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

Nup43

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs8252879	snp	A/G	0.142012	0.225474	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7665786	AAAAAGGACCCTTAA[A/G]TTACCCTGGAAGTAT	69912
rs8252880	snp	A/C	0.124444	0.216185	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7665762	GAAGTATTTTCATTA[A/C]NGTACCAANTTAATA	69912
rs8252881	snp	A/G	0.488166	0.0760073	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7665761	AAGTATTTTCATTAA[A/G]GTACCAAATTAATAT	69912
rs8252882	snp	A/C	0.124444	0.216185	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7665753	TCATTANNGTACCAA[A/C]TTAATATCTTCCTCT	69912
rs8252883	snp	C/T	0.493827	0.0552116	upstream-variant-2KB, intron-variant	Pcmt1, Nup43	GRCm38.p3	10:7665572	AAGAGGGTCTAGGAT[C/T]CCCCCTGGAACTAGG	69912
rs8252884	snp	C/T	0.124444	0.216185	upstream-variant-2KB, intron-variant	Pcmt1, Nup43	GRCm38.p3	10:7665552	ctggaactagggtta[C/T]aaaggattgtcagcn	69912
rs8252885	snp	C/T	0.124444	0.216185	upstream-variant-2KB, intron-variant	Pcmt1, Nup43	GRCm38.p3	10:7665537	naaaggattgtcagc[C/T]accacgtgggtgctg	69912
rs29310987	snp	A/C	0.32	0.24	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673898	TAGATTTACAGGCAA[A/C]TAGAATTGCCATGTG	69912
rs29313753	snp	A/G	0.375	0.216506	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667291	CTGCCTCTGCCTCCC[A/G]AGTTCTGGGATTAAA	69912
rs29314743	snp	C/T	0.5	0	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672582	GTAGCTGTCTTCAGA[C/T]ACACCAGAAGAGGGC	69912
rs29315027	snp	C/T	0.444444	0.157135	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666513	ATACATACATACATA[C/T]GAATAATTAAAATAC	69912
rs29315122	snp	C/T	0.375	0.216506	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667399	AAAGAACATCTCAAA[C/T]TCTTTCAGCCCAAGG	69912
rs29316890	snp	G/T	0.32	0.24	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676973	TTCCTCCAGTCTCCA[G/T]GCACCAGGCACACAC	69912
rs29321290	snp	C/G	0.498615	0.0262793	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7665890	CTGAAAGTTTTTATA[C/G]GTTTATTTTATGCAT	69912
rs29321996	snp	A/G	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671914	CCCTAGACCTGTTGG[A/G]TCAGAATCTCCAGGT	69912
rs29322740	snp	C/T	0.32	0.24	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666039	TCCCGGTAATGTCTT[C/T]GCCTGCATGTATGTA	69912
rs29326464	snp	A/G	0.32	0.24	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677107	TGCATGTTTATATTC[A/G]TCAATGTGTATATAA	69912
rs29326578	snp	G/T	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671706	AGCCGGAAAGGGAAA[G/T]TGGGATGGATTGCAA	69912
rs29326622	snp	A/T	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676196	GGGTAGGCCATAAAA[A/T]AACCTCTGTGGATTA	69912
rs29326656	snp	C/T	0.375	0.216506	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668202	CACCTTATAGTTTGT[C/T]TACCCTTACCCCTGA	69912
rs29328264	snp	A/G	0.5	0	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668401	GCAGGAGGGATCTCA[A/G]AGCTAGTCAGGGCTA	69912
rs29336403	snp	G/T	0.375	0.216506	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667295	CTCTGCCTCCCGAGT[G/T]CTGGGATTAAAGGCG	69912
rs29338571	snp	A/T	0.5	0	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672585	GCTGTCTTCAGACAC[A/T]CCAGAAGAGGGCGTC	69912
rs29341618	snp	A/G	0.375	0.216506	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666679	CTTACCACTAGGCAT[A/G]AACACACGCAGCACA	69912
rs29342042	snp	A/G	0.32	0.24	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668460	TAACAATATTTGTCC[A/G]TCTATGTGCCAAACG	69912
rs29343832	snp	C/T	0.375	0.216506	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671143	TCCTATTTCTTCTAT[C/T]CATTACATAGTAATT	69912
rs29345608	snp	C/T	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677877	TCAAATCTCAGCAAC[C/T]GCATGGTGGCTCACA	69912
rs29346083	snp	C/T	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671886	TTGCCTGAGAAGATT[C/T]CAGGCCCCCCCACCC	69912
rs29347471	snp	A/C	0.5	0	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673755	TATTATGATAAAAAA[A/C]TTGTTTAATTAGTTA	69912
rs29349309	snp	A/T	0.375	0.216506	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666779	TTAAAAATAATTTTT[A/T]AAAAAATTAGTTATC	69912
rs29350767	snp	A/G	0.5	0	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668450	TTATCTTAAATAACA[A/G]TATTTGTCCGTCTAT	69912
rs29355827	snp	C/G	0.375	0.216506	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674441	TGTGTAATCTTTGCT[C/G]CTTTCTTAAGAAACT	69912
rs29356449	snp	A/G	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672214	GAACAACATAGTGAA[A/G]TCCTGGCTCAAAGCT	69912
rs29366440	snp	C/T	0.32	0.24	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677154	AGGCCACATCAGATC[C/T]CCTGAAGCTGGAGTT	69912
rs29366748	snp	A/G	0.375	0.216506	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676698	AGGCCTAGAGAGAGT[A/G]TAGTCTCAGCAGTTG	69912
rs29367152	snp	C/G	0.444444	0.157135	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666528	TGAATAATTAAAATA[C/G]TAAGAAGAAAGCTGT	69912
rs29367930	snp	C/T	0.5	0	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672576	TACACTGTAGCTGTC[C/T]TCAGACACACCAGAA	69912
rs29370203	snp	C/T	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672288	TGAGGAAGCTGCTGA[C/T]GAAGGTAAAGATGGG	69912
rs29370497	snp	A/T	0.492188	0.0620098	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7666934	TAAAATCCAATATGG[A/T]GCTACACAGCTTCGG	69912
rs29373535	snp	C/T	0.375	0.216506	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669399	TTTTCGATGTTAACA[C/T]ATTTTATTTGCTTTG	69912
rs29375513	snp	A/G	0.375	0.216506	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670386	CTTAGGCATACATAT[A/G]TGCACATAAATGTTT	69912
rs29379353	snp	A/G	0.444444	0.157135	missense, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676329	TGGGATGCCTCCACA[A/G]ATGCACCTGAAAAGT	69912
rs33850652	snp	C/T	0.375	0.216506	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672768	ACCAAAATTTCTTAT[C/T]TGATCTAGGGGTTGT	69912
rs45702115	snp	A/T	0.132653	0.220748	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670130	CACTTAGCTTCTAAC[A/T]CAGATACCACAAAGA	69912
rs45710397	snp	A/G	0.444444	0.157135	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673085	TAAGATTGGATAGAC[A/G]GGAGCTTGAACATCT	69912
rs45880139	snp	A/G	0.408163	0.193609	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669906	CTGAGAATCTCAGAT[A/G]TAGTAAGCATGCATT	69912
rs46038273	snp	G/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666337	TTTCTCTGTCAGGGC[G/T]AGAGAGATGGCTCGC	69912
rs46065360	snp	C/G	0.124444	0.216185	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7665857	GCGGAACTACACACC[C/G]AGTCCTAGCTGAGGA	69912
