C/T	0.492188	0.0620098	intron-variant	Amph	GRCm38.p3	13:19094910	GAATCTTAAGGCATG[C/T]AGCAGCCCTGTTTTT	218038
rs29908056	snp	G/T	0.475309	0.108333	intron-variant	Amph	GRCm38.p3	13:19123607	AGAACTTAAGTCGCA[G/T]CCACAATTGTTAGAA	218038
rs29918119	snp	A/C	0.5	0	intron-variant	Amph	GRCm38.p3	13:19138899	CGGTCATGAACAACC[A/C]TGGCAAACCCTCGTA	218038
rs29918953	snp	C/T	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19140256	ATGGGCACAGACCAC[C/T]GAGCCTGGATGCCTA	218038
rs29927510	snp	C/T	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19097119	TGCCTCTTTGGTTCT[C/T]TTACTATCTATTGTT	218038
rs29927511	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19078765	CCGGCCCATGTTCAA[C/T]GACAGGAGAAAGTTT	218038
rs29930056	snp	C/T	0.32	0.24	intron-variant	Amph	GRCm38.p3	13:19117651	GTTGAGGGTGAACTG[C/T]CAGGAGACACTCAAG	218038
rs29941379	snp	A/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19048394	TCATCTCCTGAACCC[A/G]GATGGCACTCCACAA	218038
rs29954490	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19011542	GTTTGGAGCTGAGAT[A/G]AAAGGATGGACCATC	218038
rs29957446	snp	A/T	0.304688	0.243945	intron-variant	Amph	Mm_Celera	13:19085500	TCAGAAGGAAGGAAA[A/T]TTTAAAGAATAATGG	218038
rs29959206	snp	A/T	0.49827	0.0293608	intron-variant	Amph	GRCm38.p3	13:19114747	TGCTTCCTCCTTTGA[A/T]AAAAATGCTGCTGTA	218038
rs29961121	snp	C/T	0.188366	0.242283	intron-variant	Amph	Mm_Celera	13:19084195	TGCAGCTGTTTTTCT[C/T]CAATGCCAGGTATGC	218038
rs29962680	snp	C/T	0.492188	0.0620098	intron-variant	Amph	Mm_Celera	13:19100176	GAAAAGTTGGATTTT[C/T]CAGTAATGTTCTAAA	218038
rs29963118	snp	C/G	0.444444	0.157135	utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19151741	TCAGGGCCTTTGCTG[C/G]TGGTGGTGTTTGCAG	218038
rs29963451	snp	A/C	0.359862	0.224567	intron-variant	Amph	Mm_Celera	13:19069142	CAGCTATGATGACTT[A/C]TTTGGTTAGCTTTTG	218038
rs29968521	snp	C/T	0.33241	0.236027	intron-variant	Amph	Mm_Celera	13:19077250	TTCTGGCAATGATCA[C/T]TGAATCTTATTGCTT	218038
rs29977972	snp	A/T	0.487535	0.077957	intron-variant	Amph	Mm_Celera	13:19121345	TGGTAAGTTGATGTG[A/T]CCATATTTGGGACAG	218038
rs30004518	snp	G/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19069180	TCTTAATACACATGG[G/T]TATAGACTCAAGTTA	218038
rs30006360	snp	C/T	0.188366	0.242283	intron-variant	Amph	Mm_Celera	13:19085717	TTCAAAGTGTCTACT[C/T]ACAACAGATGATGAG	218038
rs30010392	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19077168	ACCTTTATGAGTACC[A/G]AGATGGATGGGCATA	218038
rs30018695	snp	C/G	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19133316	GGGAGAACTCTTTCA[C/G]CTTTTGGTTTTTGTT	218038
rs30020309	snp	C/T	0.487535	0.077957	intron-variant	Amph	GRCm38.p3	13:19121920	TCACTGTGTGTTTAC[C/T]CTACTGCAGAAGAGA	218038
rs30025116	snp	A/G	0.456747	0.140554	intron-variant	Amph	Mm_Celera	13:19097614	TTATGGGACAGACTT[A/G]TCATTTAATTATCAC	218038
rs30031112	snp	A/T	0.32	0.24	intron-variant	Amph	Mm_Celera	13:19137782	AAGAGCACTGTTTAG[A/T]GGGGTCTTTCCTACT	218038
rs30041911	snp	A/G	0.375	0.216506	intron-variant	Amph	GRCm38.p3	13:19112709	GCACATTTCATACTC[A/G]GTGCAGAGTATGAAA	218038
rs30048837	snp	A/G	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19138520	ACATTTCCTCCAAAC[A/G]TCACATGATGCCACT	218038
rs30050998	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19052976	ACAAACTACTAACAC[A/G]GGCTTGGCAACACAA	218038
rs30058618	snp	C/T	0.5	0	intron-variant	Amph	GRCm38.p3	13:19100035	GGGCATTGCATAGAA[C/T]TACCAACTAGTTTGC	218038
rs30074616	snp	A/G	0.231111	0.249285	intron-variant	Amph	Mm_Celera	13:19072019	CTATGAATTTTGTTT[A/G]GAATCCTATTAAATC	218038
rs30090909	snp	G/T	0.432133	0.171253	intron-variant	Amph	Mm_Celera	13:19072312	ACAGCATATATCATG[G/T]CATTTTCCTTCAGTG	218038
rs30757242	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19056626	AGGAGCTACTGACCG[C/T]ACTCTACCGACCCCT	218038
rs30767681	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19056545	TGTGCCTCTGCCTTC[A/G]TGCTGAACTTTTCTG	218038
rs30820894	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19057384	CTCCCTCCCTCCCTC[C/T]CTCTCTCTCTCTTTC	218038
rs30913940	snp	A/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19057671	TTTTACATACTTAAA[A/T]TTTTAAAACCCAGAA	218038
rs30915564	snp	A/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19055182	TGTTCTATTTACTTT[A/G]CACTTTTCTAGAATC	218038
rs30968686	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19056761	TATCCAGATGGAATA[A/G]TTTCTAGGCACTGAA	218038
rs30970142	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19057392	CTCCCTCTCTCTCTC[C/T]CTCTTTCTTTCTTTT	218038
rs30971921	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19056558	TCATGCTGAACTTTT[C/T]TGGTTCCCCTTGCTC	218038
rs30974661	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19057388	CTCCCTCCCTCTCTC[C/T]CTCTCTCTTTCTTTC	218038
rs45632673	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19046429	GTCTAGACTAACACA[A/G]TGTGAAGATATTTCT	218038
rs45636719	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18968477	CAGTCTATCTCAAAT[C/T]GAATACCAAGAAGAG	218038
rs45643209	snp	A/C	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:19119430	TGCCAAAAACTGAAA[A/C]AACTGATTCTCGGGG	218038
rs45649560	snp	A/C			intron-variant	Amph	GRCm38.p3	13:19102417	TAGCTTTCTATAGAC[A/C]GCGCCATGGCACGAC	218038
rs45652012	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18967261	TCTGGCGTCCAGTGG[A/G]ACATAAGAGTATAGC	218038
rs45652447	snp	A/G			intron-variant	Amph	Mm_Celera	13:19075484	CCAAATTCATATTTT[A/G]CATCTTTCATATATA	218038
rs45659317	snp	A/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19026297	GTCTATTTTCTCCTT[A/T]TGTTTATCTTTCTTC	218038
rs45659607	snp	A/G	0.408163	0.193609	intron-variant	Amph	GRCm38.p3	13:19001151	CTCCATGTATGGGAG[A/G]TGCTGGAGAACAGAA	218038
rs45661942	snp	A/T	0.132653	0.220748	utr-variant-3-prime, intron-variant	Amph, Gm31887	Mm_Celera	13:19153911	GAGTGGGACACTAAG[A/T]AGGGAGATAGCAATA	218038
rs45669589	snp	A/C	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19126295	CCATGCAGGCTTTGA[A/C]GCTATGAGGGAATTT	218038
rs45672047	snp	G/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19088782	AGGGAGCCACCCTAG[G/T]GATACCATACCAAAG	218038
rs45672546	snp	G/T			intron-variant	Amph	Mm_Celera	13:19050068	TTTTCAATCCCCAAT[G/T]AAGTGATTTGACAGT	218038
rs45675384	snp	A/C	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19077938	CCTAGATGGGAACTG[A/C]TAGGCCTCTGCATTG	218038
rs45680988	snp	C/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:18977609	ATGAAATGTGATCTG[C/T]TGTAGCAAACTTATA	218038
rs45697787	snp	A/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:18966986	ACACTGGGCTCTCCT[A/G]AGAGTCACCTGGCTG	218038
rs45715296	snp	A/T			intron-variant	Amph	Mm_Celera	13:19050033	ACAACTTAGAGCTCA[A/T]GTTTTCCCAACAAAT	218038
rs45716536	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19109629	TATGCTGAGCTCAGA[A/G]GGACTTTGTTTAACT	218038
rs45717409	snp	A/G	0.459184	0.136902	intron-variant	Amph	Mm_Celera	13:19010037	CTTCTCTCCTTGAAG[A/G]AGTTGAGGACTACCT	218038
rs45719677	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19028172	TCTGGGGTGCTCCCC[A/G]GCTTGGGTTAGCCAG	218038
rs45723195	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18970857	TCTTGGAGAAGTTAG[A/G]TTCAAGGATGGACCA	218038
rs45727527	snp	C/T	0.231111	0.249285	intron-variant	Amph	Mm_Celera	13:18964327	ATTTCTGGGAAACTT[C/T]GATTATTATGAAGAT	218038
rs45728928	snp	C/T	0.473373	0.11227	intron-variant	Amph	Mm_Celera	13:18992661	AACACATATGGTATG[C/T]ACTCATTGATCAGTT	218038
rs45745661	snp	G/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18964297	TCACCGGCAATCTAG[G/T]CTCCGGTTGTTGTTA	218038
rs45750956	snp	A/G	0.5	0	intron-variant	Amph	Mm_Celera	13:19097176	CTTTAGATGCAGAAA[A/G]AAGTATAGTAAGATC	218038
rs45753115	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19030718	CTTGGTGGCAGCCCT[C/T]CTGCAAGTTCTGCTT	218038
rs45753787	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19012784	CCCACTGTCCATTTG[A/G]AGCAGTCCTAATCAT	218038
rs45754100	snp	A/C			intron-variant	Amph, Gm31887	Mm_Celera	13:19146320	TATGAGCTAAGAATG[A/C]AAATACATGAGTCTG	218038
rs45754527	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19066542	GTCTCTGGTCTCTCC[C/T]TCCTAGCCCATAACA	218038
rs45767750	snp	A/G			intron-variant	Amph	Mm_Celera	13:19052583	AATGCATACACCAGA[A/G]CCAAGATACACCAGA	218038
rs45777158	snp	G/T	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:19009869	TGAGCGCCTGCCTTT[G/T]AGAAGGAAGGTAGAG	218038
rs45779644	snp	A/T			intron-variant	Amph	GRCm38.p3	13:19129781	CATGTAATAAAAATG[A/T]CAGTAGTCTTTCTGT	218038
rs45779719	snp	A/G			intron-variant	Amph	GRCm38.p3	13:19140636	GTCAGTTATATCTCT[A/G]ATAGTTTTTATTCTA	218038
rs45789867	snp	C/T	0.426035	0.177515	intron-variant	Amph	Mm_Celera	13:19003374	TACATTCCTGAGGGA[C/T]GCAAGGAAAGTGTTT	218038
rs45792360	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19088140	TGAATAAGAATACTA[C/T]GCGTCAAAGTTAACA	218038
rs45794340	snp	C/G			intron-variant	Amph	Mm_Celera	13:19126253	ATAAATATTTATTAT[C/G]TAAAAAACACTTTTT	218038
rs45799821	snp	A/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:18977460	ACGGTGCTAGACTTG[A/T]GTGATGAGATTTACT	218038
rs45800282	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18986930	AGTGGTCGGGCTTTT[C/T]CTCAGTGTGTTATCA	218038
rs45810247	snp	C/T			intron-variant	Amph	Mm_Celera	13:19052955	TGGGCCAATTTCCTC[C/T]CAGCCACAAACTACT	218038
rs45812435	snp	A/G	0.231111	0.249285	intron-variant	Amph	Mm_Celera	13:19078424	TTAGACAGTAAACTA[A/G]CCAGAAAAAGGTTTA	218038
rs45819529	snp	G/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19013069	TGACACACTTGGAAA[G/T]CATAGAAAAACTAGA	218038
rs45820024	snp	C/T	0.493827	0.0552116	intron-variant	Amph	Mm_Celera	13:19126534	GGATTATTCAGCAAA[C/T]ACCGGCTACATCATT	218038
rs45820222	snp	G/T			intron-variant	Amph	Mm_Celera	13:19101611	TCCAAGAGAGGGACA[G/T]AAACTAAAAGAATCC	218038
rs45820713	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19069446	GAACCATGATTTCCA[A/G]TGCCATTCACTCTGG	218038
rs45821286	snp	C/G			intron-variant	Amph, Gm31887	Mm_Celera	13:19148847	GCTCAGATTAAATCT[C/G]ACCATCCATTTTTGT	218038
rs45824905	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19005469	GCAAGGATGGTAGGA[C/T]AGAGTTCTTTAAGGG	218038
rs45837712	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19126044	GTGCAGGTGATGAAA[C/T]GAGGCTGCCATGTAG	218038
rs45841858	snp	A/G	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19013197	ATGCTTAATTACAAA[A/G]ACTATATGAGCATCA	218038
rs45851689	snp	G/T	0.486111	0.0821678	intron-variant	Amph, Gm31887	GRCm38.p3	13:19149473	ACCATAATGTCACGT[G/T]AAACAACTTATAACT	218038
rs45857758	snp	A/G	0.244898	0.249948	intron-variant	Amph	Mm_Celera	13:19034134	TATGGGCTAGCAGGG[A/G]TCACCATGGGACTAG	218038
rs45862972	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19026801	CTTTCAGTCCTTACT[C/T]AGTAAATGTGCAAGC	218038
rs45872154	snp	A/T			intron-variant	Amph	Mm_Celera	13:19078401	AATTGAACTAAGATA[A/T]AAAGGATTTAGACAG	218038
rs45876418	snp	G/T	0.18	0.24	intron-variant	Amph	Mm_Celera	13:19091188	CTGCTCCTGTTGCCA[G/T]TTAGGCTCAGAGATG	218038
rs45876675	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18972933	ACATGGACATGCAAA[A/G]TTATTCTCCTTTCAA	218038
rs45882607	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19036914	TACTCTTTGCCAGAC[C/T]GTAATGCTGTCTTGG	218038
rs45902881	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19124074	AGCATCTTATTTTGC[C/T]CCTATGGTATAAAGG	218038
rs45909350	snp	G/T			intron-variant	Amph	GRCm38.p3	13:19091338	ATCTTATTAACATTG[G/T]TTTTCCTCTTATTAG	218038
rs45910263	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19076563	TACATAGCTTTCATG[A/G]AAACATTATCACACT	218038
rs45912226	snp	C/T			intron-variant	Amph	Mm_Celera	13:19078978	AATTGTAATGATTAG[C/T]AAAATTAATTTTTAA	218038
rs45920424	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19082790	AGGGTGAATATGATA[C/T]ATGAGATGGTGTAGT	218038
rs45922539	snp	A/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19087109	TAAGATGTGAAAAAA[A/T]TATGTTTAAAACAAT	218038
rs45923191	snp	C/T	0.336735	0.234472	intron-variant	Amph	Mm_Celera	13:19043776	AGACCAATACAACTC[C/T]GAGTTCTACCCATTC	218038
rs45930629	snp	C/T	0.396694	0.202437	intron-variant	Amph	Mm_Celera	13:19126491	ATTGACTTCTTTAAA[C/T]GGGGTTCACAGAACA	218038
rs45933662	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18970246	TATTTGAATCCATTG[C/T]TTGTTGGAAAGCCAC	218038
rs45940737	snp	A/G	0.444444	0.157135	utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19152736	GCACCTTACCTTGGG[A/G]ACATGCCAAACACAT	218038
rs45942145	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18967004	AGTCACCTGGCTGAA[C/T]CAATAGGCTCTGGTC	218038
rs45950703	snp	A/T	0.473373	0.11227	intron-variant	Amph	Mm_Celera	13:18952477	AACCATTTAATATTT[A/T]AAAATTCTCATCAAA	218038
rs45961259	snp	A/G			intron-variant	Amph	Mm_Celera	13:19074606	AAAGAACCAAGAAGA[A/G]CACAGGCAGGCTCTA	218038
