SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3656611 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134296232 | CAGGAGAGGCAAGGA[A/G]CCTGTGAGGAGTTTC | 71007 |
rs3668877 | snp | A/G | 0.375 | 0.216506 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134515592 | TCTGCTGGGATCAGT[A/G]GATAAAGACAGATGG | 71007 |
rs3669956 | snp | A/C | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134515744 | TGAGCTACATTTCTT[A/C]GTCTAGCTTTGGAAG | 71007 |
rs3695686 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | D7Ertd443e | GRCm38.p3 | 7:134520450 | AACCAAACGAGGTCA[A/G]GGGGGATTTATGATC | 71007 |
rs6166875 | snp | C/T | 0.359862 | 0.224567 | intron-variant | D7Ertd443e | Mm_Celera | 7:134375021 | GTTACTCTATGACAA[C/T]CTTTGTGTTACTTAC | 71007 |
rs6167434 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134375127 | ctggcctgtaggcaa[A/G]catgtaatgcatttt | 71007 |
rs6167483 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134375154 | ttttcttgattgaca[A/G]ttgncatggagnggc | 71007 |
rs6167487 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134375158 | cttgattgacanttg[C/T]catggagnggcntga | 71007 |
rs6167502 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134375166 | acanttgncatggag[A/G]ggcntgatccactgt | 71007 |
rs6167517 | snp | A/C | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134375170 | ttgncatggagnggc[A/C]tgatccactgtnagt | 71007 |
rs6167536 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134375182 | ggcntgatccactgt[A/G]agtagtgcnagctct | 71007 |
rs6167552 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134375191 | cactgtnagtagtgc[C/T]agctctgggcaggtg | 71007 |
rs6167974 | snp | A/C | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134375227 | gactatataagaaag[A/C]aaactgagcaaacca | 71007 |
rs6168015 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134375248 | gagcaaaccacaggg[A/G]aaaagtcattaagca | 71007 |
rs6171478 | snp | C/T | 0.21875 | 0.248039 | intron-variant | D7Ertd443e | Mm_Celera | 7:134302334 | TCTGACAGGAGAAGC[C/T]CAGTATAAATGGGAT | 71007 |
rs6171514 | snp | G/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134302351 | AGTATAAATGGGATA[G/T]CGAGGATCTTGGCAA | 71007 |
rs6171547 | snp | A/G | 0.21875 | 0.248039 | intron-variant | D7Ertd443e | Mm_Celera | 7:134302371 | GATCTTGGCAATATA[A/G]GGTCAGCCAAGAAGG | 71007 |
rs6173829 | snp | C/T | 0.21875 | 0.248039 | intron-variant | D7Ertd443e | Mm_Celera | 7:134302783 | CACATGTAGAACTCA[C/T]GTTTCCATCACTGAT | 71007 |
rs6181754 | snp | C/G | 0.359862 | 0.224567 | intron-variant | D7Ertd443e | Mm_Celera | 7:134375432 | gaagcctgactgaaa[C/G]aGCCTTGCAGGGACT | 71007 |
rs6181921 | snp | G/T | 0.475309 | 0.108333 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134421377 | AGCAGTCCATGCTAC[G/T]CAGTTCTCTGGTCCC | 71007 |
rs6184253 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134421840 | aggggaaaggagGAA[C/T]GGTGGNTCAGGATCA | 71007 |
rs6184267 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134421846 | aaggagGAANGGTGG[A/G]TCAGGATCANGAAGA | 71007 |
rs6184698 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134421856 | GGTGGGTCAGGATCA[C/T]GAAGAAGTCAAGTGG | 71007 |
rs6190392 | snp | A/G | 0.5 | 0 | downstream-variant-500B | D7Ertd443e | Mm_Celera | 7:134265947 | GGTGGTGAAGATGCT[A/G]NCAGCTTTACTCAGT | 71007 |
rs6190393 | snp | C/T | 0.415225 | 0.187619 | downstream-variant-500B | D7Ertd443e | Mm_Celera | 7:134265948 | GTGGTGAAGATGCTN[C/T]CAGCTTTACTCAGTC | 71007 |
rs6191361 | snp | C/T | 0.290657 | 0.246672 | downstream-variant-500B | D7Ertd443e | Mm_Celera | 7:134266108 | CAGCCTCTGACACTC[C/T]AGGATGTGTACAGAA | 71007 |
rs6191930 | snp | G/T | 0.5 | 0 | downstream-variant-500B | D7Ertd443e | Mm_Celera | 7:134266199 | AGACTTTTGCAAAAA[G/T]TTTGGAAAAAAAAAA | 71007 |
rs6192011 | snp | A/G | 0.5 | 0 | downstream-variant-500B | D7Ertd443e | Mm_Celera | 7:134266250 | CCCAAAAAAAAAAAA[A/G]AAAAACAAGCATCCA | 71007 |
rs6193081 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | D7Ertd443e | Mm_Celera | 7:134266431 | TGATCCATTGCCTGC[C/T]GGACTGTTGCTTCTG | 71007 |
rs6198561 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134422156 | GTTTAAGACACTTCC[A/G]CCCCAACCAGCAGAG | 71007 |
rs6252254 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134425183 | tatttatttattttg[C/T]ggggaggagggggat | 71007 |
rs6265707 | snp | C/G | 0.429688 | 0.173817 | intron-variant | D7Ertd443e | Mm_Celera | 7:134465355 | AATCGTTACAGGTCC[C/G]AGACACATTCAGGAA | 71007 |
rs6266794 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134438548 | tctccatcaagacca[C/T]gcctcctaatccttc | 71007 |
rs6335161 | snp | A/G | 0.359862 | 0.224567 | intron-variant | D7Ertd443e | Mm_Celera | 7:134369436 | ACAAATGAGGCTGGC[A/G]CAGTGTCTGAAAGCC | 71007 |
rs6335697 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134369539 | GGGAGAGGCACCATC[A/G]CTGGGCTGGATCTGA | 71007 |
rs6335754 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134369562 | GGATCTGAGAGTACA[A/G]CACCAGAGGAAAAGC | 71007 |
rs6339111 | snp | A/G | 0.304688 | 0.243945 | intron-variant | D7Ertd443e | Mm_Celera | 7:134436089 | AAAGAGTTTGATGTT[A/G]AAGATTACAGTAAGT | 71007 |
rs6339563 | snp | G/T | 0.304688 | 0.243945 | intron-variant | D7Ertd443e | Mm_Celera | 7:134436161 | AGAAATCCATCATCA[G/T]CTGTAGAAGAAACAG | 71007 |
rs6340143 | snp | G/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134370354 | acctggtattgttag[G/T]caaacaaaccctttc | 71007 |
rs6340172 | snp | C/T | 0.304688 | 0.243945 | intron-variant | D7Ertd443e | Mm_Celera | 7:134436312 | CCATCTTGTGATTAC[C/T]TAAGCCTGTCCTGCT | 71007 |
rs6340757 | snp | A/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134436422 | AGAGCTGTTCACTCC[A/T]CGGAAGCCAAAAACG | 71007 |
rs6341159 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134436489 | TGTGTTATTTGGATC[A/G]NTTCCTTTCTTGTTT | 71007 |
rs6341161 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134436490 | GTGTTATTTGGATCN[C/T]TTCCTTTCTTGTTTC | 71007 |
rs6353727 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134370601 | GAAAGGCCTGGTTCA[A/G]tgacttcagaaaacc | 71007 |
rs6354162 | snp | A/C | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134370620 | cttcagaaaacctct[A/C]actcctcccaaagaa | 71007 |
rs6354760 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134370758 | tgaaatgacaggagg[C/T]ntggcctcgtngggc | 71007 |
rs6354762 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134370759 | gaaatgacaggaggn[A/G]tggcctcgtngggct | 71007 |
rs6354780 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134370769 | gaggnntggcctcgt[C/T]gggcttctttcattt | 71007 |
rs6354825 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134370798 | ttaacaGCTCCCTTG[C/T]GTTNTACATACACTG | 71007 |
rs6354838 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134370802 | caGCTCCCTTGNGTT[A/G]TACATACACTGTTCA | 71007 |
rs6355304 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134370853 | AAAGGGAAAGACTGC[A/G]TGGGAGCTGCTAGCC | 71007 |
rs6355352 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134370881 | GCCATTCAGCTGATG[A/G]GCATGTAGGCTGACC | 71007 |
rs6355745 | snp | A/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134370914 | GTctaccataaacat[A/T]tgtgtacaggtattc | 71007 |
rs6386154 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | D7Ertd443e | Mm_Celera | 7:134520649 | gctaagactgggcaa[A/G]tcanagacaagagaa | 71007 |
rs6386175 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | D7Ertd443e | Mm_Celera | 7:134520653 | agactgggcaantca[A/T]agacaagagaacagt | 71007 |
rs6386786 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | D7Ertd443e | Mm_Celera | 7:134520811 | TATGAGAGCTATTTA[G/T]CCATAGTTTAGTAAA | 71007 |
rs31010149 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134416717 | AGAGACAGAGACAGA[A/G]AAACTGAGACAGACA | 71007 |
rs31031889 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134405321 | CATGTGCACTGTAAT[A/G]TACCAGAACAGCTGG | 71007 |
rs31043666 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134423780 | AAGAAGAAGCCTAGA[A/G]GGCTTTCAGGGGAGC | 71007 |
rs31044124 | snp | A/G | 0.401235 | 0.199068 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134417756 | TCACAAGTTAATTTG[A/G]GTTGGTTTAATCTGA | 71007 |
rs31080497 | snp | A/C | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134513594 | GTTTATGTCTTGTAT[A/C]TCAGTCCGTTGAGTC | 71007 |
rs31087817 | snp | A/G | 0.188366 | 0.242283 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268676 | CAGGAGGCTTTTAAG[A/G]GGAAGAGAAAGGAGA | 71007 |
rs31101047 | snp | A/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134506403 | TCATCTGAGATACTG[A/G]CTTCTGGTCATGTCT | 71007 |
rs31111879 | snp | C/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134462713 | GTTAAATTTAATGGA[C/G]GAAAGATGCTCACGG | 71007 |
rs31128063 | snp | A/G | 0.456747 | 0.140554 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134425919 | CTATGTGTGCACTTC[A/G]ATAGTTTGAATGGAA | 71007 |
rs31128254 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134407555 | CTATACTATACCGGT[A/G]GTATTGTTGGTACCT | 71007 |
rs31140360 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134425603 | TCATGAGGTGTGTGA[A/G]AGTCTTACAGGAAGA | 71007 |
rs31147629 | snp | G/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134425960 | ACGGGCTGTCTTAGT[G/T]TGGGCTTTATTGCTT | 71007 |
rs31154498 | snp | A/C | 0.5 | 0 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134381524 | TATATATCTGGAAGT[A/C]CATACTGGGAGCCTT | 71007 |
rs31207027 | snp | C/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134506161 | TCTGTCATCACACCG[C/T]GGTGACTAAACATGT | 71007 |
rs31228206 | snp | A/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134513640 | AGACTGTGATCTTCA[A/G]TCTGATGAATAGGCT | 71007 |
rs31273666 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134513543 | CACCTTTGTATTCTA[C/T]CCTACCTGTCTCCCT | 71007 |
rs31311316 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134422326 | GTCCCGGTTCTGCAG[C/T]TTTAAGGATCTCTGC | 71007 |
rs31371519 | snp | C/T | 0.408163 | 0.193609 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134423531 | CAACCATCACGGTAA[C/T]GTAACAGGGTACTTT | 71007 |
rs31443773 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134406184 | TCTAAAGCCTCATGC[C/T]GTGCAGCTGAAGAGC | 71007 |
rs31455803 | snp | A/T | 0.5 | 0 | intron-variant | D7Ertd443e, Gm35970 | Mm_Celera | 7:134412436 | AACCACAGGCAACTG[A/T]GTGCATCTAAAAAAA | 71007 |
rs31488445 | snp | C/T | 0.375 | 0.216506 | intron-variant | D7Ertd443e | Mm_Celera | 7:134462054 | TATGGACATGCCCCC[C/T]GACATACACACACAC | 71007 |
rs31509277 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134398332 | GTCAGGATTCTCAGT[C/T]GCTATTCCTTTGAGG | 71007 |
rs31544678 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134408963 | ATGCTGCTGGGCAAC[C/T]TGTGAGCTGCACACA | 71007 |
rs31575300 | snp | C/T | 0.375 | 0.216506 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134417918 | GTGCATGCATGAATG[C/T]GCATGTATACAAGTA | 71007 |
rs31595542 | snp | C/G | 0.375 | 0.216506 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134461236 | AATCATTACTTTGTA[C/G]GTTCTTTATTTGTGA | 71007 |
rs31601321 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134412719 | AGGGAACCTTGGGAA[C/T]AGTCTTGCTTGCCTT | 71007 |
rs31617645 | snp | A/T | 0.359862 | 0.224567 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134508003 | TGAAATACAATACGT[A/T]TCAGCAAAACCCCTA | 71007 |
rs31622093 | snp | G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134409658 | TTGGGAACCTTCAAG[G/T]AGCTGATAGCCTAAC | 71007 |
rs31646253 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134398444 | AATCATAACTCTGAG[C/T]CCAAGGGCAGAGTTA | 71007 |
rs31650437 | snp | A/G | 0.401235 | 0.199068 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134416830 | AAGATTCACGAAACT[A/G]TATGCATAGGATAGG | 71007 |