rs46322892	snp	A/C	0.124444	0.216185	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669708	GATTGTGTTAGTAAG[A/C]GCACAGTGCTTTATA	69912
rs46365313	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667184	CTTTTTTGTTTTGTT[C/T]TTGTTTTTTCGAGAC	69912
rs46649681	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671479	CGGATTTCTGAGTTC[A/G]AGACCAGCCTGGTCT	69912
rs46726420	snp	A/G	0.497778	0.0332592	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667764	TTGCTGGTCTGGTTT[A/G]GCTGCCCGCTACTTG	69912
rs47362962	snp	A/G	0.231111	0.249285	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671819	TGACTGACACCAGTC[A/G]TGATTTGGCCAGTGT	69912
rs47824970	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668875	GCTGGGCGGGGTGGC[A/G]CAGGCCTTTAATCCC	69912
rs48019057	snp	G/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666197	AGGGTTTTTAAAGTG[G/T]TTTTTTTTTGTTTTT	69912
rs48120410	snp	A/G	0.142012	0.225474	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667819	CTGGGATCTGGTTTT[A/G]AACCCTCACCAAGTC	69912
rs48339507	snp	C/T	0.486111	0.0821678	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671656	TTTACTGTGAGCTGG[C/T]CTTAGATATTTGTTA	69912
rs48489442	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674421	TTTTTCCAGAGCTTT[C/T]TAGATGTGTAATCTT	69912
rs48937784	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668843	AAGCACACCCCAATC[A/C]AAAAAAAAAAAATCG	69912
rs49082004	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675640	GATTACAGGCATGAG[C/T]CACCACTCTTTGATA	69912
rs49346059	snp	A/G	0.277778	0.248452	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671662	GTGAGCTGGCCTTAG[A/G]TATTTGTTACTGGAG	69912
rs49897027	snp	C/G/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7668866	AAAAATCGTGCTGGG[C/G/T]GGGGTGGCGCAGGCC	69912
rs50913545	snp	C/T	0.124444	0.216185	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670125	GTTCACACTTAGCTT[C/T]TAACTCAGATACCAC	69912
rs51198283	snp	A/G	0.408163	0.193609	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667772	CTGGTTTAGCTGCCC[A/G]CTACTTGAGAGCCCT	69912
rs51745260	snp	C/G/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7668986	ATACAGTGAAACCCT[C/G/T]TCTCAAAAAACCAAA	69912
rs51833866	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677721	TGATTCCTACAGGAC[A/G]CCTTCTGACCTCCAC	69912
rs51878318	snp	C/T	0.124444	0.216185	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670061	CTTTGTGAGCTCCTC[C/T]GATAGTCTTTTGGAG	69912
rs51913429	snp	C/T	0.32	0.24	intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669336	GTAAAATTTTAAGCT[C/T]ACTCTTTATCTTTCA	69912
rs52377955	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677983	AAATAAATAATCTTT[A/T]AAAAATATATAAGAT	69912
rs52629299	snp	A/G	0.124444	0.216185	upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7665844	CTATAATTTTAATGC[A/G]GAACTACACACCCAG	69912
rs107657219	snp	G/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666221	TGTTTTTGTTTTTTT[G/T]TTTTTTTTTTTTTTT	69912
rs211889239	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669730	TGCTTTATAGTGTTG[A/G]AACATGAGGAGAGGC	69912
rs211948056	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677674	TGACAACGGAGTTTG[A/T]TTGGCAGGACTCAAG	69912
rs211993301	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678215	TTAGTGGTACAGAGT[A/C]AGCCTTGTGGTTTGA	69912
rs212263680	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670571	CATGTAAAAAAGATA[C/T]AGAGGTTAGTTCCTT	69912
rs212451693	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675903	AGAAAGGTGTGATCC[C/G]AGCAGCTAGGTCACA	69912
rs212503128	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677121	CGTCAATGTGTATAT[A/G]AGTGTAGTTGGCAGC	69912
rs212640578	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668340	TGAATTGCCCAAACC[A/G]GGCATGGTGGTACAA	69912
rs212707986	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667316	ATTAAAGGCGTGCGC[C/T]ACCACGCCGGGCAGA	69912
rs212875429	snp	A/C/G			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7675348	TATTACTACATGCTC[A/C/G]TCTTACTGAGCTGAT	69912
rs213101668	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673567	AGGAACCTGTTAACG[A/C]ATTTTTAAAACTTGC	69912
rs213279983	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674574	TAGACTATGTATTGG[C/T]GTGGCTTAGCTATGT	69912
rs213290641	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668408	GGATCTCAAAGCTAG[C/T]CAGGGCTACATATAC	69912
rs213358326	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676885	GCTCCTCTAAAGGAC[A/C]CTGTTTCAATTCACA	69912
rs213632690	snp	G/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666225	TTTGTTTTTTTTTTT[G/T]TTTTTTTTTTTTTAT	69912
rs213840176	snp	G/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667378	TTGTTCAGAGCTGCC[G/T]ACATGAAAGAACATC	69912
rs214021954	in-del	-/CT			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676794	GGGCTACATGAGACC[-/CT]GTTTCCAAAAAACAA	69912
rs214092428	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675268	CTGGCCCGTATAAGC[C/T]AGATAATCTCTTCCT	69912
rs214216043	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676006	GAGAATCTTATTCCT[A/G]TGCAGATGAGCTGGG	69912
rs214507585	in-del	-/AAG			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671559	AAAAAAAAAAGAAAA[-/AAG]AAAGACAGACAGACA	69912
rs214548640	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674654	ACTGGGCTGACATAC[A/G]ACTGGGAGCCACTGA	69912
rs214877844	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674702	GGGTCCTCTGGAACA[C/G]TATCTGCCCAGAACT	69912
rs215008147	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675309	CCTTTAATGTTCGTT[C/T]ATCATATCTACAACT	69912
rs215184904	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672687	AGTCTGTGCTCTTAA[C/G]CACTGAGCCCTCAAG	69912
rs215188603	in-del	-/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668662	TCAGATGGATGGACA[-/G]GGGTCTTTTGAACAT	69912
rs215281150	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673426	TCTCTGTGTACCCCT[A/G]GGTGTCCTGGAACTC	69912
rs215357094	in-del	-/GAAAGACAGAC			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7671561	AAAAAAAAGAAAAAA[-/GAAAGACAGAC]AGACAGACAGACAGA	69912
rs215557938	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672761	TCCGCATACCAAAAT[G/T]TCTTATTTGATCTAG	69912
rs215972543	in-del	-/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670510	CCACCTGCATTTGCT[-/C]CCCAATGTCACCGTG	69912
rs216125678	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678320	TAGGAGGTGTGGCCT[A/T]GTGGGAAGGGGTGGG	69912
rs216695073	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671203	GAAGGGTGTGAAAAT[A/G]ACACTTGGCAGGATC	69912