rs45962726	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19043467	GTCTCCAATCTACAA[C/T]GTCAAAGCCCGGGGA	218038
rs45965443	snp	A/C/G	0.260355	0.249785	intron-variant	Amph	GRCm38.p3	13:19001628	ATTTTTTTTTAAGCT[A/C/G]TTCACACATATCATC	218038
rs45972649	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19126126	CCATGGTCACTATCC[C/T]GTCTCCTATGTCTTT	218038
rs45974554	snp	G/T			intron-variant	Amph	Mm_Celera	13:19058655	ACCTATAACAAGCAT[G/T]ACAATGGTTGTGGAT	218038
rs45976244	snp	C/G			intron-variant	Amph	Mm_Celera	13:19129856	CTAGAACTCAGTAGT[C/G]TTTCTATCAGTTGTC	218038
rs45979558	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18984286	GAGGAGCCACGTTTA[C/T]ATTCTCTGTCTACTA	218038
rs45994064	snp	C/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:18989473	AGGCTCTCAAGTCAC[C/T]ATGTCCCAAGGTCAT	218038
rs45998758	snp	A/T			intron-variant	Amph, Gm31887	GRCm38.p3	13:19146159	TGGTGCTGGAAAAGG[A/T]GCTGAGAGTTCTACA	218038
rs45999675	snp	G/T			intron-variant	Amph	GRCm38.p3	13:19140939	AAGCTATTTGTTTAA[G/T]TAAATACTAATTCTT	218038
rs46004553	snp	A/G			utr-variant-3-prime, intron-variant	Amph, Gm31887	Mm_Celera	13:19153278	AGATTCAAAAGCACT[A/G]AACGTTCAAATGCAT	218038
rs46004576	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19030984	GCCCATGTTAACAAA[A/G]CATTGCATTACCAGG	218038
rs46005210	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19125353	TGGCTCTTTAAAACT[A/G]TCCCATGATTATTCT	218038
rs46007141	snp	G/T	0.165289	0.235211	intron-variant	Amph	Mm_Celera	13:19012631	CAACCACTTCCTGTT[G/T]GGCTTCCGTGCAATG	218038
rs46011784	snp	A/C	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19044258	TGTGATTTCAGGCTC[A/C]CAGTGGGTATGCAAT	218038
rs46013246	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18969236	TTTGATAGCAGCAGT[C/T]TGTCAATGGATGGTG	218038
rs46016353	snp	G/T	0.142012	0.225474	intron-variant	Amph	Mm_Celera	13:19002801	GCAGATGCTCACGAT[G/T]TGAGATTCTCGGCGA	218038
rs46020736	snp	C/G	0.231111	0.249285	intron-variant	Amph	Mm_Celera	13:18989231	GAATAAGAACGACAA[C/G]AGAAGATTTAAGAAC	218038
rs46026842	snp	A/C			intron-variant	Amph	GRCm38.p3	13:19131850	GGAGAATAGGAAGGC[A/C]AATATGCAAACATGG	218038
rs46028159	snp	G/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19115605	TCAAATTCCTCCATA[G/T]ATCAGTGAGCTTTAT	218038
rs46029523	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18966594	AAGTCATCCACTATT[C/T]TTTTCCCAAAAGGTC	218038
rs46029611	snp	C/T	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:19082811	ATGGTGTAGTTTTCA[C/T]ATCATTGGTGGCTTT	218038
rs46037550	snp	C/G	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:18982716	TGAAAACTGATGTGT[C/G]CATACCTGTGGGAAC	218038
rs46038187	snp	C/T	0.5	0	intron-variant	Amph	Mm_Celera	13:19122771	TCCTGAGCAGAATTC[C/T]CTGCTGAGGAGCACA	218038
rs46044492	snp	C/T	0.142012	0.225474	intron-variant	Amph	Mm_Celera	13:19011925	GCAGCCCTACACACA[C/T]TATTTTTCTGTCTTT	218038
rs46057375	snp	C/G	0.152778	0.230321	intron-variant	Amph	Mm_Celera	13:19119708	AGTTCAGATCAAAGC[C/G]AGGAGACAATTAGAC	218038
rs46057656	snp	A/G	0.336735	0.234472	intron-variant	Amph	Mm_Celera	13:19110333	GTCTGTCTTATTAAC[A/G]TACTATGTTGTGATT	218038
rs46058121	snp	C/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:18982491	TGTTGCCTTACCAGA[C/T]GTTAAACAATGAAAG	218038
rs46065168	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19038074	TATGCTCTGTGAGGT[A/G]AAGAGTTTAGGGTGT	218038
rs46075992	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18952368	GAGTGCAGAAGAAGG[C/T]AGTTACTGGGCTAGC	218038
rs46078108	snp	C/G			intron-variant	Amph	Mm_Celera	13:19102464	AGTGAAGCTGGTTTG[C/G]TTTTCTTCCTATGCC	218038
rs46080955	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18951689	GGATAAGTCAGAATC[C/G]TGCCAAATGTCAGGA	218038
rs46088952	snp	A/G			intron-variant	Amph	GRCm38.p3	13:19141255	GGTTCATGATATTAA[A/G]TTTATATTATGATAC	218038
rs46089296	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19121588	ATAAATCCATCAAAG[C/T]CACAGGTCTCTATGT	218038
rs46098616	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19026609	AATCTCGGCATCCTT[C/T]TTGTATCCCACCTCT	218038
rs46100575	snp	A/G			intron-variant	Amph	Mm_Celera	13:19073084	ATAAAAGATTCAATT[A/G]AAAGAAGAAAAGAAC	218038
rs46110713	snp	G/T			intron-variant	Amph	Mm_Celera	13:19105786	ACTTAGATTTCTGTT[G/T]GTCATTTTGGGTTAT	218038
rs46111143	snp	A/T			missense	Amph	GRCm38.p3	13:19137548	CAGATCCCTCCCGCA[A/T]CTGATACTGGCGAGA	218038
rs46114158	snp	A/G	0.497041	0.0383476	intron-variant	Amph	Mm_Celera	13:19095942	TTTCTCTTTAATATG[A/G]AGTGATGCTTTTATG	218038
rs46123569	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18993758	ATGCAGTATGGCCAC[A/G]TCTTGGTTATCTCTA	218038
rs46127236	snp	C/T	0.244898	0.249948	intron-variant	Amph	Mm_Celera	13:19037064	TACTCATTCCAAACA[C/T]TTTCTCTGATCCAGC	218038
rs46139304	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19091804	CTTTCATGCAATTAA[C/T]AGTAAAGGCAGGCAG	218038
rs46145578	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19125593	AAGATAAATTAATTT[A/G]CAGCAAAGTGATAGT	218038
rs46150144	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19083163	ATAGGGAAAACCTAA[A/G]GTTCCATGTCAGTTA	218038
rs46153762	snp	C/T	0.165289	0.235211	intron-variant	Amph	Mm_Celera	13:19122986	TTCAGCTGCATATCT[C/T]CTGATTCATGTTTCA	218038
rs46157272	snp	C/T			missense	Amph	GRCm38.p3	13:19137717	AGAGCCCTCAACCAG[C/T]GGAGCCCGAAGCGGG	218038
rs46157560	snp	A/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18967143	TGAGTATAATGGACA[A/T]CTTGGGGAAAGTAAA	218038
rs46162583	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18969672	TAATTTGTTTGGATG[C/T]CAGTGTCTTTCTCAA	218038
rs46163202	snp	A/G	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:18980552	CCTTCTTTTTATATC[A/G]TACAGTCTTCAGCCC	218038
rs46180410	snp	A/C	0.142012	0.225474	intron-variant	Amph	Mm_Celera	13:19004777	GAAGGAAGAGTGTGT[A/C]CTGGTGGAAGTTGTA	218038
rs46185923	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19114915	CCATCTTCCCTGTTC[C/T]TTGGTGCTAATCAAA	218038
rs46187126	snp	A/C	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19106835	TCCCAAGAACTTACA[A/C]TCCTGTGCATAAATC	218038
rs46189054	snp	A/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18967182	CTTCTTTATCTAGTT[A/T]CACTCTGCAGCCACT	218038
rs46190394	snp	C/T	0.35503	0.226867	intron-variant	Amph	Mm_Celera	13:19112326	GACTGGCACAGCACA[C/T]TCTCTGTTTTCTCCC	218038
rs46192762	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19085176	CTTCTGCAGGGGTTC[A/G]CAGTGAGTCTCTGGC	218038
rs46193983	snp	G/T			intron-variant	Amph	Mm_Celera	13:19084742	TCAACTGAACTTTAG[G/T]GCAGCCTTGGACTTA	218038
rs46194109	snp	A/G	0.444444	0.157135	utr-variant-3-prime, intron-variant	Amph, Gm31887	Mm_Celera	13:19152326	TATGTTTTATCCCAC[A/G]TGGCCTGGATCAAGA	218038
rs46196465	snp	A/C/G	0.46281	0.131194	intron-variant	Amph	GRCm38.p3	13:19092957	GCTAAAGTTAGAGGA[A/C/G]AGTCAGTCAGTGTAA	218038
rs46196946	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18957944	AGGGGCGAGTTCTCT[C/T]CTCTGCCGTGCTTTT	218038
rs46200517	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19041244	ATTTGCCTTCCACTT[C/T]GGGAACATAAACTTG	218038
rs46202266	snp	A/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19113001	GTTGTGTGTGGCTAG[A/T]CTCTATCACTGCATT	218038
rs46207575	snp	G/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19043191	TGATATGTCAGGATT[G/T]CTGAGGCATTACAAT	218038
rs46208636	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19141260	ATGATATTAAGTTTA[C/T]ATTATGATACAAAAA	218038
rs46210276	snp	C/G	0.336735	0.234472	intron-variant	Amph	Mm_Celera	13:19007733	AGAGGGCACAGATAG[C/G]TTGGAAGCTGTGAAA	218038
rs46219890	snp	A/G	0.486111	0.0821678	intron-variant	Amph	Mm_Celera	13:19094718	GTCAGAGACTGACAC[A/G]ACCTCTCCAGTTCAT	218038
rs46227379	snp	C/T			intron-variant	Amph, Gm31887	Mm_Celera	13:19147382	CTCTATGAGGGTGCT[C/T]TCCCACCCACCCACT	218038
rs46231562	snp	A/G			intron-variant	Amph	Mm_Celera	13:19102317	TTGGTAACGCTCCAA[A/G]CATAATTCAAAAGGT	218038
rs46236848	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19140757	AGGACTAGAGAGTCC[C/T]CATACTGACAGATGG	218038
rs46243795	snp	G/T			intron-variant	Amph	Mm_Celera	13:19144018	GCAAAGAAAGAACAT[G/T]TTGGGACTTCACCGG	218038
rs46245086	snp	A/T	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:19081964	ATATTATATTCTGTT[A/T]TCATAGTAAGTTCTT	218038
rs46256445	snp	A/C	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18964435	TAAATAGGTGAAGTG[A/C]TACAGTACTACTTAT	218038
rs46260165	snp	A/G	0.5	0	synonymous-codon	Amph	Mm_Celera	13:19100643	GGCCTTCAGCATTCA[A/G]GGAGCTCCCAGGTAG	218038
rs46260590	snp	C/T	0.124444	0.216185	downstream-variant-500B, intron-variant	Amph, Gm31887	Mm_Celera	13:19154058	GAATTCCTATAACTT[C/T]TGCAGAGCGATTCTA	218038
rs46261746	snp	G/T			intron-variant	Amph	GRCm38.p3	13:19140609	CTCTCATGAATTAAT[G/T]TTTGAATAACAGTCA	218038
rs46267159	snp	C/T	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:19040023	CCCTAGTATTGATAG[C/T]TGGAAGTTTCAAGTT	218038
rs46284638	snp	A/C	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19081430	AACTAAAACATCTAC[A/C]TCAAGGCTATGCAAG	218038
rs46287175	snp	C/T	0.21875	0.248039	intron-variant	Amph	Mm_Celera	13:19135133	AAATAAGTCAATGAA[C/T]AATTGCTTGCTATTC	218038
rs46288917	snp	C/T	0.32	0.24	intron-variant	Amph	Mm_Celera	13:18950629	TAATTGAATGCCAGA[C/T]GTGTTCCCCAGACCC	218038
rs46289465	snp	A/G			intron-variant	Amph	Mm_Celera	13:19142615	GAAAACTTTAAAGGG[A/G]TGTAGAAATGTTTTG	218038
rs46301159	snp	A/G			intron-variant	Amph	Mm_Celera	13:19049759	TATTTGGTCACAATG[A/G]TTAAATATAATCTAA	218038
rs46302588	snp	A/C			intron-variant	Amph	Mm_Celera	13:19090997	GAGAAGTTATGCTGA[A/C]GAGTTAGCAGAGTCT	218038
rs46306227	snp	A/C	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19074404	CACACTGTTCTGTGA[A/C]TGCTTGGGAGGTCAG	218038
rs46308405	snp	A/G	0.231111	0.249285	intron-variant	Amph	Mm_Celera	13:19118288	CTAGTCCTAGAATTG[A/G]CTGTAAACTGATTAA	218038
rs46318123	snp	A/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18984191	GTAGAGTTGCCAGGG[A/T]TCACATTGCCCAGCC	218038
rs46318357	snp	C/G	0.18	0.24	intron-variant	Amph	Mm_Celera	13:19127736	CAGGGAAGAGTTTAG[C/G]GAATTCAGAAAATGG	218038
rs46324583	snp	G/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19046745	CATATCAAAATTCAG[G/T]ACATGATAGTGCACA	218038
rs46326749	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19101123	ATGATTGAGTCAGTG[A/G]GAGAATGAGGGCCCA	218038
rs46326922	snp	C/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18978098	AGAGGCAATGCTATT[C/G]CTATGGGCTGTGTGA	218038
rs46326941	snp	A/G/T	0.297521	0.245442	intron-variant	Amph	GRCm38.p3	13:18984029	TGCTAGCTGCTTCCT[A/G/T]TATTTGTGTCAACAA	218038
rs46334281	snp	C/T	0.165289	0.235211	intron-variant	Amph	Mm_Celera	13:18988407	TTCAGGCTTCGCATT[C/T]CATACTGTATCCTCA	218038
rs46335256	snp	C/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19087078	TTTTCAGATTAAAAT[C/T]GAAATATGAGCCTTT	218038
rs46341362	snp	A/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19082167	CCTCTTGATGAGCCT[A/G]CTTGCTCAATCGTCG	218038
rs46343947	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19029082	TATACCTAGTGACTG[C/T]GAATTCTCCTGAAGG	218038
rs46351129	snp	C/T	0.489796	0.070696	intron-variant	Amph	Mm_Celera	13:19113449	TGTTTGCCTCAGAAC[C/T]GTGTCTTTCAGAGTT	218038
rs46353211	snp	A/T	0.408163	0.193609	intron-variant	Amph	GRCm38.p3	13:19118873	TAAAATATCAGATGG[A/T]GAAATAAAACAGACA	218038
rs46353783	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18972510	CTCTGGTTCTTCTGT[A/G]GGATGTCAGGATTGA	218038
rs46356010	snp	A/C			intron-variant	Amph	Mm_Celera	13:19081739	TGTAGGGAAACTGGA[A/C]TTTACATGTTTGCTC	218038
rs46364293	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19036110	AGTATTTGATGAGGA[A/G]GGAGCATAGGGGTGT	218038
rs46367901	snp	A/G	0.18	0.24	intron-variant	Amph	Mm_Celera	13:19134798	CAAGACAGATGAAAA[A/G]CAAAAATAGATTTAT	218038
rs46368749	snp	G/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19082134	GAAGTGAAGAACTCA[G/T]TCTTTAGAAGACTCT	218038
rs46370051	snp	C/T	0.48	0.0979796	synonymous-codon, intron-variant	Amph, Gm31887	Mm_Celera	13:19149822	CCTCTTTCCAGAGAA[C/T]TTCACGCGGCGCCTG	218038
rs46372590	snp	A/G	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:19089182	ATTATAATCGATTGT[A/G]CTGGTTGTTCATTTC	218038
rs46373638	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19042262	AAACACAGTAAAGCA[C/T]AATCAAATGAGGAGG	218038
rs46377743	snp	A/G			intron-variant	Amph	Mm_Celera	13:19051267	CGGAGGTTGCAGAGC[A/G]AGGGTCCCCTGGCAG	218038
rs46378140	snp	C/G	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:19077062	TCTAAATTAAAAGAA[C/G]CACTGACTTGTAAGT	218038
rs46378879	snp	C/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:18975115	AATAACAGAAACAAA[C/G]TCTCCACATTTCTCC	218038
rs46380242	snp	A/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19089242	CTCAGTAGAACTTCT[A/T]CCAAGGAGCCCCTTT	218038
