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

Psen2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs6291718	snp	A/C	0.5	0	intron-variant	Psen2	Mm_Celera	1:180250511	ACAGTGGAGAGAGGC[A/C]CAGGATTGCCCTGAT	19165
rs30473421	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263759	TTTTGCTTGCATTTA[C/T]ATCTGTGCACGGTGT	19165
rs30505573	snp	C/T	0.444444	0.157135	intron-variant	Psen2	Mm_Celera	1:180231650	TCTGTGACTTTGCCT[C/T]CTCTTGCTGCCTCCT	19165
rs30507380	snp	A/G	0.444444	0.157135	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180260443	CATGCATATATTCAC[A/G]TATACCATCTATCTA	19165
rs30616461	snp	A/G	0.48	0.0979796	intron-variant, upstream-variant-2KB	Psen2, Gm31728	GRCm38.p3	1:180255303	AGTCATTTCACAACC[A/G]TTCATATCTTTAAAG	19165
rs30667956	snp	C/T	0.260355	0.249785	intron-variant	Psen2, Gm31728	Mm_Celera	1:180262285	TAAGAGTTGTATAAC[C/T]GATGCACTTATCTTT	19165
rs30670767	snp	A/G	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180250302	TGGACCGTGTGCAGA[A/G]GACAGGCTGTTCTGG	19165
rs30984606	snp	C/T	0.345679	0.230967	downstream-variant-500B	Psen2	Mm_Celera	1:180226715	GGACATCTGTCAAAG[C/T]AACCACTCAGCTTTT	19165
rs31052399	snp	C/T	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180245470	AGGGGAGAGGACATT[C/T]CCTTATGATCTCCAT	19165
rs31126107	snp	A/T	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180251357	CTGCATAGACTAGTG[A/T]GACATGAACCATACT	19165
rs31153288	snp	A/G	0.32	0.24	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254591	GAGCAACCACAGAAG[A/G]GCCACTGGACAGGGT	19165
rs31302683	snp	C/T	0.495868	0.0452663	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180261326	AATTGTCATGGTCTA[C/T]ACTTGAAACTTTAAT	19165
rs31344197	snp	C/T	0.444444	0.157135	intron-variant	Psen2	Mm_Celera	1:180231003	ACATGAAGGGACCTA[C/T]GGGCTCCAGCTGCAT	19165
rs31417850	snp	C/G	0.375	0.216506	intron-variant	Psen2	Mm_Celera	1:180250139	AGCATAGAAAAACAA[C/G]CCCCGCTGGATCCGC	19165
rs31431681	snp	A/G	0.345679	0.230967	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180260167	TCCCAGTCATGAACA[A/G]GTATGGTTGTTTTGC	19165
rs31450547	snp	C/T	0.489796	0.070696	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255132	AAGGCCTGAGAGGCT[C/T]AGGTGTCCACAGAGG	19165
rs31462499	snp	A/G	0.48	0.0979796	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180259781	CTCTTCACAGCAATG[A/G]AACTAAGTCAGGGGG	19165
rs31548221	snp	A/G	0.5	0	intron-variant	Psen2	Mm_Celera	1:180231084	GCTCTGTGGAAGCTC[A/G]ATGCCCCAGCATAGG	19165
rs31562572	snp	C/T	0.375	0.216506	intron-variant	Psen2	GRCm38.p3	1:180233557	ACTTCCACGCCTCCA[C/T]GAAAGGCCACCTGCT	19165
rs31651455	snp	C/T	0.375	0.216506	intron-variant	Psen2	Mm_Celera	1:180228192	CAAATCACCAAAGTG[C/T]CTGCCCTGCCCTTGG	19165
rs31670154	snp	A/G	0.5	0	intron-variant, downstream-variant-500B	Psen2, Gm31728	GRCm38.p3	1:180258797	GTAGATGAACAGATG[A/G]GCAAATGGGTTCTAG	19165
rs31709105	snp	A/G	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180250776	CCCCTGGAAAGTCCC[A/G]GTCTTCCTCCACACT	19165
rs31763341	snp	A/C	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180230020	GAAAGCCTGCAGAGC[A/C]CCTCTGTCCCGAGGC	19165
rs31771102	snp	C/T	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180248549	AGTACCTCCCACTCC[C/T]ATGACTTGTAGGGAT	19165
rs31774241	snp	C/G	0.32	0.24	intron-variant	Psen2, Gm31728	Mm_Celera	1:180259758	AAGAGTTGCCATGGT[C/G]ATGGTGTCTCTTCAC	19165
rs31819863	snp	C/T	0.444444	0.157135	intron-variant	Psen2, Gm31728	Mm_Celera	1:180260404	TGCTGATAATAATTA[C/T]GTATGTATATGTGTG	19165
rs31819908	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255953	CCAGAGCTGCACCCT[A/G]CGCTCCTTCCAAGCC	19165
rs31837949	snp	C/T	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180236576	AGAATGAAAGGGAAG[C/T]CCAGGCAAGGGTGGG	19165
rs31849057	snp	C/T	0.260355	0.249785	intron-variant	Psen2, Gm31728	Mm_Celera	1:180262450	CTTTCACTCTCTTTT[C/T]CCATTTTTCCAAAGC	19165
rs31852556	snp	C/T	0.486111	0.0821678	intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258833	GTGGACAGAGTATTG[C/T]CTAAAGGAGCTGCTC	19165
rs31870962	snp	G/T	0.375	0.216506	intron-variant	Psen2	Mm_Celera	1:180250171	CAGGAGGTCCTGGGG[G/T]AGCCTGACTCAGCAC	19165
rs31893827	snp	A/G	0.277778	0.248452	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254719	TTCATTTCCACATAC[A/G]AATGGATGTACAGCC	19165
rs31947168	snp	C/T	0.32	0.24	intron-variant	Psen2	GRCm38.p3	1:180254049	TTTTGGGGATAGTGT[C/T]TCACTACATAGCTCA	19165
rs31950085	snp	C/T	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180251492	TGGCTAGTCAGTGAA[C/T]GGGAGCCTCGATGGG	19165
rs31960160	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Psen2	GRCm38.p3	1:180247870	GATCTCTTCCGTATC[C/T]CTTCTGGCAACAGTG	19165
rs31961746	snp	C/T	0.375	0.216506	intron-variant	Psen2	GRCm38.p3	1:180238316	ACGGGGTGAGGGTAC[C/T]GCTCAGTGGTACATT	19165
rs31966860	snp	A/G	0.290657	0.246672	intron-variant	Psen2	Mm_Celera	1:180232264	CTGGGTTGTTTCTCC[A/G]TGTCCAAACCGGCTC	19165
rs32001496	snp	A/C	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180237415	CTTAAGGACTGTCCG[A/C]GGTCACCAGCTCAGC	19165
rs32026433	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Psen2	GRCm38.p3	1:180247285	AGGACCAGGCGCTCC[A/G]TCTCTTGGGTCTTGA	19165
rs32085490	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254608	CCACTGGACAGGGTA[C/T]GGCTAGACACTGCTC	19165
rs32129149	snp	A/G	0.5	0	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180261260	GTGTGTACTGGGGGC[A/G]GGGAAGAGTTCCACA	19165
rs32193659	snp	C/T	0.375	0.216506	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180262014	GTCACTAGTCTTCAG[C/T]GTGTTCGCTCGGAAC	19165
rs32216262	snp	A/G	0.375	0.216506	intron-variant	Psen2, Gm31728	Mm_Celera	1:180259576	AGCATTAGAATAGAA[A/G]CAGGTACAATATTAT	19165
rs32220633	snp	C/T	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180234240	TTGTTATCATGTGAA[C/T]GTGAAATGTCCCCTA	19165
rs32230437	snp	C/T	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180249586	TGCTTGGATCACAGG[C/T]ATGAACCTCTACATC	19165
rs32315325	snp	C/T	0.48	0.0979796	intron-variant	Psen2	GRCm38.p3	1:180251851	AAACTGCCCACAGAA[C/T]GATGTCATCTCCCAG	19165
rs32378604	snp	C/T	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180229493	GAGTCTTCTTCTAAG[C/T]GTCCAGGAACAAAGG	19165
rs32435302	snp	A/G	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180228285	CTGACACACATGTGG[A/G]CAGAGACAAGCTCTT	19165
rs32456894	snp	A/G	0.32	0.24	intron-variant	Psen2	Mm_Celera	1:180254332	TACAGATGGTTGTGG[A/G]CCTCCATGTTGAACA	19165
rs32520209	snp	A/G	0.46875	0.121031	intron-variant	Psen2	GRCm38.p3	1:180240419	TATGCAGAGCTCAAA[A/G]CTACAGTACCAGAGC	19165
rs32539316	snp	A/T	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180248579	TGAAGGGGTAAACTG[A/T]ACAGCCCTTAATCCT	19165
rs32552715	snp	A/G	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180229490	TAGGAGTCTTCTTCT[A/G]AGTGTCCAGGAACAA	19165
rs32553311	snp	C/T	0.444444	0.157135	downstream-variant-500B	Psen2	GRCm38.p3	1:180226965	CGCCCCTAGCCCCTC[C/T]CACTACACAGCGGAG	19165
rs32570462	snp	A/G	0.375	0.216506	intron-variant	Psen2	Mm_Celera	1:180231257	CCAATTTTTTAAAAA[A/G]AGGAAATGATTTTCA	19165
rs32591046	snp	C/T	0.444444	0.157135	intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246468	CCAAGCTAGGCCAGG[C/T]TAGACAAGGTTAGCC	19165
rs32610029	snp	A/G	0.336735	0.234472	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254799	CTCCAAACCGGACCC[A/G]GCTTCCAGCTCAGTC	19165
rs32610934	snp	C/T	0.375	0.216506	intron-variant, downstream-variant-500B	Psen2, Gm31728	GRCm38.p3	1:180258889	GTGTCAGAATAGTCT[C/T]AGTCGGAGGTGTGGT	19165
rs32685017	snp	C/T	0.46875	0.121031	downstream-variant-500B	Psen2	GRCm38.p3	1:180226839	CCTCCCAATGCCCTG[C/T]TATGGAACTTTTTAG	19165
rs32685020	snp	G/T	0.375	0.216506	utr-variant-3-prime, nc-transcript-variant	Psen2	Mm_Celera	1:180227552	GCCCCCATAGCTCTC[G/T]GAGCCTCCGCCTGGC	19165
rs32685775	snp	C/T	0.375	0.216506	intron-variant	Psen2	GRCm38.p3	1:180230395	GGTGTCTCCGTGTTC[C/T]AGGAGACAAACCTGT	19165
rs32685778	snp	A/G	0.426035	0.177515	intron-variant	Psen2	Mm_Celera	1:180231534	TGTATTCAGATCTGC[A/G]AAAAAAAACCCAGCT	19165
rs32685781	snp	A/T	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180232925	GGGATTACCCGGCTC[A/T]GCAGCGGGCTTCCAG	19165
rs32685783	snp	A/G	0.493827	0.0552116	intron-variant	Psen2	GRCm38.p3	1:180233041	TGAACTCACATAACC[A/G]TGCCTCCTGTGAGAC	19165
rs32685945	snp	A/C	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180236630	CACTTAGTTACAACT[A/C]TCTCTTACCTTCTAC	19165
rs32685948	snp	G/T	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180236919	CTGAAGCCCTGGACA[G/T]CCTTCTCAGCTACAC	19165
rs32685951	snp	A/G	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180237067	TGTGTGCACAGGCTG[A/G]CAATCTAAACATGCA	19165
rs32686754	snp	A/G	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180237168	TAGCAGGTAGGATGA[A/G]GGTCACGCTGGTCCA	19165
rs32686757	snp	A/G	0.231111	0.249285	intron-variant	Psen2	Mm_Celera	1:180237300	GACAGGTCCGTCCTC[A/G]GGAGAGCTGTCTTTT	19165
rs32686759	snp	A/T	0.165289	0.235211	intron-variant	Psen2	Mm_Celera	1:180237452	GGTCTCCAGCAGTCT[A/T]CCTGGAGGAAGGGCC	19165
rs32686761	snp	A/G	0.132653	0.220748	intron-variant	Psen2	Mm_Celera	1:180237553	TCCCAACTATGACTT[A/G]CTTGTCTGGGCAATG	19165
rs32686925	snp	A/G	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180233073	TCTATGCCACACACA[A/G]GAGCTACGGGTAAGT	19165
rs32686927	snp	C/T	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180233288	CCTCTGAAGGTGGCA[C/T]GTTCATGCGATGTGG	19165
rs32686929	snp	A/G	0.142012	0.225474	intron-variant	Psen2	Mm_Celera	1:180233490	TATGATAAGACCCTC[A/G]TCTTTGGTTAAGATA	19165
rs32686930	snp	C/T	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180233527	ATAACCTGTCAGATA[C/T]CAAAACCACGGCCCA	19165
rs32686932	snp	A/G	0.132653	0.220748	intron-variant	Psen2	Mm_Celera	1:180233537	AGATATCAAAACCAC[A/G]GCCCACTTCCACGCC	19165
rs32687464	snp	A/C	0.132653	0.220748	intron-variant	Psen2	Mm_Celera	1:180237651	ATGACATGTACTGAC[A/C]ACAGCACGGTCATTC	19165
rs32687467	snp	A/G	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180237688	TGTTCCTAGTTTGTT[A/G]CCATGTTCTCTATAT	19165
rs32687470	snp	C/T	0.231111	0.249285	intron-variant	Psen2	Mm_Celera	1:180237961	ACACAAGGGCCCACG[C/T]TTTGCCCGTGGCAGC	19165
rs32687473	snp	G/T	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180238031	CTTTCATGTTTCAAA[G/T]CCTGCTGCCTAAAAC	19165
rs32688036	snp	C/T	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180238082	CACAGTTAGGTCTAG[C/T]AATACAGGTCTGTTT	19165
rs32688039	snp	A/C	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180238456	GAGGCTCAAGATCCA[A/C]AGGAGAACCCAACTC	19165
rs32688042	snp	C/T	0.231111	0.249285	intron-variant	Psen2	Mm_Celera	1:180238469	CAAAGGAGAACCCAA[C/T]TCACAGGCTTCCCGG	19165
rs32688324	snp	A/G	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180233699	TTTGGGGCACAGCAC[A/G]GCCACGAGATCTGGG	19165
rs32688326	snp	C/T	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180233801	CACCAGGAACCTAAG[C/T]GAACTCTGGGCCACC	19165
rs32688329	snp	A/G	0.231111	0.249285	intron-variant	Psen2	Mm_Celera	1:180233827	CCACCATGCTGCTGG[A/G]CTTGGGTCCCAAGGC	19165
rs32688331	snp	C/T	0.231111	0.249285	intron-variant	Psen2	Mm_Celera	1:180233860	CTTATCCAGTTTGCA[C/T]TGATGGAGCCGAAGC	19165
rs32688333	snp	A/G	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180234144	GTGGTCACTTGGGGT[A/G]TGTGCTTCAAGTATC	19165
rs32688755	snp	C/T	0.32	0.24	intron-variant	Psen2	Mm_Celera	1:180238787	GAGAAAGTTGCCGTG[C/T]GGTAGTAGCTCCAGC	19165
rs32688758	snp	A/G	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Psen2	GRCm38.p3	1:180238906	GTAGAGTACCACGAG[A/G]AAGATGGTCATGACT	19165
rs32688760	snp	A/C	0.391111	0.206368	synonymous-codon, nc-transcript-variant	Psen2	GRCm38.p3	1:180238951	CATGATGAGGGTGTT[A/C]AGCACGGAGTTGAGG	19165
rs32688763	snp	A/G	0.32	0.24	intron-variant	Psen2	GRCm38.p3	1:180239113	CCCTAGAAACCCCAC[A/G]CTGCTCTGTTAGAAC	19165
rs32689166	snp	C/T	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180235032	CCAGGCAGACCACTC[C/T]GGCAGGTACTTGATG	19165
rs32689169	snp	A/G	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180235143	CATGCCCACTGCCCC[A/G]AAGTTCCAGACAGCC	19165
rs32689172	snp	A/G	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180235353	CACACGTCCCAGTCT[A/G]GGTTTAATTCACAAC	19165
rs32689324	snp	C/T	0.197531	0.244432	intron-variant	Psen2	Mm_Celera	1:180253175	TTTTGTTAGAAAGAT[C/T]CATGTGACCTACACA	19165
rs32689327	snp	C/T	0.46875	0.121031	intron-variant	Psen2	Mm_Celera	1:180253361	TTTATTTTTTATTTT[C/T]CTATAGCCAGGATGA	19165
rs32689330	snp	A/G	0.48	0.0979796	intron-variant	Psen2	GRCm38.p3	1:180253434	ACAGCCAGTAGTAGT[A/G]ACATTAAACTCCAGA	19165
rs32689333	snp	C/T	0.46875	0.121031	intron-variant	Psen2	GRCm38.p3	1:180253484	CCAAGCACTGGCATA[C/T]AGGCATTTTGGGTTG	19165
rs32689336	snp	A/G	0.197531	0.244432	intron-variant	Psen2, Gm31728	Mm_Celera	1:180260764	CATCCTTTTCTCCAC[A/G]CCGTTGGATGATTTT	19165
rs32689339	snp	A/G	0.444444	0.157135	intron-variant	Psen2, Gm31728	Mm_Celera	1:180260797	TTCTCTGAGGAGGAC[A/G]TTTGTTTCCTTTTGA	19165
rs32689342	snp	G/T	0.444444	0.157135	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180260957	AAGCTTTCCATATGC[G/T]CTGACCAGCTTTCTG	19165
rs32689355	snp	A/G	0.231111	0.249285	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264842	AAAAGAGGAATCTGG[A/G]AAATGTTATTTCATT	19165
rs32689358	snp	A/G	0.124444	0.216185	upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180265150	TGACCTCATTGTGAT[A/G]GATACAGCTTGAAAT	19165
rs32689361	snp	A/G	0.231111	0.249285	upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180265168	TACAGCTTGAAATGG[A/G]TTCGTCTTACAATTC	19165
rs32689516	snp	C/T	0.32	0.24	intron-variant	Psen2	GRCm38.p3	1:180239190	TGGCTTCTGCCTCTT[C/T]CGGTCAGTGGCTTGC	19165
rs32689519	snp	C/T	0.336735	0.234472	intron-variant	Psen2	GRCm38.p3	1:180239847	CATTGGTCCCATTGC[C/T]CTAGAGAACCCAACA	19165
rs32689521	snp	C/T	0.391111	0.206368	intron-variant	Psen2	Mm_Celera	1:180239962	GAAGTAATTCACAGG[C/T]ACCTTGCTCTTCCCT	19165
rs32689855	snp	A/G	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180235418	TTTCTGGAATGTACC[A/G]GGGAGTGTATCAATA	19165
rs32689857	snp	C/T	0.48	0.0979796	intron-variant	Psen2	GRCm38.p3	1:180235443	TCAATAGCTGGTGGG[C/T]CACATGACTATGTGA	19165
rs32689859	snp	C/T	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180235549	TCAAAAATCAAAGGG[C/T]AAAAGGGCAGATAAG	19165
rs32689862	snp	A/G	0.231111	0.249285	intron-variant	Psen2	Mm_Celera	1:180235658	CCACCTGCTCAGTGC[A/G]TTCTGAGAAGGCTTC	19165
rs32690016	snp	A/G	0.277778	0.248452	intron-variant	Psen2	Mm_Celera	1:180253969	ATAATTAACTGTCTC[A/G]GTGTTCCTTTAGCTC	19165
rs32690019	snp	A/G	0.489796	0.070696	intron-variant	Psen2	Mm_Celera	1:180253998	TCTGTTTGGTGACTT[A/G]ACAGTTGTTGCTGTG	19165
rs32690021	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254573	ACTGTGCAGTGGAGT[C/T]GTGAGCAACCACAGA	19165
rs32690154	snp	A/G	0.408163	0.193609	upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180265172	GCTTGAAATGGATTC[A/G]TCTTACAATTCATTA	19165
rs32690157	snp	C/T	0.124444	0.216185	upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180265205	AAAACAAAGTGCAGT[C/T]CTTGCAGCAAGGTTT	19165
rs32690160	snp	C/G	0.124444	0.216185	upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180265216	CAGTTCTTGCAGCAA[C/G]GTTTGAAAGAAAGCA	19165
rs32690163	snp	A/T	0.231111	0.249285	upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180265238	AAGAAAGCAAAGCAG[A/T]TAGCAACCGGGAAGA	19165