rs217078082	in-del	-/AAC			downstream-variant-500B, nc-transcript-variant, intron-variant	Nup43, BC020402, Pcmt1	Mm_Celera	10:7679026	CACTTCTACAAAATA[-/AAC]AACAGTGTAGAATCC	69912
rs217366154	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669511	CCCCCCTGTTAATAT[G/T]TTCAAGTAATCTATA	69912
rs217429131	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668476	TCTATGTGCCAAACG[A/C]TGTTTGGTAAGTTTT	69912
rs217431008	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677566	CCAAGACTACAGATG[C/T]GGTACCTACCCATAC	69912
rs218062494	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668804	AGATGAGTTTGGGCA[A/T]CAGAGACAAACCCAC	69912
rs218137963	snp	C/T			upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant, intron-variant	Lats1, Nup43, BC020402, Pcmt1	Mm_Celera	10:7679319	AGTCTTGCAGAAGAC[C/T]CAGGTTCAGTCCCCA	69912
rs218159232	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678421	CTGAGCTGCTGCTCC[A/G]GGGCCTGACTGCTGT	69912
rs218341288	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667803	GGTGGTGTGTCTGAG[C/T]CTGGGATCTGGTTTT	69912
rs218534743	in-del	-/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670700	AGAATATAAAAAAAA[-/T]TAAGGGAAGTAGTTT	69912
rs219125832	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672823	GTTCTTAGCTAAAGG[A/G]GACTTCCTAGTTTCT	69912
rs219465053	snp	A/G			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666571	GAGACATGTTGCTCC[A/G]CCAGGGGACCTGAGG	69912
rs219967653	in-del	-/AGACAGACAGACAGACAGGG			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671580	GACAGACAGACAGAC[-/AGACAGACAGACAGACAGGG]AATAGCATGGAGATG	69912
rs220214801	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675590	CTAGACTTGACTATA[C/G]CACAGTCCTCCTGCC	69912
rs220472046	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673976	AGTCCCCCAGCTTTG[C/T]GTTTTAATGAATTTC	69912
rs220506615	snp	A/G			synonymous-codon, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676262	GGTTCACTTCCACCC[A/G]TCCAACCCAGATCAC	69912
rs220904594	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674343	CAAACTCAGAAATCC[A/G]CCTGCCTCTGCCTCC	69912
rs221258069	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671993	TGAGTTACAACATTC[A/G]CTTAATTGTTAAGAG	69912
rs221494911	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677160	CATCAGATCCCCTGA[A/C]GCTGGAGTTACAGGT	69912
rs221531361	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674802	TTATTTTGCCTCCTA[C/G]CCTTTAATTCTAAAC	69912
rs221556231	snp	A/C			utr-variant-3-prime, downstream-variant-500B, intron-variant	Nup43, BC020402, Pcmt1	Mm_Celera	10:7678799	AACTATTTTCATGAA[A/C]GTGAAAAAACCTAGT	69912
rs221666542	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676491	TGTTTTGCCTGCATG[C/T]ATGTGGGTGTACCAC	69912
rs221958107	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666288	GCACAAGATATATCC[C/T]CCTGCATTCTTTTTT	69912
rs221972857	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674949	GAAATGTTTCTTATT[A/G]GGCAAAGATAAATTG	69912
rs222020304	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670175	CGCCTTCATTAAGAG[A/G]GAGGGTCTACTACCT	69912
rs222180084	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677288	CCTGGAAGTTCATTC[A/G]CATGAACTAGGAACT	69912
rs222315024	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677746	CTCCACATGTGTGCT[A/G]TGGCTGTGTGTATTG	69912
rs222316994	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669261	GTAAAAAGCTGTCTA[C/T]ACTTAGGAATGAAAT	69912
rs222445736	snp	A/G			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7675426	CCTATGGACCAAACC[A/G]TCATACTTCATGTTG	69912
rs222474155	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672266	CCATGAAGGGGAAGG[A/G]TGTAGGTGAGGAAGC	69912
rs222734929	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672975	TACAAAAGCTCGGCT[A/C]GAATTTTGCTGTGTG	69912
rs223030977	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672354	GGGTCCCACTTGGGG[A/G]TGAATAATAAAGACA	69912
rs223170440	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673827	GCTTGTATATCTATG[C/T]ACCACAAGAATGTAG	69912
rs223310663	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667690	CAATGAGGTACCGGG[C/T]TTGGGCGGGCCCCGG	69912
rs223371479	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676135	GCAGACTATAAGTAA[A/C]CTTTTGGTGACTATA	69912
rs223371666	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667032	TTTTGTTGTTGTTTG[C/T]AACATTTTATAATAA	69912
rs223446408	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678466	GACTCTAAGCACAAC[A/G]AGCCCTGAGCCCCAG	69912
rs223650189	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675522	TTTGTGCAGTTTTGA[A/G]ATAGGATCTCACTTT	69912
rs223662654	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671364	TACATTCTTGATTCT[G/T]TACCATAAATAACAC	69912
rs223756564	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670291	TCCAAGCCCTCAAAT[C/G]AGGTGGCTCACAACA	69912
rs223767171	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677869	TCCGGAGTTCAAATC[C/T]CAGCAACTGCATGGT	69912
rs223887913	in-del	-/A			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677982	AAATAAATAATCTTT[-/A]TAAAAATATATAAGA	69912
rs224225732	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673189	AAAGAAAAGTAAAAA[C/G]GAAGAATTCAGTATA	69912
rs224282803	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667257	GTAGACCAGGTTGGC[C/T]TCGAACTCAGAAATC	69912
rs224296169	snp	C/G			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666441	CTGCCTCTAACTCCA[C/G]TCTAGGACATTCAGG	69912
rs224475030	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671412	AAAACATGGAATAGC[C/T]GGGCGTGGTGGTGCA	69912
rs224548025	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672605	AAGAGGGCGTCAGAT[C/T]TCATTATGGATGGTT	69912
rs224635362	in-del	-/ATATATATATATAT			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674828	AAACTTTTATTACTC[-/ATATATATATATAT]ATATATATATATATA	69912
rs224719278	in-del	-/A			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666350	CGAGAGAGATGGCTC[-/A]GCAGTTAAAACGTAT	69912
rs224747869	in-del	-/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667016	TCAGATTAATTTTGG[-/T]TTTTGTTGTTGTTTG	69912
rs225047472	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668873	GTGCTGGGCGGGGTG[G/T]CGCAGGCCTTTAATC	69912
rs225442205	snp	G/T			downstream-variant-500B, nc-transcript-variant, intron-variant	Nup43, BC020402, Pcmt1	Mm_Celera	10:7679093	CAGGGGCTAGAGATA[G/T]CTCAGTGGTTATTAA	69912
rs226953311	snp	C/T			upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant, intron-variant	Lats1, Nup43, BC020402, Pcmt1	Mm_Celera	10:7679300	CAAAAGAAAAGCACC[C/T]GCTAGTCTTGCAGAA	69912
rs227250761	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676781	TTTAAGGCCAGCCAG[G/T]GCTACATGAGACCGT	69912