rs46382269	snp	C/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19013269	ATTTGAGAAATCTTA[C/G]TGAGAGAGGAATAGG	218038
rs46392742	snp	C/T	0.18	0.24	intron-variant	Amph	Mm_Celera	13:19136573	AGGCCTCACAGGAGC[C/T]CAGGTCTCTTCAGTG	218038
rs46394480	snp	A/C	0.124444	0.216185	intron-variant, utr-variant-3-prime	Amph, Gm31887	Mm_Celera	13:19151178	GATCTCCTTCTATTG[A/C]TGGCTGTGGACACTC	218038
rs46401518	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19001568	ATGAGCCCAGATGGC[C/T]GTCACAGTGACTGCA	218038
rs46407948	snp	A/G			intron-variant	Amph	GRCm38.p3	13:19133378	TCTCCATCAAAAAAT[A/G]CTTTAGACAATGAAT	218038
rs46416668	snp	C/T	0.152778	0.230321	intron-variant	Amph	Mm_Celera	13:19101387	AGGTGATGCTCTGTT[C/T]TGAGACTCTACACTT	218038
rs46432845	snp	A/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:18982582	CAAACTTAAAGACTC[A/G]GACCACTGCAAAACT	218038
rs46440033	snp	C/G	0.165289	0.235211	intron-variant	Amph	Mm_Celera	13:19046147	AATTCCCACTGTGTA[C/G]TCTTAAGGAGGTCCC	218038
rs46440739	snp	A/G	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:19004836	CATTCTCTTAGGGAT[A/G]GTATTGTTAAATGGA	218038
rs46444412	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19001680	GGGTCATCCACAGAG[A/G]ACTGCTTTTGCAATG	218038
rs46447402	snp	A/G			intron-variant	Amph	Mm_Celera	13:19052607	CACCAGAACCAAGAT[A/G]TGCTCACAAATTGGT	218038
rs46448215	snp	C/T			intron-variant	Amph	Mm_Celera	13:19141439	GAAAATCTCCCTCTC[C/T]CGTTTTCTTCTTGGA	218038
rs46454276	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19003955	TATTCCACTGACACT[A/G]AAAGTTAGTGGCCAA	218038
rs46454902	snp	C/T	0.35503	0.226867	intron-variant	Amph	Mm_Celera	13:19030534	TTATTAGCTCATCTG[C/T]TTGAGAGGTGACACA	218038
rs46455396	snp	A/T	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:18970737	TACTTCACACCATGC[A/T]GTCCAAATTTTCTTA	218038
rs46458122	snp	A/C	0.5	0	intron-variant	Amph	Mm_Celera	13:19101143	ATGAGGGCCCAGTGG[A/C]TCAGCTGAGCTGTTT	218038
rs46467804	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19083828	CAAAAGCCGTATTTA[C/T]ACTCTTTCTACCTGT	218038
rs46471248	snp	A/T	0.32	0.24	intron-variant	Amph	Mm_Celera	13:19095758	GATCCCATTGGGAAA[A/T]TTTTCTAAATCCCCT	218038
rs46472478	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19118952	GTAGACACTGGAGCT[A/G]TTGGTATCAAGGCAA	218038
rs46476559	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19121783	GAGACTAACACCATG[C/G]ACTAAGTAGGAAAGA	218038
rs46499629	snp	C/T	0.165289	0.235211	intron-variant	Amph	Mm_Celera	13:19092305	AGTCAGTACTTCTTC[C/T]CTTCTAGGTTTATAG	218038
rs46500826	snp	C/T	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:18974968	CAGTGATCTGTGTAA[C/T]TCCAGGAAAATCCAT	218038
rs46505131	snp	A/G	0.486111	0.0821678	intron-variant	Amph	Mm_Celera	13:19011198	CAGTTATCTAGATTT[A/G]TAAAGATCTATTCAG	218038
rs46511394	snp	G/T	0.165289	0.235211	intron-variant	Amph	Mm_Celera	13:19132990	CCTGGTTCTGTGACC[G/T]CATTGTGTTTCCCTT	218038
rs46526130	snp	A/G	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:19040463	TCTGCAGTGTCAGGG[A/G]ACTATGTGTTCTCAA	218038
rs46529115	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19121069	ATCAGAAACCATACT[C/T]AGGCTGTCTTCAAGA	218038
rs46533948	snp	A/G			intron-variant	Amph	Mm_Celera	13:19098685	ATGTGACTGTGGGAT[A/G]GCAACCCCATTTCTT	218038
rs46534959	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19030624	ATATGTTTATGTCAA[C/T]GTCTAACAAATGTGA	218038
rs46539361	snp	G/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:18977791	CTGCATTCCTCTTTG[G/T]TTCCTCCCATGAGCC	218038
rs46540328	snp	A/G			intron-variant	Amph, Gm31887	Mm_Celera	13:19148466	TAGAATCCAATATAG[A/G]CTTGTGGGAGGGGAA	218038
rs46541386	snp	A/G	0.486111	0.0821678	intron-variant	Amph	Mm_Celera	13:19093068	GCTGCTTGAGCTTGT[A/G]GAGGTCTCGGCCCTG	218038
rs46548762	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19110394	AAGTTCTGAGGCCTA[A/G]ATTTGAAGTACATGT	218038
rs46562536	snp	A/G	0.142012	0.225474	intron-variant	Amph	Mm_Celera	13:19087534	CCTTTGGTGACTTCC[A/G]GGCAAGAACGTAAGT	218038
rs46562874	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19035032	TAATGGAGATTATGC[C/T]GAACAAAGAAGCTTT	218038
rs46565691	snp	C/G	0.244898	0.249948	intron-variant	Amph	Mm_Celera	13:19027248	CATCTGTAATCATGC[C/G]TCTGCCTTGTGGGTT	218038
rs46570284	snp	G/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19105256	TCGAAAATTACAGAT[G/T]CCAGGAGAGTCTTTA	218038
rs46573553	snp	A/G			intron-variant	Amph, Gm31887	GRCm38.p3	13:19146227	AAGATCTCAAAGGCT[A/G]CCTCCACAGTGACAC	218038
rs46586726	snp	A/T	0.142012	0.225474	intron-variant	Amph	Mm_Celera	13:18953515	TTTGTTTGTCTAGAA[A/T]ATTCTCTCTGTGAGT	218038
rs46587889	snp	C/G	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:18969268	TGAGATCTGACCTCC[C/G]GGCCATATTTCTGTG	218038
rs46588046	snp	C/G			intron-variant	Amph	Mm_Celera	13:19051019	TAGTGAAATTCTTAG[C/G]ACCAGATGTGTTTCA	218038
rs46588290	snp	C/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19033988	ACTCCTGTGCTAAAA[C/G]TTTTGAAAGCATTGG	218038
rs46597731	snp	A/G			intron-variant	Amph	GRCm38.p3	13:19141103	TTCAGCTATTGTGTC[A/G]ATTTGAATTGAATTA	218038
rs46599600	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19123097	CTGAGTTTGTATTAA[A/G]TAACCCTTCTAAGCC	218038
rs46600699	snp	A/T	0.152778	0.230321	intron-variant	Amph	Mm_Celera	13:19068739	TGACAGTCAAGGCAT[A/T]AACTCACCCTCATTA	218038
rs46601744	snp	A/T			intron-variant	Amph	Mm_Celera	13:19140419	AATGTATGCAAAATA[A/T]TTGAAAGTACAGGTT	218038
rs46602142	snp	A/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19109335	TGTTTCCCACACACA[A/T]TGTTTAATTTCTTGA	218038
rs46603435	snp	A/C	0.32	0.24	intron-variant	Amph	Mm_Celera	13:19025364	ACACATGGATTATAC[A/C]TTTAACAACATGAAC	218038
rs46608264	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18977557	TTCCACAGTGAGAAG[A/G]AATATTAAGCAGACC	218038
rs46614961	snp	C/T			intron-variant	Amph	Mm_Celera	13:19080561	CCTGGCTCTTTCTGC[C/T]GTCTCTCCTGTGTCA	218038
rs46616375	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18964804	AATTGTGACCGCTTA[A/G]GAATTCTGTCTTTCA	218038
rs46618632	snp	A/G	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:18977656	AGATCAAAGGGACAG[A/G]ATTTTGAATGATACA	218038
rs46622001	snp	G/T			intron-variant	Amph	GRCm38.p3	13:19130816	TGGTTTCTACTGCTG[G/T]GATAAACACCATAGC	218038
rs46626328	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19027538	AATTTAATCACTGCT[A/G]TTCATAACCTTTGGT	218038
rs46641085	snp	A/G			intron-variant	Amph	Mm_Celera	13:19053980	GAATGGCAAGTTCCC[A/G]TGCTATGCTGTGCCT	218038
rs46643136	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19076741	CTCCGAGTATTGTGA[A/G]TGAGTGTTCAGGGCT	218038
rs46644029	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19031832	GAACTAACAAAATAC[C/T]TTGCTCACAGCTAAG	218038
rs46653300	snp	C/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19091362	TTATTAGCATATTCA[C/T]TTTAAGAGGTTTTTA	218038
rs46669644	snp	A/G	0.473373	0.11227	intron-variant	Amph	GRCm38.p3	13:19099836	TATTTGTTTCATTGC[A/G]ATTAAAAACCACTTT	218038
rs46671167	snp	G/T			intron-variant	Amph	Mm_Celera	13:19074906	AACCGGACTTCTCTG[G/T]AAGGACAATCCCATC	218038
rs46672930	snp	A/C/T	0.495868	0.0452663	intron-variant	Amph	GRCm38.p3	13:19001120	AAAAGAAAAAAAGAC[A/C/T]CTCAGCCACCTCAGC	218038
rs46688403	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19120745	TCAGTACAAAACTTG[C/T]CCTCCCTGCTTACAA	218038
rs46691806	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19084707	ATCCCTCTGTAGCAC[A/G]CCTAGTCCAGTCACT	218038
rs46695406	snp	C/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19104015	GTGTTCAAATTGAGA[C/T]GAATGGACTCTCATC	218038
rs46703615	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19029657	CAGCACTGCTGGAGG[A/G]TCAGGAGGACAGTTT	218038
rs46708406	snp	C/G			intron-variant	Amph	Mm_Celera	13:19052012	AGGACAACCTTAAGA[C/G]TCTGCATTTCTGACA	218038
rs46708633	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19012773	GGCACTATGCGCCCA[C/T]TGTCCATTTGGAGCA	218038
rs46716023	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19125486	ATGCTCTGTGCTTCT[C/G]GCAGTCAGGGATGCA	218038
rs46717205	snp	C/T			intron-variant	Amph	Mm_Celera	13:19075529	TGAGGATAGTACAGA[C/T]CAATTTTTCTGAAGC	218038
rs46720018	snp	C/T	0.391111	0.206368	intron-variant	Amph	GRCm38.p3	13:19002364	TTGGACTTTCAGGTC[C/T]CGAGGAGTTGGCTTC	218038
rs46721304	snp	C/T			intron-variant	Amph	Mm_Celera	13:19116764	ATGTGGAGTTGAGTT[C/T]GTACCCTAATACTTA	218038
rs46722259	snp	A/C	0.493827	0.0552116	intron-variant	Amph, Gm31887	GRCm38.p3	13:19148346	GTTAGAATACATCTT[A/C]ATTATGGCTTTGTGG	218038
rs46722308	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19113943	TGGTGGTTCATACCT[C/T]TAATCCCCCTCACTA	218038
rs46727426	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19082837	GCTTTATCATGAGAG[A/G]ATATATCTTCACTTG	218038
rs46735711	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19072924	CCCTATGCTAGAAGA[A/G]TGTGAGAACCCCTGA	218038
rs46744891	snp	A/G			intron-variant	Amph	Mm_Celera	13:19075340	TACTGGCTCCCACCT[A/G]AGTGCTTCATGCCAC	218038
rs46746126	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18950630	AATTGAATGCCAGAC[A/G]TGTTCCCCAGACCCT	218038
rs46753983	snp	A/C	0.231111	0.249285	intron-variant	Amph	Mm_Celera	13:18969451	GAGAAAACTGTGACT[A/C]TTTGGAAGTTTAGGT	218038
rs46757111	snp	C/G	0.142012	0.225474	intron-variant	Amph	Mm_Celera	13:19004435	GACAGAAAACTTAGT[C/G]TAAAACTTGAAGGGC	218038
rs46776205	snp	A/T			intron-variant	Amph	Mm_Celera	13:19075070	GTTATTTTGTGTGTC[A/T]GCCTTCTCTACCTGT	218038
rs46776629	snp	A/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18972294	CTTATCTCCTTTGTC[A/T]CCTATTCTTTAGAAA	218038
rs46778362	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18973173	CAGCACACCAAGGAG[C/T]GATGGTGAGGCAGTC	218038
rs46779348	snp	C/G	0.48	0.0979796	utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19153177	ACTCAGCCATTATTG[C/G]AGATTTTTCTTAACC	218038
rs46781517	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19099669	AAGATGGATGGGTTC[C/T]TAGTGCCCTCCCTAT	218038
rs46782567	snp	A/T			intron-variant	Amph	Mm_Celera	13:19126370	ATACATTTTTTTTTT[A/T]AACCTTGATGCACAA	218038
rs46784050	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19002843	GAAAAATCATTGCCA[C/T]TTTATCTTCTGCTCT	218038
rs46791848	snp	C/T	0.486111	0.0821678	intron-variant	Amph	Mm_Celera	13:19101260	TCAGTTACATGCCTC[C/T]GGGGTCATTTTGCTT	218038
rs46794039	snp	A/T			intron-variant	Amph	Mm_Celera	13:19091307	GGTGACTTCTGTGTT[A/T]TGTAAAAACATAAAT	218038
rs46798048	snp	A/T			intron-variant	Amph	GRCm38.p3	13:19144160	CTAAAACATGTTTCA[A/T]GAAATTTTCTAGGCA	218038
rs46805860	snp	A/G	0.391111	0.206368	synonymous-codon, intron-variant	Amph	Mm_Celera	13:19125142	GGAGCCAAAGGAGGA[A/G]GCTGTGGTGAGCACT	218038
rs46810935	snp	C/T	0.459184	0.136902	intron-variant	Amph	Mm_Celera	13:19012637	CTTCCTGTTGGGCTT[C/T]CGTGCAATGAGAGTG	218038
rs46813049	snp	A/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19129850	GAAAGCCTAGAACTC[A/G]GTAGTCTTTCTATCA	218038
rs46813362	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19012946	CCATGGAACTGGATG[C/T]ATATTCACAGAAAAA	218038
rs46819337	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19045137	CTGTGCTCCAGACAT[A/G]GTATTTCTTCTTGTG	218038
rs46830926	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19078169	GGGAAACTCTCCAAA[C/T]ATTGAAGGCCCAATT	218038
rs46831796	snp	A/G	0.375	0.216506	utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19150615	AGATAGCGCGTCCAC[A/G]CTGCTGCCCCTTTGG	218038
rs46833184	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18951952	GATTAGGAAGAGGTT[A/G]ATGACACAATTAACT	218038
rs46833269	snp	A/G			intron-variant	Amph	Mm_Celera	13:19051878	GACCTTCTGGATTGG[A/G]ACTAAGAACCTCATT	218038
rs46839154	snp	G/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19131780	TATTGTTTGTAGATC[G/T]GAAAATGAAGACATG	218038
rs46843049	snp	A/C			intron-variant	Amph	GRCm38.p3	13:19099775	TTACTCTAAGATGTT[A/C]TTTAATTCAATATTT	218038
rs46843236	snp	A/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19030169	ATTCTTCGCAGTTGG[A/T]CTTATTAAATTGTTT	218038
rs46844396	snp	C/T	0.124444	0.216185	intron-variant	Amph	GRCm38.p3	13:18956814	AGGTGATACTTTGAT[C/T]TAAAGTTACTCAGGA	218038
rs46847377	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19073335	AGGAAAAGTAAAGGC[A/G]TATAGTACCACAGGT	218038
rs46848400	snp	C/T	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19012876	ATAACCCAGACTTTA[C/T]AACTAAGTATAAACA	218038
rs46848592	snp	C/G			intron-variant	Amph	Mm_Celera	13:19080955	TGCTACTATTGTTCC[C/G]CTGGGGATATCTTAT	218038
rs46849230	snp	A/T	0.391111	0.206368	intron-variant	Amph	GRCm38.p3	13:19124777	ATACAGTGGCAGGTC[A/T]TTGCTCGACTTTGAA	218038
rs46855703	snp	C/T	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:19003385	GGGACGCAAGGAAAG[C/T]GTTTCGTTTCGAGGA	218038