rs32690224	snp	A/G	0.493827	0.0552116	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180261009	GGAGGATTAACTTCA[A/G]AGGAGGACAGTGTCT	19165
rs32690226	snp	C/T	0.345679	0.230967	intron-variant	Psen2, Gm31728	Mm_Celera	1:180261077	TTGTCCTTGAGCCTA[C/T]ATTGACACAGAGCCA	19165
rs32690228	snp	A/G	0.197531	0.244432	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180261111	CATGTGACAGAAGAA[A/G]CCTGTTCCACTCATG	19165
rs32690230	snp	A/C	0.197531	0.244432	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180261184	TGTCTCCATCAAGGT[A/C]TTCAGTGACTGGACT	19165
rs32690434	snp	A/C/T	0.459184	0.136902	intron-variant	Psen2	GRCm38.p3	1:180240559	CATGGAAATGGAGAC[A/C/T]GGTCAGAGATGAGTC	19165
rs32690437	snp	C/T	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180240736	CCCAACTCACAGCTG[C/T]CCGTTCTTCTCAGTG	19165
rs32690442	snp	A/T	0.5	0	intron-variant	Psen2	GRCm38.p3	1:180251951	AGTGTTCTCAGGCAT[A/T]TGGATGGCGTATATC	19165
rs32690715	snp	C/T	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180235786	GGACAGCATACAGAG[C/T]CTACTCCTAGGCCAA	19165
rs32690718	snp	A/G	0.124444	0.216185	intron-variant	Psen2	Mm_Celera	1:180235827	CCAGAGCCCGGCAGC[A/G]GACTCTGAGGACCCT	19165
rs32690896	snp	C/T	0.132653	0.220748	upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180265439	ACTTAAGGTGTTATC[C/T]ACGTGATATAGAAGA	19165
rs32691106	snp	A/G	0.244898	0.249948	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254713	GAAATATTCATTTCC[A/G]CATACGAATGGATGT	19165
rs32691112	snp	C/T	0.197531	0.244432	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254890	CATTCTTCACTCTAT[C/T]CCTGCCCACCTGATT	19165
rs32691245	snp	A/G	0.277778	0.248452	intron-variant	Psen2	Mm_Celera	1:180252233	AATCCTTAATAAAGT[A/G]TCTCACACTCTCCAG	19165
rs32691247	snp	C/G	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180252643	GAGTGCCAACAGCCT[C/G]ATGCCTCCAATGACC	19165
rs32691250	snp	G/T	0.46875	0.121031	intron-variant	Psen2	GRCm38.p3	1:180252807	CATGAGGAAGTTTCT[G/T]TCTGAGGTGTAACAG	19165
rs32691253	snp	A/G	0.277778	0.248452	intron-variant	Psen2	Mm_Celera	1:180252888	GCAACCTGTTCTCTG[A/G]ATCACGGGAGAGGCC	19165
rs32691414	snp	A/G	0.244898	0.249948	intron-variant	Psen2, Gm31728	Mm_Celera	1:180261610	TGTGGTCCTGAGCCC[A/G]TGAGCCTCTTTGTCC	19165
rs32691417	snp	C/T	0.46875	0.121031	intron-variant	Psen2, Gm31728	Mm_Celera	1:180261663	GCCAGCGTTCACCAG[C/T]CTGGAAGCCCTCTGG	19165
rs32691419	snp	A/T	0.32	0.24	intron-variant	Psen2, Gm31728	Mm_Celera	1:180261665	CAGCGTTCACCAGCC[A/T]GGAAGCCCTCTGGAT	19165
rs32691421	snp	C/T	0.375	0.216506	intron-variant	Psen2, Gm31728	Mm_Celera	1:180261696	TGTGCAGTTTGTGGG[C/T]TTTTGCTTTCTCCCA	19165
rs32692006	snp	A/G	0.493827	0.0552116	intron-variant	Psen2	Mm_Celera	1:180252894	TGTTCTCTGAATCAC[A/G]GGAGAGGCCACAGAC	19165
rs32692009	snp	C/T	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180252956	TGAGGATTGACCTGG[C/T]GTTTTCTGTCTCCAG	19165
rs32692012	snp	A/G	0.444444	0.157135	intron-variant	Psen2	GRCm38.p3	1:180253060	CAGCGGCCATAGCCC[A/G]ACAGGTGAGCTGACA	19165
rs32692045	snp	A/G	0.375	0.216506	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254944	GGAATGAACCCAGAC[A/G]GTCACCTCTAGGCTA	19165
rs32692050	snp	C/T	0.46875	0.121031	intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255687	GGATTTACAAAACAC[C/T]GAACACAGCTGGTAA	19165
rs32692052	snp	C/T	0.244898	0.249948	intron-variant, upstream-variant-2KB	Psen2, Gm31728	GRCm38.p3	1:180256048	AGAGGCCGAGATCGC[C/T]GCAGGGGCCGCAGCT	19165
rs32692314	snp	C/T	0.493827	0.0552116	intron-variant	Psen2, Gm31728	Mm_Celera	1:180261825	CGTAGACCTCATTGA[C/T]TAACCCCATCTCCAG	19165
rs32692315	snp	A/G	0.375	0.216506	intron-variant	Psen2, Gm31728	Mm_Celera	1:180261854	AGCTCCTAGATGGAC[A/G]GTGCTCAAAGCCCCA	19165
rs32692318	snp	A/G	0.197531	0.244432	intron-variant	Psen2, Gm31728	Mm_Celera	1:180262093	GCTGGTGTGGAGAAT[A/G]TAGATAATAGAGCTG	19165
rs32692321	snp	A/G	0.444444	0.157135	intron-variant	Psen2, Gm31728	Mm_Celera	1:180262305	CACTTATCTTTGGGC[A/G]CAAATCCATAGGCCC	19165
rs32693374	snp	A/G	0.244898	0.249948	upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180256417	TGCACTTGCGCCTTC[A/G]TCGTCGGTTTACAGG	19165
rs32693375	snp	A/G	0.345679	0.230967	upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180256442	TACAGGAAAACACTG[A/G]GTGCAGAAGGTGCAG	19165
rs32693378	snp	C/T	0.493827	0.0552116	upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180256497	GACCGCAGCATCATA[C/T]TGACATTGAAATCTG	19165
rs32693380	snp	G/T	0.493827	0.0552116	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256660	AGTAAGCTAACATCG[G/T]GAGCCTTCTCCTGAT	19165
rs32693382	snp	C/T	0.489796	0.070696	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256828	GGAGTGAGTTGAAAT[C/T]GTCAACAATTTGCCA	19165
rs32693396	snp	C/T	0.391111	0.206368	intron-variant	Psen2, Gm31728	Mm_Celera	1:180262799	GTAGCTGGAGGCTGC[C/T]AGAGTGTCTGGACAA	19165
rs32693398	snp	C/T	0.391111	0.206368	intron-variant	Psen2, Gm31728	Mm_Celera	1:180262878	CCTCAGATAGGCACA[C/T]AATTCTCTCTCAGAT	19165
rs32693400	snp	C/T	0.336735	0.234472	intron-variant	Psen2, Gm31728	Mm_Celera	1:180262903	TCAGATCCATGGCTG[C/T]TCCAACATGCATCAC	19165
rs32693403	snp	C/T	0.231111	0.249285	intron-variant	Psen2, Gm31728	Mm_Celera	1:180263082	AAGTTAAGAAGTATA[C/T]CAGTCCTCTTAGGAT	19165
rs32694058	snp	C/T	0.32	0.24	intron-variant	Psen2, Gm31728	Mm_Celera	1:180259912	GCTTATCTTTCCTTG[C/T]TAGGGTATGAGGGCT	19165
rs32694376	snp	C/T	0.231111	0.249285	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264033	AGAATATAAAGTACC[C/T]AAGAAAAAAATCATT	19165
rs32694378	snp	C/T	0.48	0.0979796	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264149	AAAGCTTTTCCATAC[C/T]TGTTTGATATTTTGA	19165
rs32694381	snp	A/C	0.132653	0.220748	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264315	GTACAACATGTCCCT[A/C]CAAGTAATAGAACCT	19165
rs32694383	snp	A/T	0.231111	0.249285	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264367	CTCCTGGTCATTGGC[A/T]GGATACTCCCTGACC	19165
rs32694444	snp	C/T	0.197531	0.244432	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256905	GAAATTCGTATAACA[C/T]AAAATTGTCATTGTA	19165
rs32694447	snp	A/G	0.396694	0.202437	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257305	ACTTCAATGTGTGCC[A/G]ATCTGGCTTGTGTGA	19165
rs32694450	snp	A/G	0.244898	0.249948	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257511	CATAGACGCATGAAC[A/G]GAGGTCCGAAATCTC	19165
rs32694452	snp	G/T	0.408163	0.193609	upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180257678	CTGAACAGACAGTAA[G/T]TGTTTCCTTCCTCTG	19165
rs32695195	snp	A/G	0.489796	0.070696	intron-variant, nc-transcript-variant	Psen2, Gm31728	GRCm38.p3	1:180258371	AGTTCCCAAAGACTG[A/G]GCAGTTATCTGCTAC	19165
rs32695203	snp	A/G	0.197531	0.244432	intron-variant	Psen2, Gm31728	Mm_Celera	1:180260335	AGGCTTTCAAGTCTA[A/G]GCAGCTACTGGCTTC	19165
rs32695256	snp	C/T	0.124444	0.216185	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264415	AGAGATGCAAAAACA[C/T]GAATGTATTTCAAAA	19165
rs32695258	snp	A/T	0.124444	0.216185	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264514	ATGTATGTGCCTTGT[A/T]CATGCCTCAGCGCCA	19165
rs32695260	snp	A/G/T	0.124444	0.216185	upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180264518	ATGTGCCTTGTACAT[A/G/T]CCTCAGCGCCAATAA	19165
rs32695261	snp	A/G	0.124444	0.216185	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264596	ATGATCTATGTGAAC[A/G]ACATTACCATAGCGA	19165
rs32695263	snp	C/T	0.231111	0.249285	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264724	CAAATATGTGTTATC[C/T]TAAGCAAATATGTGT	19165
rs32696246	snp	C/T	0.244898	0.249948	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264754	TTATCTTAAACTTGA[C/T]CAATGAAAATTAGAA	19165
rs32696386	snp	C/G	0.244898	0.249948	intron-variant	Psen2, Gm31728	Mm_Celera	1:180260636	TTTAGAGAAATTTGT[C/G]TAATATATAGATTAG	19165
rs32696389	snp	A/G	0.197531	0.244432	intron-variant	Psen2, Gm31728	Mm_Celera	1:180260670	TTTGCCAGTAAGTCT[A/G]GGCATTGGCAGCCAT	19165
rs32717699	snp	C/T	0.375	0.216506	intron-variant	Psen2	GRCm38.p3	1:180232505	CTCCCTTTCCTCACC[C/T]GCTGGCCTCCAGATT	19165
rs32739789	snp	G/T	0.375	0.216506	intron-variant	Psen2, Gm31728	GRCm38.p3	1:180260128	AAGGCAAAGAGAGGG[G/T]CAAGCTCATCCACAG	19165
rs33901069	snp	C/G	0.124444	0.216185	upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264168	TTGATATTTTGAACA[C/G]CCTCCTCAAATCCTT	19165
rs45758727	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247455	GAGATCAGGGGACCT[A/G]CTAGGGTAGGCCATC	19165
rs45791757	snp	A/G			synonymous-codon, nc-transcript-variant	Psen2	GRCm38.p3	1:180238957	GAGGGTGTTAAGCAC[A/G]GAGTTGAGGAGCCGC	19165
rs45992368	snp	G/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256994	ATACTCAATTCTGGT[G/T]TATGCATGGCTGAGT	19165
rs46056469	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257354	CTTAAAAAATAAAAG[A/G]CAGTTGTATAATTGA	19165
rs46100144	snp	G/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	GRCm38.p3	1:180258021	TATAACAATAGAAAT[G/T]TGTTTTTCCGCTGTT	19165
rs46135292	snp	A/C/T			intron-variant, upstream-variant-2KB	Psen2	GRCm38.p3	1:180247864	ACCCGAGATCTCTTC[A/C/T]GTATCTCTTCTGGCA	19165
rs46223555	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180265368	CTTTAGTTGGCACCA[A/G]AAATAAAGGTCTGGG	19165
rs46241274	snp	A/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180257889	CACCACACTTGAAAA[A/T]GCCCAATTGTGCTGT	19165
rs46394564	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180241324	GAGCATCAAAACACG[G/T]GGCTGCCTCAGTACC	19165
rs46485321	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247856	CCCACTAGACCCGAG[A/G]TCTCTTCCGTATCTC	19165
rs46509088	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180252140	GACCAGGCTGGCCTC[A/G]AACTCAGAAATCCAT	19165
rs46617785	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180251522	GGACAGGAGGGGACA[G/T]CGAGAGGGGATTAAC	19165
rs46669465	snp	C/G/T			intron-variant	Psen2	GRCm38.p3	1:180250927	GTTCTCCTGGCTTTT[C/G/T]GGAGATCTCATGCAG	19165
rs46734385	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180229046	AAGAAAGAAAAAAAA[A/G]AAAAAAAAAGAAAAA	19165
rs46853466	snp	A/G			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180256088	GACCCTGATGCCCCG[A/G]GAGGGCAACGGAAGC	19165
rs46928203	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180250989	TCACATGGCTTATGG[C/T]CTGCATTAAACACCA	19165
rs46930996	snp	A/G			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258646	AAGAATGCTATATGG[A/G]TCTCATAATGTTGCC	19165
rs47026146	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180251392	GGACAGCTTCTAGCC[A/G]TGCAAGGTGGCAGGA	19165
rs47133965	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180251045	TGGGTTGGAGCAATT[C/T]TTCTCATTTCATGAA	19165
rs47186007	snp	G/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247260	CCACAGGCACAAGAG[G/T]GAGGTGGAGAGGACC	19165
rs47243857	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180241138	GGAGGGTCAGAGCTA[G/T]CCTGCATAGCCACAG	19165
rs47274088	snp	A/G			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258631	TTTTATTTTTCTTTT[A/G]AGAATGCTATATGGG	19165
rs47616169	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180250978	ACCCTAGACCCTCAC[A/G]TGGCTTATGGTCTGC	19165
rs47711941	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180251001	TGGTCTGCATTAAAC[A/T]CCATTAACTCTGTCT	19165
rs47719361	snp	C/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256320	CGGTTCGCCAGCGCC[C/T]CAGACACGCCCCCGG	19165
rs47726156	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247787	GGGGTCTGCAAGACT[A/G]TAAGGTCCCCTTCCT	19165
rs47753706	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180241086	TCTGATTTAAGTCTC[G/T]GGATATATAAAAAAC	19165
rs47767796	snp	A/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180256764	CGAGATCTAGGAATC[A/T]GCCTCGGGGTGAGGG	19165
rs47870145	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180241113	AAACTTAGAAGACGG[C/T]GGTGGTGGAGGAGGG	19165
rs47934392	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256776	ATCAGCCTCGGGGTG[A/G]GGGCAGGGAGGGGTT	19165
rs48027583	snp	C/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257162	AGGCAGAGACAGGCA[C/G]ATCTCTGAGTTCAAG	19165
rs48128564	snp	C/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258157	CTACGTGGCAGACAG[C/T]GCAGAATCAGTAGAC	19165
rs48145001	snp	C/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257526	GGAGGTCCGAAATCT[C/T]CCTCTTCTGCTTGTC	19165
rs48346189	snp	C/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180257657	GGGCAGGGGGCAGCG[C/T]GGATCCTGAACAGAC	19165
rs48412341	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180250980	CCTAGACCCTCACAT[A/G]GCTTATGGTCTGCAT	19165
rs48424550	snp	A/G			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180235919	CACTCACCCGAGGTA[A/G]ATGTAGGTGAACAAG	19165
rs48447626	snp	A/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263713	GGAAGTCTTTTTTTT[A/T]AAAATTGATTTCACT	19165
rs48569391	snp	A/G			synonymous-codon, nc-transcript-variant	Psen2	GRCm38.p3	1:180240940	TTCTTCGCTCTCCTG[A/G]GTCCTCTGTGGGAAA	19165
rs48661467	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180239030	CTGAAGAGGTCACCA[A/G]AAGAGACTTGGTATC	19165
rs48739697	snp	A/C			upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180257735	GGGTTTCATTTTGTT[A/C]TGTTTGACATTGAAA	19165
rs48804821	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247853	ACACCCACTAGACCC[A/G]AGATCTCTTCCGTAT	19165
rs48899525	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247328	ACAGGGCATGGGCCA[A/G]AAAGGTATATGAGCT	19165
rs49050241	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180251075	AGTCGCCTGGGAGAC[A/G]GTTAGGAGGAAGAGA	19165
rs49115767	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180252742	GGGGAGAGGGTGTCT[C/T]TTAAAGACATGTTTT	19165
rs49223379	snp	C/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180257946	CTTACAACTAACACA[C/G]ACAGGCCACTGTCTC	19165
rs49224018	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180252203	ACGTGCGCCACCACC[A/G]CCCAGCCAGCTCAAA	19165
rs49311405	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180252155	GAACTCAGAAATCCA[C/T]CTGCCTCTGCCTCCT	19165
rs49397948	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180241080	GCGAGCTCTGATTTA[A/G]GTCTCGGGATATATA	19165
rs49433470	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180242207	TAGCCCACTGCACAT[G/T]GTGACTGTGTAGCCC	19165
rs49567968	snp	A/C			intron-variant	Psen2	GRCm38.p3	1:180252781	GTATGTATTACTTTT[A/C]TTTTTAAAAGCATGA	19165
rs49584750	snp	A/G			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180235934	GATGTAGGTGAACAA[A/G]AAGAGGAGCATCAGG	19165
rs49623699	snp	C/G			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180256086	CAGACCCTGATGCCC[C/G]GGGAGGGCAACGGAA	19165
rs49668484	snp	G/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258176	GAATCAGTAGACCTA[G/T]GTCTGAAATCTCCCT	19165
rs49677445	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180252384	GACGAGTGGAAAAGT[G/T]TTTCGATAGGGGGTT	19165
rs49912783	snp	C/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257537	ATCTCCCTCTTCTGC[C/T]TGTCTGTTGCAGTTC	19165
rs49925017	snp	A/G/T			intron-variant	Psen2	GRCm38.p3	1:180243555	TAGCCCACTGCACAC[A/G/T]GTGACTGTGTAGCCC	19165
rs50109092	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180250938	TTTTGGGAGATCTCA[G/T]GCAGAGCTGGAGTTA	19165
rs50113084	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180241323	GGAGCATCAAAACAC[A/G]GGGCTGCCTCAGTAC	19165
rs50169779	snp	A/C			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255954	CAGAGCTGCACCCTA[A/C]GCTCCTTCCAAGCCC	19165