rs227381212	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668346	GCCCAAACCGGGCAT[A/G]GTGGTACAAGCCTCT	69912
rs227807535	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675725	CTCTGTCCCTGAGCT[A/G]TATCACAAGGTCCAA	69912
rs227812203	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677934	TCTTCTAGAGTGTCT[A/G]AAGACAGCTACAGTG	69912
rs227821928	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677351	TTTATGGAGTCCTGG[C/G]TGTCCTGGAACTCAC	69912
rs227822568	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675279	AAGCCAGATAATCTC[C/T]TCCTCTGTTTACGCC	69912
rs227827123	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677480	TGGTTGTTTATGGTA[C/T]CTCTCTTTCCATTAA	69912
rs228105488	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675242	CCATTTCACATCAGC[A/G]CTTTTAGTATCTGGC	69912
rs228360617	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671420	GAATAGCTGGGCGTG[A/G]TGGTGCACGCCTTTA	69912
rs228369259	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670487	AGCCTGGCCTTAAAC[G/T]CAGACATCCACCTGC	69912
rs228591800	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674586	TGGCGTGGCTTAGCT[A/C]TGTGCATGTGATTGC	69912
rs228755645	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676644	AATTATTGTGTAGAA[C/G]AGTAAGCAGACCAGA	69912
rs228953997	in-del	-/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669502	TGGACTTTTCCCCCC[-/T]GTTAATATGTTCAAG	69912
rs228997251	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675849	AAGCAAACATCAAAA[C/T]AGTACTGCAACATGA	69912
rs229284574	snp	A/G			synonymous-codon, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675135	CATGCCTGTGTCATT[A/G]CTGAAGGCTCATGAG	69912
rs229300149	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674521	GCATAAAGAATGGCT[A/G]CTGTAATTGATATTT	69912
rs229405563	snp	A/C			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666361	GGCTCGCAGTTAAAA[A/C]GTATTTGCTGTTCTT	69912
rs229639293	snp	G/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667336	CGCCGGGCAGAAGTG[G/T]ATCTTGTTGCCAAAG	69912
rs229694786	snp	A/G			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666708	CACACACATACATAT[A/G]TGCAAACAAAACATT	69912
rs229915690	in-del	-/TT			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673781	GTTATTGTAGTCAAC[-/TT]TGTATTTTTATTTGT	69912
rs230194031	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7665613	TGAGCACCAGGCTAG[C/T]GTGTGGTGCACACAT	69912
rs230280053	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673350	ATTAGTCATTTATTT[A/T]TAATATTTCAACCAG	69912
rs230769172	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670627	TAAAGAATGTGTCAA[C/T]ATTCAGCTATTTAGT	69912
rs230775048	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671757	AACAGAAGCTAGGGA[C/T]CTGTATGTGGTAAAC	69912
rs230827680	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678254	ATGAATGAGCCCATA[C/T]GCTAATATTTGAATG	69912
rs230828654	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671225	GGCAGGATCCTTGTA[A/T]AAGATAGTGTACGGA	69912
rs231009303	snp	A/G			upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant, intron-variant	Lats1, Nup43, BC020402, Pcmt1	Mm_Celera	10:7679223	CCTCTGGTCTATGGA[A/G]CAAAGTCCCAATGCA	69912
rs231108134	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671553	GTCTCGAAAAAAAAA[A/G]GAAAAAAGAAAGACA	69912
rs231482742	in-del	-/ATATATATATAT			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674829	AAACTTTTATTACTC[-/ATATATATATAT]ATATATATATTTACC	69912
rs231510649	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669343	TTTAAGCTTACTCTT[C/T]ATCTTTCATGAAAAA	69912
rs231514963	in-del	-/AT			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677987	AATAATCTTTTAAAA[-/AT]ATATATAAGATGGTC	69912
rs232076394	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669420	ATTTGCTTTGTGTGT[A/G]TGTGGAGGGGGGGCT	69912
rs232082716	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666231	TTTTTTTTTTTTTTT[C/T]TTTTTTTATGTTCAG	69912
rs232172055	snp	C/T			intron-variant, downstream-variant-500B	Nup43, BC020402, Pcmt1	Mm_Celera	10:7678478	AACAAGCCCTGAGCC[C/T]CAGTAAACATTTCCC	69912
rs232215540	in-del	-/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668134	TACAGGTAAATCTGA[-/G]TTGTCTGCCAAAGCT	69912
rs232403491	in-del	-/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671969	TCTTTGTTCTAAGTG[-/C]TTAATTTCTGAGTTA	69912
rs232559172	in-del	-/CTTCAGTCCCCTCTGTTGGC			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666644	CTCAAGTTATAGGGA[-/CTTCAGTCCCCTCTGTTGGC]CTTACCACTAGGCAT	69912
rs232701117	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667288	CGCCTGCCTCTGCCT[C/T]CCGAGTTCTGGGATT	69912
rs232898134	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678323	GAGGTGTGGCCTTGT[A/G]GGAAGGGGTGGGGCT	69912
rs232959057	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677726	CCTACAGGACACCTT[C/T]TGACCTCCACATGTG	69912
rs232980692	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671179	AAGTAAACATGATCT[G/T]AAAAGCTTGAAGGGT	69912
rs232984810	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677606	AAATGTTGAGTGCTT[A/T]CTGGCACTGAATAAG	69912
rs233212180	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667945	AAGGCAATCTGAATC[C/T]GACTTTCCTAGAGTT	69912
rs233426338	in-del	-/A			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673748	TCTCAGTATTATGAT[-/A]AAAAAACTTGTTTAA	69912
rs233842928	in-del	-/TG			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670009	CTCCTTTAAATGAAC[-/TG]TGTTAATTAGCTCTA	69912
rs234004038	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678005	ATATAAGATGGTCTG[A/G]TAAAAACTGAATGTG	69912
rs234437098	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671416	CATGGAATAGCTGGG[C/T]GTGGTGGTGCACGCC	69912
rs234613503	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675351	TACTACATGCTCCTC[C/T]TACTGAGCTGATGGC	69912
rs234628041	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676043	ATAAACTTTAAGTCT[A/G]TTGAAAATCAAAGGC	69912
rs234690310	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675497	TTTCCTAATTTATGA[A/T]TTCATTAATTTTGTG	69912
rs234717334	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676926	GATAGGTCACAACCA[C/T]CTGTAATTCCAGTTT	69912
rs234828199	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675324	CATCATATCTACAAC[C/T]GCAGTCAGTATTACT	69912
rs234892962	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674731	CTACTGAGCCAGCTC[G/T]CTTGCTGGACACATA	69912
rs234922012	snp	A/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666613	CACACACAAGGCAGG[A/T]CATAACTTTGTGTAA	69912
rs235414641	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668513	GTATGTTAATTTAGA[C/T]TACATGTCTGTGAGT	69912
rs235485247	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669652	AACTCTGTGGGAAAG[A/T]ACACTCGTCTTTTTA	69912