rs31654399 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134406441 | TCTGGCCAGCCCCAT[C/T]CTCACTGGTAGCCAG | 71007 |
rs31662356 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134513106 | GAGGTCAACCATGTG[C/T]GTTACTCCCAGTAGA | 71007 |
rs31668143 | snp | A/G | 0.375 | 0.216506 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134417523 | TTGCTAGAGGCTGAC[A/G]TCTGGTTCTTTTGAA | 71007 |
rs31670913 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134508898 | TGACAACAGCAAGGG[A/G]ATGGAAACGATGCAT | 71007 |
rs31675917 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134425679 | AGAGATGAAGATGGA[A/C]GACGAGAGGTAGGAA | 71007 |
rs31705683 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134408645 | ACTCCCCAGAAGTTC[C/T]GAGATCCGTACGCTC | 71007 |
rs31709883 | snp | G/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134461965 | CCAATGAGAGAGACT[G/T]TCTCAAAAGAATAAG | 71007 |
rs31737641 | snp | C/T | 0.359862 | 0.224567 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134442950 | AGCTATACCACCCAT[C/T]CCAGGGCCATTGGAT | 71007 |
rs31771633 | snp | A/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134511535 | AGCACCTGAAAAAAA[A/T]GTTCAACATCCTTAA | 71007 |
rs31783536 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134403985 | GCTGAATGTTCAAAG[C/T]GCAGTGACAAATAGC | 71007 |
rs31883120 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134408398 | TGGTGTCTGTCTTTC[C/T]TTCTTTCTTTTCTTT | 71007 |
rs31894912 | snp | C/T | 0.375 | 0.216506 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134515404 | GAAATTGTAAGACAG[C/T]CACAATTAAATGTTT | 71007 |
rs31897519 | snp | C/T | 0.465374 | 0.126941 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134418042 | TGCCCTCCAACTAGC[C/T]GTTAGTGACATTACC | 71007 |
rs31906567 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134412681 | CAGCAGAGAGATACC[C/G/T]GATTCTCTACAGCAC | 71007 |
rs31938763 | snp | A/G | 0.484429 | 0.0868505 | upstream-variant-2KB, intron-variant | D7Ertd443e | GRCm38.p3 | 7:134378468 | AAGAGGCGCTAGTGC[A/G]CCAATCCTTGCCTGT | 71007 |
rs31939002 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134420378 | AGGAGAGTACGGTAT[A/G]GTGAAGAGAGAGGGG | 71007 |
rs31943382 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134506868 | TCTGGTCCATGGAGA[C/T]ATATAACCAGTAGGC | 71007 |
rs31946457 | snp | C/G/T | 0.46875 | 0.121031 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134424940 | GTGAAGAAGTTGTGA[C/G/T]GATGAGGGCTGAGAC | 71007 |
rs31948352 | snp | A/G | 0.487535 | 0.077957 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134421557 | ACAGAGACATGTGCA[A/G]GTTGAAGACACACCC | 71007 |
rs31951279 | snp | C/T | 0.33241 | 0.236027 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134518753 | GAATGGCTTCGATTC[C/T]AACTGTGTTCCAACC | 71007 |
rs31957114 | snp | A/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134412717 | AGAGGGAACCTTGGG[A/T]ACAGTCTTGCTTGCC | 71007 |
rs32065383 | snp | C/T | 0.487535 | 0.077957 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134417030 | CGTGAGATTTTATTC[C/T]GGATGGGTTTTTGCA | 71007 |
rs32068690 | snp | G/T | 0.387812 | 0.208586 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134417711 | CTGGGACCCTGTAAG[G/T]TTTGTATCTTATCCA | 71007 |
rs32110108 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134407420 | CTCCCTGCCTTCCCC[C/T]TCCCTTCTTTCTCTC | 71007 |
rs32173181 | snp | C/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134516785 | AGAGAAAGTGGGGGG[C/G]GGTGTTCATAATGCC | 71007 |
rs32197586 | snp | A/C | 0.475309 | 0.108333 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134288466 | GGATGAGATGCACAA[A/C]TTAATTGAATTAGAT | 71007 |
rs32206935 | snp | A/C | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134408467 | ATCTATAAAGAAAAC[A/C]TAAGGACTTTGCAGT | 71007 |
rs32248194 | snp | A/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134506314 | TCAATGAAATGGAAA[A/G]GGGGGAGTCTTTCAG | 71007 |
rs32248200 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134451633 | AGGATAGCTAAAACA[A/G]TCCTGAACTTCCAAC | 71007 |
rs32261285 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134407476 | CTCTCCTTCTCTGTC[C/T]CCTCTCTTTCTGTCT | 71007 |
rs32278178 | snp | G/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134398756 | TTGCCTGGCATACAG[G/T]AGGTCCTAGGGATCG | 71007 |
rs32306532 | snp | C/G | 0.429688 | 0.173817 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134308696 | GATGCAGAGAGTAAT[C/G]AGGACTAAAAACATT | 71007 |
rs32367861 | snp | G/T | 0.33241 | 0.236027 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134517053 | CAGCATGACCAAGAC[G/T]GAGCAGAGGAAGGCT | 71007 |
rs32382497 | snp | A/T | 0.5 | 0 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134425616 | GAAAGTCTTACAGGA[A/T]GAGTAGATGTCTGGA | 71007 |
rs32419096 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134398667 | ACTACAGTGTGAATT[C/T]AAGGCTACCCTGGGC | 71007 |
rs32431224 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134407759 | GTGGGGGACACCACA[C/T]AATGAAGCCTGCAGA | 71007 |
rs32453275 | snp | C/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134316632 | GCAAATCAAAACTAC[C/T]TGGAGGCTTCCATTT | 71007 |
rs32454116 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134411249 | ATCCATTTACAAATT[C/T]AGGAATGGTGTTTCT | 71007 |
rs32456755 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134287443 | GAAATGGAGATCTAC[A/G]CAACATTGATGAACT | 71007 |
rs32456763 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134408064 | AAACATCAACACTAC[A/G]AGCCATTGCCAGGCT | 71007 |
rs32463380 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134408423 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTG | 71007 |
rs32467554 | snp | A/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134506317 | ATGAAATGGAAAAGG[A/G]GGAGTCTTTCAGTCA | 71007 |
rs32470818 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134407761 | GGGGGACACCACATA[A/G]TGAAGCCTGCAGAGT | 71007 |
rs32487771 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134407966 | GCCTTTAAAAACAAG[C/T]ATATATAGCTTCCCA | 71007 |
rs32502854 | snp | A/G | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134420616 | GGGGAGAGAGAGAGA[A/G]AGAAAGGGGCCAGGG | 71007 |
rs32510093 | snp | A/T | 0.359862 | 0.224567 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134443218 | TTTTGTTCATTCTTT[A/T]AATTTCCACGTATTT | 71007 |
rs32517385 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134407416 | TCCTCTCCCTGCCTT[C/T]CCCCTCCCTTCTTTC | 71007 |
rs32527725 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134518921 | AATGGGAAATGTGTG[C/T]CCTCAGTTGGAAGGG | 71007 |
rs33351215 | snp | A/G | 0.375 | 0.216506 | intron-variant | D7Ertd443e | Mm_Celera | 7:134276188 | GACCACGCTAACTGA[A/G]GCAGTCAGGAACATA | 71007 |
rs33351218 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134276193 | CGCTAACTGAAGCAG[C/T]CAGGAACATACTCTG | 71007 |
rs33351221 | snp | A/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134276442 | AAGCTTCCAAGACAA[A/G]GAGGGTCTCTTTTCT | 71007 |
rs33352084 | snp | C/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134276465 | TCTTTTCTATCCATC[C/T]ATACTGCCCAGGTCA | 71007 |
rs33352087 | snp | A/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134276526 | CACCTCTAACGGGAA[A/G]ACATAAGATGCCCCA | 71007 |
rs33352090 | snp | C/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134276591 | AAGGGATCAAGCAAT[C/T]ATCATTAGTTCCCTC | 71007 |
rs33352093 | snp | C/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134276784 | GTAAACTCCAAAGGG[C/T]GTCAACATCCAAAGA | 71007 |
rs33352996 | snp | G/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134276852 | GTTTAGGAAATAGAA[G/T]GAACTCCACTTGGAA | 71007 |
rs33352999 | snp | C/T | 0.375 | 0.216506 | intron-variant | D7Ertd443e | Mm_Celera | 7:134277055 | CTAACTTGTACTGGA[C/T]CCATGTTACTGTGGC | 71007 |
rs33353002 | snp | A/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134277108 | AAACAAGTCAAGTTC[A/T]CCTGTGGGCTTCACA | 71007 |
rs33353735 | snp | A/C | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134277170 | CTCAATTGAATTGGC[A/C]CTTACAATGAATAAC | 71007 |
rs33353738 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134277198 | AACAAAGCCCTTATA[A/G]ACATCTTAGATGCTG | 71007 |
rs33353741 | snp | A/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134277470 | ACCAGTATTCAACAT[A/T]TCCATTAGCTGAATC | 71007 |
rs33354314 | snp | C/T | 0.459184 | 0.136902 | intron-variant | D7Ertd443e | Mm_Celera | 7:134277519 | GATCATGGAAGCTCT[C/T]GATGCCATGACAACA | 71007 |
rs33354317 | snp | A/G | 0.375 | 0.216506 | intron-variant | D7Ertd443e | Mm_Celera | 7:134277532 | CTTGATGCCATGACA[A/G]CACAGCATCAGGGCT | 71007 |
rs33354319 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134277617 | CCTGGTCATTTTGTC[A/C]GCTCAAGTTCTGCTC | 71007 |
rs33354322 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134277640 | TTCTGCTCTGTCTGG[C/T]AGGCTTCTCTCTCTT | 71007 |
rs33354646 | snp | G/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134271394 | AATATGAAGGCCCTC[G/T]TAGACCCTTTAAAGC | 71007 |
rs33354649 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134271461 | CCTTTGACTAAAAAA[A/G]GTACACTAGAGTAGG | 71007 |
rs33354652 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134272108 | CTCCTAGAGTGCTAT[C/T]GCAATGGGTTATATC | 71007 |
rs33355075 | snp | G/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134277699 | TTTCCAGGGCTCTGT[G/T]ACAGGCTCTTCATAT | 71007 |
rs33355078 | snp | C/T | 0.426035 | 0.177515 | intron-variant | D7Ertd443e | Mm_Celera | 7:134277869 | AAGGGCTCCAGCCCT[C/T]ACTTCCAGGTATTGG | 71007 |
rs33355081 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134278224 | CTTGTCAAAAGAACC[A/G]TAAGAGACATGGGTT | 71007 |
rs33355094 | snp | C/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134282724 | GACAATTTGTAAACT[C/G]CTTATGAGAACTTGC | 71007 |
rs33355097 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134282763 | TACTGGTACATAGAC[C/T]AGTAAGATTTCAGTG | 71007 |
rs33355100 | snp | C/T | 0.426035 | 0.177515 | intron-variant | D7Ertd443e | Mm_Celera | 7:134286674 | TGTCTATATATGATG[C/T]TATTTGTGACATCGA | 71007 |
rs33355103 | snp | C/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134287199 | GAAGGGACAGTGCAC[C/T]ATCATGAGTTTGTAT | 71007 |
rs33355114 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134267299 | AAGTACATTTGTAAA[C/T]CTAATGAAATTCATA | 71007 |
rs33355117 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134267394 | ATCTCAATGATGCTT[C/T]CCGGGCCGTGCAGCA | 71007 |
rs33355119 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134267453 | GGAAATCACCTCTCA[A/G]CCTGCCTTACCCAAC | 71007 |
rs33355120 | snp | A/C | 0.260355 | 0.249785 | intron-variant | D7Ertd443e | Mm_Celera | 7:134267459 | CACCTCTCAGCCTGC[A/C]TTACCCAACTGGTTT | 71007 |
rs33355122 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134267608 | CTTGCTTCTCTTAGC[A/G]CATGGCACGTCTGAT | 71007 |
rs33355484 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134272183 | AGTCAGGCTTCCATG[A/G]AGGTACAGGAAGACA | 71007 |
rs33355487 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134272302 | AGTCATTAAAGAAAG[A/G]ACTATGATATTTTTA | 71007 |
rs33355490 | snp | A/T | 0.35503 | 0.226867 | intron-variant | D7Ertd443e | Mm_Celera | 7:134272325 | TATTTTTATGATTAC[A/T]AGTGCAGTTTGTAAT | 71007 |
rs33355492 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134272557 | GTCTGGATCCTGGTC[A/G]TTGTGCATATTCAAA | 71007 |
rs33355616 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291454 | AAGTTGATTTGTCTC[A/G]GATATTTGTCGTAGT | 71007 |
rs33355619 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291534 | CATCTGTCTCTGCTT[C/T]TTACACAAACCAAAG | 71007 |
rs33355622 | snp | C/G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291572 | ACGGAGATCTTCCAA[C/G/T]GTTAGCTTGTGTGTG | 71007 |
rs33355634 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134300063 | TCCTGTACAGGAAAG[C/T]GTGGATCCATGACAC | 71007 |