rs50273261	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180252036	CCAGCTCAAAATCCT[C/T]TTTTTGTTTTGTTTT	19165
rs50314381	snp	C/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257088	ACACATTAGACCTTG[C/T]CTTTAAAAGAAAAAA	19165
rs50380892	snp	C/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180257876	ACCTGGGCATGCTCA[C/G]CACACTTGAAAAAGC	19165
rs50588798	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180252271	GGCTCTCTGAGCCCC[A/T]CTCAGTCCTGCCAGT	19165
rs50590644	snp	C/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180257933	CTATTGAACAGGACT[C/T]ACAACTAACACAGAC	19165
rs50729576	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257380	ATTGAAAGGTTTCCT[A/G]TCCCTCTCCCTGACC	19165
rs50732137	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180241144	TCAGAGCTAGCCTGC[A/G]TAGCCACAGAAGGGC	19165
rs50757068	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180252515	AATTTACATTATTTT[A/G]AAACAGGGTAGTTTA	19165
rs50830341	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180243511	ACGGTACACTGTGAT[G/T]GTGTAGCCTACTGCA	19165
rs51049326	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180257589	TTTCCTCATCTGTGA[A/G]AGGATAGTGTGAGGG	19165
rs51209862	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180249759	TGAGATAAGGTCTCA[C/T]TAAGTAGCCCTGATT	19165
rs51338022	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180250959	GCTGGAGTTAGAAAG[C/T]CAGACCCTAGACCCT	19165
rs51488728	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	GRCm38.p3	1:180258098	CTGGAGAGGACTTGC[A/G]TCCTAGTTTATAGGT	19165
rs51522532	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180243486	CCACCACACTGTGAC[G/T]GGGTAGCCCACGGTA	19165
rs51775093	snp	C/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	GRCm38.p3	1:180257562	CAGTTCCTTACCCTT[C/G]CTGGGCCTCGGTTTC	19165
rs51835056	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180256519	TGAAATCTGAAGTTG[A/G]CTAGTGCCTTTTCTT	19165
rs51907823	snp	A/G			intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258310	AACTTTGAAGGGACA[A/G]AAAAGCATTAAGACT	19165
rs51931702	snp	A/G			utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	Psen2, Gm31728	GRCm38.p3	1:180256240	GCTCCGCCGCGGCGC[A/G]GGGTAGAGTTTACGC	19165
rs51978750	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180239782	CTGTTGGACTAGCTA[A/G]TCTTTGTTGTATAAG	19165
rs52030979	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180253007	ACCATCCCTAAACCC[A/G]GGGAGGAAAGACTGC	19165
rs52051123	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180240220	AGCTCACAGTTCTCT[A/G]AATTATATTTATTAA	19165
rs52081989	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180242237	CACCATACACTGTGA[C/T]TGCGTAGCCCACTGC	19165
rs52094461	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180244706	TAGCCCACTGCACAC[G/T]GTGACTGTGTAGCCC	19165
rs52095609	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180241857	TAGCCCACTGCACAC[G/T]GTGACTGTGTAGCCC	19165
rs52127914	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180241875	GACTGTGTAGCCCAC[C/T]GCACACAGTGACTGT	19165
rs52148322	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180241856	GTAGCCCACTGCACA[C/T]TGTGACTGTGTAGCC	19165
rs52175676	snp	A/T			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258511	GGTGGCAGTTATTTT[A/T]AAAATTAGGTATTTT	19165
rs52193223	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180241850	GACTGTGTAGCCCAC[C/T]GCACACTGTGACTGT	19165
rs52198403	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180242181	GTAGCCCACTGCACA[C/T]GGTGACTGTGTAGCC	19165
rs52205986	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180242387	CACTGCACACTGTGA[C/T]TGTGTAGCCCACTGC	19165
rs52211718	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244461	CACTGCACACTGTGA[C/T]TGTGTAGCCCACTGC	19165
rs52224097	snp	A/T			intron-variant	Psen2	GRCm38.p3	1:180244310	CCACTGCACACTGTG[A/T]CTGTGTAGCCCACTG	19165
rs52225351	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244686	CACTGTACACTGTGA[C/T]TGTGTAGCCCACTGC	19165
rs52228338	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180242226	ACTGTGTAGCCCACC[A/G]TACACTGTGATTGCG	19165
rs52236086	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244311	CACTGCACACTGTGA[C/T]TGTGTAGCCCACTGC	19165
rs52239321	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180244332	AGCCCACTGCACACT[A/G]TGACTGTGTAGCCCA	19165
rs52296505	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180242182	TAGCCCACTGCACAT[G/T]GTGACTGTGTAGCCC	19165
rs52308873	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180242240	CATACACTGTGATTG[C/T]GTAGCCCACTGCACA	19165
rs52345666	snp	A/C			intron-variant	Psen2	GRCm38.p3	1:180244398	TGACTGTGTAGCCCA[A/C]CACATACTGTGATTG	19165
rs52347673	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180251191	CTCACTGTATATAGC[C/T]CTGGCTGTCCTGGAA	19165
rs52390347	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180242225	GACTGTGTAGCCCAC[C/T]ATACACTGTGATTGC	19165
rs52399940	snp	A/G/T			intron-variant	Psen2	GRCm38.p3	1:180241882	TAGCCCACTGCACAC[A/G/T]GTGACTGTGTAGCCC	19165
rs52419197	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180241877	CTGTGTAGCCCACCG[C/T]ACACTGTGACTGTGT	19165
rs52459863	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180242131	GTAGCCCACTGCACA[C/T]TGTGACTGTGTAGCC	19165
rs52476659	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180241852	CTGTGTAGCCCACTG[C/T]ACACTGTGATTGTGT	19165
rs52529735	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180249461	TTTTCTGCATTTCTC[C/T]ATTTTATCTATTTTC	19165
rs52544723	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243445	ACTGTGATTGTGTAG[C/T]CCACTGCACACTATG	19165
rs52556744	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180242137	CACTGCACACTGTGA[C/T]TGTGTAGCCCACTGC	19165
rs52563269	snp	A/T			intron-variant	Psen2	GRCm38.p3	1:180244460	CCACTGCACACTGTG[A/T]CTGTGTAGCCCACTG	19165
rs52664983	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180241932	TAGCCCACTGCACAC[G/T]GTGACTGTGTAGCCC	19165
rs107599430	snp	C/G/T			intron-variant	Psen2	GRCm38.p3	1:180253205	ACACACACACACACA[C/G/T]ACACACACAGACACA	19165
rs107618984	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180253341	TCTCTCAGTTTTTTT[A/T]TTTTTTTATTTTTTA	19165
rs107664086	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180247955	CCATGCCTGAGGCCT[C/T]GGGTTTCATCCACGG	19165
rs107699460	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180244375	TTTGTGTAGTCCACT[G/T]CACACTATGACTGTG	19165
rs107701631	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180248215	TGTTCCGGTTGTTCC[C/T]ACACACACACACACA	19165
rs107724307	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180247953	TGCCATGCCTGAGGC[C/T]TTGGGTTTCATCCAC	19165
rs107740772	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180248444	AGCCTAATGTCTGGG[C/T]GACGCATTTTGAGAT	19165
rs107855748	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180241908	AGCCCACTGCACACT[A/G]TGACTGTGTAGCCCA	19165
rs107897834	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180253201	ACACACACACACACA[C/G]ACAGACACACACAGA	19165
rs107912517	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244336	CACTGCACACTGTGA[C/T]TGTGTAGCCCACTGC	19165
rs107980797	snp	A/C			intron-variant	Psen2	GRCm38.p3	1:180239609	GCTGCCACTGCCCCA[A/C]CCTTCACTAACAGCA	19165
rs108104377	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260442	ACATGCATATATTCA[C/T]ATATACCATCTATCT	19165
rs108122799	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244286	CACTGCACACTGTGA[C/T]TGTGTAGCCCACTGC	19165
rs108192044	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180248459	CGACGCATTTTGAGA[C/T]GGTGCCCTACGTTCA	19165
rs108221482	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180244369	ACTGTGTTTGTGTAG[C/T]CCACTTCACACTATG	19165
rs108229350	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180235762	AAAAAAAAAAAAAAA[A/C]CAACCCTGGGACAGC	19165
rs108298903	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180248270	CACACACACAGAGTC[C/T]GGACTGTGCCACCCA	19165
rs108411666	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180247999	TTATCCTTAAGCCTG[C/G]GTATTCTGTTGCTGG	19165
rs108437979	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247919	ATCTAGATCAGGGAT[A/G]TGCCTCGGTGGCAGA	19165
rs108461264	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180248412	CATTGAAAACGTGGA[C/T]CTGTAAGCTCCACTC	19165
rs108466411	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180235763	AAAAAAAAAAAAAAC[A/C]AACCCTGGGACAGCA	19165
rs108506532	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247942	GTGGCAGAGCCTGCC[A/G]TGCCTGAGGCCTTGG	19165
rs108584382	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180239594	TCCACCACCACCACC[A/G]CTGCCACTGCCCCAC	19165
rs108748500	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180248179	ACAGTCAGGGAGCAG[A/G]GACCGAGGAATGGAT	19165
rs108800900	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180248214	CTGTTCCGGTTGTTC[A/C]TACACACACACACAC	19165
rs108850072	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180248119	GTACAGGCACATCAC[A/G]GTGGGAGGAGCTTGA	19165
rs108885398	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180247982	ACGGCCCCACATCAA[A/G]GTTATCCTTAAGCCT	19165
rs211746071	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180234616	ACACTCATGTTTTGA[A/G]TGCTTAATCTCTAGC	19165
rs211746446	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246456	CTAAGATCCTAGCCA[A/G]GCTAGGCCAGGCTAG	19165
rs211804763	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180235519	AGTGTTTCTCTTTCA[A/G]CCTTCCGGCTGATGT	19165
rs211862168	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180227859	GCCCCTCAAGATGCA[C/T]GGGGCAGGGCTCCCC	19165
rs211984829	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260059	TGTGTGGGGAAGAAC[C/T]GCCCTGATTGAGGAC	19165
rs212047794	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180228683	TGGCATAAGATACAT[A/G]TGGTGAGTGAGATCC	19165
rs212099397	in-del	-/GC			intron-variant	Psen2	Mm_Celera	1:180236992	AAGTGTCTGGAAGAG[-/GC]GAGAGTCCTAAGGGT	19165
rs212372388	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180253079	GGTGAGCTGACAGTG[A/T]CAGAAACCTTTGCTG	19165
rs212500388	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180245457	TCACTCCAGCTCCAG[C/G]GGAGAGGACATTCCC	19165
rs212637608	in-del	-/CTC			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261987	AGGCAAATGGCCCTT[-/CTC]CTCTCCTAAGTCACT	19165
rs212842529	snp	A/C/G			intron-variant	Psen2	GRCm38.p3	1:180250700	GGCCAACAGAACAAT[A/C/G]CCCTTATCTTTCAAA	19165
rs212855523	snp	A/G/T			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180262369	CACCCCTCCCCCACC[A/G/T]CTGCCCATATCCTGC	19165
rs212903483	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180239373	AAGTCAGATTGTCCA[A/T]GTGAGTGTATCTGGA	19165
rs213026197	snp	C/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247775	TCTTGCCAAGCAGGG[C/G]TCTGCAAGACTATAA	19165
rs213088912	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180248195	GACCGAGGAATGGAT[A/G]TAGCTGTTCCGGTTG	19165
rs213172290	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180229735	TGTCAGAGTCTGGCC[A/G]TCAGGCAGTGCCACT	19165
rs213173827	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264214	GACTTCTCCCCTCTC[A/G]TCACCTCCCCTCTCC	19165
rs213193429	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180249945	CCTGCTTGGCCTGGG[A/G]AAACAAACGAGAATA	19165
rs213217418	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180238282	CCTGATCATGACAGG[A/C]GCATGCCCCGCTTCC	19165
rs213308769	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259242	TAATTTCTATATTCC[A/G]TCTTGGCTGCTCTTG	19165
rs213531103	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180233362	CACGGGACTGTCCAC[A/T]CCCCTCTAGTATCCC	19165
rs213584464	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243726	CTGTGTAGCCCACTG[C/T]ACACTGTGACTGTGT	19165
rs213644721	snp	A/G			downstream-variant-500B	Psen2	Mm_Celera	1:180226625	TGCCTGCCTTTCATC[A/G]CAGGCAGGAACCGGA	19165
rs213723953	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180231506	ACTTTTAAATGCAGT[A/G]CCTGCATCCCTGTGT	19165
rs213728105	in-del	-/TCTCT			intron-variant	Psen2	Mm_Celera	1:180248907	ACTGAAGTTTCTGAC[-/TCTCT]TCTCTGGTACAGGAA	19165
rs213784337	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180231999	CCTGTTTCCAGTTCC[C/T]TGCTGAGATTTCCAC	19165
rs213791374	in-del	-/GAG			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246141	AATGGCACATCGACA[-/GAG]GATGAAGGAACTTGT	19165
rs213902691	snp	A/G			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180240751	CCCGTTCTTCTCAGT[A/G]TAGAAACGCACAGAC	19165
rs213982626	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259794	TGAAACTAAGTCAGG[A/G]GGGCTCCAGAGAAGG	19165
rs214084194	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180236597	CAAGGGTGGGCAGAG[C/T]CATGCCTTGACCAGG	19165
rs214086251	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180227965	CTAGGGACAGTGGGC[A/G]AATAGATGGTGGGAG	19165
rs214143915	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180228827	AGTGCCCACACCCAC[C/T]ACACAGCCCACTCAC	19165
rs214161125	in-del	-/ACAC			intron-variant	Psen2	Mm_Celera	1:180253185	AGATCCATGTGACCT[-/ACAC]ACACACACACACACA	19165
rs214205034	snp	A/G			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180229474	TTCTCCAAAACTGTC[A/G]TAGGAGTCTTCTTCT	19165
rs214229155	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261633	CTTTGTCCCTGCACC[A/G]TGCTCCTGACACAAG	19165
rs214422262	snp	C/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180256401	GTGCCAGGTTCCCCT[C/G]TGCACTTGCGCCTTC	19165
rs214429916	snp	A/C			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180263867	GCTGCGATTTTGGGG[A/C]TGAGAATTGAACCCA	19165
rs214489444	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262964	AACTCACCGGGAGGA[C/T]GTAGCTGTACTATTT	19165
rs214554878	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262453	TCACTCTCTTTTCCC[A/G]TTTTTCCAAAGCAGA	19165
rs214587967	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180230445	GGTTGAACCCCTCCA[-/C]CCCTTCCTTTAGAGC	19165
rs214631096	in-del	-/TGCGACTGTGGCCATGGAAGCTTTCCATATGCGC			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260924	ACAGACACTGGCTTA[lengthTooLong]TGCGACTGTGGCCAT	19165
rs214730074	in-del	-/TCCCG			intron-variant	Psen2	Mm_Celera	1:180232055	TAATATCGCCCCCCC[-/TCCCG]CCACATACCCACACC	19165
rs214948726	snp	C/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180257956	ACACAGACAGGCCAC[C/T]GTCTCAGTCCATTCA	19165
rs215084350	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180254057	ATAGTGTTTCACTAC[A/G]TAGCTCAATTGGCCT	19165
rs215127247	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180251343	ACAGCAGCCAGTGGC[C/T]GCATAGACTAGTGTG	19165
rs215157695	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246565	GAGTGTCTGTGGGTT[A/G]AAAATGGGATACCAT	19165
rs215361476	in-del	-/ACAC			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180259100	GTTCCCGAATGAAAG[-/ACAC]ACACACACACACACA	19165
rs215384835	in-del	-/ACACACACAC			intron-variant	Psen2	Mm_Celera	1:180253293	CACACAGACACACAG[-/ACACACACAC]ACACACACACAGTGT	19165
rs215446475	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180230538	AACTTAAAATGCTGC[C/T]TTTGGTTACAGTTAC	19165
rs215503619	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180231302	GAGCTGGCTCGGTGG[C/T]TGAGAGCACTTGCTG	19165
rs215591356	snp	A/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260505	TAAACATACATATAG[A/T]ATGTATACATATATA	19165