rs46866280	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19144167	ATGTTTCATGAAATT[C/T]TCTAGGCATTTATTA	218038
rs46870892	snp	A/G			intron-variant	Amph	Mm_Celera	13:19126533	AGGATTATTCAGCAA[A/G]TACCGGCTACATCAT	218038
rs46878434	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18981011	AAATGGGAATTGTGG[A/G]TTGAGCAGGGATCGC	218038
rs46879832	snp	A/C	0.21875	0.248039	intron-variant	Amph	GRCm38.p3	13:19127207	ATTTCACGACTCTTC[A/C]AAAAGAACTCAGACA	218038
rs46883879	snp	A/G	0.152778	0.230321	intron-variant	Amph	Mm_Celera	13:18983806	ATCTCTTTCCCTTTG[A/G]AGTCCTATTGGTCCT	218038
rs46888111	snp	C/G	0.35503	0.226867	intron-variant	Amph	GRCm38.p3	13:19125789	ACCCTAAAAGAGGAT[C/G]CTTTTGTCTTACTAC	218038
rs46892517	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18978257	TTGAAAGGTCACACA[C/T]TACAGGTAGTAGGGT	218038
rs46903157	snp	A/C	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19042023	TATCGAGAATATGGG[A/C]CATTAAGAAGACCTG	218038
rs46903579	snp	A/G			intron-variant	Amph	Mm_Celera	13:19116139	CAAAAGTAGAGCTAT[A/G]GAAGAGAGCTGCTAC	218038
rs46908615	snp	G/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19082969	ACTCTCTCTGCCTTC[G/T]CTCCAGCATATCCAT	218038
rs46909498	snp	C/T	0.489796	0.070696	synonymous-codon	Amph	Mm_Celera	13:19099935	CAAAAATGTCTCCAG[C/T]CTTGAGGCCAAGTTT	218038
rs46919382	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18950582	ATCTACTTCTTTGGT[C/T]TCTTTCTCCCAATGC	218038
rs46920099	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19035663	TGAGCTTCATGGAGA[A/G]AATTTCTGGTTAGTT	218038
rs46921414	snp	A/G			intron-variant	Amph	GRCm38.p3	13:19132045	AGTGAGGCCTGCTTC[A/G]CACTCACCCTTCTCT	218038
rs46923804	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18969525	CCTAGTTGTGGGGTG[C/G]TCAACACTTCCTAAA	218038
rs46930208	snp	C/T	0.459184	0.136902	intron-variant	Amph	Mm_Celera	13:19095090	GTGACCAGAATAACT[C/T]TGAGCCTGTTTCAGT	218038
rs46931129	snp	C/T	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19119718	AAAGCGAGGAGACAA[C/T]TAGACCACTGAGTCA	218038
rs46935800	snp	C/T			intron-variant	Amph	Mm_Celera	13:19081927	AGACATGCGCCATCA[C/T]GCCTGGCTTATTTGC	218038
rs46942083	snp	A/T			intron-variant	Amph	GRCm38.p3	13:19121167	TTGTGTTTTTTTTTT[A/T]AATAATTTAAAGGGA	218038
rs46943357	snp	C/G	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:18989851	GCACCGAAGTTCTTA[C/G]CTTTGTGAATTGCTC	218038
rs46951833	snp	A/C	0.336735	0.234472	intron-variant	Amph	Mm_Celera	13:19068228	GGGAGAGTTCTGGTA[A/C]TATTGAACAACCCAG	218038
rs46952603	snp	A/C	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19082909	CTTGTCCATACTTGT[A/C]TGCCTCTGCTTCCTC	218038
rs46953271	snp	A/T	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19113606	AGAATTTGGATAACT[A/T]CCAGACCATGTCCCC	218038
rs46953615	snp	A/G	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19012507	TAGGGAAAGTGACTT[A/G]CAAGGTGGTCAGTTG	218038
rs46960162	snp	A/G			intron-variant	Amph	Mm_Celera	13:19051542	AATAAAAAGTATGTT[A/G]GCCTATGCACTGACA	218038
rs46961649	snp	C/T			intron-variant	Amph	Mm_Celera	13:19053348	TCACCAGCTGACAGT[C/T]CCCCTTGTCTGGGAC	218038
rs46964570	snp	G/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19074227	TTTTCCTCACTGTTA[G/T]ATTAAAAACTCATCT	218038
rs46965130	snp	C/T	0.18	0.24	intron-variant	Amph	Mm_Celera	13:19135095	AATCTCCATCCCAGC[C/T]TAAAATTGCTGATTT	218038
rs46969237	snp	C/T			intron-variant	Amph	Mm_Celera	13:19083201	GCTTTCACACACTCT[C/T]CAAGGACGAATTCTA	218038
rs46969516	snp	C/T	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19096992	TCTCTCTGAAACCTG[C/T]CCCAGATCCCTGTTG	218038
rs46973968	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19039705	GTGCATTGACGAGTA[C/T]AAACCCTTCCTGGGT	218038
rs46973995	snp	A/G	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:18984391	AAGGTACTCATCCCC[A/G]ATGGCTCTGGGTTCA	218038
rs46991642	snp	C/T	0.152778	0.230321	intron-variant	Amph	Mm_Celera	13:19100679	TGGTCCTCTGAGCTG[C/T]ATGTGCAAGTGATGT	218038
rs46999056	snp	C/T	0.244898	0.249948	intron-variant	Amph	Mm_Celera	13:19030427	CCTGTGTAAGATGTG[C/T]ACTGGAAAACAGACA	218038
rs47004699	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19029977	TTTTATTGGAACAAA[C/G]GAGGGGCCTCCAGGC	218038
rs47012053	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18980198	CCATGTGCACTGTCT[C/T]GGTTTTAGGCCAGTA	218038
rs47019018	snp	G/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19082029	TTAAAGAATAGAAAC[G/T]GAATTGGCTCATCTG	218038
rs47021386	snp	G/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18952641	TGTTTCTACAGCTAT[G/T]TATTGACTTCCCTGT	218038
rs47024051	snp	C/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19123806	AGGCAATGATCCAAA[C/T]ATTGTTCTGTATTTT	218038
rs47026506	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19113508	TGTAGGTTCTGATAA[C/T]ACACCTCATGGCTTC	218038
rs47026814	snp	A/G/T			utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19153261	CAGCAAGGGGGCTGA[A/G/T]CAGATTCAAAAGCAC	218038
rs47027886	snp	G/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19044679	AATGCCAAGAATCTC[G/T]TCCTTCAAATTGTGA	218038
rs47028385	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19089872	TATCACGTACCATTC[C/G]TGAGGATGATGTTTG	218038
rs47028631	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19074523	GATTCTCATGAGATG[C/T]TGAGGGCAAAACATC	218038
rs47036153	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19082678	AGACTTAATGAAAAT[A/G]CCAGGAGCCCTTGTT	218038
rs47042798	snp	A/T	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:18975022	GGTGTTCATCTCAAT[A/T]CTGCCTAGACTCTCT	218038
rs47043570	snp	A/G	0.473373	0.11227	intron-variant	Amph	Mm_Celera	13:19096486	CAGTATTCTCAGTCC[A/G]CATCTTACCTTCTGA	218038
rs47046535	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19083353	CTGCCTTAGCCTCTA[C/T]CAACCTCCTAGTGAT	218038
rs47046667	snp	C/T	0.459184	0.136902	intron-variant	Amph	Mm_Celera	13:19034585	ATCCATAAGGAGCAG[C/T]ATCTCAGATACCAGT	218038
rs47048763	snp	G/T	0.493827	0.0552116	intron-variant	Amph	GRCm38.p3	13:19124883	AGTGACACTAGATGA[G/T]AGAACTCGTTTTTCT	218038
rs47048925	snp	A/T			intron-variant	Amph	Mm_Celera	13:18981780	ATCTCATAATATATG[A/T]AAAAGCAGAAATCAC	218038
rs47056563	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19083333	TGATTTCAATCTCTG[C/T]TTCACTGCCTTAGCC	218038
rs47066730	snp	C/T			intron-variant	Amph, Gm31887	GRCm38.p3	13:19146068	AAGGACAGCATTTAA[C/T]TGGGGTTGGCTTACA	218038
rs47067921	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19125411	TTCTGTGATCCACCT[A/G]AGACAGTTGGAAACG	218038
rs47069616	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18984345	ATCACCAAATTTAAT[A/G]CCTGTGAGTCTGAAA	218038
rs47069624	snp	A/C			intron-variant	Amph	Mm_Celera	13:19053893	GATCCCCACCCATAC[A/C]ATTATTTTTGTTGCT	218038
rs47079263	snp	A/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18955702	TTTGGTTATGTGGTT[A/T]GATCTGGACATGAAG	218038
rs47083223	snp	C/T			intron-variant	Amph	Mm_Celera	13:19049797	AGTGACCAATTCACT[C/T]AGTTAGATTATATTT	218038
rs47084426	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19030888	CATAATTTAGATTCA[C/T]GATGAACTTCATATT	218038
rs47090762	snp	A/G	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19012459	GGTTAAGAAGCCTCT[A/G]TAGCAATCTAGCCTA	218038
rs47090855	snp	C/T	0.35503	0.226867	intron-variant	Amph	Mm_Celera	13:19039811	TGTCTCTGGAACATC[C/T]GGCTAATGGGACATG	218038
rs47096729	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19035483	GCTCAGTCATTGGGG[A/G]ATTCCATTGCTGCAG	218038
rs47100963	snp	C/G	0.336735	0.234472	intron-variant	Amph	Mm_Celera	13:19036716	CAACAATTCTAATAA[C/G]TAATATTTCTGAGCA	218038
rs47105326	snp	A/G	0.391111	0.206368	intron-variant	Amph	GRCm38.p3	13:19112977	CAAGTGTGTGGTCCA[A/G]GGACATGAGTTGTGT	218038
rs47106976	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18979437	GAACAGGATATCAAA[A/G]AGGAAAGAAGACAGA	218038
rs47112236	snp	C/T	0.35503	0.226867	intron-variant	Amph	Mm_Celera	13:18966665	GTGTACTCCTAGGGA[C/T]ACGTCTCCCCATAGA	218038
rs47119034	snp	G/T			intron-variant	Amph	Mm_Celera	13:19021521	CGCAACATGGAAATT[G/T]GAGAGTGGCCAAGCA	218038
rs47119071	snp	A/T			intron-variant	Amph	Mm_Celera	13:19116368	ATACATTCAGTGATA[A/T]TGTATTCCCCTAGAA	218038
rs47119766	snp	A/G			intron-variant	Amph	GRCm38.p3	13:19129799	GTAGTCTTTCTGTGC[A/G]CCAGAATTATTATTC	218038
rs47125835	snp	A/T	0.46281	0.131194	utr-variant-3-prime, intron-variant	Amph, Gm31887	Mm_Celera	13:19152813	CACAAAAGGCGTGAC[A/T]GCACACCTTGGAGCT	218038
rs47129443	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19111177	GATATTCATCTTCAA[C/T]ATTCCCTCTTCAACT	218038
rs47132775	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19117728	TAGTGAAATAGACCC[A/G]AGTGAAGAACGAGTG	218038
rs47135003	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18953301	AGTGATAGACTCGGG[C/T]GGTTCTTTCCAGTGT	218038
rs47135443	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19121102	GTGGTGTTTCCTGGG[C/T]AGTCTGCTAGTACAG	218038
rs47150129	snp	C/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19073793	CTTTTCTATTATAAG[C/G]CACCAACAACCAAGC	218038
rs47153911	snp	C/T			intron-variant	Amph	Mm_Celera	13:18993239	TTACATACTCTGCTG[C/T]GTGCTTGACAGAGAT	218038
rs47172755	snp	A/C	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:18978290	CTAGGAATGACCCTT[A/C]GGGGTGATTTCCTGA	218038
rs47175180	snp	A/T			intron-variant	Amph	GRCm38.p3	13:19115998	GCTCTCACAGTATCT[A/T]CATGTGGATAAGCTA	218038
rs47182097	snp	A/G	0.48	0.0979796	intron-variant	Amph	GRCm38.p3	13:19089447	CATGTGAAGAGGATG[A/G]ATCAATCTCGCCTCT	218038
rs47182160	snp	C/T	0.124444	0.216185	downstream-variant-500B, intron-variant	Amph, Gm31887	Mm_Celera	13:19154104	GTACCCAGCACATGG[C/T]GGAATCTTGGACCTG	218038
rs47195559	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19118110	CACTACACTGAAGTG[C/T]CTTCTCATTCTTTTG	218038
rs47206686	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19105971	TCACTCTGAGAACTA[C/G]TATTTTGATCAGTTG	218038
rs47219058	snp	A/G	0.197531	0.244432	intron-variant	Amph	Mm_Celera	13:19128266	CTATGTCAAAGTACC[A/G]GTATCTTCTCTATGA	218038
rs47224279	snp	A/T	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:18983048	TTTGTGGAAAATAAC[A/T]AAATAGAGAAGTCAC	218038
rs47231039	snp	A/G	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:18979969	TCTGTTAGGTTTGTC[A/G]AACTTGTATCTCTCG	218038
rs47237300	snp	A/G	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:18968367	GAGGGATTGTAGTTT[A/G]CATTCTTAGGGCCTG	218038
rs47240466	snp	C/T			intron-variant	Amph	Mm_Celera	13:19053217	CGGTAACAGTTTTTC[C/T]GACACTAGTGTATAG	218038
rs47244929	snp	C/T			intron-variant	Amph	Mm_Celera	13:19078140	TAGGATGAAACATCT[C/T]ATAAAGAGTGTTAGG	218038
rs47245961	snp	G/T	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:19029321	ATAGGTAATGGATTG[G/T]AATACATCGCAAATG	218038
rs47246583	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19034163	AGAATGCTTAGACTT[C/G]CTTATCATGTGCAAT	218038
rs47247670	snp	G/T	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:18969244	CAGCAGTCTGTCAAT[G/T]GATGGTGTTGAGATC	218038
rs47250105	snp	C/T			intron-variant	Amph	Mm_Celera	13:19050151	GTTGTTTTAAAATTC[C/T]ACTTTTCTAAAATAG	218038
rs47251055	snp	A/T	0.32	0.24	intron-variant	Amph	Mm_Celera	13:19036688	CTGTTTAAAATTTTG[A/T]CTGTTAGGGTATCAA	218038
rs47256454	snp	C/T	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19012572	AGGGACCAAAGGAGG[C/T]GGTGGATACTGCACC	218038
rs47257774	snp	C/T	0.32	0.24	intron-variant	Amph	Mm_Celera	13:18955105	TTCACCTTATTCTGA[C/T]GCAGTTATTTAGTTG	218038
rs47261770	snp	A/T			intron-variant	Amph	GRCm38.p3	13:19131841	GAAGATGGGGGAGAA[A/T]AGGAAGGCCAATATG	218038
rs47261995	snp	A/G			intron-variant, nc-transcript-variant	Amph, Gm31887	Mm_Celera	13:19145569	GCCCTCTGCCAAATA[A/G]CTTAGCCCATTGATT	218038
rs47264224	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19073163	ATAAGGGACTTTGTC[A/G]GTAGCAAATCCTTCT	218038
rs47268486	snp	A/T			intron-variant	Amph, Gm31887	Mm_Celera	13:19147692	GCCCCACTCAGGAGA[A/T]AAACTGCACACTCTC	218038
rs47271796	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19033587	TCTTAACAACCCAGT[A/G]TGCAATTTGATTTCC	218038
rs47274250	snp	A/G	0.48	0.0979796	intron-variant	Amph	GRCm38.p3	13:19115829	TTAGTTAAGGATTAA[A/G]GTCTGCATTTGCTCA	218038
rs47284514	snp	A/G			intron-variant	Amph	Mm_Celera	13:19081618	TTCTTCCTATATATG[A/G]TACTGTGTAGTTTAT	218038
rs47294451	snp	A/T			intron-variant	Amph	Mm_Celera	13:19081298	CTGGGGTTTCTGTTA[A/T]GTAGTCTGTGGCTCT	218038
rs47297684	snp	A/C	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19002453	TTTGAGAATAAAAAA[A/C]GTTATATTGCTGAAG	218038
rs47300348	snp	A/C			intron-variant	Amph	Mm_Celera	13:19036529	ATGTAAGACATAAAT[A/C]CCTGTGTAGAGAGAA	218038
rs47300565	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19103343	CCTTTGCCTGGGATG[C/T]CCCGTGCTCTGAGCA	218038