rs33355637 | snp | A/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134300605 | AAAAAGATGTACAAA[A/T]CCCAACTAATTATCA | 71007 |
rs33355640 | snp | A/C | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134300644 | ATCTCTGCTAGCTAA[A/C]AGAGGTGATCTGCAC | 71007 |
rs33355643 | snp | C/T | 0.260355 | 0.249785 | intron-variant | D7Ertd443e | Mm_Celera | 7:134300679 | GGTTATTTGAATCAA[C/T]GTATTTCATATAGAT | 71007 |
rs33355875 | snp | C/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134296422 | GTCAATGTCACACTA[C/G]TTAGAGGTGCTTAGA | 71007 |
rs33355878 | snp | C/T | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134296458 | CTTCCAGTCTCCAAG[C/T]TCTTTCTCTTCTTCC | 71007 |
rs33355881 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134296497 | GATTTCCTCATTGTC[C/T]TACTTTCTCTTTAGG | 71007 |
rs33355906 | snp | C/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134287317 | CGAGCTGTTGAAGCC[C/G]TTGTTGGTCAAATAC | 71007 |
rs33355908 | snp | C/T | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134287522 | GACACGAAAAAGTCA[C/T]TTGAAAAACAAAACC | 71007 |
rs33355911 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134287779 | TGGGAAGGAAGGGCT[C/T]TGCACCAGAAGTCTT | 71007 |
rs33355944 | snp | C/T | 0.35503 | 0.226867 | intron-variant | D7Ertd443e | Mm_Celera | 7:134278328 | CCATCAGAGTTCATC[C/T]GAATTTTCCAAAATT | 71007 |
rs33355947 | snp | G/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134278329 | CATCAGAGTTCATCC[G/T]AATTTTCCAAAATTA | 71007 |
rs33355950 | snp | A/G | 0.18 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134278942 | GAGATTCTCTCTACA[A/G]TTTAAATTTTCTGGA | 71007 |
rs33355953 | snp | A/C | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134278947 | TCTCTCTACAATTTA[A/C]ATTTTCTGGAATATA | 71007 |
rs33356085 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134267740 | CTGGAAGGTTGTTTC[C/T]GCCTCCTCAACACAA | 71007 |
rs33356087 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134267775 | TTCAGGTGCTGATGT[C/T]GATTGGTTTTCCTCC | 71007 |
rs33356090 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134267929 | TTATAAGCATGAACA[C/T]AAAGTATGAAAGAAC | 71007 |
rs33356092 | snp | A/C | 0.408163 | 0.193609 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268005 | TAGTCACACTCAATG[A/C]GCATGATAGCTGGAA | 71007 |
rs33356295 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291638 | TGTCTATATATAGCC[C/T]AACTCTTTTTGACCA | 71007 |
rs33356298 | snp | A/C | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291728 | TGGCCTCTGGTCTTC[A/C]CAGTGCCTTGAGATA | 71007 |
rs33356301 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291788 | TTGTTGAGCCAGAGA[C/T]TAAACAGTCCCCTAG | 71007 |
rs33356416 | snp | C/T | 0.260355 | 0.249785 | intron-variant | D7Ertd443e | Mm_Celera | 7:134300743 | TGACATATCTGTCTT[C/T]TCCTAGGCCCTTGTT | 71007 |
rs33356418 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134300802 | ATTGTTCTAATATAA[C/T]AGCTGTGAGTTTATG | 71007 |
rs33356421 | snp | A/G | 0.336735 | 0.234472 | intron-variant | D7Ertd443e | Mm_Celera | 7:134301045 | GGAATGAGCAAAGTG[A/G]AATAAGAAAAGTTAG | 71007 |
rs33356505 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134272586 | AATATGTGCACAATT[A/G]GAGACTTCCCTCCAG | 71007 |
rs33356508 | snp | A/G | 0.297521 | 0.245442 | intron-variant | D7Ertd443e | Mm_Celera | 7:134272607 | TTCCCTCCAGAGAAG[A/G]AGAGAAGACCTTAAG | 71007 |
rs33356510 | snp | A/G | 0.165289 | 0.235211 | intron-variant | D7Ertd443e | Mm_Celera | 7:134272633 | TTAAGCAGAGACTCA[A/G]ACCCAATTTTGAATT | 71007 |
rs33356513 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134273648 | AGTTGACAAACTATT[C/T]CACCAATGGCACTTT | 71007 |
rs33356614 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134287808 | TTCAAGTAGCTCCTA[C/T]TTCCTGTTTCCTCTG | 71007 |
rs33356617 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134288029 | CTGCTGTTATCACTT[A/G]TCAACTGAGTCACAT | 71007 |
rs33356619 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134288220 | GGAGGTGTGGATAAC[C/T]CAATTCAGATGAAGT | 71007 |
rs33356622 | snp | C/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134288264 | GAGATACAGCGGGGA[C/G]GCTGGTGAGCCATGT | 71007 |
rs33356624 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134296535 | AGTAGCTCAGGCTAG[C/T]TCAGGTCCAGCCACC | 71007 |
rs33356627 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134296581 | TCCAAAGTTAATTCT[A/G]CTCTCTACCACTCTG | 71007 |
rs33356630 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134296785 | TCACCCAGACCTTCC[C/T]ACCTTAGAGATCTTC | 71007 |
rs33356633 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134296796 | TTCCCACCTTAGAGA[C/T]CTTCTTGACTGAGTC | 71007 |
rs33356656 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134279924 | AACTCCCCAAACCCA[A/G]CCTAAGATCTTAGAA | 71007 |
rs33356659 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134280174 | TGAATAAGTTCACTC[A/G]CCCTGCTTTGCAAGA | 71007 |
rs33356662 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134280206 | ATGGCGAAGGACATT[C/T]TTCACCAGCAGAAAC | 71007 |
rs33357015 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268122 | GGGCCAGCATTGGAA[C/T]CTCAAGAGGAACGCT | 71007 |
rs33357018 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268134 | GAACCTCAAGAGGAA[C/T]GCTTCCTACTTAACT | 71007 |
rs33357021 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268149 | CGCTTCCTACTTAAC[C/T]GTGAAGCACTGTGTT | 71007 |
rs33357164 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291823 | CACACCTAGACCAAG[C/T]CTGTGTCTACACCTA | 71007 |
rs33357167 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291864 | CTAGCTAGACACACA[A/G]TGTGATGGGCCAGCC | 71007 |
rs33357170 | snp | C/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291961 | ACAGGTAACTTGTCA[C/G]ATCCCTTGAATGGAA | 71007 |
rs33357173 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134292150 | TAAGCTTTGCTAAGC[C/T]GCACTTTATTGAATA | 71007 |
rs33357186 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B | D7Ertd443e | Mm_Celera | 7:134265820 | TTCCACGTTGGTTGC[A/G]AAAACTAATCTGTTC | 71007 |
rs33357191 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | D7Ertd443e | Mm_Celera | 7:134266059 | CTCTTCTGCTTCTTC[C/T]GTGTTCTGCCTCTCC | 71007 |
rs33357365 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134296858 | CCACATACTGCTCCT[A/G]AAACCATCGTCTGGA | 71007 |
rs33357367 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134296867 | GCTCCTGAAACCATC[A/G]TCTGGAATGTAAACC | 71007 |
rs33357369 | snp | A/G | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134296945 | CCTGCGATGGGTGTA[A/G]AGGGCCTTCCGACCA | 71007 |
rs33357372 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134297199 | GCTCAGAATCATTTG[A/G]ACAAAGATGTCTACT | 71007 |
rs33357396 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134273945 | GGTGAGTTTTACCTG[C/T]TCAGGTTCACAGTAG | 71007 |
rs33357399 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134273978 | CAGTGAGAAGCAGGA[C/T]TGGGTTCCAACTCCT | 71007 |
rs33357402 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134274218 | TTCTTACATGTCTGC[C/T]GTTTGCTCATGTGGT | 71007 |
rs33357404 | snp | C/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134301232 | AATTTTCTCAAAGTT[C/G]TGACTAAAATACATA | 71007 |
rs33357407 | snp | A/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134301964 | AGAGCATAGGGTCAT[A/T]ATGTGTCATCCACTT | 71007 |
rs33357413 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134302764 | ACAGTCCAGGCCAGG[C/T]TATCACATGTAGAAC | 71007 |
rs33357415 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134280240 | AGGCTTCAAACTGGT[C/T]ATGGAAAAACGCATG | 71007 |
rs33357418 | snp | A/G | 0.426035 | 0.177515 | intron-variant | D7Ertd443e | Mm_Celera | 7:134280251 | TGGTCATGGAAAAAC[A/G]CATGGTGTGAGAATC | 71007 |
rs33357421 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134280297 | AGGCAGCACAAATCA[A/G]CATATTCTAATGCCA | 71007 |
rs33357455 | snp | A/C | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134288399 | TGGGAGCATTGAAGA[A/C]GGAGAGGCTTAGGGA | 71007 |
rs33357459 | snp | C/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134288722 | TGCCATATTAAGTGT[C/G]GAGTCATCTCTTCAG | 71007 |
rs33357462 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134288871 | AAGGCCAAGTCTGAG[A/G]AGCTACAGTGAGAAC | 71007 |
rs33357754 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268260 | TGAGGGTTATGTAAA[C/T]GTGTGAATAAAGAAA | 71007 |
rs33357757 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268278 | GTGAATAAAGAAACA[C/T]GCCTTTGCTTCACGT | 71007 |
rs33357760 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268306 | CGTGAGAGTGACTGG[A/G]ACAAGGAACGAGAGA | 71007 |
rs33357763 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268324 | AAGGAACGAGAGAAA[A/G]CCACAAGGGAACTGG | 71007 |
rs33357866 | snp | A/C | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134292264 | AGATCTCATCCCTGT[A/C]TTCACAGTCATAAAC | 71007 |
rs33357869 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134292328 | TTGAGTTGGCAGGCC[C/T]TTCATAAGTTTCCTG | 71007 |
rs33357872 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134292410 | CTGTTTATGAGGGTC[C/T]ATGAAAATAAAAAAA | 71007 |
rs33358116 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134312278 | AGAAAGGGCCTCTGA[A/G]ATCCCAAAGGCTCTT | 71007 |
rs33358119 | snp | A/G | 0.277778 | 0.248452 | intron-variant | D7Ertd443e | Mm_Celera | 7:134318996 | CAGAAGTTCTTGGTG[A/G]TGCTTAAGGTTCTGC | 71007 |
rs33358122 | snp | G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134319464 | CCTCAAGCCTGGAGA[G/T]AAGTCCACCTCACTT | 71007 |
rs33358136 | snp | G/T | 0.32 | 0.24 | downstream-variant-500B | D7Ertd443e | Mm_Celera | 7:134266142 | GAACTTTGACTTAAA[G/T]TTCAGAACTGGCAGC | 71007 |
rs33358138 | snp | C/G | 0.32 | 0.24 | utr-variant-3-prime | D7Ertd443e | Mm_Celera | 7:134266568 | TCCATCCAGCGTCGT[C/G]GTCAGAAGTGTTCCC | 71007 |
rs33358140 | snp | A/C | 0.32 | 0.24 | utr-variant-3-prime | D7Ertd443e | Mm_Celera | 7:134266588 | GAAGTGTTCCCAGAT[A/C]CAGGGCTAGCAGAGC | 71007 |
rs33358141 | snp | G/T | 0.32 | 0.24 | synonymous-codon | D7Ertd443e | Mm_Celera | 7:134266764 | CTTCTGCTCGGAGCC[G/T]GTTACTCTGTAAGAT | 71007 |
rs33358194 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134280466 | CCAACCTGGTAGTGA[C/T]GAAGTAAAAATATTA | 71007 |
rs33358197 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134282185 | CCATCACTACAAACC[A/C]TCAACACAGGAGACA | 71007 |
rs33358200 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134282294 | TCACCAATTATCTGG[A/C]GTGTAAATGAATTAA | 71007 |
rs33358205 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134274705 | GGAAAAAGAGTACAA[C/T]TATATCTACTCCATT | 71007 |
rs33358208 | snp | A/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134274738 | CAGTGAAATGGAGGG[A/G]ACTTTTCGACAGTAC | 71007 |
rs33358211 | snp | A/C | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134274753 | GACTTTTCGACAGTA[A/C]AATTAGGAAGGTAAT | 71007 |
rs33358438 | snp | A/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134303206 | GAGGAAATAAAATGT[A/T]GAACGGGCTCTTTCC | 71007 |
rs33358441 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134305023 | AATAAAAGGAGTCTA[C/T]GCAAACACAATGTAT | 71007 |
rs33358445 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134297378 | ATAAGAACCAACTCC[A/C]TGTAACATTACTTTT | 71007 |
rs33358448 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134297584 | CAGAATTGTTCACTA[C/T]GGTATTTAGGAGTGG | 71007 |
rs33358450 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134297637 | TATGATGCCTATGTC[C/T]AGTTTGGCTATTTCT | 71007 |
rs33358453 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134297696 | TCCTGCCTATGTACA[C/T]TAGGGCCCAAATTGC | 71007 |
rs33358524 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134288911 | TCCCCAGTGTGTCAG[C/T]GGAGAACGGCAAGGG | 71007 |