rs215631987	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180253023	GGGAGGAAAGACTGC[A/T]TGTGGACTGAGCACC	19165
rs215689630	snp	C/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247510	CCAAGGGGAAGGGAG[C/T]GTAATTCAGCCTAGG	19165
rs215743653	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180240438	CAGTACCAGAGCTGG[C/T]CTCTGGTAAGATCCC	19165
rs215844321	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180227736	CACAAGCCCTGCAGG[A/G]AGGACATCAAGGTGA	19165
rs215901194	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180237811	AGATGTAACTGGTGA[G/T]GTCAGCTTCAGGAAC	19165
rs215923000	in-del	-/ATT			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246995	TGTGATCTTCAAGTG[-/ATT]AGACAGGGTCCCTTC	19165
rs216027811	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180232048	CCAGGCTTAATATCG[-/C]CCCCCCCCCACATAC	19165
rs216056027	snp	C/T			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180238996	CGAGGGCGTGTCCTC[C/T]GTGAAGGGCGTGTAG	19165
rs216113022	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180239921	CTTCTCCCCCAACTG[C/T]AGCTGCAGGTACCGT	19165
rs216178110	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180232096	CCCTGGCTCACCAGC[C/T]TGGCCCCTTCTCTGC	19165
rs216345576	in-del	-/TTTTTTTT			intron-variant	Psen2	Mm_Celera	1:180253334	TCTCTCCTCTCTCAG[-/TTTTTTTT]TTTTTTTATTTTTTA	19165
rs216350742	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180249155	GTTCAGAAACCAAAC[C/T]AAACCAAAACACAAT	19165
rs216377168	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180245227	CCACAAGGTTCCATT[C/T]CTTAAAGGTTCTAAG	19165
rs216433605	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180238342	ACATTTTACTAGCAC[A/G]GACAAGGGTCAGAAC	19165
rs216454536	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180234279	GGATGGTTTGTATAT[A/G]CTCGGCCCAGGGAGT	19165
rs216616343	in-del	-/TATCTATA			intron-variant	Psen2	GRCm38.p3	1:180244971	ATCTATCTATCTATC[-/TATCTATA]TATCTATCTATCTAT	19165
rs216688464	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180249228	CATCTGACGAGGACT[A/C]TTACAGGAGCACCGA	19165
rs216777569	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180232618	TTTGCAAAACTTGGC[C/T]GTGAAGTCCTTGACC	19165
rs216787719	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180241417	ATAAGAAAAGAATGA[C/G]CTTGAACTGTGAACC	19165
rs216795891	in-del	-/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259333	TCTTCTTCCTGCATG[-/T]TTTTACCCTTCAGGG	19165
rs216796414	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180240673	TGAGGGAGCCTTTGA[-/C]CCCCCCTCAAAACAA	19165
rs216820565	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180254149	TATGCACTGGAATTA[C/T]AGACATGAGCTATCA	19165
rs216874871	snp	A/G			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255087	AGCAACTTATACAGA[A/G]CCTTTAATTACTGCC	19165
rs216933996	snp	C/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247616	TCCACTGCCCTCATA[C/T]TTGGCATTCTGGAAG	19165
rs217004544	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180235431	CCAGGGAGTGTATCA[A/G]TAGCTGGTGGGCCAC	19165
rs217183122	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180250852	ACACATTCCAGACTT[A/G]CTTCTAACCCTCAGC	19165
rs217243378	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180251391	TGGACAGCTTCTAGC[C/T]ATGCAAGGTGGCAGG	19165
rs217358371	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180241216	CCACTAACTAACATG[C/G]CCTTATTGGTCTAGG	19165
rs217705145	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180229554	CATGAAGAGTGGCAG[A/G]GAGAGACAAAGGCTG	19165
rs217938031	in-del	-/CAATGTCTCCAT			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180261166	AAGTGGCCGGTATTC[-/CAATGTCTCCAT]CAAGGTCTTCAGTGA	19165
rs217945602	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261672	CACCAGCCTGGAAGC[C/T]CTCTGGATTGTGCAG	19165
rs218143602	in-del	-/T			intron-variant	Psen2	GRCm38.p3	1:180237622	GGTCAAGCCACTCTG[-/T]TGGGACTGGCCCTAT	19165
rs218165489	in-del	-/A			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260983	TTCTGGGGCTGAGAG[-/A]AAAATGTCTGGGAGG	19165
rs218176140	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180245812	CATGGGGGATGGTTT[A/G]GTGGCTTGAACACCA	19165
rs218212401	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180241055	CTGCGGCTTTCTAGA[C/T]GTGAGAAGCGCGAGC	19165
rs218269952	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180241729	GGTGGGAGGCGAAGG[A/G]AGATGTGCCAGCCAG	19165
rs218303436	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264137	AAAATGGAGAGCAAA[A/G]CTTTTCCATACTTGT	19165
rs218322287	in-del	-/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259320	TGGCTGCTCTGCTTC[-/T]TCTTCCTGCATGTTT	19165
rs218340914	snp	A/C			intron-variant	Psen2, Gm31728	Mm_Celera	1:180263068	AAAAGACACAACAGA[A/C]GTTAAGAAGTATACC	19165
rs218527587	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180236792	TACTATTAACTTGGG[C/T]TTTTTAATTAGCTTG	19165
rs218611009	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180237446	CCACTGGGTCTCCAG[A/C]AGTCTTCCTGGAGGA	19165
rs218614137	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180238623	AGAGCAGGAGTGTGT[A/G]TCAGAAACACTGTGG	19165
rs218614242	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180230210	TGCATCTTTAAAAAC[G/T]TGTCTTATTTTTCAG	19165
rs218630909	snp	A/G			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180228876	ACAGGCCAGCGTAGT[A/G]TTCCAGTCTCCGTTG	19165
rs218671469	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180230811	GCCCTCTTGTGGCCT[A/C]CATGGGTACTGCAGG	19165
rs218944155	snp	C/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246914	TTGAGCTTTGTGCTA[C/T]GGAGGTAGAAGCAGG	19165
rs219000605	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180235984	CATGGATGAACTGGA[C/T]AACAGAAACAAGAGG	19165
rs219024136	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180232661	TTGTCTTCAACAGAG[A/C]ACCTGCCACCTTCTG	19165
rs219060552	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180236851	TTAGGACTGACAGAC[A/G]CACAGGTTCCACTGC	19165
rs219174780	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180263330	TTTTCTGGTAGAAAT[C/T]GACAAGTCGCTTATA	19165
rs219202051	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180233185	TTAGAAATGACTAAC[G/T]TCCACTCTAAGCCAC	19165
rs219232594	snp	C/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262726	AGACTGTCTGTGGCA[C/G]CTTGTGGGTGGGGGA	19165
rs219296838	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180240202	GAGCGCTGGGGTTAG[G/T]GAAGCTCACAGTTCT	19165
rs219344329	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180232295	TGGATTGTGCTGCTG[C/T]CCCAGTCTTTCAGGG	19165
rs219357256	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180231434	TCTGGCCTCTGTACA[C/T]GGGGTGTATGCATGA	19165
rs219399682	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180232866	TCAAGCCAAGGGGCA[C/T]GCTGCAGGCAATTCT	19165
rs219487062	in-del	-/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180257842	CTTATCATGTGGAAG[-/T]TGTGGACAGAAGTTC	19165
rs219553551	snp	A/T			intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258469	GTTGGACTTTTATAA[A/T]ATTTTTAGTTACATA	19165
rs219600827	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180231808	GAATTACCATATTTC[A/G]GTCATCCACTGACAC	19165
rs219641898	snp	A/C			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259166	TCAATAGCTGGGAAG[A/C]TGCCTAACTTCATGT	19165
rs219674240	in-del	-/TGC			intron-variant	Psen2	Mm_Celera	1:180239563	GTGCATCTACTCCAT[-/TGC]TGCTGCTGCTGCCTC	19165
rs219885873	in-del	-/ACACACACAC			intron-variant	Psen2	GRCm38.p3	1:180235587	GCACCCCCGGCTTAT[-/ACACACACAC]ACACACACACACACA	19165
rs219953487	in-del	-/AG			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247353	TGAGCTGTGACAGAC[-/AG]AGACAGAACATTCTG	19165
rs220008989	snp	A/T			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255359	GACATTTCATTTAAC[A/T]GGCAAAGGACTTATG	19165
rs220052490	snp	C/T			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258791	CACGAGGTAGATGAA[C/T]AGATGAGCAAATGGG	19165
rs220102920	in-del	-/TCTTATAT			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258116	CTAGTTTATAGGTAG[-/TCTTATAT]AGTATCCTTCTATGA	19165
rs220162124	in-del	-/C			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258746	GGTGGGCGTTGGGGG[-/C]GAATGTGGGAAGTTG	19165
rs220219409	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261757	TGAGATGTGTTCTAC[C/T]CATCTCTAGTTTAGG	19165
rs220237826	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259387	CACACACTCCTAAAG[C/T]ATAGAGTCTCCTCTC	19165
rs220239479	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260129	AGGCAAAGAGAGGGT[C/T]AAGCTCATCCACAGG	19165
rs220295140	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259427	TCAGGGTCCCAACCC[C/T]AAATCCTACCTCTAT	19165
rs220334781	in-del	-/AGAGAGAGAGAGAGAGAG			intron-variant	Psen2	Mm_Celera	1:180248263	CACACACACACACAC[-/AGAGAGAGAGAGAGAGAG]AGAGTCCGGACTGTG	19165
rs220341727	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180234775	TCCTGATCCACTACA[A/G]GGAGCTTCTGCCACT	19165
rs220363892	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180253787	GGTAGCAGTTTGGAT[A/G]CAGGTCAGAGGTGAC	19165
rs220403275	snp	A/C			downstream-variant-500B	Psen2	Mm_Celera	1:180226919	AGATATTTGTGCAGG[A/C]ACAGAAACCCTAAGA	19165
rs220522233	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180232984	CACAGGCTCTATACT[C/T]AGATAGCGGCCACTG	19165
rs220563888	in-del	-/CT			intron-variant	Psen2	Mm_Celera	1:180230575	CTCCTTCAATCAAGA[-/CT]CTGTCAAAAGGCAGA	19165
rs220607353	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261055	AGAAGTCTGAGTCCA[C/T]AGTCACTTGTCCTTG	19165
rs220705490	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180231571	CTTACAAGATGGGAA[C/T]CCAAGCTCACTGATG	19165
rs220719158	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180251795	AGCTGGGGATGAAGC[A/G]AGACTCAAGGAGACA	19165
rs220730082	snp	A/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180263712	AGGAAGTCTTTTTTT[A/T]AAAAATTGATTTCAC	19165
rs220781523	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256598	ATTTCAGGAGCCTCT[A/G]CTGCCCCTCCCTCCT	19165
rs221050083	in-del	-/ACACACACACACACACACACACAC			intron-variant	Psen2	GRCm38.p3	1:180248216	GTTCCGGTTGTTCCT[-/ACACACACACACACACACACACAC]ACACACACACACACA	19165
rs221139533	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180229233	ACGGACTGAGTGACT[G/T]GCAGCCTAGGCAGAA	19165
rs221250409	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259347	GTTTTTACCCTTCAG[A/G]GCCACTCTCTTCTCT	19165
rs221301843	in-del	-/AT			intron-variant	Psen2	Mm_Celera	1:180232120	TCTCTGCAAAAGGCA[-/AT]ATGTCTTCCTTGTTC	19165
rs221310723	snp	A/G			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258749	TGGGCGTTGGGGGGA[A/G]TGTGGGAAGTTGGAA	19165
rs221332557	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180249396	AAAATATTAAAAGTC[A/G]TTATCTTTAAACTGG	19165
rs221359286	snp	G/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258149	TATGATGACTACGTG[G/T]CAGACAGCGCAGAAT	19165
rs221419605	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180229187	ACTTCCTAGAAAAAG[A/T]CTGGGGGCATCGGGG	19165
rs221430974	snp	C/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264265	CCTCCCCTCCCTCCT[C/T]CACCCTTTCCCACCC	19165
rs221467755	in-del	-/TAAA			intron-variant	Psen2	Mm_Celera	1:180239644	CCAGCCACTGTGCAC[-/TAAA]TAAAGGCCAGCAGCT	19165
rs221672529	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180251703	ACTTCCACAGATGGC[A/G]TCAAAGCTGGAGTGA	19165
rs221775662	in-del	-/GTAGAAAT			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263322	CCAATTAATTTTCTG[-/GTAGAAAT]TGACAAGTCGCTTAT	19165
rs221802411	snp	A/C/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	GRCm38.p3	1:180258097	TCTGGAGAGGACTTG[A/C/G]GTCCTAGTTTATAGG	19165
rs221847156	snp	C/T			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255727	TGCCTCAGGCCCTGT[C/T]GGGCGCCTCGCTCCT	19165
rs221886374	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180228206	GCCTGCCCTGCCCTT[G/T]GAACAACGGGTCCCA	19165
rs221903242	in-del	-/TAAG			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262516	ACTAAGGGGGTTTAC[-/TAAG]AGTCTAATCAATGGC	19165
rs221922586	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180248500	GCCTCCCTGGGTTGG[G/T]TCAGACTCAGGAAGG	19165
rs222073345	in-del	-/G			intron-variant	Psen2	Mm_Celera	1:180253482	TCCAAGCACTGGCAT[-/G]ATAGGCATTTTGGGT	19165
rs222093145	in-del	-/TTTG			intron-variant	Psen2	Mm_Celera	1:180252053	TTTGTTTTGTTTTGT[-/TTTG]TTTTGTTGTTGTTGT	19165
rs222291462	in-del	-/TTTGT			intron-variant	Psen2	Mm_Celera	1:180253378	ATAGCCAGGATGACC[-/TTTGT]TTTGTTTTGTTTTGT	19165
rs222332512	in-del	-/ACACACACAG			intron-variant	Psen2	Mm_Celera	1:180249360	CACACACACACACAC[-/ACACACACAG]AGGACTTGGAAAACT	19165
rs222415439	in-del	-/AGG			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255316	CATTCATATCTTTAA[-/AGG]AGAAAAATCCCTAAG	19165
rs222606607	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180250351	AGGGTGGCTGAGGGA[C/G]TAAGGACCTACCTAC	19165
rs222755075	in-del	-/TGTG			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260413	AATTATGTATGTATA[-/TGTG]TGTGTGTGTATACAC	19165
rs222768808	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180253560	GGGGTGGGTGTTAAG[A/C]TGAAGGGATGGCACT	19165
rs222799355	in-del	-/G			intron-variant	Psen2	Mm_Celera	1:180252056	GTTTTGTTTTGTTTT[-/G]TGTTGTTGTTGTTGT	19165
rs222833173	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180245787	CAGGGACAGGCATAG[A/G]CAGTGGGGACATGGG	19165
rs222866233	in-del	-/TC			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263196	GTCTCTCTGTCTCTG[-/TC]TCTCTCTCTCTCTCT	19165
rs222903080	snp	C/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246763	TCTCAATAATGTACT[C/G]TGACACAGCATCACC	19165
rs223117602	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180249572	CTCCACCTCTCAAGT[A/G]CTTGGATCACAGGTA	19165
rs223177957	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180250247	CCAGCTCCGCATCCC[G/T]AGAGTCCACAGGAAG	19165
rs223241405	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180239579	GCTGCTGCTGCTGCC[G/T]CCACCACCACCACCG	19165
rs223246289	in-del	-/AT/TTTT/TTTTT			intron-variant	Psen2	Mm_Celera	1:180249422	CTGGTTTGTGGGTGA[-/AT/TTTT/TTTTT]TTTTTTTTTTTTTGG	19165
rs223341520	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247083	GGATAACTTCCATAA[A/G]GACTTCCCTCAATCT	19165
rs223396134	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180237623	GTCAAGCCACTCTGT[G/T]GGGACTGGCCCTATG	19165
rs223440729	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180236013	GGACCACTGTAACCC[C/T]CAACAGGATGAAGAC	19165
rs223467877	snp	A/C			missense, nc-transcript-variant	Psen2	Mm_Celera	1:180245622	AACCTACCCACTGGG[A/C]AGTGCTCTCTCCATC	19165
rs223586640	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180250610	GAAATCATACTCCAA[A/G]CGTGAACTGGAAACT	19165
rs223618651	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180252808	ATGAGGAAGTTTCTT[G/T]CTGAGGTGTAACAGG	19165
rs223632276	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180239819	TAATGCATTCTTTTT[C/T]ATAATACACACGCAT	19165
rs223678917	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180240330	TACTTAAGGGGGCAG[A/G]GACCCAGGCAGGACG	19165
rs223702909	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180241772	GGTGACTGTGTAGCC[C/T]ACTGCACATGGTGAC	19165
rs223798527	in-del	-/TAGCCACCACT			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261284	TCCACACTAACCACC[-/TAGCCACCACT]AATTATCTGACCCTC	19165
rs223889409	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180249502	TCGTGTATCCCTCAT[G/T]GACTTCTAGCTCACT	19165