rs47307314	snp	C/T	0.152778	0.230321	intron-variant	Amph	Mm_Celera	13:18989055	AGAGTTTTTAATAGG[C/T]ATAAATTTACTAATG	218038
rs47312890	snp	C/T	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19030846	CAGACTGTTTATATA[C/T]TAAGGTAGTCTGAAG	218038
rs47313861	snp	A/G	0.5	0	intron-variant	Amph	GRCm38.p3	13:19137265	GAATTCTGTTTTTAC[A/G]TTGTTATACTTTCAA	218038
rs47318364	snp	G/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19037901	TTGAGTTGTGTCATG[G/T]AGGAGACAATTAATT	218038
rs47325598	snp	A/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19083992	TTGCAGTTTTCAGAC[A/G]AATGACACTGTTAAC	218038
rs47326003	snp	A/G	0.244898	0.249948	intron-variant	Amph	Mm_Celera	13:19127200	GATAGTAATTTCACG[A/G]CTCTTCAAAAAGAAC	218038
rs47326292	snp	C/T			intron-variant	Amph	Mm_Celera	13:19053283	ACATCATCCCTTCTT[C/T]TTCTTTCTACCCCCA	218038
rs47332321	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19117873	ATTTTCATTTCTTGG[C/T]TTCCTAAGGGAGAAA	218038
rs47333469	snp	A/G	0.152778	0.230321	intron-variant	Amph	Mm_Celera	13:19082464	ATTCTCTGTGTATAC[A/G]CCCTGTAATGGACAG	218038
rs47334105	snp	G/T			intron-variant	Amph	GRCm38.p3	13:19140631	TAACAGTCAGTTATA[G/T]CTCTAATAGTTTTTA	218038
rs47346411	snp	A/G	0.336735	0.234472	intron-variant	Amph	Mm_Celera	13:18952322	GGCCTTGAACTGTGT[A/G]GACTCACAGTGGAAG	218038
rs47348182	snp	A/G			intron-variant	Amph	Mm_Celera	13:18964204	GGGCTCGAGTCGAGC[A/G]GAAGGGACTTGTGCC	218038
rs47350979	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19089764	GCATAGACCAAAACT[A/G]ACTTCCTTGACTCCC	218038
rs47355484	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18970579	TTTGAATATAGTAAG[C/T]TTTAGGAGATGCTTA	218038
rs47358401	snp	C/T	0.473373	0.11227	utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19153148	TGTTCAGCTTGGAGA[C/T]ACTCTCTTTCCTGAC	218038
rs47367526	snp	A/C	0.142012	0.225474	intron-variant	Amph	Mm_Celera	13:18966836	GGTCATTTGTTCTGC[A/C]TATTTTTGTCTCCTG	218038
rs47374102	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19045811	GCCACCAAGCACACT[C/G]CCACAATAGGAAAGG	218038
rs47374405	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19036613	TTGAATTCTCTATTC[A/G]AGGGCTGCTGTATAG	218038
rs47374660	snp	A/G/T			utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19152990	GCATCATACTGTTCC[A/G/T]CTGTTCCACGTGTGG	218038
rs47374698	snp	C/T			intron-variant	Amph, Gm31887	GRCm38.p3	13:19146228	AGATCTCAAAGGCTG[C/T]CTCCACAGTGACACA	218038
rs47378848	snp	C/T	0.495868	0.0452663	utr-variant-3-prime, intron-variant	Amph, Gm31887	Mm_Celera	13:19153309	GAAAAACCTGAGTAG[C/T]CTCCCCAAATATTTT	218038
rs47385935	snp	C/G	0.244898	0.249948	intron-variant	Amph	Mm_Celera	13:19026436	GAAGAGCCTAGCATG[C/G]AAGTATAGGTACAGC	218038
rs47390839	snp	C/T	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:19101925	GGTGAGTTAGCTCTG[C/T]GGGCAATCTCTAGAC	218038
rs47394320	snp	A/T	0.152778	0.230321	intron-variant	Amph	Mm_Celera	13:19127484	AGTGCTGCTGTGCAA[A/T]ATGAGGAAGGCAAAT	218038
rs47400751	snp	C/T	0.32	0.24	intron-variant	Amph	Mm_Celera	13:18990351	TTCCTCTCCTTTTGA[C/T]TGTACTTATGATAAC	218038
rs47401702	snp	C/T			intron-variant	Amph	Mm_Celera	13:19081258	CCCTGACCAACAATA[C/T]GAAGGGAGGTTTCTT	218038
rs47412378	snp	C/T			intron-variant	Amph	Mm_Celera	13:19053867	TTTAACACAGCTCTT[C/T]ATGTTGCAGTGATCC	218038
rs47413028	snp	A/C	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19043897	CATATCATCCAAGGA[A/C]TGAAATTTCAGTGAG	218038
rs47418574	snp	C/T			intron-variant	Amph	Mm_Celera	13:19053406	TTACTTTAGGGTCTC[C/T]GATCCCATCTTAGTT	218038
rs47420251	snp	A/C	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19074720	TGGCCCAGATTCTCT[A/C]GGTTGCTGGTTTGAG	218038
rs47422020	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19006436	GCTGCCGAGTATACA[A/G]AATCATTCTAAGCCA	218038
rs47422979	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19076811	CCATTAGGCTTTGTG[C/T]TGGATGATGACTTGG	218038
rs47427717	snp	C/G	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19084709	CCCTCTGTAGCACAC[C/G]TAGTCCAGTCACTAA	218038
rs47430901	snp	G/T			intron-variant	Amph	Mm_Celera	13:19088221	CTTCGACATGGAAGC[G/T]ATGAAGGTTCGCATC	218038
rs47432703	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19081343	TTTCCAATGTAGTGT[A/G]ACTCCAGTGACAATA	218038
rs47438987	snp	G/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19036929	CGTAATGCTGTCTTG[G/T]GTCATACACCCCTTC	218038
rs47439148	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19125248	GTCTTAGCTGCCCTG[C/G]ATATTTCTCTGACAT	218038
rs47449272	snp	C/T			intron-variant	Amph	Mm_Celera	13:19053715	ACATCAGGACTTTGG[C/T]GACATGCCCTTTAAA	218038
rs47451544	snp	A/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19117408	TATCCCTGAATTTTG[A/T]AACTTTATTTATAAC	218038
rs47454683	snp	A/G	0.489796	0.070696	intron-variant	Amph	GRCm38.p3	13:19125743	CATAGTAGAGCAATG[A/G]CATAACCTAATCAAC	218038
rs47455348	snp	A/C	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19071735	CTGCTACCTTAAGGT[A/C]ATTTCCTGACTCAAA	218038
rs47455999	snp	C/T	0.48	0.0979796	intron-variant	Amph	GRCm38.p3	13:19105929	TGTCACTTTAACATA[C/T]CTCCAGCAGTCCTTA	218038
rs47461423	snp	A/G	0.165289	0.235211	intron-variant	Amph	Mm_Celera	13:19027356	ATAGTGTTTACATTA[A/G]GAAAGCCTGATCATG	218038
rs47462825	snp	A/G	0.459184	0.136902	intron-variant	Amph	Mm_Celera	13:19092969	GGACAGTCAGTCAGT[A/G]TAAGGCCAGTGTAAG	218038
rs47463123	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18982553	CTTAGTGGAGGGACG[A/G]TGCTCAAATACTACA	218038
rs47465928	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18953562	CAGAAGAATAGCTTA[C/T]CTGGTTGTGATTATG	218038
rs47468490	snp	A/G			intron-variant	Amph	Mm_Celera	13:19053400	TACTGTTTACTTTAG[A/G]GTCTCTGATCCCATC	218038
rs47478200	snp	C/T	0.32	0.24	intron-variant	Amph	Mm_Celera	13:19026605	TCTCAATCTCGGCAT[C/T]CTTCTTGTATCCCAC	218038
rs47478259	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19059165	AATCATCAGCTGGGG[C/T]CCTTTAAATGCTGAT	218038
rs47483646	snp	C/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18971038	AAGATCAGAAGAGTT[C/G]CAAATGCAGGCCCAT	218038
rs47490841	snp	A/C	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19083210	CACTCTTCAAGGACG[A/C]ATTCTATCATCTCAG	218038
rs47495050	snp	C/T			utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19149862	TGCAGATGCTGCAAA[C/T]GGGTCACGTGACTGG	218038
rs47495283	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19120847	CTCATTAAGTGCTCC[A/G]TGATGCTATACCAAT	218038
rs47503214	snp	A/G	0.444444	0.157135	intron-variant	Amph	GRCm38.p3	13:19130287	CTTGAGCACTGAGGT[A/G]CCTTCCTACAGCACC	218038
rs47503915	snp	C/G	0.152778	0.230321	intron-variant	Amph	Mm_Celera	13:18980276	AACTAGGAATGTTTA[C/G]GCAGCAGGAAGACAC	218038
rs47509180	snp	A/C	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19122742	TTTCCGTCTAGTCCT[A/C]TCCTCATGTATTCTC	218038
rs47513968	snp	C/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:18989635	ACGCGCTGAGTACAG[C/T]TGCAGGCTTGCCAAT	218038
rs47517848	snp	A/G	0.21875	0.248039	intron-variant	Amph	Mm_Celera	13:19127935	ACAGTTATTGCCATG[A/G]CAACAGTGTAGCAAT	218038
rs47521597	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19125235	GCTTCCTATCCGGGT[C/T]TTAGCTGCCCTGCAT	218038
rs47526547	snp	G/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19109417	TTAAATGTCATGGTA[G/T]TCAGGGAGCGATTTG	218038
rs47530127	snp	A/G			intron-variant	Amph	Mm_Celera	13:19049880	GCTGGAAAAGGTGTG[A/G]TGTTTATGTGCAAAT	218038
rs47531565	snp	A/G			intron-variant	Amph	Mm_Celera	13:19075435	TCCTATTCCTATCAC[A/G]GTAATTTTGAGATAT	218038
rs47531942	snp	A/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19043835	GGAACTCTTTTTACA[A/T]GTGGGAACTATTTCA	218038
rs47534320	snp	C/G			intron-variant	Amph	Mm_Celera	13:19075301	CTGTGGATTTGAAAG[C/G]AAAGCAAAGACATGT	218038
rs47535511	snp	G/T	0.32	0.24	intron-variant	Amph	Mm_Celera	13:19008806	TTTCTTGTCCACAGG[G/T]GAAAATTCTTAGCAG	218038
rs47535803	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18967482	GCTTTAGAGGCTAGC[A/G]CTTCCAGGTTTTATT	218038
rs47538663	snp	C/T	0.497778	0.0332592	intron-variant	Amph	GRCm38.p3	13:19113045	GCATGGCTCGGGCAT[C/T]TCAGTGAGCCATTCT	218038
rs47540801	snp	C/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:18975349	ATAATTAAGAAATTA[C/T]GGTGACCATAGGGCT	218038
rs47542264	snp	G/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18992748	GAATTTGAATAATGG[G/T]CCAAATTATAGTGCT	218038
rs47545720	snp	C/T	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19034126	TGAAAATGTATGGGC[C/T]AGCAGGGATCACCAT	218038
rs47552529	snp	C/T			intron-variant	Amph	Mm_Celera	13:19004720	TTTTCTTTCCTCCCT[C/T]GTTCCCTGACTCAAG	218038
rs47553291	snp	A/G			intron-variant	Amph	Mm_Celera	13:19053474	AATATCTTGGTCATT[A/G]ACTATTAACTACTTC	218038
rs47553633	snp	A/G			intron-variant, nc-transcript-variant	Amph, Gm31887	GRCm38.p3	13:19145899	TTGTCCCAGTCATAC[A/G]GCCAGCTCACAGCAA	218038
rs47554360	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18976204	GAGAAATGGCTTGAA[A/G]TACACAGGTGGGATA	218038
rs47555417	snp	A/G			intron-variant	Amph	Mm_Celera	13:19075374	TAATAACATTCCACA[A/G]CCCAAGAGAAGTTCT	218038
rs47566309	snp	A/G	0.336735	0.234472	intron-variant	Amph	Mm_Celera	13:19008916	GATTTTAAGACATTT[A/G]TCCTTTAGTTTCTTA	218038
rs47568914	snp	A/G	0.277778	0.248452	intron-variant	Amph	Mm_Celera	13:19126886	TCCTATTTACTGAGC[A/G]CTTTCCTCCAGGTGT	218038
rs47582880	snp	A/G			intron-variant	Amph	Mm_Celera	13:19083126	GTGTGAGGACCGTTG[A/G]TTATGTAGACTTGCC	218038
rs47584607	snp	C/T			intron-variant	Amph	Mm_Celera	13:18992362	AAATTGGACATAGTA[C/T]TACCTGAGAACCCAG	218038
rs47592408	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18969610	GTTAGAATAGAGCCA[A/G]TGTCTCAAAATTTGG	218038
rs47592844	snp	A/G	0.124444	0.216185	utr-variant-3-prime, intron-variant	Amph, Gm31887	Mm_Celera	13:19153120	AGTTAGACAACTGAG[A/G]GCCATGTGGTTCTGT	218038
rs47595528	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19105407	GCTATGCACCACTTT[C/T]TGTAGGACCTCATGA	218038
rs47596814	snp	A/G	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:19010571	GGATTATAATTTCCC[A/G]TATATTCAATTTCTC	218038
rs47598036	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18970600	GAGATGCTTATGGAA[C/T]GAATGAATTGATGAT	218038
rs47598897	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19109426	ATGGTAGTCAGGGAG[C/T]GATTTGCTCAGCAGC	218038
rs47603958	snp	G/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18952264	GACCATAGTTCATTG[G/T]ACCCGAGTTATAAGC	218038
rs47608058	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18952948	TTGTTTGTTTCCTTT[A/G]GGGACTTGTCTCTTA	218038
rs47609912	snp	C/T	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:19039207	GCTGTTACACATTAG[C/T]TTCATGGCTCTCAAC	218038
rs47610219	snp	C/T	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:19029242	GTGGCTAACAAGGCT[C/T]GGTATACACCTTGTT	218038
rs47612138	snp	G/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19123088	ACCAATCCTCTGAGT[G/T]TGTATTAAATAACCC	218038
rs47619057	snp	C/T	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:18972996	TAATGAGTGTGCTAC[C/T]AAGTTATATATTGGA	218038
rs47619192	snp	C/T	0.459184	0.136902	intron-variant	Amph	Mm_Celera	13:18988646	ATATAGGTTCTTTCA[C/T]GTTTGTCTTTGGTTA	218038
rs47620747	snp	A/G	0.32	0.24	intron-variant	Amph	Mm_Celera	13:19039273	GCTTCATCAATGAAA[A/G]AGGACAACCATAGTA	218038
rs47620748	snp	G/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19105191	ATTTGAAGTTTTCTG[G/T]CTCGGTTACAAGGAC	218038
rs47628955	snp	A/C	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18953620	CTGGAGCACATCACG[A/C]TTCTGCTTTCTAATT	218038
rs47634423	snp	A/G	0.345679	0.230967	intron-variant	Amph, Gm31887	Mm_Celera	13:19148042	TGGTGCCTTCAGCTG[A/G]CTCTGCACAGGATTT	218038
rs47637699	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19111491	AAAGCAGACTAGAAA[A/G]GAATGAGAGAAAGAA	218038
rs47640434	snp	A/G	0.408163	0.193609	intron-variant	Amph	GRCm38.p3	13:19127562	TGCTCAGGAATAGCA[A/G]GTTACCAGCCTGGTT	218038
rs47656558	snp	A/G	0.444444	0.157135	intron-variant	Amph, Gm31887	GRCm38.p3	13:19149101	TGTGAGAGAAACAAG[A/G]CTCATTTAGAAAGAA	218038
rs47667343	snp	A/C	0.42	0.183303	intron-variant	Amph	Mm_Celera	13:19131267	TACATAGGGCGTATA[A/C]ATCAACACAAAAGAA	218038
rs47682026	snp	A/G	0.497041	0.0383476	intron-variant	Amph	Mm_Celera	13:19059122	CATACAATGATAGAC[A/G]CAGTGAAGAATTGAA	218038
rs47684456	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19140327	TGGGATTGAATATCT[C/T]TATCTATTTTCTTTG	218038
rs47685039	snp	A/G			intron-variant	Amph	GRCm38.p3	13:19142461	CAATTAGATGAGATG[A/G]CTTTTTCTTAAGATA	218038
rs47691643	snp	A/C			intron-variant	Amph	Mm_Celera	13:19078264	ATTAAAGCACAAAGT[A/C]TTTATTTTTGGGTGA	218038
rs47693863	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18978520	TTCAGTCCACAAACT[C/T]AGTGAAGGTGAGGTA	218038
rs47696259	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19006086	TATGTAACATCTACC[A/G]TTTTTTCTAAGCCTT	218038