rs33358527 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134289110 | GGTTAGCTTTTGTAC[A/G]TGGCTCAGTCTAACC | 71007 |
rs33358530 | snp | A/C | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134289280 | TCAGTTTTTCTCACG[A/C]AGCTCAATAATTGCC | 71007 |
rs33358533 | snp | C/G | 0.35503 | 0.226867 | intron-variant | D7Ertd443e | Mm_Celera | 7:134289348 | ATGTCTACACACCAG[C/G]ACCTTCCTGGCCTCT | 71007 |
rs33358586 | snp | C/T | 0.165289 | 0.235211 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268365 | CTCGCATGGGCAGTT[C/T]CTGAGATCCACAGGC | 71007 |
rs33358589 | snp | C/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268426 | ACTGGGAAGTTGAAA[C/G]AAAAGCTTCCATGTC | 71007 |
rs33358592 | snp | C/T | 0.408163 | 0.193609 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268452 | ATGTCCCACCTCTGG[C/T]CCTGCACTGTTTCCT | 71007 |
rs33358685 | snp | A/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134292758 | agtgagtgagtgagt[A/G]CCCTGCCTCTCAGGG | 71007 |
rs33358688 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134293002 | ACAGTGGTGTGGCTC[C/T]TTTCCCAGCTACAAT | 71007 |
rs33358691 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134293028 | ACAATGGTGAATTTG[C/T]GTCCCAAGTTATTTC | 71007 |
rs33358693 | snp | G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134293490 | ATTTACTCCATGGGA[G/T]CCAATCAAGATCACA | 71007 |
rs33358945 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134319839 | GATACTTGTAGAAAA[C/T]AGCTGGAAATTGTGA | 71007 |
rs33358948 | snp | G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134320081 | CTTAGCCATGGAAGA[G/T]CGATTACCAGGAAAG | 71007 |
rs33358951 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134321843 | AACCACACTATTTTC[A/G]CTGGCATCACCAAGC | 71007 |
rs33359034 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134274995 | AGGAAGGTATTTATT[A/G]CAATTCTGACATCAA | 71007 |
rs33359037 | snp | G/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134275053 | TGACCTCAGCGTGCA[G/T]CCTCTTGACAGTGTC | 71007 |
rs33359040 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134275109 | ACCCTGATGCCAGTA[C/T]AGCTGGTTGCTTGGG | 71007 |
rs33359043 | snp | A/C/G | 0.165289 | 0.235211 | intron-variant | D7Ertd443e | Mm_Celera | 7:134275184 | GCTGGCAAAGCTTCA[A/C/G]CCTCCCTCTGCAGTC | 71007 |
rs33359156 | snp | A/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134297707 | TACATTAGGGCCCAA[A/G]TTGCTCATTTTAAAT | 71007 |
rs33359158 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134297734 | AAATGTTGGCTGTAT[A/G]TCAGGGGCTGTATCC | 71007 |
rs33359161 | snp | G/T | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134297884 | CCTGGGCTTTAGCTG[G/T]CACTAGCCTTGGGTT | 71007 |
rs33359163 | snp | A/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134297946 | GAGCTGCCATCTATC[A/T]GTTTGCAGAGTATAA | 71007 |
rs33359174 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134363099 | ACACATTGTCTAACA[C/T]GACTCAGGCTGTCCC | 71007 |
rs33359177 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134363666 | AAGCTTACAGCTCAG[A/C]TCTTCCAAGTCATTG | 71007 |
rs33359180 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134363821 | TCCCTGCCTTCTCTC[A/G]TCTGCTGGATCCTCC | 71007 |
rs33359182 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134363835 | CATCTGCTGGATCCT[C/T]CCAAAAAGTAAAGTT | 71007 |
rs33359296 | snp | C/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134289417 | AAGCTGCCCCATCTT[C/G]TGACCATTGCATAAG | 71007 |
rs33359299 | snp | C/T | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134289424 | CCCATCTTGTGACCA[C/T]TGCATAAGACCAAAC | 71007 |
rs33359302 | snp | C/T | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134289603 | CTTAGTTTCCAATCA[C/T]CTCCACACAATGGGA | 71007 |
rs33359314 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134341728 | CATCTTTGTGAAAAC[C/T]CTCTACATCTTTGTG | 71007 |
rs33359316 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134346492 | ATGCCAGTTGCTGAC[A/G]GGAAATGCACAGGTA | 71007 |
rs33359318 | snp | C/T | 0.5 | 0 | intron-variant | D7Ertd443e | Mm_Celera | 7:134350132 | GGTGGCTCAGCAAGA[C/T]CTGTTTGGCCCTGCC | 71007 |
rs33359321 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134350428 | ATAAAAAGGATAATC[C/T]GTCTCTTCTTGTGTT | 71007 |
rs33359354 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134305034 | TCTATGCAAACACAA[C/T]GTATACAGAGGCAGA | 71007 |
rs33359357 | snp | A/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134305127 | TACATTGCGAGCACC[A/G]TCACCAAGACACACG | 71007 |
rs33359360 | snp | G/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134305740 | TGGTACCTTAGTGTA[G/T]CTTAGTCATCCCAAA | 71007 |
rs33359362 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134307325 | TGCCAAAGGCTTAAC[A/G]TCAGAAATGAAAGAC | 71007 |
rs33359425 | snp | A/G | 0.408163 | 0.193609 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268639 | GCATGGTTGAAGATC[A/G]GGTGCCTGTGTAATG | 71007 |
rs33359430 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268723 | GGTCTGGGGCCAAGC[A/G]AAGAAGCGCTGGCTA | 71007 |
rs33359433 | snp | G/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268861 | CTGTGGAAAGCTGGG[G/T]TCAGTGCCTAGCCAT | 71007 |
rs33359465 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134375496 | ATGATTTTCCCTGAG[A/G]GCAAAGAGGCTGGGG | 71007 |
rs33359468 | snp | A/C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134376288 | CTCTCTCTCTGACTT[A/C/T]GCATAGGTCCTTCCC | 71007 |
rs33359470 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134376307 | TAGGTCCTTCCCTGG[A/G]CCTGCTTAAAGAAGA | 71007 |
rs33359473 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134376343 | CTCAGATCGACTCCC[C/T]GTAAGTGAAGTCTGG | 71007 |
rs33359476 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134369321 | GTGTATGGGACTGCT[A/G]ACTTCTTGTCGTCGA | 71007 |
rs33359479 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134369368 | ATTGGCCATAACTGC[A/G]AGCCTGGTTCCTGGA | 71007 |
rs33359482 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134369401 | CCACAGAGATGATTA[A/C]AAGCTCTGCCAAGAA | 71007 |
rs33359566 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134293579 | TAAAAATGGTATGGA[C/T]ATATTGATGACAAGG | 71007 |
rs33359569 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134293607 | AGGTACTGGAGGTCA[A/G]TGCTGGCCAGCGCAC | 71007 |
rs33359572 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134293868 | AGGGATTGTGTCCCT[A/G]GTGTAGAAAATGGTG | 71007 |
rs33359587 | snp | G/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134417070 | TTCTTGATACAATTT[G/T]ACACCGCGCAAATTT | 71007 |
rs33359589 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134417464 | CACAGTGAAGCTGTG[A/G]ACACACTACTCTATC | 71007 |
rs33359592 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134417477 | TGAACACACTACTCT[A/G]TCAACCTGTTCTTCC | 71007 |
rs33359624 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134383287 | CTTAGTTTGTGAAAG[A/G]GAGACCTCAAGCCAG | 71007 |
rs33359626 | snp | A/C | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134383754 | CTTGTTGTCCATTTA[A/C]AGCCACACTCAATGT | 71007 |
rs33359629 | snp | C/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134383855 | TTCCTGGGCTTCTTT[C/G]TTTGTAGTGATGGTT | 71007 |
rs33359632 | snp | A/C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134384589 | ACTGACAAAGATCTA[A/C/T]GACAGAAATGAAAGC | 71007 |
rs33359633 | snp | A/C | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134384615 | AAAGCCACAGTGCAG[A/C]TGGGCCTGGTGGCAT | 71007 |
rs33359804 | snp | A/C | 0.336735 | 0.234472 | intron-variant | D7Ertd443e | Mm_Celera | 7:134324763 | CAAGGAAATGCTGCA[A/C]AGTTTCAAAACAGAC | 71007 |
rs33359807 | snp | A/T | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134325323 | TGATCTCAAAAAAGC[A/T]AAAAGTCCTAGAAAT | 71007 |
rs33359810 | snp | C/T | 0.375 | 0.216506 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134325419 | AGAACTATAATTTTA[C/T]TGAACACAGAGTCAG | 71007 |
rs33359813 | snp | A/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134325711 | GGTAAAGCCCAAAGG[A/T]ATAATAGGTACAGGA | 71007 |
rs33359856 | snp | A/T | 0.277778 | 0.248452 | intron-variant | D7Ertd443e | Mm_Celera | 7:134275394 | CCTTAAGTCTTCTAT[A/T]AAAAAGTATTAAGGA | 71007 |
rs33359859 | snp | A/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134275429 | CCTTTTCATAAAGAG[A/T]GAAAATGTGGTGTGT | 71007 |
rs33359861 | snp | A/C | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134275518 | TCAGCTAAGCAGCTG[A/C]CTGAAGCCATCACAC | 71007 |
rs33359925 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134289628 | ATGGGAAACTCCCCA[A/G]TCAGGAGCCGGGGAC | 71007 |
rs33359928 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134289889 | GCCACAGATCCCTTT[C/T]GTCATTGCTCCTGCA | 71007 |
rs33359931 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134290344 | CAGGGACAGTTGGAA[C/T]GGCCATAAAAATCCA | 71007 |
rs33360045 | snp | A/C | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134293892 | AATGGTGCTTTTCAG[A/C]GGTCTCTCTGTGGCT | 71007 |
rs33360048 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134294699 | CATGTGACCTCTGGG[C/T]GCCCTTTCATTGCCA | 71007 |
rs33360051 | snp | A/C | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134294730 | TTGCCATTGCCATTG[A/C]CATGGTGGCAGTAGC | 71007 |
rs33360136 | snp | G/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134268876 | GTCAGTGCCTAGCCA[G/T]GTATGTTCCACAGAG | 71007 |
rs33360139 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134269016 | CTTTAGAGACTTGCC[C/T]GGACAGAACTCTGTC | 71007 |
rs33360142 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134269198 | AAGCCGTATACAACT[C/T]TTCACTTATCAAACA | 71007 |
rs33360165 | snp | C/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134307407 | TTGAATGGTCTACAT[C/G]CATCTAGCTTCCTAG | 71007 |
rs33360168 | snp | A/C | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134307869 | GTTGTTCTTATCCAC[A/C]TACTTAAAATAAGTC | 71007 |
rs33360171 | snp | C/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134307897 | GTCAAGGGCAGGCAG[C/G]ATAGACCTAAGGTTG | 71007 |
rs33360216 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134298023 | TGATACCTCCATAAG[A/G]TCAGCTTGTGTGAAC | 71007 |
rs33360218 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134298039 | TCAGCTTGTGTGAAC[C/T]ATCCCAGAAAGGCAT | 71007 |
rs33360221 | snp | G/T | 0.124444 | 0.216185 | missense, intron-variant | D7Ertd443e | Mm_Celera | 7:134298235 | ATGAAGTATGGGTGT[G/T]GCCTCTCATTGGACT | 71007 |
rs33360255 | snp | A/C | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134363951 | AACCATACCTCCTTG[A/C]AAGCTTGGCTAAATT | 71007 |
rs33360257 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134364006 | GTATAGAGAGGCTCC[A/G]TGGTTCCTCTTGTTA | 71007 |
rs33360260 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134364106 | CTCAAAGAAACTGGT[A/G]CAGGAACCCTTGAAA | 71007 |
rs33360262 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134364202 | ACAAAGACTGTCTCG[A/C]AGCCTTTCCTTAGGA | 71007 |
rs33360307 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134369743 | TTCTTGGGCTTTTTA[C/T]CTCAGTTGAATGCAG | 71007 |
rs33360310 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134369825 | AACCTCACAATGGGT[C/T]AAGAATCATAGAAAC | 71007 |
rs33360313 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134369888 | AAAGCCTCCAAAAAA[C/T]ATCTTCATAGCCACT | 71007 |
rs33360385 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134376430 | TAACTCCGGACTGTG[A/G]AAACCTGGGGTTCAC | 71007 |
rs33360388 | snp | A/T | 0.32 | 0.24 | utr-variant-5-prime, intron-variant | D7Ertd443e | Mm_Celera | 7:134376807 | AGCATTCTGACCCTG[A/T]CAGGGCCTCTCTTCT | 71007 |
rs33360391 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134376905 | CAAGTGCCTGCCACA[C/T]AGCAGAAGCTACGAA | 71007 |
rs33360404 | snp | A/G | 0.345679 | 0.230967 | intron-variant | D7Ertd443e | Mm_Celera | 7:134352013 | CTCTAGGCTTAAGTT[A/G]ATTCAGGACCTGTTG | 71007 |