rs223916946	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180248785	CGCTATGCAAAGATT[C/T]AGACCTTTTAGATCC	19165
rs223971099	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180238724	ACAGTGCCAGAGAGC[A/G]CAAAGAGGCAATCTA	19165
rs223974023	in-del	-/CCCC			intron-variant	Psen2	GRCm38.p3	1:180250803	ACTAGGGAAGGGTTT[-/CCCC]CCCCCCCAAACAGGG	19165
rs224077372	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180236464	TTAGAATTCCCCTAG[C/G]AATTTCATGCTTCCA	19165
rs224086825	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180239540	CCTTCATCACTCCTT[G/T]CTAGTGAGTGCATCT	19165
rs224118889	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180241296	GACTAACTAGAAGAC[C/T]CAGCACTTCTTGGAG	19165
rs224163548	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180237338	GGCTGAGCATGGAGG[A/G]GTCAAAAACAAGACT	19165
rs224174809	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180244860	TGTTTTGCTCTTCCT[A/G]AGTGGCTGGTTTCAT	19165
rs224233817	snp	G/T			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180229429	TGGGTAGCCAGGCAG[G/T]GGGGCTTCGAAGGCT	19165
rs224234323	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180234184	GGAAGGAAGGTTTTC[A/T]TTCTTAGGACAGGAG	19165
rs224283839	in-del	-/TTTGCT			intron-variant	Psen2, Gm31728	Mm_Celera	1:180263097	CCAGTCCTCTTAGGA[-/TTTGCT]GAAAAACAGTCTCTC	19165
rs224299228	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180237114	TGAAGGGAGCCTGCA[C/T]AATTGCCATAGAAAG	19165
rs224307708	in-del	-/A			intron-variant	Psen2	Mm_Celera	1:180249964	AAACGAGAATATAGG[-/A]AAGCCAATGACATAA	19165
rs224670122	snp	G/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262044	CAACAGAAAGGAAAC[G/T]GAAACTCCTTGCTTT	19165
rs224865129	in-del	-/AA			upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180264115	CACACAAACAAACAG[-/AA]AAAAAAAAATGGAGA	19165
rs224872377	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180233489	TTATGATAAGACCCT[C/T]ATCTTTGGTTAAGAT	19165
rs225057625	snp	A/G			intron-variant	Psen2, Gm31728	GRCm38.p3	1:180260225	AGCCTTTGCATGTGG[A/G]CAGGCATGGGATGCT	19165
rs225130872	snp	A/C			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180265441	TTAAGGTGTTATCTA[A/C]GTGATATAGAAGAAT	19165
rs225136818	in-del	-/G			intron-variant	Psen2	Mm_Celera	1:180229056	AAAAAAAAAAAAAAA[-/G]AAAAAAAAAAAGGAA	19165
rs225230100	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180263828	ACCCTGGGAGCCGGA[A/G]TGGAGTTACCGACAG	19165
rs225294579	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262955	AGAAGAGAGAACTCA[C/T]CGGGAGGACGTAGCT	19165
rs225445329	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180231693	GCCTGTCCTTTTGTC[A/G]ATAGCTCAATTCACT	19165
rs225532251	in-del	-/G			intron-variant	Psen2	Mm_Celera	1:180236700	GGTATCAATAGATTT[-/G]GGGGGGGGGTCACTG	19165
rs225611859	in-del	-/CT			intron-variant	Psen2	GRCm38.p3	1:180248214	CTGTTCCGGTTGTTC[-/CT]ACACACACACACACA	19165
rs225631349	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180240239	TATATTTATTAAGTC[A/C]TAAAAGGGCCTGATA	19165
rs225705217	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180232371	TCTGCAGGGCTCATA[A/C]TGTCCAGACCTTCCC	19165
rs225712293	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180237205	AGGCAGCTCACTGGC[C/T]GCTGTTTAGACTGAG	19165
rs225783061	in-del	-/TTTT			intron-variant	Psen2	Mm_Celera	1:180231246	TAATAAAACAACCAA[-/TTTT]TTAAAAAAAGGAAAT	19165
rs225810208	in-del	-/GG			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256336	AGACACGCCCCCGGT[-/GG]GGGGGACACGCCCAC	19165
rs225855789	in-del	-/TC			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258728	TTTATTATATGAGGA[-/TC]TGGGTGGGCGTTGGG	19165
rs225914531	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180253855	GTAGCAATGTCCAAA[G/T]CCTGTGCTAACAGAC	19165
rs225922488	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258213	GATCTCATCCATGAG[A/G]CCTGTGTTCCTGTGG	19165
rs226031412	in-del	-/ATAT			intron-variant	Psen2	GRCm38.p3	1:180245008	TCTGTGTGTGGACAC[-/ATAT]ATATATGTATATATA	19165
rs226071959	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180238303	CCCCGCTTCCAACAC[A/G]GGGTGAGGGTACCGC	19165
rs226077758	snp	A/G			utr-variant-3-prime, nc-transcript-variant	Psen2	Mm_Celera	1:180227034	CTGTTTATTGGTATC[A/G]TTATTAAGCCACTTC	19165
rs226153788	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261931	GCTTCAAGCTACTCC[C/T]TCAGTTCCTGCCCTG	19165
rs226197168	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180231264	TTTAAAAAAAGGAAA[C/T]GATTTTCAGTCCTGA	19165
rs226214768	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180237842	ATGTCCTGGGACTCC[C/T]TTCCATGGTTCCTCC	19165
rs226216903	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260858	AGCCAGCAGTTCTCA[A/G]ACTGTTTGGATTTAC	19165
rs226237741	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180232522	CTGGCCTCCAGATTT[C/G]TACCTAATGCTAACC	19165
rs226249389	snp	A/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258019	CTTATAACAATAGAA[A/T]TGTGTTTTTCCGCTG	19165
rs226318454	in-del	-/ACAC			intron-variant	Psen2	Mm_Celera	1:180239863	CTAGAGAACCCAACA[-/ACAC]ACCCCACTGAAGTTT	19165
rs226416676	snp	A/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260503	CATAAACATACATAT[A/T]GAATGTATACATATA	19165
rs226458389	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180234259	AAATGTCCCCTAAAG[A/G]CTCAGGATGGTTTGT	19165
rs226470277	snp	A/C			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259859	AGACATTAGCCATGC[A/C]TCCCTTGTTACATCA	19165
rs226487515	in-del	-/ATCTATCT			intron-variant	Psen2	GRCm38.p3	1:180244954	TCCCTCCCTCCTTCC[-/ATCTATCT]CTATCTATCTATCTA	19165
rs226520188	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180235417	TTTTCTGGAATGTAC[C/T]AGGGAGTGTATCAAT	19165
rs226524316	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180235826	ACCAGAGCCCGGCAG[C/T]GGACTCTGAGGACCC	19165
rs226529664	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262567	TCCCACAGACAATAT[C/T]GATCAACTCTGGACA	19165
rs226548735	in-del	-/T			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258587	AATCATGTGTTCATC[-/T]TTTTTTTTTCTAATA	19165
rs226581162	snp	G/T			utr-variant-3-prime, nc-transcript-variant	Psen2	Mm_Celera	1:180227566	CGGAGCCTCCGCCTG[G/T]CTCCTGTCAGATGTA	19165
rs226599573	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180228032	TGTTTGCATTTACAA[G/T]AGACCCAGATGAGCT	19165
rs226673767	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180230317	GTAATTTCGGTCTGC[A/T]CACTGTCCAGGAACG	19165
rs226792727	in-del	-/CCCCT			intron-variant	Psen2	Mm_Celera	1:180250808	GGAAGGGTTTCCCCC[-/CCCCT]CCAAACAGGGTACGC	19165
rs226848692	snp	C/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264288	TCCCACCCGACCATG[C/T]ATGGCCTCCAAGTAC	19165
rs226872550	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180230749	CTTCCCAGCACCCAC[A/G]TGGCAGCTCACAAGA	19165
rs227103702	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262819	TGTCTGGACAATACT[A/G]CAAGAGTCAGGGCTG	19165
rs227159498	snp	A/C			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262201	AGACAGGAGGTAGCT[A/C]ATGAGAGTTGCAGGT	19165
rs227265438	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180230170	ACACTGGCAATAATG[A/G]TGCTCAGTGAGCGGC	19165
rs227330931	in-del	-/GATAGATAGATAGATA			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260565	ATGGATGGATGGATG[-/GATAGATAGATAGATA]GATAGATAGATAGAT	19165
rs227415977	in-del	-/AGTG			intron-variant	Psen2	Mm_Celera	1:180233211	CCACTGTCCATGAAC[-/AGTG]CCCAGAGGGAAGTGG	19165
rs227489004	in-del	-/GA			intron-variant	Psen2	Mm_Celera	1:180235254	GCACTCAGGGGTGGG[-/GA]GAGAGGTGCCACACT	19165
rs227612715	snp	C/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257502	GGCAGATAGCATAGA[C/T]GCATGAACGGAGGTC	19165
rs227646418	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258158	TACGTGGCAGACAGC[A/G]CAGAATCAGTAGACC	19165
rs227725824	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180249749	TTTCTCCTCTTGAGA[A/T]AAGGTCTCACTAAGT	19165
rs227780086	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180250477	CCGGGTGACCTAATT[C/T]TCTCAGACCTGCTTT	19165
rs227790687	in-del	-/AGAC			intron-variant	Psen2	Mm_Celera	1:180234928	ATGCAAGAGCACTTG[-/AGAC]ACCGCTCCATCAATG	19165
rs227976272	in-del	-/TATATAG			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258119	TTTATAGGTAGTCTT[-/TATATAG]ATCCTTCTATGATGA	19165
rs228010253	in-del	-/AA			intron-variant	Psen2, Gm31728	Mm_Celera	1:180263242	CAGATAGATTTTAAT[-/AA]AAAAAAATACCATGC	19165
rs228023149	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180253909	CTGGGCCCCCATCCC[G/T]GACACCCACACCCCA	19165
rs228023545	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180252951	TTTCCTGAGGATTGA[C/T]CTGGTGTTTTCTGTC	19165
rs228025516	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180251350	CCAGTGGCTGCATAG[A/T]CTAGTGTGACATGAA	19165
rs228028568	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180232476	GCCTACCTCGGGGTC[A/T]TTGTACCAGCTGCCT	19165
rs228030108	in-del	-/G			intron-variant	Psen2	Mm_Celera	1:180254348	CCTCCATGTTGAACA[-/G]GGGTTCTCTGGAATT	19165
rs228096162	snp	A/G			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254609	CACTGGACAGGGTAT[A/G]GCTAGACACTGCTCC	19165
rs228096169	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246178	AGAAGCTGAAATTCC[A/G]TGCTTCCTAGACAGG	19165
rs228141589	in-del	-/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260504	ATAAACATACATATA[-/G]AATGTATACATATAT	19165
rs228175389	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259612	TCAAGTCTGGCCAGT[A/G]TGACAGGGCCTCTTC	19165
rs228184252	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247261	CACAGGCACAAGAGG[A/G]AGGTGGAGAGGACCA	19165
rs228216061	snp	A/G			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258914	TGTGGTGGTTTGAAT[A/G]TGCTTGGCCCATGAG	19165
rs228298107	in-del	-/CTTCTTC			utr-variant-3-prime, nc-transcript-variant	Psen2	Mm_Celera	1:180227449	ATTCTTTTTTTTTTT[-/CTTCTTC]TTCTTCTTCTTCTTT	19165
rs228332578	in-del	-/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256337	AGACACGCCCCCGGT[-/G]GGGGACACGCCCACT	19165
rs228403604	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261595	GGGCAGTAGGCCTGC[C/T]GTGGTCCTGAGCCCA	19165
rs228523371	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180228692	ATACATATGGTGAGT[G/T]AGATCCAAGCCTCCC	19165
rs228536870	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180231869	GATACAGACACAATG[C/T]GCACATGCTTGTTTG	19165
rs228656113	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260565	GATGGATGGATGGAT[A/G]GATAGATAGATAGAT	19165
rs228882156	snp	C/T			downstream-variant-500B	Psen2	Mm_Celera	1:180226546	GCTTCTGTGGTCTCA[C/T]GTCCCCACCCAGAGG	19165
rs228898841	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180238256	CCCACATGATAAAAG[A/G]AGAGCGGACTCCTGA	19165
rs228951025	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180238783	TTTTGAGAAAGTTGC[C/T]GTGCGGTAGTAGCTC	19165
rs229355191	in-del	-/T			intron-variant	Psen2	Mm_Celera	1:180248555	TCCCACTCCTATGAC[-/T]TGTAGGGATGAAGGG	19165
rs229387272	snp	A/G			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255320	TCATATCTTTAAAGA[A/G]AAATCCCTAAGCAGA	19165
rs229415637	snp	A/C			utr-variant-3-prime, nc-transcript-variant	Psen2	Mm_Celera	1:180227228	GATCATCCCTGGAGA[A/C]TTACAGACGTGGACA	19165
rs229551654	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180248935	ACAGGAACTCCCTCC[C/T]CCTCCCCCTCCCCCA	19165
rs229746100	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180240039	CATCTCTTGTTTCTA[C/T]GAGTCCTCCACAGGC	19165
rs229774964	in-del	-/GGT			intron-variant	Psen2	Mm_Celera	1:180241111	AAAAACTTAGAAGAC[-/GGT]GGTGGTGGAGGAGGG	19165
rs229783729	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180240650	CTCTGCAGAGCTACA[A/G]CAGTAGCTGAGGGAG	19165
rs229823051	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180232728	TACCTCCATCCTCCA[C/T]CCAAGAATGAATTCT	19165
rs229845084	in-del	-/GGGG			intron-variant	Psen2	Mm_Celera	1:180238662	CAGAAGACAGTGGGT[-/GGGG]GGGGGGGGGGCGTAC	19165
rs229861535	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180233286	AGCCTCTGAAGGTGG[C/T]ATGTTCATGCGATGT	19165
rs230021649	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180238482	AACTCACAGGCTTCC[C/T]GGGACCAGAAGACCT	19165
rs230024401	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180249787	ATTAGTCTGGAACTG[G/T]ATGGGTAAACCAAGC	19165
rs230037764	in-del	-/AAA			intron-variant	Psen2	GRCm38.p3	1:180229038	GCAGGCAAAAGAAAG[-/AAA]AAAAAAAAAAAAAAA	19165
rs230084051	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180239241	CATCATGGCAGAATC[A/G]ACAGTCTGTACCTCA	19165
rs230171988	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180250701	GCCAACAGAACAATA[C/T]CCTTATCTTTCAAAA	19165
rs230370141	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180249614	ATCCAGTTCACGATG[C/T]ACTAGGGGTACAGCC	19165
rs230385473	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180234751	CCTAGCTCTGGTAAA[C/T]GCTCTGCTTCCTGAT	19165
rs230421149	snp	A/C			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256805	TTGTGATCGCAGGAT[A/C]GGTCTGTGGAGTGAG	19165
rs230444672	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180235635	TAGAATGTGACTCTG[A/G]GGGGTTTCCACCTGC	19165
rs230493189	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180249069	TGCAGTATATTGCTG[C/T]AATTGCTGGTTTGTT	19165
rs230504466	in-del	-/C			intron-variant	Psen2, Gm31728	Mm_Celera	1:180263354	CTTATAAATGTTTAA[-/C]AGGCACTAGGTGTGG	19165
rs230690358	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180253014	CTAAACCCGGGGAGG[A/G]AAGACTGCATGTGGA	19165
rs230744413	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180245150	ATGCAAGCTGCTCAC[C/T]TCACAGTCAGGATAC	19165
rs230783927	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262400	ATGTCTCAGACTTAC[A/G]TGGGATTTAGTGCTA	19165
rs230841575	snp	C/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261808	TCCTGGAGGCTTCAT[C/G]CCGTAGACCTCATTG	19165
rs231043594	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180245460	CTCCAGCTCCAGGGG[A/G]GAGGACATTCCCTTA	19165
rs231048424	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246132	AACTTGACAAATGGC[A/G]CATCGACAGAGGATG	19165
rs231394733	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180239381	TTGTCCAAGTGAGTG[G/T]ATCTGGAATCAACTA	19165
rs231839000	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259321	GGCTGCTCTGCTTCT[C/T]CTTCCTGCATGTTTT	19165
rs231977158	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180236861	CAGACACACAGGTTC[C/T]ACTGCTAAGGCTAGT	19165
rs231986469	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247513	AGGGGAAGGGAGTGT[A/G]ATTCAGCCTAGGTAT	19165
rs232062182	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180237690	TTCCTAGTTTGTTAC[C/T]ATGTTCTCTATATAT	19165
rs232110893	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264815	GTTTTTCTCCCCCAC[A/G]CAGTCTAAGATAAAA	19165
rs232145212	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180229747	GCCGTCAGGCAGTGC[C/G]ACTCTGCCATGCTGA	19165
rs232201466	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264217	TTCTCCCCTCTCATC[A/G]CCTCCCCTCTCCTGT	19165
rs232218720	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180232072	CACATACCCACACCC[A/C]CACAGCATCCCTGGC	19165
rs232235860	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180230438	CACTGACCGGTTGAA[C/T]CCCTCCACCCTTCCT	19165
rs232371949	in-del	-/CTGGATCCGCAT			intron-variant	Psen2	GRCm38.p3	1:180250144	GAAAAACAAGCCCCG[-/CTGGATCCGCAT]CTGAGCGATGCCAGG	19165