rs47696494	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18982741	GGGAACTGAGGGTCT[A/G]GGAGTCTCTGGAGCC	218038
rs47708087	snp	A/C/T	0.444444	0.157135	utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19152909	ACTAAAATCTGCCTT[A/C/T]TGGTTTTTACTTAGA	218038
rs47709751	snp	C/T			intron-variant	Amph	Mm_Celera	13:19054518	AATTACTCTGTTCCA[C/T]CATGATCAGTAAGAG	218038
rs47722997	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19084399	CTCAGAGCATGAATC[C/G]CAAACCAAGATGAGA	218038
rs47725219	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18967096	TGTCAGGTTTCCCAA[C/T]CTAACTTTCAAGTAT	218038
rs47728580	snp	A/G	0.18	0.24	intron-variant	Amph	Mm_Celera	13:19128715	CAATGGAGAAATCCC[A/G]CAAAGATCAGAAGGC	218038
rs47731666	snp	C/G			utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19152551	TTTGTCAAAGCTAGA[C/G]AGGCTTTGAAGTAAG	218038
rs47737949	snp	C/T	0.32	0.24	intron-variant	Amph	GRCm38.p3	13:19127169	CAGATAAAGTTATTT[C/T]CCTAAAAGCAGAAGA	218038
rs47743892	snp	C/T			intron-variant	Amph	Mm_Celera	13:19126960	GTTCTAAGCATATTA[C/T]AAAAAGCAGTCATGA	218038
rs47745203	snp	A/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19027364	TACATTAGGAAAGCC[A/T]GATCATGCCAGGAAT	218038
rs47758667	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18972178	AAGTCCTTGATTTGT[C/T]TTTAAGTAACACACT	218038
rs47762526	snp	A/T	0.231111	0.249285	intron-variant	Amph	Mm_Celera	13:19077950	CTGCTAGGCCTCTGC[A/T]TTGGTTTCTGATCTT	218038
rs47776878	snp	A/T			intron-variant	Amph	Mm_Celera	13:19052606	ACACCAGAACCAAGA[A/T]GTGCTCACAAATTGG	218038
rs47777208	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19080281	CACATTTTGGATTGG[A/G]AAACACACTTAAACA	218038
rs47777371	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19004740	CCTGACTCAAGGTTT[C/T]ATGCAAGAATGATCC	218038
rs47782865	snp	C/T	0.18	0.24	intron-variant	Amph	Mm_Celera	13:18952999	TGTGACTTGTGGTTG[C/T]CTTGCTTTATAGAAG	218038
rs47789330	snp	A/C	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18970807	GTTTTAGACATACAT[A/C]TTCTTGTTTGGTACT	218038
rs47790402	snp	C/T	0.35503	0.226867	intron-variant	Amph	Mm_Celera	13:19029433	AAGAATGCAAGCTAT[C/T]TGTTTATAACCGTGT	218038
rs47799335	snp	C/G	0.35503	0.226867	intron-variant	Amph	Mm_Celera	13:18988426	ACTGTATCCTCAGTG[C/G]TCAGAGCAGCATGAA	218038
rs47810725	snp	G/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18983251	CGAGGTTAAGGATTT[G/T]TAAGAGCTTCTTTTC	218038
rs47812309	snp	C/T	0.408163	0.193609	intron-variant	Amph	GRCm38.p3	13:19133864	TAATCATGCAAAGAA[C/T]TGAGAAGAACTCTTT	218038
rs47812648	snp	A/C/G	0.459184	0.136902	intron-variant	Amph	GRCm38.p3	13:18956175	TAACATGTTCCGACC[A/C/G]TACTAACAGTTGATC	218038
rs47813493	snp	C/G			intron-variant	Amph	GRCm38.p3	13:19130267	AGCCTACAAGGCAGA[C/G]GATGCTTGAGCACTG	218038
rs47814907	snp	C/G/T			intron-variant	Amph	GRCm38.p3	13:18982059	AGCATGAGGAGTCTC[C/G/T]GCAAGAAGCTAGGAA	218038
rs47821764	snp	C/T	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:19085088	TGTCAGGTGGGTCAA[C/T]ACAGCTCCTCTAGAA	218038
rs47828566	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19119550	ACACAAGCACATTTG[C/T]TGAGTGGCAGGAATC	218038
rs47828721	snp	A/G	0.165289	0.235211	intron-variant	Amph	Mm_Celera	13:19134748	AGATATCGAACTATT[A/G]AAACCATTTGGCTGG	218038
rs47832045	snp	G/T	0.459184	0.136902	intron-variant	Amph	Mm_Celera	13:18988868	GGGTATGGTTTTATA[G/T]TGAAGCAATGATTTC	218038
rs47834693	snp	A/T			intron-variant	Amph	Mm_Celera	13:19075198	TCTAACTTTTGGAAA[A/T]GCAAAAATGTAGCTG	218038
rs47835488	snp	A/G	0.46875	0.121031	intron-variant	Amph	Mm_Celera	13:19095007	TCTCTAAGCCACTTT[A/G]ATTAAAAAATACGTT	218038
rs47844138	snp	A/G			intron-variant, nc-transcript-variant	Amph, Gm31887	Mm_Celera	13:19145582	TAGCTTAGCCCATTG[A/G]TTTTCAATTTTTACT	218038
rs47847501	snp	C/T	0.142012	0.225474	intron-variant	Amph	Mm_Celera	13:18966807	CTGTGGTACAAATGG[C/T]CCATGGTGGTAGGGG	218038
rs47852750	snp	G/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19031649	GTAATACAACATCAT[G/T]GTTGCCTATTTTATG	218038
rs47853215	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18985304	CCAGATGTTTCTGAG[C/T]CAGTCTTTCCCTACT	218038
rs47853670	snp	C/T	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:19028075	TGGGAACAGATACTG[C/T]TTTCATTCATCATGA	218038
rs47862114	snp	A/C	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19034646	TGGGTAGGCTATATT[A/C]CTTGGTTGAACACAA	218038
rs47862615	snp	A/G			intron-variant	Amph	Mm_Celera	13:18963899	CCTCGCAGAAGTTGT[A/G]TTCCACTCACTAGAG	218038
rs47866274	snp	C/T	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19008643	GAATGGAGACTTTTA[C/T]ATAACTGTTTCTTTG	218038
rs47869514	snp	C/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19012929	GGGGCAGTAGAGAGT[C/G]TCCATGGAACTGGAT	218038
rs47876657	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19035542	CCGCAGCAGTCGCCA[A/G]CCAGGTTCTGTCTGT	218038
rs47879138	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19114008	CCAGCCTGGCTTAAA[A/G]AGACTCAGAACAAAT	218038
rs47886209	snp	A/G			intron-variant	Amph	Mm_Celera	13:19021399	TAGCCACTTAAGAGC[A/G]AGGGAAGAGAGATTC	218038
rs47899022	snp	A/C			intron-variant, nc-transcript-variant	Amph, Gm31887	Mm_Celera	13:19145645	AAACACAGTCTGGTT[A/C]TTTGGCAAAATAAAA	218038
rs47901749	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18990208	CAATGTCACCATTGT[C/T]AGTAGAGCTCCCTTT	218038
rs47902606	snp	A/T			intron-variant	Amph	Mm_Celera	13:19126654	TTTATTGTTGCTTTT[A/T]TAGCTCCAGTTCAAT	218038
rs47904519	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19118699	TCAGGATGAGGATGC[C/T]CCTCCAGCTAGAAAT	218038
rs47911050	snp	A/G	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:18987700	CTAACAAAACACTAA[A/G]CATCTACTTACTTGT	218038
rs47914390	snp	A/G	0.197531	0.244432	intron-variant	Amph	Mm_Celera	13:19101261	CAGTTACATGCCTCC[A/G]GGGTCATTTTGCTTT	218038
rs47914689	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19085954	GTTGTGGGCCAGTGT[C/T]TCCACCTTTAGATTA	218038
rs47919250	snp	A/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19012402	TAATTCTTAATTTTG[A/T]CTCTTAACACTCCTG	218038
rs47932018	snp	A/T			intron-variant	Amph	Mm_Celera	13:19096742	TGAAAATATATATAT[A/T]TTACTCATTCTTTTA	218038
rs47937278	snp	A/T	0.486111	0.0821678	intron-variant	Amph	Mm_Celera	13:19093719	GAAGATGGTAGTACT[A/T]GAGAAACAGACTGAG	218038
rs47937288	snp	C/T			intron-variant	Amph	Mm_Celera	13:19091346	AACATTGTTTTTCCT[C/T]TTATTAGCATATTCA	218038
rs47938911	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18966888	TAGTGGCTTTTCCTT[C/T]ATTTGTACATAGCAT	218038
rs47943429	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19004634	CACACAAGGAAAGTT[C/T]CCACAAAGGCTGAGT	218038
rs47947875	snp	A/G	0.35503	0.226867	intron-variant	Amph	Mm_Celera	13:19124914	AGAATGAATTCAGTG[A/G]AACTGGCTGCCTGCT	218038
rs47962229	snp	C/T			intron-variant, utr-variant-3-prime	Amph, Gm31887	Mm_Celera	13:19151399	AAATGTCTACTAATA[C/T]ACTTCTGTATCCAGT	218038
rs47967235	snp	C/T			intron-variant	Amph	Mm_Celera	13:18981957	CAGGGGAATGAGCTC[C/T]GGCCACAGTATACAG	218038
rs47968406	snp	C/T	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:18980389	TTTTATGATAATTTT[C/T]TGCCTTATGTTGTAT	218038
rs47973872	snp	C/T	0.391111	0.206368	intron-variant	Amph	GRCm38.p3	13:19125946	TCAGAAGTGGAAACA[C/T]ATGGAGCCTGGTGCA	218038
rs47982117	snp	A/T	0.375	0.216506	intron-variant	Amph, Gm31887	Mm_Celera	13:19148037	TGTCTTGGTGCCTTC[A/T]GCTGACTCTGCACAG	218038
rs47985520	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19130853	ATCCTGGGGAAAGGG[C/T]TTATCTGATTTACAT	218038
rs47993094	snp	A/G			intron-variant	Amph, Gm31887	GRCm38.p3	13:19149246	GTAGTGGTGAGCCCT[A/G]TATTGGGGACTTTGT	218038
rs47996525	snp	C/T	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:18951777	TAACTTATATTTGGA[C/T]CTTGCATAGACATCT	218038
rs47997607	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19117896	GGGAGAAATTGTAAA[C/G]TAGCCATGATACATC	218038
rs48001718	snp	C/T	0.152778	0.230321	intron-variant	Amph	Mm_Celera	13:19099980	AGTGGTGAGTAATGG[C/T]GACTGTTGCTGTTAT	218038
rs48006058	snp	A/G	0.124444	0.216185	utr-variant-3-prime, intron-variant	Amph, Gm31887	Mm_Celera	13:19152930	TTTACTTAGAGCTGA[A/G]AGAAAATTCTTACAA	218038
rs48008268	snp	C/T			intron-variant	Amph	Mm_Celera	13:19049313	GATCTAAATTTGGGG[C/T]CTGAAAAATTTTTGC	218038
rs48010968	snp	G/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18975190	GGGAGGGCTTCGGAT[G/T]CTTCTCTAGCCACGG	218038
rs48018646	snp	C/T	0.444444	0.157135	intron-variant	Amph, Gm31887	GRCm38.p3	13:19149537	ATTAGAAGGTTAAAA[C/T]TTACCTTCAGTTAAG	218038
rs48021757	snp	A/G	0.244898	0.249948	intron-variant	Amph	Mm_Celera	13:18990589	AGTATTATGAAAAGA[A/G]TAATACCAGATTTAT	218038
rs48023808	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19091178	CTCGCCTCATCTGCT[C/T]CTGTTGCCATTTAGG	218038
rs48024547	snp	C/T			intron-variant	Amph	Mm_Celera	13:19075694	ACACTACTTTTCTTC[C/T]TTTTAATGTCCAGAA	218038
rs48028052	snp	A/G			intron-variant	Amph	Mm_Celera	13:19081113	CCCAGGTCAGCTCTA[A/G]CTTGATTCCTCTGAG	218038
rs48030153	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19026630	TCCCACCTCTTTATG[C/G]AGCTTTTCTATTCTG	218038
rs48044689	snp	A/G	0.152778	0.230321	intron-variant	Amph	Mm_Celera	13:19099800	ATATTTTTCAAAGTT[A/G]TATATTGGAAACATA	218038
rs48050864	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18969636	TTTGGCAGAGTTTTC[A/G]GAATTAAATGCTAGC	218038
rs48067022	snp	C/T			intron-variant	Amph	Mm_Celera	13:19078408	CTAAGATATAAAGGA[C/T]TTAGACAGTAAACTA	218038
rs48068085	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19125364	AACTATCCCATGATT[A/G]TTCTGTTGTCAGTGG	218038
rs48068406	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19045210	CATTTCTGTCCATTG[C/G]AGTCACTAACAGCAG	218038
rs48078896	snp	C/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19123771	AAGATCCAGAATTTC[C/G]CCAGCTTTCTAGAAA	218038
rs48089122	snp	A/G	0.46281	0.131194	intron-variant	Amph	Mm_Celera	13:19095875	TTACAAAATGGTGTG[A/G]ATTTCAACAAATGTC	218038
rs48090697	snp	A/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19090327	TTTATTTATTTATTT[A/G]TTGCTCCAAACTTCC	218038
rs48096031	snp	A/G			intron-variant	Amph	GRCm38.p3	13:19129307	TAGTACAGAAAATAA[A/G]AAAAGTTATGTAGAT	218038
rs48105248	snp	A/G			intron-variant	Amph	Mm_Celera	13:19140474	AGTTGTTTAAGCAGT[A/G]CACATAAAACCCAGG	218038
rs48112156	snp	C/G	0.459184	0.136902	intron-variant	Amph	Mm_Celera	13:19010455	TTTGCCATAAGGGAA[C/G]TTAATATCCCAGAGT	218038
rs48116467	snp	A/G	0.345679	0.230967	intron-variant	Amph	GRCm38.p3	13:19127213	CGACTCTTCAAAAAG[A/G]ACTCAGACATAATTT	218038
rs48120738	snp	A/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19135067	GGGCCTCAGCTGGGA[A/G]CTCTGTACCACTAAT	218038
rs48122281	snp	C/T	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:19003666	CACTGGCACAGCAGA[C/T]TGCTAGCCTAGCTAA	218038
rs48124582	snp	A/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18956210	GTGCAATCAGATTTC[A/T]GCTCATATACTGAAG	218038
rs48125406	snp	A/G	0.391111	0.206368	intron-variant	Amph	GRCm38.p3	13:19118767	TTGCTATTACTACGT[A/G]CATGGAGATGGACCA	218038
rs48128041	snp	C/T			intron-variant	Amph	Mm_Celera	13:19130516	TTCCCAGCCCAGGGG[C/T]TGAGCTGCCCTTCCC	218038
rs48128569	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19080133	TGTTTAAGCAGATGC[C/T]TGGTGATCTTCCCAT	218038
rs48130858	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19047834	AACTGGATAATCTAA[C/T]AGTGCCTGACTGTAC	218038
rs48131347	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19029627	ATCAAAGGCTGGAAG[C/T]ACAGATGACCCTGTC	218038
rs48133338	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18964275	ATTTTACAGATGTTG[A/G]GAGAATTCACCGGCA	218038
rs48143230	snp	C/T			intron-variant	Amph	Mm_Celera	13:19081282	GTTTCTTTGCCTGGG[C/T]CTGGGGTTTCTGTTA	218038
rs48143879	snp	C/T	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:19039473	TCCTCCAGGGACCCT[C/T]TCCATCTGTTTCCTA	218038
rs48150820	snp	C/T	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:19013109	TCACTCAGAGTTCTA[C/T]AGCAGGAAAGTATCA	218038
rs48152141	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19086013	GATCAAGATTTACCA[C/T]TCACTTAAAGAAATT	218038
rs48157186	snp	C/G			intron-variant	Amph	Mm_Celera	13:19053816	GTTTGTATTCATCCT[C/G]AACAGCGTTTCTCAG	218038
rs48157384	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19040962	TGCCATCTGCATCCT[C/T]TGCCCTTATCAACTT	218038
rs48157867	snp	C/T			intron-variant	Amph	Mm_Celera	13:19098394	TCAGCTTCTTTTAGC[C/T]TTCCCTAATTCAACA	218038
rs48160357	snp	A/G			intron-variant	Amph	Mm_Celera	13:19116127	TGTTTCTATAACCAA[A/G]AGTAGAGCTATGGAA	218038
rs48161232	snp	G/T	0.336735	0.234472	intron-variant	Amph	Mm_Celera	13:18952037	ACAGTACCTTATTTC[G/T]ATTAAGACCAGGCAA	218038