rs33360407 | snp | G/T | 0.375 | 0.216506 | intron-variant | D7Ertd443e | Mm_Celera | 7:134352401 | TGGCAGTGACAGTCT[G/T]GTTCCTCCAGGCAGA | 71007 |
rs33360410 | snp | A/G | 0.277778 | 0.248452 | intron-variant | D7Ertd443e | Mm_Celera | 7:134354193 | AGTTTTGAAAGTGAT[A/G]CATGTTAAAATGAGC | 71007 |
rs33360413 | snp | A/G | 0.277778 | 0.248452 | intron-variant | D7Ertd443e | Mm_Celera | 7:134354815 | ACCCCATGCTGCAGT[A/G]TCCTGGATGCAAGAG | 71007 |
rs33360616 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134326046 | CGGAGCAGAGCAGGT[A/G]GACCGGATGCGAAAG | 71007 |
rs33360618 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134326184 | AATCTGTTCAACACA[C/T]GGCAATGAAGGAGAT | 71007 |
rs33360621 | snp | C/T | 0.42 | 0.183303 | intron-variant | D7Ertd443e | Mm_Celera | 7:134326806 | ATATTGTTAAATGTC[C/T]CTGTAGACTTATACA | 71007 |
rs33360694 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134275588 | CTACCACATTCATCA[C/T]GTCTTTCTACCTCAC | 71007 |
rs33360697 | snp | A/C | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134275613 | CCTCACCACTGTGGA[A/C]CCTCTAGTTCATCTG | 71007 |
rs33360700 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134275761 | TAGGTTTTCTAAAGT[A/G]TCTCACCTCTCTCAC | 71007 |
rs33360703 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134275784 | TCTCTCACACCCTGC[C/T]CTGCTTATGTGAAAT | 71007 |
rs33360716 | snp | A/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134384650 | ACATAATCCGAGTAC[A/T]GGGGAGACAGAGAAT | 71007 |
rs33360719 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134385399 | AGCACAGACACAAAT[A/G]CCATGTGCACACAGT | 71007 |
rs33360721 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134385426 | CAGTCAAATATAACA[C/T]GTGCACACATTCAAT | 71007 |
rs33360724 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134290516 | ACACGAACTTATAAG[A/G]ATATTTGCTTTGGGA | 71007 |
rs33360727 | snp | A/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134290631 | CCCAAACTGTGACTG[A/T]GACCTTCTCTTGACC | 71007 |
rs33360730 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291079 | CCCAGCTAGAAGGTC[C/T]ACCTCAGAAGAGAAG | 71007 |
rs33360733 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291103 | AGAGAAGGAGCTCAG[C/T]ATGGCGCCTGCTACC | 71007 |
rs33360817 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134417528 | AGAGGCTGACGTCTG[A/G]TTCTTTTGAATGAGT | 71007 |
rs33360820 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134417603 | CATAGCAGAGACAAA[C/T]CTCCAGGGTAGAAAA | 71007 |
rs33360914 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134295317 | CCAGTGAGTTATTAA[C/T]GGGCCTTGTTAAGCT | 71007 |
rs33360917 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134295426 | TTAGGCCATGGAGGT[A/G]TTCCTTAGATTGCAG | 71007 |
rs33360919 | snp | A/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134295739 | TGGAAAGGGTCAAAA[A/T]TTAATTGATTCCTTG | 71007 |
rs33360922 | snp | G/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134295907 | CTACTCTGCAGTACC[G/T]TCTCAGTTCCAGCCT | 71007 |
rs33360975 | snp | G/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134269227 | CAGCAAGTCTTCAAA[G/T]GCAGGGACTGACCGC | 71007 |
rs33360978 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134269632 | AGAGTTAGTGGGAGT[C/T]TTGAATGGTGACTGG | 71007 |
rs33360981 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134270025 | AAACATTCCGAGGCA[C/T]AGTTCGACAACTTTG | 71007 |
rs33361074 | snp | A/C | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134307986 | ATCTGCACTGGGCAG[A/C]GTAGTCCATCTCACC | 71007 |
rs33361077 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134308257 | CTCTTGAAGACATCT[A/G]AGCGTTATTCTCACC | 71007 |
rs33361080 | snp | C/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134308441 | GCCATGCTGCCTCCT[C/G]CATTAGCAAGACCAC | 71007 |
rs33361082 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134308475 | TCATGTTTAGATGCT[A/G]TTTGCTGGCAATAAT | 71007 |
rs33361134 | snp | A/G | 0.124444 | 0.216185 | missense, intron-variant | D7Ertd443e | Mm_Celera | 7:134298311 | CTTCAGGAGGGAAGT[A/G]TTTAATGGTCTTCTG | 71007 |
rs33361137 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134298416 | CTATTAAAAATAAAA[C/T]GAGAGTTGACTCACA | 71007 |
rs33361140 | snp | C/T | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134298449 | ATTAGATGAGCCGAC[C/T]TCTCGCGTACCTGAT | 71007 |
rs33361143 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134298503 | ACAGCAGGGCTTCCG[A/G]AACAGTAGGTAGTAG | 71007 |
rs33361204 | snp | G/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134377045 | TCTTTCCTATGAGAC[G/T]CAGACCCTGTGGGCG | 71007 |
rs33361207 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134378049 | CCCAAAGCAAGCACA[A/G]CAGCAGAATGTTACA | 71007 |
rs33361212 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134378471 | AGGCGCTAGTGCGCC[A/G]ATCCTTGCCTGTGGC | 71007 |
rs33361276 | snp | C/T | 0.46875 | 0.121031 | intron-variant | D7Ertd443e | Mm_Celera | 7:134354936 | CTCAAAGCCATTGTC[C/T]TTCTGCACAGTCACT | 71007 |
rs33361279 | snp | C/T | 0.297521 | 0.245442 | intron-variant | D7Ertd443e | Mm_Celera | 7:134355212 | ACAGCCACTGGAAAC[C/T]AAGAAGAATCAATGC | 71007 |
rs33361282 | snp | A/G | 0.46875 | 0.121031 | intron-variant | D7Ertd443e | Mm_Celera | 7:134355369 | GCATGAAAGAAGAAA[A/G]CCATGAAAATTGAAG | 71007 |
rs33361296 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134369947 | AGATCAGAGATGGGC[A/G]GAGCTTTCCCAAGAA | 71007 |
rs33361299 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134370511 | GCATTCTCCACACTC[C/T]CCAAACGATTAACTG | 71007 |
rs33361302 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134370572 | GTTTTCCACAACATT[C/T]CTATCTTGAACTGGA | 71007 |
rs33361385 | snp | C/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134364301 | CCTACCTTTAGCCAC[C/G]TGCTTCAGATTTCTA | 71007 |
rs33361388 | snp | C/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134364649 | GTACCTAGGATGTCT[C/G]GGCAGCTGAAGACAT | 71007 |
rs33361391 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | D7Ertd443e | Mm_Celera | 7:134365017 | TTCATTTGACAAGTA[C/T]GATGAGTTTCAAGAG | 71007 |
rs33361506 | snp | A/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134275892 | CTGTGGTGATTTTGA[A/G]ACAAAGCTGTGCACC | 71007 |
rs33361509 | snp | A/C | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134275978 | TTCTGGACAAAAGGA[A/C]AAAAAAATCCCAAGG | 71007 |
rs33361512 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134276030 | GAGGAATAAGATGGC[A/G]AAGAAGTTCCAGGGG | 71007 |
rs33361516 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291151 | CCTCCTGTGTGTGAA[A/G]TGCTCAGTCCCCAGG | 71007 |
rs33361519 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291298 | TCTCATTTGCTTCCT[A/G]GTTGCCATGAGATGG | 71007 |
rs33361522 | snp | G/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291299 | CTCATTTGCTTCCTG[G/T]TTGCCATGAGATGGA | 71007 |
rs33361614 | snp | G/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134328693 | ATAGACAGTCTTATG[G/T]AGATGGAATCTACAT | 71007 |
rs33361617 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134328758 | AATGCTGTCTCTCAG[C/T]ACCTCTCTTTATATC | 71007 |
rs33361620 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134328782 | TTATATCCTACTTGC[A/G]ATGATGCCTTATGCA | 71007 |
rs33361623 | snp | A/C | 0.260355 | 0.249785 | intron-variant | D7Ertd443e | Mm_Celera | 7:134328851 | CTTCTAGAGCCTTTC[A/C]CCATCTCTCATCTCC | 71007 |
rs33361634 | snp | A/C | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134386229 | CATGCCACATACATA[A/C]AAAACATACAGCACA | 71007 |
rs33361637 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134386297 | ATATATTCACACATA[C/T]CGCACATGTGCACTT | 71007 |
rs33361640 | snp | A/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134386458 | AAAATGCACATTCCT[A/T]GTGACCGTCACTTAT | 71007 |
rs33361642 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134387338 | CTCTGGCTGGAGACA[A/G]AGAGCCAAGCATCTC | 71007 |
rs33361835 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134295986 | GCCTCTGATCTCCAT[C/T]AAGTGCTTTTGGTTC | 71007 |
rs33361838 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134295992 | GATCTCCATTAAGTG[C/T]TTTTGGTTCTTCTTC | 71007 |
rs33361840 | snp | A/C | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134296030 | ATTCCCATCTCCAGA[A/C]TGAGTTCTAATGACC | 71007 |
rs33361854 | snp | C/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134270158 | TCTCCAAACCCCTCT[C/G]GAGCTCTTTCCATAC | 71007 |
rs33361857 | snp | C/T | 0.260355 | 0.249785 | intron-variant | D7Ertd443e | Mm_Celera | 7:134270268 | GTTATCTGGAAGAAA[C/T]AGAAAAAGGATTAAT | 71007 |
rs33361860 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134270444 | ACAGTTAAATAGAGT[A/G]GAAGCAAATGCCCTA | 71007 |
rs33361863 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134270902 | TTCCTGAATTTATTC[A/G]CTGACTGCTCTTGAC | 71007 |
rs33361968 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134418114 | GATTGACATTTACAT[C/T]TGTAACAGGAGGCAC | 71007 |
rs33361971 | snp | A/C | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134418330 | TTTACAGTGAGGGAC[A/C]AACAGAAATTTGTGT | 71007 |
rs33361996 | snp | C/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134298993 | GCAGGCAGCTACATA[C/G]TGTTACCATGAATTT | 71007 |
rs33361999 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134299019 | AATTTGGCTTCATTT[A/G]TATACATTGTTACCA | 71007 |
rs33362002 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134299509 | ACACATGAAGCAGAG[A/G]ATCATGCCCTTGTCA | 71007 |
rs33362055 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134308587 | AGTGAGGAAGGAAAG[A/G]GACCTTAGTTAGCAT | 71007 |
rs33362057 | snp | A/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134308830 | CTAGGACCATTTTCC[A/G]CTAAGAATTTGTTAT | 71007 |
rs33362059 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134309327 | CCTGCGACTTTCAGA[C/T]GTGGACACTTAACAC | 71007 |
rs33362060 | snp | C/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134310239 | TTTGTGGATAGAGGA[C/G]AGCTCATTAGTTTTC | 71007 |
rs33362063 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134310571 | CAAAGGAGGTTTTTA[A/G]ACTTTCTTGTCCCAT | 71007 |
rs33362085 | snp | G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134371659 | TGCAGCATTCACTAT[G/T]GACAGGACCCTAGCC | 71007 |
rs33362088 | snp | C/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134371982 | CCTTTCTCTCTGAGA[C/G]CACAAGGAGAGGGGC | 71007 |
rs33362091 | snp | A/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134372159 | TGAGAGGGGGAGAGA[A/T]TGATTTAGCATCTCT | 71007 |
rs33362125 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134378509 | ACTCAGGACCAAGCT[A/G]AGCCAGGCACTGTGG | 71007 |
rs33362128 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134378711 | TCCTCAGTCCGGACA[C/T]AATCTCTTCTATTCA | 71007 |
rs33362131 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134378788 | AGAGAGTCTTCCTCA[A/G]CACCACACAGCACAG | 71007 |
rs33362204 | snp | A/G | 0.408163 | 0.193609 | intron-variant | D7Ertd443e | Mm_Celera | 7:134356149 | TATGGAATAGATTAA[A/G]TGGATTCAGGCAATT | 71007 |
rs33362206 | snp | A/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134356431 | GAACAGCAGGGAACT[A/G]TGGTCAACTAGAATA | 71007 |
rs33362209 | snp | C/G/T | 0.375 | 0.216506 | intron-variant | D7Ertd443e | Mm_Celera | 7:134358097 | TAATCCTAGACAAAA[C/G/T]GAGATGACACGGCTA | 71007 |
rs33362212 | snp | G/T | 0.375 | 0.216506 | intron-variant | D7Ertd443e | Mm_Celera | 7:134360462 | GCACATTGCTAAGCG[G/T]ACCCGGGTTCCTCCC | 71007 |
rs33362264 | snp | G/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | D7Ertd443e | Mm_Celera | 7:134365152 | CAACTGGAGTCAGAA[G/T]ATTTCTTTCCAACCT | 71007 |
rs33362267 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | D7Ertd443e | Mm_Celera | 7:134365189 | ACGTTCTCGTATTTC[A/G]CTTGCTTTGACTATA | 71007 |