rs232504575	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180232867	CAAGCCAAGGGGCAT[A/G]CTGCAGGCAATTCTC	19165
rs232521707	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180228013	GAGTTTTGTTGTTTT[A/G]TTTTGTTTGCATTTA	19165
rs232577683	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180233451	CCAGAGGTGGAACCC[C/T]CCTGCAGGTGGCGAC	19165
rs232579643	snp	A/G			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180228861	GAGGATGGCGATAAA[A/G]CAGGCCAGCGTAGTG	19165
rs232648529	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180239788	GACTAGCTAATCTTT[A/G]TTGTATAAGCCAATC	19165
rs232705015	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180231792	GATACTCTGTTGTAT[A/G]GAATTACCATATTTC	19165
rs232767425	snp	C/T			downstream-variant-500B	Psen2	Mm_Celera	1:180226673	GTGGCCCCCTAGCCC[C/T]TTGGCTTTCTGGCTT	19165
rs232818785	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260531	ATATAAACATACATA[C/T]ATAATGTACATATAG	19165
rs232952534	in-del	-/G			intron-variant	Psen2	GRCm38.p3	1:180239524	GCTCTTTGCCTGCCT[-/G]CCTTCATCACTCCTT	19165
rs232976403	snp	A/C			intron-variant	Psen2, Gm31728	Mm_Celera	1:180263028	ACATGTGAAGTGAAA[A/C]TTTGCACCCAGGAAG	19165
rs233032748	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262484	TAGTTTCATTTTAAC[A/G]TAGTTTTGAGTCCTG	19165
rs233050054	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180240471	TTAGCCTTTGGTGAG[C/T]CCTGTATGACAGCTC	19165
rs233133822	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180229305	GGGACTGCAGGCTGC[C/G]GTGCAGTTTGGCATA	19165
rs233144016	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180241143	GTCAGAGCTAGCCTG[C/T]ATAGCCACAGAAGGG	19165
rs233200603	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180233104	AGGAACATCTGTCAA[A/C]TACATGTATAATCCC	19165
rs233463682	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180231344	GAAGCAGGGCTCACA[C/T]TCCTGTGCCCTTTAA	19165
rs233666259	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180249185	TTTACACAGGACTTG[A/G]TATTCACCACCACTT	19165
rs233685739	snp	G/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180263770	TTTACATCTGTGCAC[G/T]GTGTGCATGCAGTGC	19165
rs233755432	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261654	CTGACACAAGCCAGC[A/G]TTCACCAGCCTGGAA	19165
rs233833388	snp	A/C			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260806	GAGGACATTTGTTTC[A/C]TTTTGAGGAGTCTGC	19165
rs233936539	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180236129	GCACACCTTTGATCC[C/T]AGTACTTGAGGCAGA	19165
rs233962782	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180241638	GAAGGAGTTATCTCA[A/G]TGTTTCTGTGACATT	19165
rs234016024	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180245275	ACACTAGGGACCAAA[C/T]CTTCAGCACAAAGGT	19165
rs234019496	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180228506	TCCCTTGGGGTCCTG[A/G]TGGCACTGAGAATAT	19165
rs234053396	in-del	-/A			intron-variant	Psen2	GRCm38.p3	1:180236136	TTGATCCTAGTACTT[-/A]GAGGCAGAGGCAGAG	19165
rs234157381	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180253514	GGTCTTGAACTCAGA[A/G]ATCTACCTGCCTTGC	19165
rs234157570	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256788	GTGAGGGCAGGGAGG[A/G]GTTGTGATCGCAGGA	19165
rs234179477	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180248282	GTCCGGACTGTGCCA[-/C]CCACCATGAGCTTGT	19165
rs234185138	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180244759	CCCACTGCACACTGT[A/G]TTTGTGTAGTCTATT	19165
rs234226652	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180254070	ACATAGCTCAATTGG[C/T]CTGAAACTCACTACA	19165
rs234268204	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180234050	GACAGACAGCGTCAC[A/G]GGGCACCCAAGCCCG	19165
rs234329943	in-del	-/TT			intron-variant	Psen2	Mm_Celera	1:180251136	AGGTAAAAACTAGAA[-/TT]TTTTTCCTTTCTTTT	19165
rs234490494	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180257967	CCACTGTCTCAGTCC[A/G]TTCAGGCTGCTATAA	19165
rs234519190	snp	G/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261376	TCTGGAGCTAGGGCA[G/T]ATCTCACAAACTAAG	19165
rs234554934	snp	A/C/T			intron-variant	Psen2	GRCm38.p3	1:180250143	TAGAAAAACAAGCCC[A/C/T]GCTGAGCGATGCCAG	19165
rs234609965	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180230368	ATAATCTTTGTCGTC[C/T]AGAACTACTTTGGTG	19165
rs234618461	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180250804	ACTAGGGAAGGGTTT[C/T]CCCCCCAAACAGGGT	19165
rs234682918	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180251766	TCACAGTTCAGGAAA[C/G]CAAAGCCCAGGGGAG	19165
rs234741472	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180243886	CACTGCACACTGTGA[C/T]TGTGTAGCCCACTGC	19165
rs234837441	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180231485	GTATGCACACCCAAA[A/C]TAAACACTTTTAAAT	19165
rs234949538	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180230148	CCTTTTGCAATCCTC[C/T]CAAGCAACACTGGCA	19165
rs234973266	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180240084	GTGGGAACTTTCCTA[-/C]CCTCCGCTTTTCTAA	19165
rs235018298	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180230606	AGAAACCTAAAAGCC[C/T]GTCTGTCCTCAGGCC	19165
rs235070078	snp	A/C			intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258317	AAGGGACAAAAAAGC[A/C]TTAAGACTTCAGCAT	19165
rs235113029	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264666	GGACTGTGGTGTGAC[A/G]TTACTGGGTTAGGGT	19165
rs235171625	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180249242	TATTACAGGAGCACC[A/G]AAGTCTCACTTCAAA	19165
rs235184544	snp	C/T			downstream-variant-500B	Psen2	Mm_Celera	1:180226848	GCCCTGTTATGGAAC[C/T]TTTTAGTTAAAGAAC	19165
rs235249801	snp	C/G			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180256161	GCTCTCCATGCTGCC[C/G]GCTACCCGCGATCGG	19165
rs235345731	snp	G/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260097	TGTAATAGGATGGGG[G/T]CCTGGGAGGAGTGGA	19165
rs235453837	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180244475	ACTGTGTAGCCCACT[G/T]CACACTGTGACTGTG	19165
rs235528647	in-del	-/TTTTT			intron-variant	Psen2	Mm_Celera	1:180231245	TAATAAAACAACCAA[-/TTTTT]TTTTTTAAAAAAAGG	19165
rs235642748	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180252801	TAAAAGCATGAGGAA[C/G]TTTCTTTCTGAGGTG	19165
rs235898385	in-del	-/CTTTATAACCTATTCAGT			intron-variant	Psen2	Mm_Celera	1:180237513	AAGGGACGGCGTGGC[-/CTTTATAACCTATTCAGT]CTCTTTATCCCAACT	19165
rs236079218	in-del	-/AAGA			intron-variant	Psen2	Mm_Celera	1:180234164	CTTCAAGTATCACAG[-/AAGA]AGGAAGGAAGGTTTT	19165
rs236125301	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180250012	AACAAGGGATGCTTG[C/T]GTCTTCCACTCCCTT	19165
rs236310346	snp	A/G			utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180256268	CGCCGCGGGCGGAGC[A/G]CCTCTCCTGGGCTAG	19165
rs236366524	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180248306	AGCTTGTCTTCACAC[C/T]CCAGCTAACAAAATC	19165
rs236377443	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180230790	TCAATTCAACGGGAA[C/T]CCAATGCCCTCTTGT	19165
rs236445234	in-del	-/ATGCCTCAGCGCCAA			upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180264516	GTATGTGCCTTGTAC[-/ATGCCTCAGCGCCAA]TAACTAAACAGAACA	19165
rs236500224	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180254234	GTGTCTGTCTGTATG[C/T]CTGTCTAGAACAGAT	19165
rs236565700	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246803	CCAGTAAAGCTCCAA[A/G]TCCCCACATTTTGGG	19165
rs236630470	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180251542	AGGGGATTAACAAAG[C/G]CAGCAGCTGCCCTTC	19165
rs236633477	snp	C/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247721	CAGCTTAAGGGGACA[C/T]AGCTTCAAAGGTCAC	19165
rs236667471	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259211	TCCCACCGATAACTC[C/T]GAGTTACTAGTTTAC	19165
rs236695828	snp	C/T			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180240850	CCCATACTTGAGGGT[C/T]AGCTCTTCCTCCAGG	19165
rs236901761	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180239582	GCTGCTGCTGCCTCC[A/G]CCACCACCACCGCTG	19165
rs236961908	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180227900	TCAGGACACCTGCAT[A/G]TTGGTTACTAGGTGG	19165
rs237007984	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180241734	GAGGCGAAGGGAGAT[A/G]TGCCAGCCAGCCCAC	19165
rs237008012	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180232992	CTATACTCAGATAGC[A/G]GCCACTGCTACCACA	19165
rs237014459	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260721	GGTCACCTGGTGACA[C/T]TTTCTTGTCATCAGG	19165
rs237069105	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180233575	AAGGCCACCTGCTGA[C/T]CCCCCAGTGTCTGGC	19165
rs237265751	in-del	-/T			intron-variant	Psen2	Mm_Celera	1:180252536	GGTAGTTTACTTTGC[-/T]TTCAGATTTATAAGC	19165
rs237307592	in-del	-/T			intron-variant	Psen2	Mm_Celera	1:180253958	TTAAAGGAGTCATAA[-/T]TAACTGTCTCAGTGT	19165
rs237346122	in-del	-/A			intron-variant	Psen2	Mm_Celera	1:180241385	CTTGACACCAAGGAG[-/A]AAAAAAAACCTAATA	19165
rs237369762	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180238055	CTAAAACCAGGGTCT[A/G]AAAGCTGGTGGCACA	19165
rs237454781	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180230223	ACGTGTCTTATTTTT[C/T]AGGCTTCAGTTTATT	19165
rs237457661	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180238662	ACAGAAGACAGTGGG[G/T]GGGGGGGGGGCGTAC	19165
rs237487548	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180236708	ATAGATTTGGGGGGG[A/G]GTCACTGGATCTCTT	19165
rs237507233	in-del	-/CT			intron-variant	Psen2	GRCm38.p3	1:180228815	AATGACCCACGAGTG[-/CT]CCCACACCCACCACA	19165
rs237544095	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180230876	CAAGTTTTTAAAAAT[C/T]CAGTCCTTGGAGGAG	19165
rs237584918	in-del	-/T			intron-variant	Psen2	Mm_Celera	1:180253712	CAAAACACAAAAACA[-/T]TTTTTTTTTCTCCCA	19165
rs237783833	snp	G/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257211	GTGAGTTCCAGGACA[G/T]CCAGGCTATATAGAG	19165
rs237861680	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180249458	TATTTTTCTGCATTT[C/T]TCCATTTTATCTATT	19165
rs237904049	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180235380	CAACATTCCCATCAA[-/C]CCCACAACTAACTAC	19165
rs238122968	snp	A/G			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180245686	AGATGTGGGGCTCTC[A/G]GCTGACATCAAGGAC	19165
rs238126761	snp	A/G			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255319	TTCATATCTTTAAAG[A/G]AAAATCCCTAAGCAG	19165
rs238243653	snp	A/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180265373	GTTGGCACCAAAAAT[A/T]AAGGTCTGGGGGTAG	19165
rs238305026	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264370	CTGGTCATTGGCAGG[A/G]TACTCCCTGACCTAA	19165
rs238324611	in-del	-/T			intron-variant	Psen2	Mm_Celera	1:180253481	CTCCAAGCACTGGCA[-/T]TATAGGCATTTTGGG	19165
rs238382696	in-del	-/T			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254860	TCAGCTTCCTTCCCA[-/T]TCCTGCACCTCTGCC	19165
rs238385932	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180237663	ACAACAGCACGGTCA[-/C]TTCCCTTGCTGTTCC	19165
rs238518818	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262747	GGGTGGGGGAGCTAA[C/T]GCTGGTCATGGCTAT	19165
rs238584515	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180239924	CTCCCCCAACTGTAG[C/T]TGCAGGTACCGTCCC	19165
rs238649668	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180232099	TGGCTCACCAGCCTG[A/G]CCCCTTCTCTGCAAA	19165
rs238728692	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180252397	GTTTTTCGATAGGGG[G/T]TTAGTAAAAGCAATG	19165
rs238836479	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180238460	CTCAAGATCCAAAGG[A/G]GAACCCAACTCACAG	19165
rs238882996	in-del	-/GTT			intron-variant	Psen2	Mm_Celera	1:180253333	TTCTCTCCTCTCTCA[-/GTT]TTTTTTTTTTTTTAT	19165
rs238920026	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180235399	ACAACTAACTACTCA[A/G]TATTTTCTGGAATGT	19165
rs239005634	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180235987	GGATGAACTGGATAA[C/T]AGAAACAAGAGGACC	19165
rs239011284	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180253883	GACTGTAGGGCCACA[C/T]ATCTGGGCAGCTGGG	19165
rs239021652	snp	A/C			intron-variant	Psen2	GRCm38.p3	1:180239870	ACCCAACAACACACC[A/C]CACTGAAGTTTTTCA	19165
rs239072263	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180228208	CTGCCCTGCCCTTGG[A/G]ACAACGGGTCCCAAG	19165
rs239138805	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180229195	GAAAAAGTCTGGGGG[C/T]ATCGGGGTGTGGGGA	19165
rs239290473	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259363	GCCACTCTCTTCTCT[C/T]CTCTCCTGCACACAC	19165
rs239302993	snp	A/C			utr-variant-5-prime, intron-variant	Psen2, Gm31728	Mm_Celera	1:180263398	AAGTCCATAGGTGGC[A/C]GAAGCCAGTGAATCT	19165
rs239351385	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180231694	CCTGTCCTTTTGTCG[A/C]TAGCTCAATTCACTT	19165
rs239378328	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180227741	GCCCTGCAGGAAGGA[C/T]ATCAAGGTGAGGGAA	19165
rs239412701	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180232317	CTTTCAGGGGCTTAC[A/C]TTTCCTTCAGGAAGA	19165
rs239472926	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180233876	TGATGGAGCCGAAGC[A/G]GGTAGCTGCAGAGTG	19165
rs239489797	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261894	ATGATGCAGCCATCT[A/G]CGGCATCCCTCTAAA	19165
rs239548035	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261296	CACCAATTATCTGAC[C/T]CTCTAGACCCCAGCA	19165
rs239773783	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259441	CTAAATCCTACCTCT[A/G]TCTCTCTTCCCCAGC	19165
rs239930689	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180229719	CCCTCTCTGAGACAG[A/G]TGTCAGAGTCTGGCC	19165
rs240124928	in-del	-/A			upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180264444	AAGTATCATAGTAAG[-/A]AAAAAAAAATCTACC	19165
rs240141937	in-del	-/ACTT			intron-variant	Psen2	Mm_Celera	1:180249272	AGACTACTTAATAAC[-/ACTT]ACGTGACGTTAAATT	19165
rs240221775	in-del	-/TCACACACACAC			intron-variant	Psen2	Mm_Celera	1:180249327	ATAAACATCTGAATT[-/TCACACACACAC]ACACACACACACACA	19165
rs240221820	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257096	GACCTTGTCTTTAAA[A/G]GAAAAAAATACGGCT	19165
rs240354030	snp	C/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246689	GATCCCTGGAAGTAC[C/T]CACACTGAGGGTTGG	19165
rs240431805	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180235774	AAACCAACCCTGGGA[A/C]AGCATACAGAGTCTA	19165
rs240558310	snp	A/C			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264268	CCCCTCCCTCCTTCA[A/C]CCTTTCCCACCCGAC	19165
rs240558948	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180235874	CTCTCAGGCAGCTGC[A/G]AGCGGCACAGGAGGC	19165
rs240633992	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180252814	AAGTTTCTTTCTGAG[A/G]TGTAACAGGAAGGCG	19165
rs240703569	snp	C/T			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258778	AAGCCTTGCTTCTCA[C/T]GAGGTAGATGAACAG	19165
rs240764940	snp	C/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258150	ATGATGACTACGTGG[C/T]AGACAGCGCAGAATC	19165
rs240813657	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180239575	CATTGCTGCTGCTGC[C/T]GCCTCCACCACCACC	19165
rs240901496	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180231655	GACTTTGCCTCCTCT[C/T]GCTGCCTCCTTAATC	19165
rs240914476	in-del	-/TTG			intron-variant	Psen2	Mm_Celera	1:180252056	TGTTTTGTTTTGTTT[-/TTG]TTGTTGTTGTTGTTT	19165
rs240924366	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264289	CCCACCCGACCATGC[A/G]TGGCCTCCAAGTACA	19165