rs235547054	snp	C/T			upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant, intron-variant	Lats1, Nup43, BC020402, Pcmt1	Mm_Celera	10:7679371	CATCTGTACCTCTAG[C/T]TCCTGGGGATCTGAC	69912
rs235649575	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676163	ATAACATGAAGATAG[C/G]TAAGGGCCACTACTT	69912
rs235794538	snp	A/G			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7665954	TTACTATGTAGCTCT[A/G]GCTGGCCTGGAACTT	69912
rs235842203	in-del	-/AG			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670249	GTGTGTACTGCTCCT[-/AG]AGAGAGAGAGAGACC	69912
rs235926431	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675913	GATCCCAGCAGCTAG[A/G]TCACAGAGGCAGGAG	69912
rs235929239	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674655	CTGGGCTGACATACG[A/C]CTGGGAGCCACTGAT	69912
rs236321935	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672688	GTCTGTGCTCTTAAG[C/T]ACTGAGCCCTCAAGC	69912
rs236360132	in-del	-/TTT			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7666214	TTTTTTTTGTTTTTG[-/TTT]TTTTTTTTTTTTTTT	69912
rs236566510	in-del	-/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670802	AACTGAAAAATACTA[-/T]TATTAGGTAGGCATG	69912
rs236692827	in-del	-/TTTTTTT			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7672518	TCCAGCCTTAAGCTC[-/TTTTTTT]TTTTTTTTTTTTTTT	69912
rs236736017	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673507	CCTCCTGAGCACAGC[A/G]ATTGAAGGCAAGTGC	69912
rs236923049	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672916	AACCACTGACAAAAG[C/G]CTACTTCAAAGCTTA	69912
rs237033171	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670226	TGGGGAGGTGGCTCA[C/G]CAATTGAGTGTGTAC	69912
rs237098258	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669283	GAATGAAATATTTCT[A/C]AACTTTTATTATTGT	69912
rs237197042	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677136	AAGTGTAGTTGGCAG[A/C]TGAGGCCACATCAGA	69912
rs237510586	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678463	ATGGACTCTAAGCAC[A/C]ACAAGCCCTGAGCCC	69912
rs237776631	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671456	AGCACTTGGGAGGCA[A/G]AGGAAGGCGGATTTC	69912
rs238059491	in-del	-/A			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678077	TTCAAAGAACAAAAC[-/A]AAAAAAAGATGACAT	69912
rs238082127	in-del	-/TACT			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677388	CCCAGGCTGACATTG[-/TACT]TACTCAAAGGTCCTC	69912
rs238523090	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671897	GATTCCAGGCCCCCC[A/C]ACCCTAGACCTGTTG	69912
rs238803149	in-del	-/CC			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671890	TGAGAAGATTCCAGG[-/CC]CCCCCCCACCCTAGA	69912
rs238920147	in-del	-/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673863	CCAGAGGTCAGAAGA[-/G]GGCATTGAAGCCTTA	69912
rs238947342	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669840	TACAACCTTACCTTA[C/T]GGAGAAAAAGTCATG	69912
rs239003074	in-del	-/ACTAGAACCTATGGACCAAACCGTCAT			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675404	TTCTTTTTTCTCAAA[-/ACTAGAACCTATGGACCAAACCGTCAT]ACTTCATGTTGTCAG	69912
rs239138252	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677686	TTGATTGGCAGGACT[A/C]AAGTGGAGGAGGAGA	69912
rs239174306	in-del	-/A			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671496	ACCAGCCTGGTCTAC[-/A]AAATGAGTTCCAGGA	69912
rs239554417	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677225	AACTGAACCCAGGTC[C/T]TTTGTAAGAATAGCA	69912
rs239617517	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676492	GTTTTGCCTGCATGT[A/G]TGTGGGTGTACCACA	69912
rs239817821	in-del	-/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672797	GTCTTGAAAGACCCA[-/T]CCCCTAAGCAGTTCT	69912
rs240227319	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677944	TGTCTAAAGACAGCT[A/G]CAGTGTACTTACATT	69912
rs240252473	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671415	ACATGGAATAGCTGG[A/G]CGTGGTGGTGCACGC	69912
rs240315373	snp	C/T			downstream-variant-500B, intron-variant	Nup43, BC020402, Pcmt1	Mm_Celera	10:7678923	CTCCCCCAACACTTA[C/T]TAGAATCTGATCAAT	69912
rs240673318	in-del	-/AGGT			downstream-variant-500B, nc-transcript-variant, intron-variant	Nup43, BC020402, Pcmt1	Mm_Celera	10:7679170	GCACTTGGAAGGCAG[-/AGGT]AGGTAGGTAGGTGGA	69912
rs241059119	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674368	GCCTCCCAAGTGCTG[A/G]GATTAAAGGTGTGTG	69912
rs241386654	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674973	TAAATTGTTTTTTAC[C/T]ATATCTTTTGATATT	69912
rs241496383	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674045	TAACACAATGGAGTT[C/G]ATTCTACCATCTTAC	69912
rs241557527	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673144	GACATAACTATAGTT[C/T]CATCACTAGGGAAGC	69912
rs241986509	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677059	AGGGCGAATGCAAAA[C/G]GAAAGACTCATTTAA	69912
rs242099824	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675167	CTGAAAGTAAGTATT[G/T]TGGGGACACAAAGCT	69912
rs242125375	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667070	TTAAAAGAACAAAAA[C/T]CCTAATTTTGTAAAG	69912
rs242191173	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675587	AAACTAGACTTGACT[A/T]TACCACAGTCCTCCT	69912
rs242650842	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677748	CCACATGTGTGCTGT[A/G]GCTGTGTGTATTGTG	69912
rs242787072	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672994	TTTTGCTGTGTGAGT[A/C]TGAACAACAGTATAG	69912
rs243062663	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672010	TTAATTGTTAAGAGC[C/T]GTTGGCCTGCTAGCA	69912
rs243363106	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668275	CATATTAGGCACTTA[C/G]TCTCAGAAGTGGGGC	69912
rs243434506	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671403	GACACACAGAAAACA[G/T]GGAATAGCTGGGCGT	69912
rs243488246	in-del	-/TTTGTTTTG			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673384	GGGACGTGGTTTACT[-/TTTGTTTTG]TTTGTTTTGTTTTGT	69912
rs243735115	snp	A/T			upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant, intron-variant	Lats1, Nup43, BC020402, Pcmt1	Mm_Celera	10:7679227	TGGTCTATGGAGCAA[A/T]GTCCCAATGCAGCAA	69912
rs243871799	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677444	CTCTGTGTACATTTT[A/G]GGTTCTTCTTTCCTT	69912
rs243988016	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678288	GGTCCCCAGTTGGTA[A/G]AACTGTTTGGAAGGG	69912
rs244015458	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674855	TATATATATATTTAC[C/T]ATTTAGTTGAAATTT	69912
rs244256004	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670537	CGTGACCAGCTTTAA[C/T]TAGTTTTCTTAATGG	69912
rs244258652	snp	A/G			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667260	GACCAGGTTGGCTTC[A/G]AACTCAGAAATCCGC	69912