rs33362270 | snp | C/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | D7Ertd443e | Mm_Celera | 7:134365246 | GTTGGTATAAAAGTT[C/G]CTCAGGAGAACAGCT | 71007 |
rs33362273 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | D7Ertd443e | Mm_Celera | 7:134365606 | TAGCTATTATGGTTG[A/G]CTTTTATACAATCAA | 71007 |
rs33362365 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291327 | GGACAGCTTTGCTCC[C/T]TCCGCTTTGCACGGC | 71007 |
rs33362368 | snp | A/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134291405 | ATCCGAAACTTCAAA[A/G]ACCCAGAGCCTAAGT | 71007 |
rs33362385 | snp | C/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134276078 | GTCCCCAGAGAGTCA[C/T]CCTCAAGCTGAGAGC | 71007 |
rs33362388 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134276154 | GTTGAAGGGTCCTTT[A/G]GGAAGGCTGAATGAA | 71007 |
rs33362555 | snp | A/C | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134387501 | ATGTGAGATGTTATT[A/C]GGCACTCAATGGTTG | 71007 |
rs33362558 | snp | G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134387564 | TTTCCTGTAATTCCA[G/T]TTGAAGAGGGCTGTG | 71007 |
rs33362560 | snp | A/C | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134387622 | AAATTCATGGGAATG[A/C]TGGGCCCACTTTACT | 71007 |
rs33362563 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134387734 | TAATGTGTTTTCCCT[C/T]GGTGGTCAGATTCAT | 71007 |
rs33362604 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134328906 | GCAACATAAATTGTT[C/T]GACCATTAGAGAACT | 71007 |
rs33362607 | snp | C/T | 0.277778 | 0.248452 | intron-variant | D7Ertd443e | Mm_Celera | 7:134329097 | AATCAATTATGTATG[C/T]GTTGAGAAATTAATT | 71007 |
rs33362609 | snp | A/T | 0.277778 | 0.248452 | intron-variant | D7Ertd443e | Mm_Celera | 7:134329125 | ATTGTTTAAAGCTCA[A/T]TATTAGCATTCATAA | 71007 |
rs33362610 | snp | A/G | 0.297521 | 0.245442 | intron-variant | D7Ertd443e | Mm_Celera | 7:134335584 | ATTTCATGTCTCTGT[A/G]TAATTGCTTTTAATA | 71007 |
rs33362612 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134336295 | ATGTGGGCTAGAGGA[A/G]CCTTTCTAAGCCTGT | 71007 |
rs33362626 | snp | G/T | 0.336735 | 0.234472 | intron-variant | D7Ertd443e | Mm_Celera | 7:134271387 | CCTCTGTAATATGAA[G/T]GCCCTCTTAGACCCT | 71007 |
rs33362864 | snp | A/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134372191 | GATATCTAAATAAAG[A/G]ATTCCTGAGCCACTT | 71007 |
rs33362867 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134372246 | AATAAAGTGGTAAAA[C/T]TATAAAATCGCaaaa | 71007 |
rs33362869 | snp | A/C/G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134372294 | ATCAAATAAAGAGGG[A/C/G/T]GCATGGGAGCAAAGG | 71007 |
rs33362872 | snp | G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134372336 | GGTGCAAGATGCTTG[G/T]GATGCACAGCAGGGC | 71007 |
rs33362875 | snp | A/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134296236 | AGAGGCAAGGAGCCT[A/G]TGAGGAGTTTCTCCT | 71007 |
rs33362878 | snp | A/C | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134296334 | TGGATCCTTTCCCTA[A/C]TCAGGTCCCTTCAGC | 71007 |
rs33362895 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134299545 | TGATGAAGAGGTGGT[C/T]CCATAACTGTATGGC | 71007 |
rs33362897 | snp | A/G | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | Mm_Celera | 7:134299884 | CATGTTTTAAATAAA[A/G]TCATGACTCTTCTGG | 71007 |
rs33362899 | snp | C/T | 0.336735 | 0.234472 | intron-variant | D7Ertd443e | Mm_Celera | 7:134299954 | GGTTCATTGGAGGTG[C/T]AGGCCGCTAAATGCT | 71007 |
rs33362901 | snp | A/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134299991 | TTGAGTCAGGGAAAA[A/G]TAGTGGGTAGCACTG | 71007 |
rs33362914 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134418431 | GGAGAGTTCACTTGA[C/T]CAATGCATGTGTGTT | 71007 |
rs33362917 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134418507 | ATACATCCTCCAGCT[A/G]GGGAACCAGGCCATG | 71007 |
rs33362920 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134418946 | TCTCATAGGCTGGTC[A/G]TCTTCCCCACAGACA | 71007 |
rs33362923 | snp | A/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134419020 | GCTGGTATCAAACAT[A/G]GATGCAGTACACAGG | 71007 |
rs33363014 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134378808 | ACACAGCACAGAAGA[A/G]TACTCACTGGCCAGC | 71007 |
rs33363017 | snp | C/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134378856 | CCCCCTCTGGATGCT[C/G]TGAGTGTGTAAGCAT | 71007 |
rs33363020 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134378949 | AAGAGAAGGAGTGAG[A/G]TATTGCGGTCTACAA | 71007 |
rs33363022 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134379435 | CCAGGGAGTGAAGCC[A/G]CAGCTGTGTGTTCAC | 71007 |
rs33363114 | snp | C/T | 0.336735 | 0.234472 | intron-variant | D7Ertd443e | Mm_Celera | 7:134360524 | CACAGGTTACGGAAA[C/T]GTTTGAGTGACACAA | 71007 |
rs33363117 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134361602 | GATATAAAAGATCAT[A/C]GTGGAACATTAACCA | 71007 |
rs33363120 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134361721 | ACTGTCTCCTGGCTT[C/T]GATTCTTGGGGGAAA | 71007 |
rs33363122 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134361752 | GCTGTGATGGCTAAC[C/T]ACCCCTCAAGGCTAT | 71007 |
rs33363166 | snp | A/G | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | D7Ertd443e | Mm_Celera | 7:134365677 | TGCGACTTATATGTG[A/G]CAGTGTGAAGTGACT | 71007 |
rs33363169 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | D7Ertd443e | Mm_Celera | 7:134366453 | AAACACAGTCAGTGA[A/G]GCTACAGGAAGGGAG | 71007 |
rs33363172 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | D7Ertd443e | Mm_Celera | 7:134366714 | ATGAGGCATCAACAG[C/T]GTGGTCATTATCCAG | 71007 |
rs33363456 | snp | A/C | 0.336735 | 0.234472 | intron-variant | D7Ertd443e | Mm_Celera | 7:134387758 | GATTCATCTTCTACA[A/C]ACCCCTGCTATCTCC | 71007 |
rs33363458 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134387992 | TCACCTTACAGAGAC[C/T]GTGTACCAAAGTCAC | 71007 |
rs33363461 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134388808 | GAGTTATTTTACTTT[C/T]GCTAAAACACACAAC | 71007 |
rs33363475 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134310674 | GAACAGATAGATCAG[C/T]TTTTCATATCAAGTC | 71007 |
rs33363478 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134312101 | ATTACACTAATTTCT[C/T]AGCAAACTCTGGTCA | 71007 |
rs33363666 | snp | C/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134419127 | ATCAAAGAATTAAGA[C/G]ATACACTCCCAGCCT | 71007 |
rs33363669 | snp | G/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134419548 | GTCTGTGACCTGTGA[G/T]AAATGCATCTAGAGA | 71007 |
rs33363672 | snp | A/G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134419714 | CCACTCAGGAAACCC[A/G/T]CGTCAAAGCACGTAG | 71007 |
rs33363675 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134372485 | CGTTCAGAGGTCAGC[A/G]AAGCCATGATGGGCC | 71007 |
rs33363678 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134372498 | GCGAAGCCATGATGG[A/G]CCAGCATTCTCTGCC | 71007 |
rs33363681 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134372642 | CTAACATTCTATCTC[A/G]AGAGCCTTTCCACAT | 71007 |
rs33363835 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134336523 | ATGCTTCAGTTTAGA[C/T]CTGTGATTATCCACA | 71007 |
rs33363838 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134336901 | CATGCACGTCTTATT[A/G]TGCCTGCCTATATTA | 71007 |
rs33363840 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134336922 | GCCTATATTATGCTA[C/T]AGAAATGTCTCATTA | 71007 |
rs33363843 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134337023 | GGCAACACTACTGTG[C/T]CAAGAAATCTATACC | 71007 |
rs33363895 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134379469 | GCAGAGTATTCTTGA[A/G]TCATTCACAACCCTG | 71007 |
rs33363897 | snp | A/C | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134379562 | AATCCCACAGGTTAG[A/C]GGATGGGCCAGGCTC | 71007 |
rs33363900 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134379736 | AGGAAGGTAAAACTC[C/T]AGAGGCCTGAAAGCA | 71007 |
rs33363903 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134379875 | ACGCCGTGCAGCACA[C/T]AGATCCTCAAGGGCC | 71007 |
rs33364055 | snp | C/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134367076 | CAACTGCGAAGGTCA[C/G]TCAACATGGTAAGGC | 71007 |
rs33364058 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134367147 | TCAGTACCACTGCCA[C/T]CCAGCCTTAGTTCAG | 71007 |
rs33364061 | snp | A/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134367166 | GCCTTAGTTCAGTAC[A/T]TGTTCATTAAGGTCT | 71007 |
rs33364194 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134361800 | CCAAGTATGCCCCTC[C/T]AGCCGCAGGACCAAC | 71007 |
rs33364197 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134361835 | GAGGAATAGATAAGA[A/C]ACATCTGCTCTAGTA | 71007 |
rs33364200 | snp | C/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134361891 | CATCCACCAAGTGAG[C/G]ATCCCATACAGGAGT | 71007 |
rs33364202 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134361983 | GGTCTTAGACTAGTA[A/G]CACCCCTTATGGACA | 71007 |
rs33364203 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134362031 | GAAAGGAACCGTGGT[A/G]CCTTGATTCAAAAGC | 71007 |
rs33364366 | snp | C/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134400672 | GCTGGACCCACGGAC[C/T]TCAGCATCATGTGTA | 71007 |
rs33364368 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e, Gm35970 | Mm_Celera | 7:134413016 | GTTTTTTGAGCTCTT[A/G]CAAATCACTCTCAAG | 71007 |
rs33364371 | snp | A/C/T | 0.244898 | 0.249948 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | Mm_Celera | 7:134413150 | GCCTGGGTCCTCTGC[A/C/T]GAGCCCTGTGAGTAT | 71007 |
rs33364373 | snp | C/T | 0.473373 | 0.11227 | intron-variant | D7Ertd443e, Gm35970 | Mm_Celera | 7:134413351 | GAATCTTTCCCAGAA[C/T]ACATTTTCTCAGTGC | 71007 |
rs33364434 | snp | A/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134388836 | AACAGAATGTGTGAC[A/T]CCCAGAGTCTTTGCT | 71007 |
rs33364437 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134388908 | AAGAATAATGGTGTC[A/G]GGCAGAAGAAAACTC | 71007 |
rs33364440 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134389107 | CTGGTGATATTTTTT[C/T]CTTCTTGGTCAGCAC | 71007 |
rs33364484 | snp | G/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134372682 | TGACTTCCAGGGTCC[G/T]GTGGGATTACCTGCA | 71007 |
rs33364486 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134372692 | GGTCCGGTGGGATTA[C/T]CTGCAGTCTGATGAG | 71007 |
rs33364488 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134373110 | AAAGACAACCTCAGA[C/T]GTATGGAAATGCAGA | 71007 |
rs33364490 | snp | G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134373136 | GCAGAAAATAATAAC[G/T]AGGCATAGCATTTTA | 71007 |
rs33364493 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134373205 | GTGACTGAGCAACCC[A/G]TTATTATTTTGAAAA | 71007 |
rs33364505 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134419781 | TCTGCCATGATCTTG[A/G]AAAACAGCGAGTGGG | 71007 |
rs33364508 | snp | G/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134419788 | TGATCTTGGAAAACA[G/T]CGAGTGGGAGCTGGT | 71007 |
rs33364511 | snp | C/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134419809 | GGGAGCTGGTGCCTC[C/G]AGGTCCCATTTTAAA | 71007 |
rs33364666 | snp | C/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134380183 | AAACAGAATATCTTC[C/G]ACAGATGGAGCTTCT | 71007 |
rs33364669 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134380262 | TGCACATGTACGCAC[A/G]CACCCAGAGGCCTCT | 71007 |
rs33364672 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134380423 | CCAGCACAGATTGCT[C/T]TCTTTCATCTGGACT | 71007 |
rs33364706 | snp | A/G | 0.277778 | 0.248452 | intron-variant | D7Ertd443e | Mm_Celera | 7:134337057 | GAGCATTATGATCAT[A/G]TCTGTCTTCTCACCA | 71007 |
rs33364708 | snp | C/T | 0.260355 | 0.249785 | intron-variant | D7Ertd443e | Mm_Celera | 7:134337078 | CTTCTCACCAAAGTC[C/T]TAGGAATCTTGCTAA | 71007 |
rs33364711 | snp | A/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134337113 | TTCCATGGCTCTTTT[A/T]AAGGATGTTTGTCAA | 71007 |