rs48171267	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19117626	CTTGTGGGCAGAAAT[C/T]GGCTTCTAGGTTGAG	218038
rs48179177	snp	C/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19116927	GTATATAGCATGTAT[C/T]GACAAAAGGCACCAA	218038
rs48180119	snp	A/C	0.165289	0.235211	intron-variant	Amph	Mm_Celera	13:18992930	CAAACTCAACAATTG[A/C]GTTTTAACTATTACA	218038
rs48181499	snp	A/G			intron-variant	Amph	Mm_Celera	13:19081016	TTATATTTCGAGAGG[A/G]CTATTGATTGCTTTT	218038
rs48183169	snp	A/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19078062	TGCTCTCCATTGATC[A/G]CCAGTCCTTCTCTAA	218038
rs48190457	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18966709	TAGGTGGTGGGAGAG[C/T]GGTCACTTTTTAATT	218038
rs48196028	snp	A/T	0.142012	0.225474	intron-variant	Amph	Mm_Celera	13:19100725	TTCTGGAGCCTGGAG[A/T]CCACATTATACTATT	218038
rs48198464	snp	A/G			intron-variant	Amph	GRCm38.p3	13:19144042	TCACCGGATTTCTCA[A/G]TTTCCCTTTTTATTT	218038
rs48199091	snp	A/C	0.408163	0.193609	intron-variant	Amph	GRCm38.p3	13:19133203	GCAGCTCACCACCTC[A/C]AAGAAGGCTTCTACA	218038
rs48199555	snp	A/C			intron-variant	Amph	GRCm38.p3	13:19102326	CTCCAAGCATAATTC[A/C]AAAGGTACCCCCCAA	218038
rs48212367	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19040149	TACTTGGGTTGTGTT[C/T]AGAGAATAGACCCTT	218038
rs48220820	snp	A/G			intron-variant	Amph	Mm_Celera	13:19083028	AACCTCATTATCAAG[A/G]GCATCTTGAGCCTGC	218038
rs48221781	snp	C/T	0.260355	0.249785	intron-variant	Amph	GRCm38.p3	13:19116559	AGTGGAAGGCATGCA[C/T]GCATATGGTACTCTT	218038
rs48228879	snp	A/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19040255	ACTGTTGCCATGCCT[A/T]TCTACCACAATGGAC	218038
rs48249069	snp	A/C			intron-variant	Amph	Mm_Celera	13:19126815	ACTTATCACCTTTGC[A/C]TATACTGTTTCATCA	218038
rs48258767	snp	A/T			intron-variant	Amph, Gm31887	GRCm38.p3	13:19147518	GATGTGTGCACATGA[A/T]GCAGGTACCTAGGTG	218038
rs48260748	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19074716	GCAATGGCCCAGATT[C/T]TCTCGGTTGCTGGTT	218038
rs48261448	snp	A/C	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19119315	TTCAGTAACATGCCT[A/C]TGCAGATTGCCCCCA	218038
rs48263645	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19120533	TCTTCAGCCTGTCTA[A/G]TGGCTATTCATTCAT	218038
rs48267144	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19027865	TGTTTGCTAACTCCA[A/G]GACCCGAGGCTCCAT	218038
rs48269034	snp	C/T	0.426035	0.177515	intron-variant	Amph	Mm_Celera	13:19086233	GAATTCTCAATCTTT[C/T]ACTCCAGTGGCCATT	218038
rs48272851	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19034998	ACCAGCCAAGGACTC[A/G]TGTAGTTGCTGGCAC	218038
rs48280118	snp	C/T	0.408163	0.193609	intron-variant	Amph	GRCm38.p3	13:19129757	TTCTTACCCAAGCTA[C/T]AGGATGGACATGTAA	218038
rs48280851	snp	A/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19038729	AAGCTGGGACCTCCC[A/T]CATCAGTCATCAATC	218038
rs48291090	snp	A/G	0.426035	0.177515	intron-variant	Amph	Mm_Celera	13:18970649	GTGAAATGAAACTAA[A/G]TTGTTATTTTTAGAA	218038
rs48299097	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19090178	AATTTAAGGTGATGA[A/G]GAATTTCAATTAAGT	218038
rs48303557	snp	C/T	0.336735	0.234472	intron-variant	Amph	Mm_Celera	13:18951582	CTACCTTTTCATTTA[C/T]TCTTTAAAAGTCTTT	218038
rs48304664	snp	A/C	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18972546	ATTGTCTGTAATGGC[A/C]GTGACAGTGATATCA	218038
rs48307741	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19114344	CCAAATACAATTAGC[C/T]CTACTGGTGCTTTGT	218038
rs48309098	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18993837	TGGGAAGCAGGTTTC[C/T]TGAAAATATTTTTTT	218038
rs48311758	snp	A/T	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19084431	ACTGAAAATGCAGCC[A/T]AGAGTTCTAGTACCT	218038
rs48314358	snp	G/T			utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19152645	CTCCTTAAAAACATA[G/T]AGAAGCCATGGATTG	218038
rs48321174	snp	A/G	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19087780	CTCACGATTAAGAAT[A/G]AGGAGTTTGATGAGG	218038
rs48331533	snp	A/C			intron-variant	Amph	Mm_Celera	13:19116775	AGTTCGTACCCTAAT[A/C]CTTATAATCTTGTAA	218038
rs48334423	snp	C/T			intron-variant	Amph	Mm_Celera	13:19126208	GGCTCAATACTGAAC[C/T]AATAGTATATATTTT	218038
rs48335553	snp	A/G			intron-variant	Amph	Mm_Celera	13:19126966	AGCATATTACAAAAA[A/G]CAGTCATGAATCTGT	218038
rs48337785	snp	A/G	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19003886	GAATCTTCTTACTTT[A/G]CAAGAGGGTCACTTT	218038
rs48340144	snp	C/T	0.297521	0.245442	intron-variant	Amph	Mm_Celera	13:18981342	CTAGACGAAGAGTGA[C/T]AAAAGTGAAAGAGCA	218038
rs48348940	snp	C/T			intron-variant	Amph	Mm_Celera	13:18981939	AAGTACATATAGACA[C/T]GACAGGGGAATGAGC	218038
rs48350255	snp	C/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19067883	ACTCAATTTTGGCAT[C/G]TTGAATTATAATTGA	218038
rs48350874	snp	G/T	0.142012	0.225474	intron-variant	Amph	Mm_Celera	13:19115527	AGCAGCGATTCTCAG[G/T]CTCAGGGAGAAAGGA	218038
rs48353061	snp	C/T	0.336735	0.234472	intron-variant	Amph	Mm_Celera	13:19074060	TAGAATTTTATATGG[C/T]GCTCATTGGGGTTGC	218038
rs48360911	snp	A/G			intron-variant	Amph, Gm31887	GRCm38.p3	13:19146158	ATGGTGCTGGAAAAG[A/G]AGCTGAGAGTTCTAC	218038
rs48370832	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19087543	ACTTCCAGGCAAGAA[C/T]GTAAGTGGATCTCTC	218038
rs48383397	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19124835	GAAGCTCAACACAAT[C/T]GCACACTATCACTTT	218038
rs48386742	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19131569	AGAAAGAAACTTTAG[C/T]GAAGTTAACAAATTG	218038
rs48389827	snp	C/T	0.142012	0.225474	intron-variant	Amph	Mm_Celera	13:19038975	TAGTTTGGATGCAAT[C/T]GAAGTCAAATGGCTC	218038
rs48390579	snp	C/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19078119	AGACCTCAAGATGTG[C/T]GGAGGTAGGATGAAA	218038
rs48391719	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18951774	TAATAACTTATATTT[A/G]GACCTTGCATAGACA	218038
rs48396153	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19073106	GAAAAGAACTTTTGA[C/T]CAACATTGGAACGGT	218038
rs48396268	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19032088	ATTCTTTCTGAAATC[C/T]AAAGCCAGATGCAGC	218038
rs48397623	snp	G/T			intron-variant	Amph	Mm_Celera	13:19013476	GGGGGTGGGGTGGGG[G/T]GGGATATCTCAGCTC	218038
rs48397713	snp	C/T			intron-variant	Amph, Gm31887	GRCm38.p3	13:19148877	TAATCGGCTGCCTTC[C/T]CTGCCTTGGTTAACA	218038
rs48397982	snp	A/G	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:19039578	TTCCTTAAAACTTGG[A/G]AAACAGTCCGTGATT	218038
rs48400426	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19106260	AGTAATAAAATGTTT[C/T]GGGCAATGTACAGAT	218038
rs48405890	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19114811	TTAGAGAGACCATCA[A/G]GATAGTCAAAAAACC	218038
rs48407129	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18973263	CTTAGGAAAGCTGTA[A/G]AAACAGTCATTTACA	218038
rs48407447	snp	A/G	0.336735	0.234472	intron-variant	Amph	Mm_Celera	13:18982948	TCTTTCAGCTCATTG[A/G]AAATAATGATTTTCT	218038
rs48423279	snp	G/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18978817	CCATCTCTGCAGCCC[G/T]GTCATGATCTCTGTC	218038
rs48433712	snp	A/G			intron-variant	Amph	GRCm38.p3	13:19101090	ACAGGCTTTCTTAGC[A/G]CTCCATTGCATGTTA	218038
rs48435629	snp	C/G			intron-variant	Amph	Mm_Celera	13:19075143	TTGGCCCACATCCCA[C/G]TGATGTCAAACTATT	218038
rs48439774	snp	C/T	0.124444	0.216185	intron-variant	Amph	GRCm38.p3	13:19001227	AAAAAAGCCTGCATC[C/T]TGACAAGTTTGCTTT	218038
rs48450450	snp	A/C	0.336735	0.234472	intron-variant	Amph	GRCm38.p3	13:19125347	ATGGTGTGGCTCTTT[A/C]AAACTATCCCATGAT	218038
rs48454327	snp	G/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19110090	ATTATCGACTGTTTT[G/T]TTAAGTTTCAATATC	218038
rs48455292	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18964667	AAAAGACTGGACTTA[C/T]AAATCTTGTCTTTTG	218038
rs48455379	snp	C/G	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:18970317	AAGCTCTTAGCTTCA[C/G]AGAATATTGGAAATC	218038
rs48456646	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18953128	GAGCCTTAAATATCA[C/T]GCTTTCTCGGATTTT	218038
rs48460402	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19073891	ACAGATGAATATGAA[A/G]TGAGCACACATACAT	218038
rs48461373	snp	C/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18990863	GTTACTTCACCTCAC[C/G]TTATTTTAAGAGTTA	218038
rs48462209	snp	A/C			intron-variant	Amph	Mm_Celera	13:18965951	TTTTTTTTTTTTTTC[A/C]GGACAGGGTTTCTCT	218038
rs48463262	snp	A/C			intron-variant	Amph	Mm_Celera	13:19116090	TGACGAGTGTCCACC[A/C]AAATTGGTAACAGAA	218038
rs48463485	snp	C/T	0.124444	0.216185	utr-variant-3-prime, intron-variant	Amph, Gm31887	Mm_Celera	13:19152004	ACCTACTAAGTTCAT[C/T]CAAGACAACATGCTT	218038
rs48467433	snp	A/T	0.459184	0.136902	intron-variant	Amph	Mm_Celera	13:19089132	AGATCTGGAAGTCAG[A/T]CGAGAATAAGGAAAA	218038
rs48467927	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19086819	GGCCTCTTAGTGAAC[A/G]CTTCAATGCTTCTTT	218038
rs48474350	snp	G/T	0.142012	0.225474	intron-variant	Amph	Mm_Celera	13:19115894	TACTTTAATGACATG[G/T]GTGTATTGAAATAAC	218038
rs48486269	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18978875	GTTGTCTCTAGATTT[A/G]TGACTATTCTTAATC	218038
rs48486319	snp	A/C			intron-variant	Amph	Mm_Celera	13:19021506	TGGAGGGGAGGTTTT[A/C]GCAACATGGAAATTG	218038
rs48486715	snp	A/G	0.336735	0.234472	intron-variant	Amph	Mm_Celera	13:19075047	TTAGCAGCTCCACTG[A/G]ATCTTTTGTTATTTT	218038
rs48492072	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19003746	AAATAAATTGCAGAG[C/T]CCAGCAGAAAGAGCG	218038
rs48498232	snp	A/G	0.21875	0.248039	intron-variant	Amph	Mm_Celera	13:19068266	AGACTTTGTAAGTAT[A/G]TTACCATATTAATGA	218038
rs48498524	snp	C/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19076338	GAGAACCCTAGAATG[C/T]TTGTTTTACACCATG	218038
rs48510723	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18956397	AGAGAATCACAAAAT[C/T]CTCAAATGTTACACA	218038
rs48511495	snp	C/T			intron-variant, nc-transcript-variant	Amph, Gm31887	Mm_Celera	13:19145613	TCAATACCACTCATA[C/T]TTTCAGGTCACAAGC	218038
rs48514143	snp	A/G	0.152778	0.230321	intron-variant	Amph	Mm_Celera	13:19075097	CTGTCAACCCTCTCA[A/G]TGTACTCTGTGACTC	218038
rs48515452	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19013151	TCTATGTTCTAGTGG[A/G]GTTATCCATTGCTGT	218038
rs48519255	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19010991	TAAGGTGAATGGCTG[A/G]ACTCCATACAAGAGT	218038
rs48519961	snp	A/G	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:19129670	ATAGAGATGTTAACA[A/G]ACTAATATGCAATAA	218038
rs48520167	snp	A/G	0.497041	0.0383476	intron-variant	Amph	Mm_Celera	13:19123219	TTCTCATCACTGAGC[A/G]TTTTCAGAATATGTG	218038
rs48527896	snp	A/C			intron-variant	Amph	Mm_Celera	13:18983404	ATTATTTAACATTGC[A/C]CAAGGAAGCACTAGG	218038
rs48527930	snp	G/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19083624	GCCACCTACCAATGT[G/T]CAAGGAAAATTTAGA	218038
rs48531567	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19109538	GCAAAGCAGCCATCC[A/G]TCTTCCTTGCCCTCT	218038
rs48535941	snp	A/C	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:18970970	CTACCCATAAACTTC[A/C]TAAACTAGAAGCCAC	218038
rs48544774	snp	C/T	0.231111	0.249285	intron-variant	Amph	Mm_Celera	13:19079048	AGGCAGATACTTCTA[C/T]TGTCTGCATTTTAAA	218038
rs48552456	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19141480	GGCCCTTTGAGAAAC[C/T]TGCTAATTCTTTTGA	218038
rs48555353	snp	C/T	0.35503	0.226867	intron-variant	Amph	Mm_Celera	13:19030152	ACGGTCTTGATGTAC[C/T]CATTCTTCGCAGTTG	218038
rs48555612	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19038843	CTGACGTAAAACCAG[C/G]TAGTACATCCTGTTA	218038
rs48563145	snp	C/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19086405	AATTAGGTCATAGTT[C/T]ATATTGCCTCTTCTA	218038
rs48571057	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19005679	TGTTTTGCTAGTATT[C/T]CCTCTTGACTGCCAA	218038
rs48571493	snp	A/G			intron-variant	Amph	Mm_Celera	13:19116131	TCTATAACCAAAAGT[A/G]GAGCTATGGAAGAGA	218038
rs48579227	snp	C/T	0.18	0.24	intron-variant	Amph	Mm_Celera	13:19122902	GATACTGGGTGACAT[C/T]TCAGGAACAGCAGAA	218038
rs48582936	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19090409	CTATCTGTGTCAAGC[A/G]AATGACAGATCTTAA	218038
rs48584949	snp	A/T	0.277778	0.248452	intron-variant	Amph	Mm_Celera	13:19002014	TGTCAAGAATGGTCT[A/T]CGTTGATACTAAGCA	218038
rs48592020	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18950758	TGCCTTACTGTGTAA[C/T]GACTCTTAGAGATGA	218038
rs48596710	snp	A/G	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:19138357	TTACAGCTGTCGTGG[A/G]AAGTGTGGTGCCATG	218038
rs48608553	snp	C/T	0.459184	0.136902	intron-variant	Amph	Mm_Celera	13:18988632	GAGCAGTCACCAGGA[C/T]ATAGGTTCTTTCACG	218038
rs48623189	snp	A/G			intron-variant	Amph	Mm_Celera	13:19140471	GTTAGTTGTTTAAGC[A/G]GTACACATAAAACCC	218038
rs48623707	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19010228	CACTTGCCAATCAAG[A/G]GCTACAAGACCAGCT	218038