rs244530464	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675616	CTGCCTTAGCTTCCT[A/G]TGTGCTGAGATTACA	69912
rs244545010	in-del	-/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678199	AATAGCAGCTTTATA[-/T]TTAGTGGTACAGAGT	69912
rs244589436	in-del	-/TTC			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674941	AGTGGAATGAAATGT[-/TTC]TTATTAGGCAAAGAT	69912
rs244685989	in-del	-/A			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678398	AGTCTGGATCAGGAC[-/A]ATAAACTCTGAGCTG	69912
rs244998880	snp	C/G			downstream-variant-500B, nc-transcript-variant, intron-variant	Nup43, BC020402, Pcmt1	Mm_Celera	10:7679192	TAGGTAGGTGGATCT[C/G]TGAATTCAAGGCCAG	69912
rs245386811	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677322	ATTTTGTTTGTTTGT[A/T]GAGACAGGTTCTCTT	69912
rs245544106	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675819	TCTGGCTTTTACTCA[A/G]ATAGAAATACAAGAA	69912
rs245605223	in-del	-/GCTTGCT			downstream-variant-500B, intron-variant	Nup43, BC020402, Pcmt1	Mm_Celera	10:7678892	CAGTGCCCAATGTTG[-/GCTTGCT]GCTTGCTTCCTCCCC	69912
rs245614735	in-del	-/TT			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675649	CATGAGCCACCACTC[-/TT]TGATAAAATATATTC	69912
rs245734587	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667946	AGGCAATCTGAATCT[G/T]ACTTTCCTAGAGTTG	69912
rs245772149	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675292	TCTTCCTCTGTTTAC[A/G]CCCTTTAATGTTCGT	69912
rs245876722	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672395	TATAGTCTAAGTCTG[C/T]TAGCCTTTTTTGCTT	69912
rs246085746	snp	A/G			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7665629	GTGTGGTGCACACAT[A/G]TATGTGCAGGCAAAC	69912
rs246187779	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669428	TGTGTGTGTGTGGAG[G/T]GGGGGCTATTTGCTT	69912
rs246262932	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670403	GCACATAAATGTTTT[A/G]TTATTTTTGTCTTAA	69912
rs246306891	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666312	CTTTTTTAATTTTTA[C/T]TCTTAGATTTTTCTC	69912
rs246323634	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670346	ATCTAAATCCCACTG[A/G]CCTTGGCAGGCACCT	69912
rs246438113	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677524	ACAATAAGCAAAGAT[A/G]CAGAACACCTACATT	69912
rs246452024	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676941	TCTGTAATTCCAGTT[G/T]TAGGGGATCCAATGC	69912
rs246498132	snp	A/G			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667307	AGTTCTGGGATTAAA[A/G]GCGTGCGCTACCACG	69912
rs247003931	snp	C/T			synonymous-codon, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676277	GTCCAACCCAGATCA[C/T]CTGTTCACTTGTTCT	69912
rs247135267	in-del	-/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668661	ATCAGATGGATGGAC[-/G]AGGGTCTTTTGAACA	69912
rs247484924	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678358	GGTTTCCAAAGCCAA[G/T]GCCATTCTCCAGTGT	69912
rs247612494	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671677	ATATTTGTTACTGGA[C/G]AGATGACAGGTGAAG	69912
rs247624273	snp	C/T			upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant, intron-variant	Lats1, Nup43, BC020402, Pcmt1	Mm_Celera	10:7679318	TAGTCTTGCAGAAGA[C/T]CCAGGTTCAGTCCCC	69912
rs247686070	in-del	-/GGC			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668911	TGGGAGGCAGAGGCA[-/GGC]GGATTTCTGAGTTCA	69912
rs248108731	in-del	-/TACC			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677569	AGACTACAGATGTGG[-/TACC]TACCCATACTCTCCC	69912
rs248201294	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666369	GTTAAAACGTATTTG[C/T]TGTTCTTGCAGAGAG	69912
rs248314966	in-del	-/A			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677179	GAGTTACAGGTGGTT[-/A]GTAAGCCATCTGTCT	69912
rs248372409	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674534	CTGCTGTAATTGATA[C/T]TTAGTTTTACTTTTA	69912
rs248383156	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673524	TTGAAGGCAAGTGCT[G/T]CCACACCTGGCTGGA	69912
rs248534518	in-del	-/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671499	AGCCTGGTCTACAAA[-/G]TGAGTTCCAGGACAA	69912
rs248762188	snp	A/G			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666940	CCAATATGGAGCTAC[A/G]CAGCTTCGGAATGAC	69912
rs249278603	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672663	TGAACTCAGGACCTT[C/T]GGAAGAGCAGTCTGT	69912
rs249701989	in-del	-/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670212	CTTTCTGTTGGGGCT[-/G]GGGAGGTGGCTCAGC	69912
rs249880308	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677720	CTGATTCCTACAGGA[C/T]ACCTTCTGACCTCCA	69912
rs249881755	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678188	TTTGAAATATCAATA[A/G]CAGCTTTATATTTAG	69912
rs250277208	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668638	CAAGTAAGACTCACT[A/G]CTTCGCTGATCAGAT	69912
rs250696392	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671554	TCTCGAAAAAAAAAA[A/G]AAAAAAGAAAGACAG	69912
rs250770527	in-del	-/AAAA			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668842	AAGCACACCCCAATC[-/AAAA]CAAAAAAAAAAAATC	69912
rs250996691	snp	A/T			missense, downstream-variant-500B, intron-variant	Nup43, BC020402, Pcmt1	Mm_Celera	10:7678600	TTCCTGTCACATAGC[A/T]TAAGTAACCAGGCCG	69912
rs251477430	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675988	CACTAAAAGATAAAA[A/G]CTGAGAATCTTATTC	69912
rs251629322	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673915	AGAATTGCCATGTGG[A/G]TACTAGGATTGAACC	69912
rs251760154	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674689	GGGGCATGAACTTGG[A/G]TCCTCTGGAACAGTA	69912
rs251804186	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674618	GGTACCCACAGGCCA[A/G]GTTTGTAGGATACTC	69912
rs251980303	in-del	-/AGTGG			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676573	AAGAACACTGACCAT[-/AGTGG]AATAAGACAGGAAAT	69912
rs252103593	in-del	-/AGAC			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7671564	AAAAAGAAAAAAGAA[-/AGAC]AGACAGACAGACAGA	69912
rs252119258	in-del	-/A			downstream-variant-500B, intron-variant	Nup43, BC020402, Pcmt1	Mm_Celera	10:7678948	TCAATGACTGATGAC[-/A]AAAAAATCTTGAGAG	69912
rs252349091	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675343	GTCAGTATTACTACA[C/T]GCTCCTCTTACTGAG	69912
rs252467392	snp	C/G			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666623	GCAGGTCATAACTTT[C/G]TGTAACTCAAGTTAT	69912
rs252603463	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674797	TTATGTTATTTTGCC[A/T]CCTAGCCTTTAATTC	69912
rs252612492	snp	G/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666535	TTAAAATACTAAGAA[G/T]AAAGCTGTGTTTAAA	69912