rs240965613	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180248861	CAAAAATATGTGCTG[C/T]AGTTATTTGTTATCA	19165
rs241009100	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180250499	ACCTGCTTTTCAACA[A/G]TGGAGAGAGGCACAG	19165
rs241018391	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180249511	CCTCATTGACTTCTA[A/G]CTCACTATGTAGCTA	19165
rs241168242	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180240963	GTGGGAAAACACATG[G/T]TGAGGGCCACAGAGG	19165
rs241208284	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180237817	AACTGGTGATGTCAG[C/T]TTCAGGAACATGTCC	19165
rs241233847	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180230173	CTGGCAATAATGGTG[A/C]TCAGTGAGCGGCTTG	19165
rs241297462	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180228439	CCAGCTTGAGTGCCA[A/G]CCATCAGAGCCTCCA	19165
rs241350452	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247272	GAGGGAGGTGGAGAG[A/G]ACCAGGCGCTCCGTC	19165
rs241359239	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180229250	CAGCCTAGGCAGAAG[A/C]CTGGTACCTCAGGGA	19165
rs241413809	snp	C/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247875	CTTCCGTATCTCTTC[C/T]GGCAACAGTGAATTC	19165
rs241416298	in-del	-/A			intron-variant	Psen2	Mm_Celera	1:180253706	CCTGTCTCAAAACAC[-/A]AAAACATTTTTTTTT	19165
rs241454420	in-del	-/G			intron-variant	Psen2	Mm_Celera	1:180236682	TTAGGAGATGGGGGT[-/G]GGGGGTATCAATAGA	19165
rs241475220	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180248521	CTCAGGAAGGCCAGG[A/G]AACCTCTTACCCAGT	19165
rs241477244	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180237234	AGTGGTGAGGGCAAG[A/T]CTCCTGAGGGGCTTG	19165
rs241480601	in-del	-/CTGAT			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261960	GACTTCCCTCGATGC[-/CTGAT]CTGTAAGCCTAAGGC	19165
rs241538598	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180237887	TGAGCCAATAGCCAG[C/G]TCCCTCCCTGAACCA	19165
rs241562386	in-del	-/CACA			intron-variant	Psen2	Mm_Celera	1:180235290	TTGCTTGACGCACAG[-/CACA]CACACACACACACAC	19165
rs241773506	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259953	ATCTGCTTCACTGCC[C/T]TGAGTGACACTTGAG	19165
rs241804446	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180234283	GGTTTGTATATACTC[G/T]GCCCAGGGAGTGGCA	19165
rs241874409	snp	C/T			downstream-variant-500B	Psen2	Mm_Celera	1:180226793	GCCATAGCCAGGGAT[C/T]TATGTGGTTCCAGCA	19165
rs242114161	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180232619	TTGCAAAACTTGGCT[A/G]TGAAGTCCTTGACCT	19165
rs242122445	in-del	-/G			intron-variant	Psen2	Mm_Celera	1:180240159	CCATGGGGCAGGGGT[-/G]GGGTGGGGTGGGGGT	19165
rs242165655	snp	A/G			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254380	AAGCCAGCCCTCTTA[A/G]CTGCTGAGCCATCTC	19165
rs242178887	snp	A/G			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258792	ACGAGGTAGATGAAC[A/G]GATGAGCAAATGGGT	19165
rs242607470	in-del	-/AC			intron-variant	Psen2	Mm_Celera	1:180231462	TGATCGTATGCTCAT[-/AC]AGACACGTATGCACA	19165
rs242792567	snp	C/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256625	TCCTCCGGTTTCATG[C/T]ACTTTAAAATGGAGT	19165
rs242807698	snp	A/T			intron-variant	Psen2	GRCm38.p3	1:180244760	CCACTGCACACTGTG[A/T]TTGTGTAGTCTATTA	19165
rs242809835	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180253671	AGAGTACCAACCCAA[C/G]CAGGGCTACGCACCA	19165
rs242861493	in-del	-/A			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257254	CACCACCATCACTGC[-/A]AAAAAAGTAATCATT	19165
rs242874650	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180245804	AGTGGGGACATGGGG[A/G]ATGGTTTAGTGGCTT	19165
rs243011664	in-del	-/CCACGGCC			intron-variant	Psen2	Mm_Celera	1:180247965	GGCCTTGGGTTTCAT[-/CCACGGCC]CCACATCAAAGTTAT	19165
rs243040838	in-del	-/A			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254958	GGTCACCTCTAGGCT[-/A]AAAGTCGGGATGCTG	19165
rs243052821	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261684	AGCCCTCTGGATTGT[A/G]CAGTTTGTGGGTTTT	19165
rs243120574	in-del	-/TC			intron-variant	Psen2	Mm_Celera	1:180228814	AAATGACCCACGAGT[-/TC]GCCCACACCCACCAC	19165
rs243125956	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180239371	TTAAGTCAGATTGTC[C/T]AAGTGAGTGTATCTG	19165
rs243185082	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180239830	TTTTCATAATACACA[C/T]GCATTGGTCCCATTG	19165
rs243204906	snp	G/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246929	TGGAGGTAGAAGCAG[G/T]CCTGCTCTTTGTTGA	19165
rs243242626	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180240370	TGAAGTCGCTCAGTG[C/T]TTGAAACACAGTGGG	19165
rs243244676	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180231875	GACACAATGTGCACA[G/T]GCTTGTTTGAACTCT	19165
rs243416028	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180236830	TAAACAGCCAAACCT[G/T]GCTTGTTAGGACTGA	19165
rs243490253	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180229086	AGTGAGGGGCCAGGA[C/T]TTGAGCCAAGCGACC	19165
rs243615782	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180237410	CTTCACTTAAGGACT[A/G]TCCGCGGTCACCAGC	19165
rs243617382	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180228787	TTGCCCTAAGAGGGG[A/G]GACAGCAACAATAAA	19165
rs243652054	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180231218	CGGGAAGGGGGGCAT[A/T]TGAAATGTAAATTAA	19165
rs243673074	snp	A/G			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180229432	GTAGCCAGGCAGGGG[A/G]GCTTCGAAGGCTTCA	19165
rs243760079	snp	C/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264213	CGACTTCTCCCCTCT[C/G]ATCACCTCCCCTCTC	19165
rs243767585	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180248184	CAGGGAGCAGGGACC[A/G]AGGAATGGATGTAGC	19165
rs243801738	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180232265	TGGGTTGTTTCTCCG[C/T]GTCCAAACCGGCTCT	19165
rs243813378	in-del	-/ATAT			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260528	CATATATAAACATAC[-/ATAT]ATAATGTACATATAG	19165
rs243826236	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180263807	AGGCCAGAAGAGGGC[A/G]TCAGAACCCTGGGAG	19165
rs243829070	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180249001	TCAGTGGTCAAGAAC[A/G]TGAAGTGGAAAATTC	19165
rs243875716	snp	G/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262957	AAGAGAGAACTCACC[G/T]GGAGGACGTAGCTGT	19165
rs243883747	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180238272	AGAGCGGACTCCTGA[C/T]CATGACAGGCGCATG	19165
rs244139999	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180241322	TGGAGCATCAAAACA[C/T]GGGGCTGCCTCAGTA	19165
rs244167757	in-del	-/CTCTCTCTCA			intron-variant	Psen2, Gm31728	Mm_Celera	1:180263209	TGTCTCTCTCTCTCT[-/CTCTCTCTCA]CACACACACAGATAG	19165
rs244197861	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180244892	CACAAGAGTCAGCTC[G/T]CTCTCTCTCTTCCCC	19165
rs244259286	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180234213	AGGGGAATGTCCTGT[A/G]TGCCTTCCCACTTGT	19165
rs244341547	snp	G/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180256794	GCAGGGAGGGGTTGT[G/T]ATCGCAGGATCGGTC	19165
rs244513006	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180250374	CTACCTACCCTCTGC[C/T]GACTTTTACTAACTT	19165
rs244553164	snp	A/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180263849	TTACCGACAGTCTTG[A/T]GAGCTGCGATTTTGG	19165
rs244606726	in-del	-/CGA			intron-variant	Psen2	Mm_Celera	1:180239583	TGCTGCTGCCTCCAC[-/CGA]CACCACCACCGCTGC	19165
rs244622451	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180239771	GCAGAGAGCCACTGT[C/T]GGACTAGCTAATCTT	19165
rs244740821	snp	A/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262064	CTCCTTGCTTTATAC[A/T]CACCCGGGATCTTGC	19165
rs244933708	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180253793	AGTTTGGATACAGGT[A/C]AGAGGTGACTGAGCA	19165
rs244947085	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259413	CTCTCCCCTCTTCTT[C/T]AGGGTCCCAACCCTA	19165
rs244957135	snp	A/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259878	CTTGTTACATCAGTC[A/T]TGAGGTAGATACGCT	19165
rs244967312	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180252412	GTTAGTAAAAGCAAT[A/G]AAGACATTTTCAATG	19165
rs245008355	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246062	GTGCTTGGCTCCGGA[A/G]CTCTAGCCTCGAATA	19165
rs245026044	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180253015	TAAACCCGGGGAGGA[A/T]AGACTGCATGTGGAC	19165
rs245139318	in-del	-/G			intron-variant	Psen2	Mm_Celera	1:180250115	GAAAAATCACCACTC[-/G]AACTAATGAGCATAG	19165
rs245238473	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180251844	GGTCTCTAAACTGCC[C/T]ACAGAACGATGTCAT	19165
rs245311748	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180252012	GCCCCTGCCCACTCC[C/T]AGATCATTCCAGCTC	19165
rs245372059	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180232612	CCATCTTTTGCAAAA[C/T]TTGGCTGTGAAGTCC	19165
rs245427621	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180233075	TATGCCACACACAGG[A/G]GCTACGGGTAAGTAG	19165
rs245556215	in-del	-/A			intron-variant	Psen2, Gm31728	Mm_Celera	1:180263049	ACCCAGGAAGGAAGT[-/A]AAAAAAAGACACAAC	19165
rs245612532	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260504	ATAAACATACATATA[A/G]AATGTATACATATAT	19165
rs245693110	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180234898	TAGCTTCTGTCAATG[A/G]CTTTGGTCACAGCAA	19165
rs245851873	in-del	-/AA			upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180264443	AAGTATCATAGTAAG[-/AA]AAAAAAAAAATCTAC	19165
rs245893614	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258217	TCATCCATGAGGCCT[A/G]TGTTCCTGTGGGCTG	19165
rs245977210	snp	G/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257044	CAAGGTCATTCCTAG[G/T]TACATAGCAAGTTCG	19165
rs246015538	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180230502	CTCTTGCTTGCCAAA[C/T]TCTTTCATGGGATTT	19165
rs246078754	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180231265	TTAAAAAAAGGAAAT[A/G]ATTTTCAGTCCTGAG	19165
rs246083742	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	Psen2	Mm_Celera	1:180227439	GACACGTTTTTATTC[-/T]TTTTTTTTTTTTCTT	19165
rs246094299	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180238725	CAGTGCCAGAGAGCA[C/T]AAAGAGGCAATCTAT	19165
rs246197935	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180231004	CATGAAGGGACCTAT[A/G]GGCTCCAGCTGCATA	19165
rs246384037	snp	C/G			downstream-variant-500B	Psen2	Mm_Celera	1:180226678	CCCCTAGCCCTTTGG[C/G]TTTCTGGCTTCTACT	19165
rs246444413	snp	A/G			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180227684	GGGGAGGGCGGGCAG[A/G]GCCTTCTTGAACACA	19165
rs246739318	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180236910	CTCTGTGGCCTGAAG[-/C]CCTGGACAGCCTTCT	19165
rs246755229	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180249211	CACTTACAGTATCCA[C/T]CCATCTGACGAGGAC	19165
rs246755584	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180257656	GGGGCAGGGGGCAGC[A/G]TGGATCCTGAACAGA	19165
rs246810198	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180249752	CTCCTCTTGAGATAA[A/G]GTCTCACTAAGTAGC	19165
rs246837877	in-del	-/GTGTGTGTGTGTGTATGCATGC			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264876	TTTTTACATGCGTGA[-/GTGTGTGTGTGTGTATGCATGC]GTGTGTGCGTGTGTG	19165
rs246893598	in-del	-/AATATCGT			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261087	CCTATATTGACACAG[-/AATATCGT]AGCCAAGACATGTGA	19165
rs247116612	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180253913	GCCCCCATCCCTGAC[A/G]CCCACACCCCAGAAC	19165
rs247116648	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180245441	AGCTCACAAGTGCGG[A/G]TCACTCCAGCTCCAG	19165
rs247120757	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262271	TTTACATGACACACT[A/G]AGAGTTGTATAACCG	19165
rs247170968	snp	C/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246213	TTGCTGGAGGTGGAG[C/G]GAAGAGTGTGCAGAT	19165
rs247291437	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180236426	ACTCTGTTTCGAAAA[A/C]CCAAATGATGGACCC	19165
rs247435413	snp	C/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180265446	GTGTTATCTACGTGA[C/T]ATAGAAGAATCACTT	19165
rs247497987	snp	C/T			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254987	TGGCCCCTTCACCAA[C/T]GGAAAACACAGGATC	19165
rs247625742	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180248069	TGTTGTGGTAAGTAC[A/T]CAGTTCAAGAGTTTA	19165
rs247663199	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259641	TCCTGACTGTGGAAG[A/G]CAGTGTCCTCACTGC	19165
rs247696067	snp	C/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247245	GACAGCTGCAGAATA[C/T]CACAGGCACAAGAGG	19165
rs247769791	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180236035	GATGAAGACACTCCA[G/T]CGAGAGAGATACTTC	19165
rs247805178	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180253064	GGCCATAGCCCGACA[A/G]GTGAGCTGACAGTGA	19165
rs247854430	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180240292	TGTGCTAAGACATCA[C/T]TGGGTCCAACCCTGT	19165
rs247928977	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180240472	TAGCCTTTGGTGAGT[A/C]CTGTATGACAGCTCA	19165
rs247949646	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180232470	GCCCAAGCCTACCTC[A/G]GGGTCTTTGTACCAG	19165
rs248014125	snp	A/C/T			intron-variant	Psen2	GRCm38.p3	1:180244161	CACCGCACACTGTGA[A/C/T]TGTGTAGCCCACTGT	19165
rs248060696	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180248535	GGAACCTCTTACCCA[A/G]TACCTCCCACTCCTA	19165
rs248109967	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180237960	AACACAAGGGCCCAC[A/G]TTTTGCCCGTGGCAG	19165
rs248111656	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180249374	ACAGGACTTGGAAAA[C/T]TATTACAAAATATTA	19165
rs248138569	snp	C/T			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255735	GCCCTGTTGGGCGCC[C/T]CGCTCCTCATACAGG	19165
rs248162072	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180238580	AGGGAAACTAAAACA[C/G]AACTTCAGAAGAAGT	19165
rs248452586	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180234105	TGCAGGCTGCTTGAT[A/G]AGCGGCAAATGTGGG	19165
rs248568061	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180238194	AGAGATAGCCCAGAG[A/G]GTGAAGGTGCTTGCT	19165
rs248667866	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180228112	GGTGTTGTGTAAGCC[A/G]TCCCTTTGGAAGCAA	19165
rs248683989	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262834	ACAAGAGTCAGGGCT[A/G]AACCGAAGACAGCTG	19165
rs248698373	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262704	TATAGCTCTCCTCGG[A/G]GAGGACAGACTGTCT	19165
rs248814876	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180231601	GGTCCCTCCCTGCCT[C/T]GGCCACTGTATCAAG	19165
rs248828129	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180230388	CTACTTTGGTGTCTC[C/T]GTGTTCTAGGAGACA	19165
rs249013019	in-del	-/A			intron-variant	Psen2	Mm_Celera	1:180250516	GGAGAGAGGCACAGG[-/A]TTGCCCTGATGTTTA	19165
rs249016811	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180231492	CACCCAAACTAAACA[C/T]TTTTAAATGCAGTGC	19165
rs249022704	in-del	-/ACTCGGACA			intron-variant	Psen2	GRCm38.p3	1:180248066	TCTGTTGTGGTAAGT[-/ACTCGGACA]ACACAGTTCAAGAGT	19165
rs249078846	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262896	TTCTCTCTCAGATCC[A/G]TGGCTGCTCCAACAT	19165
rs249133274	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180249920	AGGGTTTCCTCCCCC[G/T]CCAGAATCACCTGCT	19165
rs249163592	in-del	-/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180263834	GGAGCCGGAATGGAG[-/T]TACCGACAGTCTTGA	19165