rs33364713 | snp | A/T | 0.260355 | 0.249785 | intron-variant | D7Ertd443e | Mm_Celera | 7:134337228 | TAGAAGGCTTTACAA[A/T]GATTAGATGTTTAAC | 71007 |
rs33364854 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134367312 | CAGGTGACTTTAAAA[C/T]GTTGTAAACATACAT | 71007 |
rs33364856 | snp | C/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134367774 | CTCGTCCTTTCTTGC[C/G]GGTTCCCCTTTGCCT | 71007 |
rs33364859 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134367798 | TTTGCCTTTCAGTCA[A/G]TGGCTCCATCTTGAT | 71007 |
rs33364861 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134367852 | CACAGCACTCTTTGA[C/T]ACAAGGAAGCCAGGG | 71007 |
rs33365066 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134423532 | AACCATCACGGTAAC[A/G]TAACAGGGTACTTTG | 71007 |
rs33365069 | snp | C/T | 0.42 | 0.183303 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134423559 | TTTGTAGATAATTAA[C/T]CAATCATCTGTAATG | 71007 |
rs33365072 | snp | C/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134423612 | CTTTATGGAGCTGGT[C/G]AGATGATTCTGTGGG | 71007 |
rs33365227 | snp | C/T | 0.336735 | 0.234472 | intron-variant | D7Ertd443e | Mm_Celera | 7:134381591 | TTCCCTTCAGAGTAA[C/T]CAAAAGCAAAGCCAT | 71007 |
rs33365230 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134381887 | TGGAGCACTTGGGAA[A/G]GGCTTTTCACATTGG | 71007 |
rs33365233 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134382120 | GGAGCCTCTTCAGTC[A/G]TACTTCATGGCAGGA | 71007 |
rs33365245 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134362075 | TCAAGGATCTGGGCC[C/T]CAAATGTATGCATGG | 71007 |
rs33365248 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134362153 | TATGATGCAGCAAAT[C/T]AAAACCATGCAGTGG | 71007 |
rs33365251 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134362222 | CTGGTCGGTTGTCCA[C/T]TTACTAACTCACTAG | 71007 |
rs33365284 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134420866 | CCAAAGCCCGCAGCT[C/T]GAGAAAAGCCTCACA | 71007 |
rs33365287 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | D7Ertd443e | Mm_Celera | 7:134421371 | AGGACAAGCAGTCCA[G/T]GCTACTCAGTTCTCT | 71007 |
rs33365293 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134421680 | TATGGTATTTAACAG[C/T]GCAAGTGACAGAAAT | 71007 |
rs33365375 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | D7Ertd443e | Mm_Celera | 7:134398367 | AAAAGAAGGAGCCGG[A/G]ATGTTAAATGCCCAT | 71007 |
rs33365378 | snp | A/T | 0.21875 | 0.248039 | intron-variant | D7Ertd443e | Mm_Celera | 7:134398368 | AAAGAAGGAGCCGGG[A/T]TGTTAAATGCCCATG | 71007 |
rs33365383 | snp | C/T | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | Mm_Celera | 7:134398962 | CATGGCCCTATTGTA[C/T]AAGTGTGCAGCTCTT | 71007 |
rs33365446 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | D7Ertd443e, Gm35970 | Mm_Celera | 7:134413359 | CCCAGAATACATTTT[C/T]TCAGTGCTGCTCTCC | 71007 |
rs33365449 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e, Gm35970 | Mm_Celera | 7:134413419 | GTCCTTCTTTCTGCA[C/T]AGCCCCATCCTTGGC | 71007 |
rs33365452 | snp | A/C | 0.489796 | 0.070696 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | Mm_Celera | 7:134413521 | TGTGTTTGGCACCCG[A/C]TCCTCCCGGAGAAGT | 71007 |
rs33365576 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134373229 | TTGAAAACACAAATA[C/T]CATCCGTATTGCTTA | 71007 |
rs33365577 | snp | G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134373583 | ATCGTTTCTCATTAC[G/T]TCTCACTTGTCACCA | 71007 |
rs33365579 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134373684 | AAGTTTAGCATCAGA[A/G]TTAATTTTTAAAGCT | 71007 |
rs33365581 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134373719 | AAAATGAATCTGGAG[A/G]AAGGCAATAGGAAAA | 71007 |
rs33365684 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134368107 | CCCCAGTCTTGTGGT[A/G]TCTTCTTGAAAAAAT | 71007 |
rs33365686 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134368680 | TCTGCTTGGGCTGCA[A/G]AGCAATGTCCCGTTC | 71007 |
rs33365689 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134368691 | TGCAGAGCAATGTCC[C/T]GTTCTCTCTTGGAGT | 71007 |
rs33365692 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134368719 | AGTCCTATCCTTCCA[C/T]GGCTGGGACATGTGT | 71007 |
rs33365695 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134338983 | GAATGGGAGAATTTA[C/T]ATAACCAATGGGAGG | 71007 |
rs33365697 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134339272 | TAGAAGCAGAGAAGA[A/G]AGGTGCTGATTCATT | 71007 |
rs33365700 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134340702 | CTCTCAACATCAGTC[C/T]CATATTATGCACTAC | 71007 |
rs33365705 | snp | A/G | 0.336735 | 0.234472 | intron-variant | D7Ertd443e | Mm_Celera | 7:134423692 | AGTACAGCACCTACA[A/G]GACACACACTGGGAA | 71007 |
rs33365708 | snp | A/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134423715 | ACTGGGAAGTGCAGT[A/T]CAGTGGCAGGCACCC | 71007 |
rs33365711 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134423910 | TAAGATGGTTTCCTC[A/G]AGAGTATTATTTATT | 71007 |
rs33366156 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134382133 | TCATACTTCATGGCA[A/G]GACAAAGGTTTCATT | 71007 |
rs33366159 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134382156 | GTTTCATTCAAAGCA[A/G]TCACCTCCAGCTACT | 71007 |
rs33366161 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134382326 | AACTCTGAGGGAAAA[A/G]AAGCAAAATAAATAA | 71007 |
rs33366164 | snp | A/C | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134362232 | GTCCATTTACTAACT[A/C]ACTAGCTTATACTGA | 71007 |
rs33366167 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134362259 | CTGAGAGATGCTTTT[C/T]TGAGTCTGTTGCAAT | 71007 |
rs33366170 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134362336 | TACTCCCTGGTCTCT[C/T]TCCAAGTATCCACAG | 71007 |
rs33366173 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134362409 | AGCAGCTGAGCAGCC[A/G]AAGGTGGGAGGAATT | 71007 |
rs33366176 | snp | A/G | 0.375 | 0.216506 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134399043 | ATTCTGTAAGGCTTC[A/G]CTTTTGATGCTCAGT | 71007 |
rs33366179 | snp | A/C | 0.46281 | 0.131194 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134399702 | CCAAGACTAACAGCC[A/C]GTCTCAGCTGTCCCC | 71007 |
rs33366182 | snp | A/G | 0.375 | 0.216506 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134399818 | TTGTTGCCTTTGTGT[A/G]GCTCTCCTCCACCTT | 71007 |
rs33366289 | snp | A/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134422869 | GCAGCCTGTGACATC[A/T]TGGCGTTCATTAAGT | 71007 |
rs33366292 | snp | G/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134423178 | CCAGAAGTTCAGAGA[G/T]GTGTTAAATGTAGAA | 71007 |
rs33366375 | snp | A/G | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | Mm_Celera | 7:134413552 | CACAGGCAGATATAA[A/G]GAGCCGTTAGAAGCA | 71007 |
rs33366378 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134413613 | GGCAGTCCCTGCAAA[A/G]TCCTTCCTGAAGATT | 71007 |
rs33366381 | snp | C/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134413704 | ATCTACTTCCAAATA[C/G]AGGCATAGGTGATAC | 71007 |
rs33366466 | snp | A/C | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134428998 | ACACTATGACTGAAA[A/C]GACCCAAAACAAAAC | 71007 |
rs33366468 | snp | A/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134428999 | CACTATGACTGAAAC[A/G]ACCCAAAACAAAACG | 71007 |
rs33366470 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134429322 | GATGAATGGCACTTT[A/G]AGGGCAGAAAGAATA | 71007 |
rs33366473 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134429753 | GTGCTGGGAAGATTA[C/T]AAGCTTTAAGGAAGC | 71007 |
rs33366635 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134368827 | GGCCTAGTGTGCATC[A/G]GGCTTCTTATATACA | 71007 |
rs33366637 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134369093 | TGAGCAAGGGTGATT[A/C]GATTCTAGTTCAAGG | 71007 |
rs33366639 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134369109 | GATTCTAGTTCAAGG[A/C]TAGAGGATGTCCTAA | 71007 |
rs33366642 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134369152 | AAATAGGACATTTTT[A/G]AAACTTCTTCATAAG | 71007 |
rs33366734 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134424405 | TTGTTTCCTTACACA[C/T]GCCTTCTCTGAAAAC | 71007 |
rs33366737 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134424406 | TGTTTCCTTACACAC[A/G]CCTTCTCTGAAAACA | 71007 |
rs33366740 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134424425 | TCTCTGAAAACATTG[C/T]GATCTTCAAGTCTTT | 71007 |
rs33366743 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134424443 | TCTTCAAGTCTTTGG[C/T]TAGGATTCCATATTT | 71007 |
rs33366774 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134373999 | TGTTACCTATGCTCA[C/T]GTTTGTACCTCAAGT | 71007 |
rs33366777 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134374392 | AGCAGACAGGCTCAC[C/T]TTAACCATTTCCTCT | 71007 |
rs33366994 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134382515 | CCAAACAAGATGTAA[A/G]AATCGGGGAAGTAAG | 71007 |
rs33367045 | snp | A/G | 0.375 | 0.216506 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134399852 | TCATCTTAACTACAA[A/G]TATCCCAGACCAGGC | 71007 |
rs33367048 | snp | C/T | 0.375 | 0.216506 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134399896 | TGTTTGTGTGACCTG[C/T]CTTACCAGCTCCATA | 71007 |
rs33367051 | snp | C/T | 0.375 | 0.216506 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134400205 | TCTCTCCTTCCTTCC[C/T]GAGCCCAGCCAGTAA | 71007 |
rs33367066 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134362443 | TGCTCTGCATAGGAC[A/G]TCAAGGCAATGTCAC | 71007 |
rs33367069 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134363049 | ACTCACGCATGGATG[A/G]CTTGTAGGATGTACC | 71007 |
rs33367124 | snp | A/G | 0.391111 | 0.206368 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134413728 | GTGATACAGGGCCAG[A/G]GAAGGCAGGCTGAGA | 71007 |
rs33367127 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | Mm_Celera | 7:134413916 | AGGCAGAAGGCAACG[C/T]ATGAATAATGAATGA | 71007 |
rs33367129 | snp | A/C | 0.459184 | 0.136902 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134414096 | TGACACTCTGCAACT[A/C]TGAAGCAGCTCACTA | 71007 |
rs33367132 | snp | A/G | 0.459184 | 0.136902 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134414125 | TATGACAGAGGGGAT[A/G]TCCAGGGAACCTAAG | 71007 |
rs33367284 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134423444 | AGGCAGACAATTGAG[C/T]CCATCTATCTGGAAA | 71007 |
rs33367287 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134423509 | CAATCAAGTTGTCCA[C/T]GTAGATCAACCATCA | 71007 |
rs33367466 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134429767 | ATAAGCTTTAAGGAA[A/G]CAAGAGTGGAGGCTG | 71007 |
rs33367469 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134429857 | TGCATGTGGAATCGA[C/T]GTGGACAAGCTTATC | 71007 |
rs33367472 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134429907 | GTGAGTTGAGAAGGG[C/T]GCTCCACTGGCTCCG | 71007 |
rs33367526 | snp | A/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134424574 | ACCCAGAGCAACGTC[A/T]CTAGCTGTGGTCTAG | 71007 |
rs33367529 | snp | C/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134424719 | CAAGAGGTTACATAG[C/G]CCATTCCCAAGTGGT | 71007 |
rs33367545 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134369288 | CTTAAGATGTCATGG[C/T]GGAGCAACGTGACAC | 71007 |
rs33367884 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134400306 | GCCAGTTCACTGTCA[A/G]GTCCCAGGGATTCAG | 71007 |
rs33368045 | snp | A/G | 0.336735 | 0.234472 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134414149 | ACCTAAGACTTCAGC[A/G]AAGCAAACCAATAAC | 71007 |
rs33368048 | snp | C/T | 0.459184 | 0.136902 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134414222 | GGTGCCTGCAGATAG[C/T]GTCTGAGTACTTCCA | 71007 |
rs33368051 | snp | A/G | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | Mm_Celera | 7:134414240 | CTGAGTACTTCCAAA[A/G]AAAGCCAGCACCTGC | 71007 |