rs252646056	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674329	GACCAGGCTGGCCTC[A/G]AACTCAGAAATCCGC	69912
rs252654243	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676125	GTAAAGAGATGCAGA[C/G]TATAAGTAACCTTTT	69912
rs252943212	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673209	AATTCAGTATAAAAA[A/C]CAAACGGCCAATCAG	69912
rs253009587	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675521	TTTTGTGCAGTTTTG[A/C]GATAGGATCTCACTT	69912
rs253270717	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673365	ATAATATTTCAACCA[A/G]TAGGGGGACGTGGTT	69912
rs253321127	in-del	-/AGGTAGGT			downstream-variant-500B, nc-transcript-variant, intron-variant	Nup43, BC020402, Pcmt1	Mm_Celera	10:7679169	GCACTTGGAAGGCAG[-/AGGTAGGT]AGGTAGGTAGGTAGG	69912
rs253354510	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671196	AAAGCTTGAAGGGTG[G/T]GAAAATGACACTTGG	69912
rs253508151	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677734	ACACCTTCTGACCTC[C/T]ACATGTGTGCTGTGG	69912
rs253559753	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677238	TCCTTTGTAAGAATA[C/G]CATGTGTTCTTAACA	69912
rs253718336	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676661	GTAAGCAGACCAGAT[A/G]GATAAAGAAAAAGGG	69912
rs253750721	in-del	-/A			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7668843	AGCACACCCCAATCC[-/A]AAAAAAAAAAAATCG	69912
rs253820697	in-del	-/AA			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676447	TTTGGCCTCAAACTC[-/AA]AGAGATTTACCTGCC	69912
rs253886333	in-del	-/TTTTTTTTTTTTTTTTTT			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674228	ATTATTCTTTTTTTC[-/TTTTTTTTTTTTTTTTTT]TTTTTTTTTTGGTTT	69912
rs253960908	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677665	TACCAAACTTGACAA[C/T]GGAGTTTGATTGGCA	69912
rs254112902	in-del	-/AA			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7669196	AATAAATAAATCTTT[-/AA]AAAAAAAAAAAAAAA	69912
rs254180201	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674233	TCTTTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT	69912
rs254248697	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670227	GGGGAGGTGGCTCAG[A/C]AATTGAGTGTGTACT	69912
rs254683317	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672819	AGCAGTTCTTAGCTA[A/T]AGGAGACTTCCTAGT	69912
rs255132663	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670667	CATTAGTTTGAGATA[A/T]ATGTGCTGAGTCTAT	69912
rs255284668	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672971	CAGATACAAAAGCTC[G/T]GCTAGAATTTTGCTG	69912
rs255322207	in-del	-/TA			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668168	TAGGAAATTTGAGAC[-/TA]TATTTAGAGGTAACA	69912
rs255847094	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671351	AAGTGGCAATTAGTA[C/T]ATTCTTGATTCTGTA	69912
rs255856819	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7678465	GGACTCTAAGCACAA[C/T]AAGCCCTGAGCCCCA	69912
rs255911341	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676849	GGAGAGTTGGTTCAA[C/T]AGTTAAGAAGAGCAC	69912
rs256663198	snp	A/C			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666497	ACATATACACATGCA[A/C]ATACATACATACATA	69912
rs256739589	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675259	TTTTAGTATCTGGCC[A/C]GTATAAGCCAGATAA	69912
rs256818381	snp	C/G			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666401	TAGAGTTGGCTTCTC[C/G]GCACTCACAAGGGTA	69912
rs257190590	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677462	TTCTTCTTTCCTTAC[A/G]TTTGGTTGTTTATGG	69912
rs257243473	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669861	AAAAGTCATGAGAGG[A/G]GAATATGCTGTCGAA	69912
rs257370054	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677900	GGCTCACAACCATCC[A/G]TAATGAGATTTGACT	69912
rs257568246	snp	G/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667342	GCAGAAGTGTATCTT[G/T]TTGCCAAAGGGTTTG	69912
rs257712059	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674934	TTTAGTTAGTGGAAT[A/G]AAATGTTTCTTATTA	69912
rs257760361	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667289	GCCTGCCTCTGCCTC[C/T]CGAGTTCTGGGATTA	69912
rs257760409	in-del	-/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674673	GGGAGCCACTGATGT[-/G]GGGGCATGAACTTGG	69912
rs257983613	snp	C/T			upstream-variant-2KB, downstream-variant-500B, nc-transcript-variant, intron-variant	Lats1, Nup43, BC020402, Pcmt1	Mm_Celera	10:7679298	CACAAAAGAAAAGCA[C/T]CCGCTAGTCTTGCAG	69912
rs258053120	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673045	CTGTCAGTGGGTAAA[A/G]TTTTCTGCCAAGTAC	69912
rs258216161	in-del	-/ATTTTAGAAT			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666741	TACACATAAAATAAG[-/ATTTTAGAAT]CTCTTCTAAAAAATT	69912
rs258497480	snp	A/G			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666948	GAGCTACACAGCTTC[A/G]GAATGACTATGCTAA	69912
rs258719090	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672689	TCTGTGCTCTTAAGC[A/G]CTGAGCCCTCAAGCT	69912
rs258800895	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673164	ACTAGGGAAGCTGAA[C/G]GCAGGAGGAAAAGAA	69912
rs258969552	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675890	GAGATGTTCATCCAG[A/G]AAGGTGTGATCCCAG	69912
rs259126953	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674483	TCAGACTAGAAAAAA[A/T]TTATATGAACTAATT	69912
rs259338735	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674974	AAATTGTTTTTTACC[A/G]TATCTTTTGATATTG	69912
rs260109945	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7676573	TAAGAACACTGACCA[C/T]AATAAGACAGGAAAT	69912
rs260171547	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675848	AAAGCAAACATCAAA[A/C]CAGTACTGCAACATG	69912
rs260293458	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667951	ATCTGAATCTGACTT[G/T]CCTAGAGTTGATGTT	69912
rs260415865	in-del	-/TT			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7672519	TCCAGCCTTAAGCTC[-/TT]TTTTTTTTTTTTTTA	69912
rs260696661	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673818	GTTTTGCCTGCTTGT[A/C]TATCTATGCACCACA	69912
rs260983038	snp	A/G			downstream-variant-500B, nc-transcript-variant, intron-variant	Nup43, BC020402, Pcmt1	Mm_Celera	10:7678972	TTGAGAGCATCAGAG[A/G]GTCCCAGTGCTGTTT	69912
rs260984260	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670423	TTTTGTCTTAAAGAC[A/T]GGATATCACTATGTA	69912
rs261021213	snp	A/C			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666663	AGTCCCCTCTGTTGG[A/C]CTTACCACTAGGCAT	69912
rs261083660	snp	C/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677841	TAAGAGCACCCGACT[C/G]CTCTTCCGAAGGTCC	69912
rs261131562	snp	A/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671417	ATGGAATAGCTGGGC[A/G]TGGTGGTGCACGCCT	69912