rs249283710	snp	A/C			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180256168	ATGCTGCCGGCTACC[A/C]GCGATCGGTGACAGG	19165
rs249359686	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180235643	GACTCTGGGGGGTTT[C/T]CACCTGCTCAGTGCA	19165
rs249361024	snp	A/C			downstream-variant-500B	Psen2	Mm_Celera	1:180226859	GAACTTTTTAGTTAA[A/C]GAACCCAGTGCAGAG	19165
rs249415404	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180227905	ACACCTGCATATTGG[C/T]TACTAGGTGGACAGA	19165
rs249703879	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180232974	ACCCCAGAATCACAG[A/G]CTCTATACTCAGATA	19165
rs249741839	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246811	GCTCCAAGTCCCCAC[A/G]TTTTGGGTTCAGGCA	19165
rs249806863	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180235876	CTCAGGCAGCTGCAA[A/G]CGGCACAGGAGGCTG	19165
rs249810934	snp	A/C			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247736	TAGCTTCAAAGGTCA[A/C]CTTGCCCTGACATAT	19165
rs249876446	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180236850	GTTAGGACTGACAGA[A/C]ACACAGGTTCCACTG	19165
rs249889157	in-del	-/CC			intron-variant	Psen2	GRCm38.p3	1:180251415	TGGCAGGAGCTATTT[-/CC]CCCCCTCTATGAACA	19165
rs250098670	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180234765	ACGCTCTGCTTCCTG[A/G]TCCACTACAGGGAGC	19165
rs250156289	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180240191	GGGAGGGGGGAGAGC[A/G]CTGGGGTTAGGGAAG	19165
rs250217896	snp	A/G			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180240748	CTGCCCGTTCTTCTC[A/G]GTGTAGAAACGCACA	19165
rs250220161	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180232274	TCTCCGTGTCCAAAC[C/T]GGCTCTGGATTGTGC	19165
rs250245783	in-del	-/CGG			intron-variant	Psen2	Mm_Celera	1:180241110	AAAAAACTTAGAAGA[-/CGG]TGGTGGTGGAGGAGG	19165
rs250275292	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259241	CTAATTTCTATATTC[C/T]ATCTTGGCTGCTCTT	19165
rs250286225	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180232845	GAACATTTCTGGGAC[A/G]TGCTTTCAAGCCAAG	19165
rs250324709	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260372	TTTCTCTGATTCTCT[A/G]GGTTAATCTTAAGTC	19165
rs250475271	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180231538	TTCAGATCTGCGAAA[A/C]AAAACCCAGCTCTAA	19165
rs250806669	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180243605	GTAGCCCACTGCACA[C/G]GGTGACTGTGTAGCC	19165
rs250817542	snp	C/T			utr-variant-3-prime, nc-transcript-variant	Psen2	Mm_Celera	1:180227392	GGTAGCACCGAAGGG[C/T]GGCTTCTGCTTCCTC	19165
rs250820221	snp	C/T			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254618	GGGTATGGCTAGACA[C/T]TGCTCCAGGCTGACA	19165
rs250861222	in-del	-/T			intron-variant	Psen2	Mm_Celera	1:180232050	AGGCTTAATATCGCC[-/T]CCCCCCCACATACCC	19165
rs250967397	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259323	CTGCTCTGCTTCTTC[C/T]TCCTGCATGTTTTTA	19165
rs251028682	snp	A/G			intron-variant, downstream-variant-500B	Psen2, Gm31728	Mm_Celera	1:180258748	GTGGGCGTTGGGGGG[A/G]ATGTGGGAAGTTGGA	19165
rs251193948	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180259414	TCTCCCCTCTTCTTC[A/G]GGGTCCCAACCCTAA	19165
rs251267146	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180229331	GCATAGCATCTGACT[A/G]AAGGTATTTTTAAAT	19165
rs251272802	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180232088	CACAGCATCCCTGGC[C/T]CACCAGCCTGGCCCC	19165
rs251295634	in-del	-/ACAA			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264103	TGTGCATGGGGACAC[-/ACAA]ACAAACAGAAAAAAA	19165
rs251441380	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180250758	TTCCCAGAACTTCCA[A/T]AACCCCTGGAAAGTC	19165
rs251502252	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180239894	TTTTTCAGCCTAAGA[C/T]TCCCGCACCCTCTTC	19165
rs251589720	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180251594	AGGCCACCAGACTCA[C/T]GAACAAGAACAGAAC	19165
rs251619487	in-del	-/TT			intron-variant	Psen2	Mm_Celera	1:180249423	CTGGTTTGTGGGTGA[-/TT]TTTTTTTTTTTGGCT	19165
rs251622913	snp	A/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263548	AAATAGTTTTGCAAT[A/G]GTTGGATGACTCACA	19165
rs251629474	snp	C/T			synonymous-codon, nc-transcript-variant	Psen2	Mm_Celera	1:180228870	GATAAAACAGGCCAG[C/T]GTAGTGTTCCAGTCT	19165
rs251692660	snp	C/G			utr-variant-3-prime, nc-transcript-variant	Psen2	Mm_Celera	1:180227149	TTCATGACTGCACAC[C/G]GGCTTTCCACCTCTG	19165
rs251696105	in-del	-/TTATC			intron-variant	Psen2	Mm_Celera	1:180248044	GGCTAGAGTAGACTA[-/TTATC]TTATCTGTTGTGGTA	19165
rs251697227	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180249091	TGGTTTGTTGTTATC[A/C]ATCTTTTGCTGTGCC	19165
rs251746076	snp	C/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180257234	ATATAGAGACCATGT[C/G]TTCACCACCACCATC	19165
rs251844695	snp	A/T			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255726	CTGCCTCAGGCCCTG[A/T]TGGGCGCCTCGCTCC	19165
rs251884457	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261958	CCTGACTTCCCTCGA[C/T]GCCTGTAAGCCTAAG	19165
rs251893081	snp	C/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180256426	GCCTTCATCGTCGGT[C/T]TACAGGAAAACACTG	19165
rs251941122	in-del	-/C			intron-variant	Psen2	Mm_Celera	1:180234752	TAGCTCTGGTAAACG[-/C]CTCTGCTTCCTGATC	19165
rs251993872	in-del	-/TT			intron-variant	Psen2	GRCm38.p3	1:180251149	AATTTTTTTCCTTTC[-/TT]TTTGTTTTGTTTTTT	19165
rs252126792	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246134	CTTGACAAATGGCAC[A/G]TCGACAGAGGATGAA	19165
rs252148310	in-del	-/GGAAGCTAGGGAACTGCTAGGCCAC			intron-variant	Psen2	Mm_Celera	1:180251561	CAGCTGCCCTTCTTT[-/GGAAGCTAGGGAACTGCTAGGCCAC]CAGACTCACGAACAA	19165
rs252168139	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180236938	TCTCAGCTACACAGG[A/T]AAGGCAGACCCCTCA	19165
rs252235334	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180237767	TCTCTCTGGAGTATC[A/C]ATGGGAACCCTGCCT	19165
rs252235436	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180229198	AAAGTCTGGGGGCAT[C/T]GGGGTGTGGGGATGG	19165
rs252292229	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180229981	TGACCTGGAGGAAGT[A/G]GAGCCGGGCTATCTA	19165
rs252294907	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180228031	TTGTTTGCATTTACA[A/G]GAGACCCAGATGAGC	19165
rs252409230	snp	C/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264238	CCTCTCCTGTCTTTT[C/T]TCTTCTCCACTCCTC	19165
rs252543631	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262316	GGGCACAAATCCATA[A/G]GCCCCAGGAGTGCTT	19165
rs252779450	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180237445	CCCACTGGGTCTCCA[A/G]CAGTCTTCCTGGAGG	19165
rs252854933	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180244307	AGCCCACTGCACACT[A/G]TGACTGTGTAGCCCA	19165
rs252866227	snp	G/T			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255212	ACTCCAAGAGACTAT[G/T]CTGGGGACGGAGTTA	19165
rs252878557	snp	A/G			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260187	GGTTGTTTTGCTGCT[A/G]TGCTAAGGAAATCTG	19165
rs253221492	in-del	-/TTTTCTTC			utr-variant-3-prime, nc-transcript-variant	Psen2	Mm_Celera	1:180227448	TTATTCTTTTTTTTT[-/TTTTCTTC]TTCTTCTTTTGTAAG	19165
rs253277815	snp	G/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264132	AAAAAAAAATGGAGA[G/T]CAAAGCTTTTCCATA	19165
rs253402134	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180229732	AGGTGTCAGAGTCTG[C/G]CCGTCAGGCAGTGCC	19165
rs253424479	in-del	-/A			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247809	CCCTTCCTCTTTGAG[-/A]AACTGGCTGTCTGTC	19165
rs253430353	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180251780	ACCAAAGCCCAGGGG[A/T]GCTGGGGATGAAGCG	19165
rs253482497	snp	C/T			intron-variant	Psen2	GRCm38.p3	1:180241016	TCCTGCAGCGGCTTT[C/T]CGAAGTAGGCCTGAG	19165
rs253535562	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180241702	CAGCCTACATCAGAA[A/C]GGCAGGTGAGGGGTG	19165
rs253584605	snp	A/C			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260837	TCTTATCCTTTCAGT[A/C]ATTTAAGCCAGCAGT	19165
rs253700929	in-del	-/A			intron-variant	Psen2	Mm_Celera	1:180238167	TACAGAGAATTGTAG[-/A]AAGTGGGCTGGAGAG	19165
rs253728956	snp	A/G			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247876	TTCCGTATCTCTTCT[A/G]GCAACAGTGAATTCT	19165
rs253730480	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180236427	CTCTGTTTCGAAAAC[C/T]CAAATGATGGACCCC	19165
rs253736159	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180253527	GAAATCTACCTGCCT[C/T]GCAGTTTGGGGTTTT	19165
rs253790681	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180254128	CAGTTCTCTTGCTTC[A/G]GTGATTATGCACTGG	19165
rs253902672	in-del	-/G			intron-variant	Psen2	Mm_Celera	1:180229037	AGCAGGCAAAAGAAA[-/G]AAAAAAAAAAAAAAA	19165
rs253903218	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180232637	AAGTCCTTGACCTCT[A/T]GCCCTCCCTTGTCTT	19165
rs254039498	snp	C/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258001	ACCACCAGAGGCAGG[C/T]AACTTATAACAATAG	19165
rs254122977	in-del	-/CA			intron-variant	Psen2	Mm_Celera	1:180249328	TAAACATCTGAATTT[-/CA]CACACACACACACAC	19165
rs254159050	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180231398	CTCTCATACTAGCTC[G/T]GAGGGAGCGGATGTC	19165
rs254162411	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180250840	CTGCGACATCTCACA[C/G]ATTCCAGACTTACTT	19165
rs254230416	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180239934	TGTAGCTGCAGGTAC[C/T]GTCCCCACTCTGGAA	19165
rs254279849	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180250634	GGAAACTCTGGGCCA[C/T]AAACAAGTCTATCTG	19165
rs254283661	in-del	-/T			intron-variant	Psen2	Mm_Celera	1:180245548	ACGCATAATTACAAA[-/T]TAAAAAAAAAGACAC	19165
rs254359027	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180261403	TAAGGGCTTGGTCCC[C/T]TGAGACTTACCCCTC	19165
rs254378713	snp	A/G			intron-variant	Psen2	GRCm38.p3	1:180242433	AGCCCACTGCACACT[A/G]TGACTGTGTAGCCCA	19165
rs254531291	snp	C/G			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180263824	CAGAACCCTGGGAGC[C/G]GGAATGGAGTTACCG	19165
rs254629268	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180228645	AACCAAGGGACAAGG[C/G]CCTAAAGCTCTCATC	19165
rs254644395	in-del	-/GC			utr-variant-3-prime, nc-transcript-variant	Psen2	Mm_Celera	1:180227399	CGAAGGGTGGCTTCT[-/GC]GCTTCCTCATCACGA	19165
rs254861102	in-del	-/TAA			intron-variant	Psen2	GRCm38.p3	1:180251275	CCCCAGTGCTAGGAT[-/TAA]AGGAGTGTGCCACCG	19165
rs254870990	snp	C/T			downstream-variant-500B	Psen2	Mm_Celera	1:180226529	GCCCCAGCAGGGCAG[C/T]AGCTTCTGTGGTCTC	19165
rs254889420	in-del	-/CC			intron-variant	Psen2	Mm_Celera	1:180230942	TGTCAACTAACCAGA[-/CC]CCCCCCCCCAGAGCT	19165
rs255220702	in-del	-/TT			upstream-variant-2KB, intron-variant	Psen2, Gm31728	GRCm38.p3	1:180263704	TTGATAAAGGAAGTC[-/TT]TTTTTTTTAAAAATT	19165
rs255296567	snp	G/T			downstream-variant-500B	Psen2	Mm_Celera	1:180226610	AGGCAGAGAGAAGCT[G/T]GCCTGCCTTTCATCG	19165
rs255554526	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180240374	GTCGCTCAGTGTTTG[A/T]AACACAGTGGGCCAG	19165
rs255559943	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180254283	TGTGCCTGGTATCCA[C/G]AGAGGTCAGAAGAGG	19165
rs255626003	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180232510	TTTCCTCACCCGCTG[G/T]CCTCCAGATTTGTAC	19165
rs255626075	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180241085	CTCTGATTTAAGTCT[C/T]GGGATATATAAAAAA	19165
rs255730413	snp	A/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260502	ACATAAACATACATA[A/T]AGAATGTATACATAT	19165
rs255755126	snp	A/C			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180246482	GCTAGACAAGGTTAG[A/C]CCAGGCTAGACCAAG	19165
rs255794771	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180263303	CTATAAATCCATTAT[C/T]GTCCCAATTAATTTT	19165
rs255804327	snp	C/G			intron-variant	Psen2	Mm_Celera	1:180229161	AGTATTGCAGACTAG[C/G]GACAAGATGGACTTC	19165
rs256094264	snp	G/T			intron-variant	Psen2	GRCm38.p3	1:180245809	GGACATGGGGGATGG[G/T]TTAGTGGCTTGAACA	19165
rs256149166	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180235246	GGGTATGGGGCACTC[A/G]GGGGTGGGGAGAGGT	19165
rs256151030	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180230310	TTCAACAGTAATTTC[A/G]GTCTGCTCACTGTCC	19165
rs256228721	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180231001	ACACATGAAGGGACC[C/T]ATGGGCTCCAGCTGC	19165
rs256271930	snp	G/T			intron-variant	Psen2	Mm_Celera	1:180251323	TTTTTTTCTTTAAAT[G/T]AGACACAGCAGCCAG	19165
rs256332347	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180230797	AACGGGAATCCAATG[C/T]CCTCTTGTGGCCTCC	19165
rs256515736	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180231691	ATGCCTGTCCTTTTG[C/T]CGATAGCTCAATTCA	19165
rs256577939	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180249641	AGCCCAGGGCCTGCC[C/T]GCTAGGTAAGTACTT	19165
rs256633000	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258031	GAAATGTGTTTTTCC[A/G]CTGTTCTGGAGGCTG	19165
rs256696518	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180250319	ACAGGCTGTTCTGGA[A/C]GCCCTGCCGGCATGG	19165
rs256856446	in-del	-/CTGTTTCCTCT			intron-variant	Psen2, Gm31728	Mm_Celera	1:180260877	GTTTGGATTTACACA[-/CTGTTTCCTCT]CCTACAACAAACAGA	19165
rs256990714	snp	A/T			intron-variant	Psen2	Mm_Celera	1:180245198	TGGGGCCTCCTCCAA[A/T]GATTTGCCACTCTCC	19165
rs257047440	snp	C/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258100	GGAGAGGACTTGCGT[C/T]CTAGTTTATAGGTAG	19165
rs257067878	snp	A/C			intron-variant	Psen2	Mm_Celera	1:180234275	CTCAGGATGGTTTGT[A/C]TATACTCGGCCCAGG	19165
rs257081729	snp	A/G			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180255321	CATATCTTTAAAGAA[A/G]AATCCCTAAGCAGAG	19165
rs257109324	in-del	-/CCCCCCCA			intron-variant	Psen2	Mm_Celera	1:180233575	AGGCCACCTGCTGAC[-/CCCCCCCA]CCCCCAGTGTCTGGC	19165
rs257116329	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180265377	GCACCAAAAATAAAG[A/G]TCTGGGGGTAGTTGG	19165
rs257184686	snp	C/T			upstream-variant-2KB, intron-variant	Psen2, Gm31728	Mm_Celera	1:180264493	TCTACAGGTTGGGGG[C/T]GGAGCATGTATGTGC	19165
rs257221418	in-del	-/GGG			intron-variant	Psen2	Mm_Celera	1:180238663	CAGAAGACAGTGGGT[-/GGG]GGGGGGGCGTACAGT	19165
rs257285016	in-del	-/AGGGGGC			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180257638	CATTACAGAGAAATG[-/AGGGGGC]AGGGGGCAGGGGGCA	19165
rs257311972	in-del	-/AAA			intron-variant, upstream-variant-2KB	Psen2, Gm31728	Mm_Celera	1:180254442	GTGATAACCACTGGG[-/AAA]AAAAAAATGGCTCTT	19165
rs257315024	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180240423	CAGAGCTCAAAACTA[C/T]AGTACCAGAGCTGGC	19165
rs257543692	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180235416	ATTTTCTGGAATGTA[C/T]CAGGGAGTGTATCAA	19165
rs257732379	snp	A/G			intron-variant	Psen2	Mm_Celera	1:180238704	CAGCACTTGGTCATC[A/G]TCCCACAGTGCCAGA	19165
rs257825642	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180253903	GGGCAGCTGGGCCCC[C/T]ATCCCTGACACCCAC	19165
rs257927407	snp	C/T			intron-variant, upstream-variant-2KB	Psen2	Mm_Celera	1:180247841	TATCTTAAACACACA[C/T]CCACTAGACCCGAGA	19165
rs257965950	snp	C/T			intron-variant	Psen2	Mm_Celera	1:180230320	ATTTCGGTCTGCTCA[C/T]TGTCCAGGAACGTCA	19165
rs258107659	snp	G/T			upstream-variant-2KB, intron-variant, nc-transcript-variant	Psen2, Gm31728	Mm_Celera	1:180258106	GACTTGCGTCCTAGT[G/T]TATAGGTAGTCTTAT	19165
rs258111338	snp	C/T			intron-variant	Psen2, Gm31728	Mm_Celera	1:180262069	TGCTTTATACACACC[C/T]GGGATCTTGCTGGTG	19165

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