rs48629987	snp	A/C			intron-variant	Amph, Gm31887	GRCm38.p3	13:19147393	TGCTCTCCCACCCAC[A/C]CACTCACCCACTCCT	218038
rs48632028	snp	C/T			intron-variant	Amph	Mm_Celera	13:19043577	ATTTTTTGTGAAGTT[C/T]CAGTTTATCCATCTT	218038
rs48649373	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19112936	TTCCTTTTATCTGTG[C/T]GGCATTCCAATACTT	218038
rs48651755	snp	C/T	0.231111	0.249285	intron-variant	Amph	Mm_Celera	13:18978837	TGATCTCTGTCTCAT[C/T]ATCATTTGGTAGCTA	218038
rs48652568	snp	A/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18981738	GGAATATTCATATCG[A/T]TAATACTGTATTAAG	218038
rs48655758	snp	C/T	0.489796	0.070696	intron-variant	Amph	GRCm38.p3	13:19131998	TGTTAAAAATGTAAT[C/T]CAAAGCTTTAAAAGT	218038
rs48656218	snp	C/T			intron-variant	Amph	Mm_Celera	13:19075133	GTTGGGCATTTTGGC[C/T]CACATCCCACTGATG	218038
rs48658107	snp	A/G	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:19115537	CTCAGTCTCAGGGAG[A/G]AAGGAAGGTCCCTCC	218038
rs48658331	snp	A/C	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18950519	ATGCAGCGGCCCAGC[A/C]GAACCCATGTGGCAA	218038
rs48658487	snp	A/T	0.473373	0.11227	intron-variant	Amph	Mm_Celera	13:19092121	TAGTTACACTGTTTT[A/T]AAATTACTTCTTATG	218038
rs48671147	snp	A/C	0.197531	0.244432	intron-variant	Amph	Mm_Celera	13:19113388	CGTTATTAGTACCAA[A/C]TATCTTACACTTCTC	218038
rs48674658	snp	G/T			intron-variant	Amph	Mm_Celera	13:19078409	TAAGATATAAAGGAT[G/T]TAGACAGTAAACTAA	218038
rs48678285	snp	C/T			intron-variant	Amph	Mm_Celera	13:19051935	ATGTGAGTCACAATT[C/T]AGCTTCTTCAGAATC	218038
rs48684169	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18970631	TGTTGAGCTATTTTT[A/G]ATGTGAAATGAAACT	218038
rs48684947	snp	C/T	0.495868	0.0452663	intron-variant	Amph	Mm_Celera	13:19100399	ATTCACTAAATAAAG[C/T]TATTTCAGCTTAGGT	218038
rs48690265	snp	C/T			intron-variant	Amph	Mm_Celera	13:19126742	TTTGAAGTTTTAAAG[C/T]ACTCCAGGCAAACTG	218038
rs48693102	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19090221	CTTAAATTGACTTAC[C/T]TAAGTTTAGTATTGG	218038
rs48693459	snp	C/T	0.21875	0.248039	intron-variant	Amph	Mm_Celera	13:19135166	CTCGGGATTGAAATG[C/T]CTTCTTAAGTTGTTA	218038
rs48696203	snp	A/G			intron-variant	Amph	Mm_Celera	13:19053582	TTTATTATATACACA[A/G]TTATACTGAATTGAA	218038
rs48699617	snp	A/T	0.277778	0.248452	intron-variant	Amph	Mm_Celera	13:19008035	TTTAAAGTACTATTT[A/T]CATGTAGATACACCA	218038
rs48703021	snp	A/G	0.165289	0.235211	intron-variant	Amph	Mm_Celera	13:19128062	AAGAAGGGAAAATCC[A/G]GTCACTCTCTTTGGA	218038
rs48704039	snp	A/C	0.489796	0.070696	intron-variant	Amph	GRCm38.p3	13:19131397	GTGCAATTGAAGATG[A/C]CGTCGCTGAGAGGAA	218038
rs48709231	snp	A/G	0.142012	0.225474	intron-variant	Amph	Mm_Celera	13:19122980	CTGGCATTCAGCTGC[A/G]TATCTCCTGATTCAT	218038
rs48714289	snp	A/G			intron-variant	Amph	Mm_Celera	13:18964139	CCCGTGGGGAGTCCC[A/G]TGTGGGCCCTTTGCG	218038
rs48714651	snp	A/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18978207	GGTGAGGAGTGGGTT[A/T]CAAGGGTCACTCACT	218038
rs48721390	snp	C/T	0.408163	0.193609	intron-variant	Amph	Mm_Celera	13:18980639	CAGTTTGCATGCCTA[C/T]TTCCTTATGATTCTG	218038
rs48728805	snp	G/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19117452	TTCCCCTCTCTAAAA[G/T]GACTGTGGTAAGGGC	218038
rs48734841	snp	A/G	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:19013121	CTACAGCAGGAAAGT[A/G]TCATTGGCATCCATT	218038
rs48734867	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19086294	TGCATTCCTCAGTAT[C/T]GCAGAATCAGCGACG	218038
rs48735467	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19106416	TTTCAGTGTTGCCTT[A/G]GAGTTTTGCTAAGTG	218038
rs48738289	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19077721	GAGGGAGTTAGGCCC[C/T]AAGAGTACAATACTC	218038
rs48738636	snp	C/T	0.231111	0.249285	intron-variant	Amph	Mm_Celera	13:19076771	TAACTGCCATTTGTG[C/T]ATGATACATAGTTTC	218038
rs48738773	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19035275	TAATTAATTAGTAGA[C/T]GTGTTGATTAATAAG	218038
rs48740026	snp	G/T	0.48	0.0979796	intron-variant	Amph	GRCm38.p3	13:19126064	CTGCCATGTAGAGTA[G/T]TACAAATTGGGGGAT	218038
rs48740035	snp	A/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19086072	TGAACTGACAAGTAC[A/T]GGAGACATTTTCTTT	218038
rs48759356	snp	C/T	0.142012	0.225474	intron-variant	Amph	Mm_Celera	13:19044051	GATGTGTGGGTCTTA[C/T]CTGCTTCTTCTGAGA	218038
rs48762425	snp	C/G	0.32	0.24	intron-variant	Amph	Mm_Celera	13:18954714	ATAATGGTGAACATT[C/G]CAAGATGAAAATGCT	218038
rs48765962	snp	A/C	0.132653	0.220748	utr-variant-3-prime, intron-variant	Amph, Gm31887	Mm_Celera	13:19150776	AAAAGCTCCTATATA[A/C]TTCCACGTTCTATTT	218038
rs48769903	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19086359	TTAACTAGAACACTG[A/G]CCACATTGCCTTGAC	218038
rs48777417	snp	C/T	0.426035	0.177515	intron-variant	Amph	Mm_Celera	13:18983172	TTTCACAAGACCACA[C/T]GTGGTGTACGTTGAA	218038
rs48779366	snp	C/T	0.165289	0.235211	intron-variant	Amph	Mm_Celera	13:18981504	TAAATGTTAAATGCA[C/T]AATTAAAATGTTTCA	218038
rs48796942	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19027954	ATGGGAGGACCGTGC[C/T]GTCACTTTACACACA	218038
rs48799726	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19131930	TACAATGAATATATT[C/T]TATCAAAACATCATA	218038
rs48803758	snp	G/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:18966614	CCCAAAAGGTCTCAT[G/T]AATCTGTCAGTTTGT	218038
rs48805825	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19042501	ACTGGAGATACAAAA[A/G]TCCAGGTAGATCTTA	218038
rs48810954	snp	C/T	0.18	0.24	intron-variant	Amph	Mm_Celera	13:18973295	TTTTTTTTTTGTCAC[C/T]TAGGAGATCTCTTAT	218038
rs48812199	snp	A/G			intron-variant	Amph	GRCm38.p3	13:19115848	TGCATTTGCTCAATG[A/G]TATGATAATCCTAGT	218038
rs48813067	snp	C/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19106710	GAGAAATGCTTCTTG[C/T]ATGCTCACAGGCATA	218038
rs48818514	snp	C/T			intron-variant	Amph	Mm_Celera	13:19078343	ATTTGATTATATAAA[C/T]GTGAATTTAAAATTA	218038
rs48819829	snp	C/T	0.35503	0.226867	intron-variant	Amph	Mm_Celera	13:19068681	ATACTCTGTAAGCGG[C/T]GGCTACACGAACATT	218038
rs48825353	snp	A/G	0.375	0.216506	intron-variant	Amph	Mm_Celera	13:19093829	CATCTCCTAAGCACA[A/G]TCATTGGAAGGTTAG	218038
rs48830517	snp	C/T	0.336735	0.234472	intron-variant	Amph	Mm_Celera	13:18952133	AAAGCACATTTCTTT[C/T]CTTCAGGCTTTTCAT	218038
rs48839870	snp	A/G			intron-variant	Amph	GRCm38.p3	13:19130514	ACTTCCCAGCCCAGG[A/G]GCTGAGCTGCCCTTC	218038
rs48843294	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19066760	ACAGCCTATAATCTC[A/G]TGCATAAAATGTTCC	218038
rs48846799	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18977886	TTGGAAGTAGTACAC[A/G]TTAGCCAGCAGATAT	218038
rs48847682	snp	A/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19040581	GCTTACTCTGGCTAC[A/T]TATAAATCCCAGTCA	218038
rs48852762	snp	G/T			intron-variant	Amph	GRCm38.p3	13:19102345	GGTACCCCCCAAAAT[G/T]ATTTATTAACTCTCT	218038
rs48857198	snp	C/T	0.48	0.0979796	intron-variant	Amph	Mm_Celera	13:19086784	ATCGTGAAATAAAAT[C/T]CAGCTACAGAAATCA	218038
rs48874344	snp	A/G			intron-variant	Amph	Mm_Celera	13:19075088	CTTCTCTACCTGTCA[A/G]CCCTCTCAGTGTACT	218038
rs48874604	snp	C/T	0.277778	0.248452	intron-variant	Amph	Mm_Celera	13:19038990	CGAAGTCAAATGGCT[C/T]CCATTTAAGAAGTCT	218038
rs48874661	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18978395	GAAGACCCAAAGGCT[C/G]AGAGCCCATGCTCAG	218038
rs48875571	snp	C/T	0.489796	0.070696	utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19150668	AGCTGCCCAGCTGCT[C/T]AGTCCAGATAAATAC	218038
rs48881168	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18978220	TTACAAGGGTCACTC[A/G]CTACAGGTAGGATTT	218038
rs48883279	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19025291	CACAGGCTGAATGAC[A/G]AAATACTGATAGCTT	218038
rs48891276	snp	A/G	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19110957	TCTCCCATTATATTC[A/G]CTTCTAGGTCTGATT	218038
rs48891716	snp	C/G			intron-variant	Amph	Mm_Celera	13:19072892	GAGAAGGCAATTTAT[C/G]GGAGTGCCCCCTTCT	218038
rs48892618	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18972403	GATGCAGTCCGGTCA[C/T]GAAGTTTAAAGGGAT	218038
rs48893355	snp	C/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18964797	CTGATAAAATTGTGA[C/G]CGCTTAAGAATTCTG	218038
rs48895590	snp	A/G	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19119257	AATAATTTATCAAAA[A/G]AAGGCAGAAGGCTCT	218038
rs48902572	snp	C/T			intron-variant	Amph, Gm31887	GRCm38.p3	13:19149399	CCACCAAGGAATATT[C/T]CCTTACTCCTTACTT	218038
rs48906294	snp	A/C	0.21875	0.248039	utr-variant-3-prime, intron-variant	Amph, Gm31887	Mm_Celera	13:19153007	TGTTCCACGTGTGGT[A/C]GTTGCTACTGTCTTC	218038
rs48906800	snp	C/T			intron-variant	Amph	Mm_Celera	13:19053470	GGGAAATATCTTGGT[C/T]ATTGACTATTAACTA	218038
rs48908430	snp	C/T			intron-variant	Amph	Mm_Celera	13:19050029	CTAGACAACTTAGAG[C/T]TCATGTTTTCCCAAC	218038
rs48909621	snp	A/G			intron-variant	Amph	Mm_Celera	13:19140401	GGGTATAATAAAGGG[A/G]TTAATGTATGCAAAA	218038
rs48916853	snp	A/T	0.459184	0.136902	intron-variant	Amph	Mm_Celera	13:19008953	AAGACAATTATACTT[A/T]AAAAATTCAGTCGTA	218038
rs48922181	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19080500	GAAATTTTGGGAGAA[A/G]CTTTGAGCCACTGTC	218038
rs48923390	snp	A/G	0.260355	0.249785	intron-variant	Amph	Mm_Celera	13:19029445	TATTTGTTTATAACC[A/G]TGTTGTGGTGGTTAA	218038
rs48924491	snp	G/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19114559	GGAAGAAGGCAGGTT[G/T]AAGGAGACTACATGA	218038
rs48928020	snp	A/G	0.46281	0.131194	intron-variant	Amph, Gm31887	GRCm38.p3	13:19149291	ATGAGCTGTGGGGCA[A/G]TGTTTTCCTATAAGA	218038
rs48931117	snp	A/G			intron-variant	Amph	Mm_Celera	13:18964133	TAGGATCCCGTGGGG[A/G]GTCCCATGTGGGCCC	218038
rs48939179	snp	C/T	0.459184	0.136902	intron-variant	Amph	Mm_Celera	13:18989623	TGAGCAGAATGAACG[C/T]GCTGAGTACAGTTGC	218038
rs48942438	snp	A/G	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19044787	TCTAGCTCTGAGACA[A/G]TAATAATAACACAAG	218038
rs48943967	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18950544	TGGCAACTGTGCTTG[C/T]TGGATTTCCCACTTG	218038
rs48947070	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19129791	AAATGTCAGTAGTCT[C/T]TCTGTGCGCCAGAAT	218038
rs48951155	snp	A/C	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:18977843	TGCTTTGTCCTGCAC[A/C]TCAGCTTGATCTTGG	218038
rs48951162	snp	A/G	0.244898	0.249948	intron-variant	Amph	Mm_Celera	13:19102808	CCTCTGGGCTAAAGA[A/G]TCTTGGGTTTTAGGA	218038
rs48956147	snp	A/G			intron-variant	Amph	GRCm38.p3	13:19130785	CAGCAACAACTTGAT[A/G]AATTCCAGCTTTGGA	218038
rs48960341	snp	C/T	0.46281	0.131194	intron-variant	Amph	Mm_Celera	13:19110603	GCCATTCTGTTATAT[C/T]ATACTATTCTCTTTA	218038
rs48968726	snp	A/G			intron-variant	Amph	Mm_Celera	13:19126539	ATTCAGCAAATACCG[A/G]CTACATCATTTTTTC	218038
rs48971691	snp	C/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19044169	AATGTGATTCCAATC[C/T]TTCAGGTGTCGCATG	218038
rs48973002	snp	G/T	0.336735	0.234472	intron-variant	Amph	Mm_Celera	13:19071526	GCTCAAGTCATACCT[G/T]TCTGGCTTCTTGTCT	218038
rs48977948	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:19002765	ACACGAGGGACTATC[C/T]AGAGTAGTTTTAAAA	218038
rs48980186	snp	A/T	0.486111	0.0821678	intron-variant	Amph	Mm_Celera	13:19093282	AAAGTTCAGTCCTGA[A/T]CAAAATCTTGGTCAA	218038
rs48981375	snp	C/T			intron-variant	Amph	GRCm38.p3	13:19140716	GGTGTTTGTAAGGAA[C/T]CAACCCAGGAGAAAT	218038
rs48981788	snp	A/T			intron-variant	Amph	Mm_Celera	13:19075216	AAAAATGTAGCTGTA[A/T]TGCATGTTTTTCTCT	218038
rs48982231	snp	A/T			utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19152674	TGGCTCATTGGAAAC[A/T]ATCTCATCGTAACTC	218038
rs48985197	snp	C/T	0.459184	0.136902	intron-variant	Amph	Mm_Celera	13:19004489	ACAGATGCCCTTGCA[C/T]ATTGGAGTCAAGCCC	218038
rs48988359	snp	A/G			intron-variant	Amph	Mm_Celera	13:19141206	TTCCAAGTGTTGTGA[A/G]GCTTTCTCATCCCCT	218038
rs48994755	snp	A/G	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:18985355	AGACTTTCTGCTACC[A/G]TGTTTCTGTCTTGCC	218038
rs48995075	snp	A/G			intron-variant	Amph	GRCm38.p3	13:19057150	CTGTTGCATCCATGA[A/G]TTCACACAAGCAGTG	218038
rs48996980	snp	A/G	0.132653	0.220748	intron-variant	Amph	Mm_Celera	13:19039258	CATAGCACTCATGTG[A/G]CTTCATCAATGAAAG	218038
rs49012432	snp	A/T	0.391111	0.206368	intron-variant	Amph	Mm_Celera	13:19085759	TGATGAATTTAATAA[A/T]TTTGTTTGGGCATTA	218038
rs49015583	snp	C/T	0.444444	0.157135	intron-variant	Amph	Mm_Celera	13:18968662	CTGAGTAGTGGCTTA[C/T]TTTTAACTGAATTTT	218038
rs49024225	snp	G/T	0.124444	0.216185	intron-variant	Amph	Mm_Celera	13:19123691	ATAGCTGTGCTTTTT[G/T]ATTTTAACAAGGAAA	218038
rs49029206	snp	A/G			utr-variant-3-prime, intron-variant	Amph, Gm31887	GRCm38.p3	13:19152550	TTTTGTCAAAGCTAG[A/G]GAGGCTTTGAAGTAA	218038

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