rs261517291	snp	C/T			downstream-variant-500B, nc-transcript-variant, intron-variant	Nup43, BC020402, Pcmt1	Mm_Celera	10:7679204	TCTGTGAATTCAAGG[C/T]CAGCCTCTGGTCTAT	69912
rs261815663	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677331	GTTTGTTGAGACAGG[C/T]TCTCTTTATGGAGTC	69912
rs261965437	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675588	AACTAGACTTGACTA[G/T]ACCACAGTCCTCCTG	69912
rs262246329	snp	G/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670350	AAATCCCACTGACCT[G/T]GGCAGGCACCTGTAC	69912
rs262392096	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667830	TTTTAAACCCTCACC[A/T]AGTCTGTAGTCATAC	69912
rs262440249	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675425	ACCTATGGACCAAAC[C/T]GTCATACTTCATGTT	69912
rs262678189	in-del	-/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666197	AGGGTTTTTAAAGTG[-/T]TTTTTTTTTGTTTTT	69912
rs262881729	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7673214	AGTATAAAAAACAAA[C/T]GGCCAATCAGCTCTG	69912
rs262892944	snp	A/G			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667438	GTGCTCCTGCTGACG[A/G]GAATTGGCTGTCTGC	69912
rs263077547	in-del	-/A			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677790	ATAAATAGGTGTAAT[-/A]AAAAAATGTAAGGGC	69912
rs263500019	snp	A/C			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7671407	CACAGAAAACATGGA[A/C]TAGCTGGGCGTGGTG	69912
rs263582951	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672401	CTAAGTCTGCTAGCC[C/T]TTTTTGCTTTGGGAC	69912
rs264468373	snp	A/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7672315	TGGGTGGATTTGACA[A/T]GAGTCTGTCTTGGGG	69912
rs264952679	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7675168	TGAAAGTAAGTATTG[C/T]GGGGACACAAAGCTT	69912
rs265023840	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7669404	GATGTTAACACATTT[C/T]ATTTGCTTTGTGTGT	69912
rs265165736	snp	C/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7667272	TTCGAACTCAGAAAT[C/T]CGCCTGCCTCTGCCT	69912
rs265267082	in-del	-/A			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668998	CTTTCTCAAAAAACC[-/A]AAAAAAAAAAAAAGT	69912
rs265328533	snp	C/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674384	GATTAAAGGTGTGTG[C/T]CACCACCGCCCGGCA	69912
rs387007844	in-del	-/T			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670803	ACTGAAAAATACTAT[-/T]ATTAGGTAGGCATGG	69912
rs387027967	in-del	-/AT			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668171	GAAATTTGAGACTAT[-/AT]TTAGAGGTAACAAGG	69912
rs387300786	in-del	-/G			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670226	TGGGGAGGTGGCTCA[-/G]CAATTGAGTGTGTAC	69912
rs387353197	in-del	-/T			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666206	AAAGTGTTTTTTTTT[-/T]GTTTTTGTTTTTTTT	69912
rs387447804	in-del	-/CGG			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7668913	GGAGGCAGAGGCAGG[-/CGG]ATTTCTGAGTTCAAG	69912
rs387549613	in-del	-/AT			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7674850	TATATATATATATAT[-/AT]TTACCATTTAGTTGA	69912
rs387709659	in-del	-/A			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7677796	AGGTGTAATAAAAAA[-/A]TGTAAGGGCTGGTGA	69912
rs387714822	in-del	-/CAGTCCCCTCTGTTGGCCTT			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	Mm_Celera	10:7666647	AAGTTATAGGGACTT[-/CAGTCCCCTCTGTTGGCCTT]ACCACTAGGCATAAA	69912
rs387794059	in-del	-/GT			intron-variant	Nup43, Pcmt1	Mm_Celera	10:7670012	CTTTAAATGAACTGT[-/GT]TAATTAGCTCTACTG	69912
rs578401453	snp	A/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7672534	TTTTTTTTTTTTTTT[A/T]AAGATTTATTTATTA	69912
rs578432380	snp	A/G			downstream-variant-500B, nc-transcript-variant, intron-variant	Nup43, BC020402, Pcmt1	GRCm38.p3	10:7679033	TACAAAATAAACAGT[A/G]TAGAATCCAAGTAGA	69912
rs579011834	snp	C/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7672780	TATTTGATCTAGGGG[C/T]TGTCTTGAAAGACCC	69912
rs579446963	snp	A/G			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7674383	GGATTAAAGGTGTGT[A/G]CCACCACCGCCCGGC	69912
rs579584444	snp	C/G			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7666213	TTTTTTTTTGTTTTT[C/G]TTTTTTTTTTTTTTT	69912
rs580905399	snp	G/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7670543	CAGCTTTAATTAGTT[G/T]TCTTAATGGAATCAT	69912
rs581154071	snp	A/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7677840	GTAAGAGCACCCGAC[A/T]GCTCTTCCGAAGGTC	69912
rs581269287	snp	A/G			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7668906	AGCACTTGGGAGGCA[A/G]AGGCAGGATTTCTGA	69912
rs581598189	snp	C/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7675663	CTTTGATAAAATATA[C/T]TCCCATTCCCTATTA	69912
rs581774813	snp	C/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7668827	AAACCCACACACACA[C/T]AAGCACACCCCAATC	69912
rs582407157	snp	A/C			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7672789	TAGGGGTTGTCTTGA[A/C]AGACCCATCCCCTAA	69912
rs582881871	snp	C/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7672586	CTGTCTTCAGACACA[C/T]CAGAAGAGGGCGTCA	69912
rs583161061	snp	A/G			upstream-variant-2KB, intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7666241	TTTTTTTTTTTTTAT[A/G]TTCAGTGAAGTACAA	69912
rs583163633	snp	A/G			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7673375	AACCAGTAGGGGGAC[A/G]TGGTTTACTTTTGTT	69912
rs583772100	snp	A/C			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7675678	TTCCCATTCCCTATT[A/C]CTGGGGAATGAGCCA	69912
rs584187736	snp	A/G			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7677849	CCCGACTGCTCTTCC[A/G]AAGGTCCGGAGTTCA	69912
rs584368953	snp	A/G			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7670686	TGCTGAGTCTATTCA[A/G]AATATAAAAAAAATT	69912
rs584392835	snp	C/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7668969	CCAGGACAGCCAGGG[C/T]TATACAGTGAAACCC	69912
rs585697607	snp	C/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7674288	TTTCTCTGTGTAGCC[C/T]TGGCTGTCCTGGAAC	69912
rs586208120	snp	A/G			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7668659	CTGATCAGATGGATG[A/G]ACAGGGTCTTTTGAA	69912
rs586260224	snp	C/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7672612	CGTCAGATTTCATTA[C/T]GGATGGTTGTGAGCC	69912
rs586799856	snp	A/C			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7676440	GACCAGGTTTGGCCT[A/C]AAACTCAAAGAGATT	69912
rs586818057	snp	C/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7672809	CCATCCCCTAAGCAG[C/T]TCTTAGCTAAAGGAG	69912
rs587339867	snp	G/T			intron-variant	Nup43, Pcmt1	GRCm38.p3	10:7668868	AAATCGTGCTGGGCG[G/T]GGTGGCGCAGGCCTT	69912
rs864293474	snp	A/G			utr-variant-3-prime, downstream-variant-500B, intron-variant	Nup43, BC020402, Pcmt1	GRCm38.p3	10:7678843	TCACCAGAAAGTGGC[A/G]TTTGTAAGGAAACAA	69912