rs33368194 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134477026 | TACCTGACCATTTCT[C/T]AACTGTTGTCCATGA | 71007 |
rs33368196 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134477156 | AAAGAAATAAATGAG[C/T]GTGGAAATAAATAAA | 71007 |
rs33368199 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134477239 | ACTTGACTTAGAGAC[C/T]TCACCCATCAGGATG | 71007 |
rs33368202 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134477442 | tctgcctctgcctct[C/T]AAATTGAATAAACTC | 71007 |
rs33368225 | snp | A/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134437006 | ATTTATGACTTAATG[A/G]CTTTTTCTTAGAGTC | 71007 |
rs33368228 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134437938 | TGAAGTCAACACTCT[A/G]CAAGAGGCATACACA | 71007 |
rs33368231 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134438980 | TAAGGAAATGGAAAG[A/G]CTTTCTCAAGCTGAA | 71007 |
rs33368285 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134463672 | ACAGCCTGGCACTCC[A/G]TGTTCCCACAGGAGC | 71007 |
rs33368288 | snp | C/T | 0.489796 | 0.070696 | intron-variant | D7Ertd443e | Mm_Celera | 7:134463701 | GCCAATGCGACAGCA[C/T]AACCCAAGTCCTGCC | 71007 |
rs33368291 | snp | C/T | 0.459184 | 0.136902 | intron-variant | D7Ertd443e | Mm_Celera | 7:134463739 | GGAGTCACGATGATG[C/T]GCTCACTTAATGAGC | 71007 |
rs33368295 | snp | G/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134479727 | TGATTAGTCATCAGA[G/T]CAAAGGAAAGACTAT | 71007 |
rs33368298 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134479874 | CTAAACTATCATTTC[C/T]CGGGAACACAGAAAG | 71007 |
rs33368301 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134481961 | TGGTTAATGCAACCT[C/T]GGCACCTATAATCGC | 71007 |
rs33368305 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134430053 | GACATTGAAATAACC[C/T]GAGGAACACTGGGAG | 71007 |
rs33368308 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134430107 | ACTACTGACAATAAT[C/T]GCACTCTTGAAGGGA | 71007 |
rs33368311 | snp | A/C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134430118 | TAATTGCACTCTTGA[A/C/T]GGGAAGTTAGGGAGA | 71007 |
rs33368344 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134425441 | CTTCCAAGCTGCTGG[A/G]TGATACTGAAGACAG | 71007 |
rs33368350 | snp | A/G | 0.260355 | 0.249785 | intron-variant | D7Ertd443e | Mm_Celera | 7:134425674 | CCTGCAGAGATGAAG[A/G]TGGAAGACGAGAGGT | 71007 |
rs33368564 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134455129 | TTTTCTTCCCAGTGG[A/G]TATTTACCAGTTTAG | 71007 |
rs33368567 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134457513 | CAATATGCTGTAGTA[C/T]TAAAGAAAAAAGGAG | 71007 |
rs33368570 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134457807 | TGAAGGCTGGCACTA[C/T]ACCTGCCTGTCAGCA | 71007 |
rs33368573 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134457892 | CCCTTACCTGAATCC[C/T]GGTGGCCTCCACCCT | 71007 |
rs33368924 | snp | C/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134414308 | CGGCCGACCGGCAAA[C/T]CAGCAAACCCCTCAG | 71007 |
rs33368927 | snp | C/T | 0.489796 | 0.070696 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134414327 | CAAACCCCTCAGGAA[C/T]GTCCACTCCTGGCAT | 71007 |
rs33368930 | snp | C/T | 0.35503 | 0.226867 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134414485 | GGAGACAGAGAGCAC[C/T]TTGCCCTGCCCTGAA | 71007 |
rs33368933 | snp | G/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | Mm_Celera | 7:134414561 | TGACTTCCGACATTT[G/T]ATCTGATATCAGTTG | 71007 |
rs33369034 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134439023 | AACTTCGAAACTGTA[C/T]CTGTAAGCTGAAAGG | 71007 |
rs33369037 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134439153 | ACAGGACATGATACA[A/G]TTGCCAAGAAAGCAG | 71007 |
rs33369040 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134439380 | GCTACACATTGGTTG[C/T]GACATATTGTGGATA | 71007 |
rs33369043 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134439491 | TTTGCGGTCTCTCAC[C/T]GTTCCCATGGATTCC | 71007 |
rs33369054 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134464790 | CTTGCAGCTAAAAGC[A/G]TGAGCACATCTCCAC | 71007 |
rs33369057 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134464883 | GTATTATGTAGAGCC[C/T]TGGATTGAGGCATTG | 71007 |
rs33369061 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134465638 | TCAGGCGAGAGAGCC[C/T]GCCTGGGGCAATGCT | 71007 |
rs33369063 | snp | C/T | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134467127 | TGTAATCCTAAAGCA[C/T]CTGTGGCCTGAAGAA | 71007 |
rs33369084 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134477459 | AATTGAATAAACTCC[C/T]TCTCTCTTAGACATT | 71007 |
rs33369086 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134477508 | CTCCCCACAAACTCA[C/T]GGCAAGGGAGCCAGC | 71007 |
rs33369089 | snp | G/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134477562 | GTTTGTCAGTCCTCA[G/T]TGAGCTACCAGGCAA | 71007 |
rs33369091 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134477650 | ATGGCTTCTACCAGC[C/T]GCTCTTAATGGCTAC | 71007 |
rs33369104 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134481986 | AATCGCTCAAATCTG[C/T]GCTTTCTCTCTCCAC | 71007 |
rs33369107 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134482344 | TAAAGTCTTCAGGCT[C/T]TTCCGCAGCTACCTA | 71007 |
rs33369110 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134482348 | GTCTTCAGGCTCTTC[C/T]GCAGCTACCTAATGA | 71007 |
rs33369113 | snp | A/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134482349 | TCTTCAGGCTCTTCC[A/G]CAGCTACCTAATGAA | 71007 |
rs33369184 | snp | A/C | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134430170 | AGAAGTCTGCTCCTG[A/C]GATGAAGTCTTCTTG | 71007 |
rs33369187 | snp | G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134430269 | TAGGAAAAGGCGCTG[G/T]TCCAGGGGCCCTATT | 71007 |
rs33369190 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134430408 | TCTTTCCCAGATGTT[C/T]AATTCTGCCACGCAC | 71007 |
rs33369193 | snp | C/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134431309 | AAGAACTAACAGCAC[C/G]CAGTTACAACTCTCT | 71007 |
rs33369405 | snp | A/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134458358 | AAACTCAAAAGAAAT[A/T]ATATGAACTCTCACT | 71007 |
rs33369408 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134458952 | CCAAAGACCTTTGAC[C/T]GTACCCTCCAACTTA | 71007 |
rs33369411 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134458980 | TTATGGCTGCTCATT[C/T]CTGATAAATCTCAAC | 71007 |
rs33369676 | snp | G/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | D7Ertd443e, Gm35970 | Mm_Celera | 7:134414621 | TAGCCTTAATAAACG[G/T]TTGTATTATGAATGT | 71007 |
rs33369679 | snp | C/T | 0.48 | 0.0979796 | intron-variant, downstream-variant-500B | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134414689 | TTTGAAGTAAACAAA[C/T]CCAGCCCAGCTCTTC | 71007 |
rs33369682 | snp | A/G | 0.35503 | 0.226867 | intron-variant, downstream-variant-500B | D7Ertd443e, Gm35970 | Mm_Celera | 7:134414823 | TAAACAGAAGGTTAG[A/G]CATTAAGAATCAACA | 71007 |
rs33369804 | snp | G/T | 0.473373 | 0.11227 | intron-variant | D7Ertd443e | Mm_Celera | 7:134427286 | CTATTAGAGCTGGAG[G/T]CAGAGGCTAGTTCTG | 71007 |
rs33369807 | snp | A/C | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134427293 | AGCTGGAGTCAGAGG[A/C]TAGTTCTGCTCCTAG | 71007 |
rs33369810 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134427682 | ATAATGTAGGGAATG[C/T]TGGCACCATCAAAGA | 71007 |
rs33369813 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134427764 | CAGTGGAATGGTGGA[A/C]TTTGGCCCTCTTTGT | 71007 |
rs33369816 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134439567 | TGAAAACCCTACTTC[C/T]GAACGTTGTGCTACT | 71007 |
rs33369818 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134441364 | CTCTAAATTAATGCA[A/G]CTACGTGAGTTATTG | 71007 |
rs33369821 | snp | G/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134441560 | AAAACAAGAAGTAAC[G/T]CAGGAGGTGGCTGCT | 71007 |
rs33369946 | snp | A/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134431427 | AAATGAAGGGTCCTC[A/T]TAGGGCATGCCATTC | 71007 |
rs33369949 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134431883 | TAGTACCAACTGATA[A/G]CACTAGCAGAGGGAA | 71007 |
rs33369952 | snp | G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134432297 | CACGATGGTCTACTT[G/T]TGCTTGGTGTGTGAG | 71007 |
rs33369955 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134482445 | CAGGTAGAAATGACA[A/G]CAGCCAAGAACAGAA | 71007 |
rs33369958 | snp | G/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134482502 | TACCAGGCATGTTGG[G/T]CAGAATCATTTCAAA | 71007 |
rs33369961 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134482577 | AACGTCTGTATTCAG[A/G]TGATATTCCCTGATT | 71007 |
rs33369963 | snp | C/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134482621 | TTCCATCATGTTCCA[C/G]CATGTTCTATCATGT | 71007 |
rs33369964 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134477651 | TGGCTTCTACCAGCC[A/G]CTCTTAATGGCTACC | 71007 |
rs33369967 | snp | G/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134477699 | CATCCCATATCCATG[G/T]TTTCCACAGCCTTAA | 71007 |
rs33369970 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134477813 | ATTCCAGCTCTGTGA[C/T]TCCTTGGCTTCCAAC | 71007 |
rs33369972 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134477897 | TTTCATGAGCTTTTC[C/T]GGAGTAGAGTAGTTC | 71007 |
rs33370135 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134468764 | AGAGATGGTCAGGTG[C/T]CTCTTAATAAGCATG | 71007 |
rs33370137 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134469599 | CTAGTTACAGAGAAA[C/T]GAGACAGTACTCTTC | 71007 |
rs33370139 | snp | A/G | 0.408163 | 0.193609 | intron-variant | D7Ertd443e | Mm_Celera | 7:134469962 | TAACCTGTTTCCCAG[A/G]TTTGAGCTAGCAAGG | 71007 |
rs33370141 | snp | A/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134470102 | AAGGGGCTCTCTACC[A/G]TTTCCTGATTTGAAA | 71007 |
rs33370264 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134459144 | GGCCTAGCAAAAACC[A/G]TCCTTTAGCAAATGG | 71007 |
rs33370266 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134459270 | AGTGCTTAAGCAAAC[A/G]TGCCCATCAGTACAC | 71007 |
rs33370269 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134459312 | TAAAGGAACTAACTC[A/G]TCTCAGAATCAAGTA | 71007 |
rs33370272 | snp | A/C | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134459443 | CATATCTTACTGGTT[A/C]CAAATGTTCAGGAGA | 71007 |
rs33370405 | snp | C/T | 0.297521 | 0.245442 | intron-variant, downstream-variant-500B | D7Ertd443e, Gm35970 | Mm_Celera | 7:134414824 | AAACAGAAGGTTAGG[C/T]ATTAAGAATCAACAC | 71007 |
rs33370408 | snp | A/G | 0.48 | 0.0979796 | intron-variant, downstream-variant-500B | D7Ertd443e, Gm35970 | Mm_Celera | 7:134414963 | GTTTGAGTGTTTTTT[A/G]AAGTAAGAAAATATA | 71007 |
rs33370411 | snp | C/T | 0.396694 | 0.202437 | intron-variant, downstream-variant-500B | D7Ertd443e, Gm35970 | Mm_Celera | 7:134415036 | TGTATTAAACACTCA[C/T]GCGTTAGATAAAAGG | 71007 |
rs33370526 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134427797 | GACCACCTGCTCTCA[C/T]AGTTACTAGCTCAGT | 71007 |
rs33370529 | snp | A/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134427928 | TGGCCTCTGCTCCAC[A/G]GAGCTTGATAGATTG | 71007 |
rs33370532 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134428025 | TCCCATCTTTTATCT[C/T]CCCTGCTATTGACAG | 71007 |
rs33370704 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134432362 | ACAGATGTGCTTATT[C/T]GACAGCGGCATGTCT | 71007 |
rs33370707 | snp | A/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134432440 | CTGGGATGTGACCCT[A/G]AACTTGGCATTAGGA | 71007 |
rs33370710 | snp | G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134432684 | GTGCTGGCTAACTTT[G/T]TATTGGTATTTTGCT | 71007 |
rs33370713 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134433142 | TCAGCTCAACTCTGC[C/T]TATAATCTCACCCAT | 71007 |
rs33370745 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134477916 | GTAGAGTAGTTCATA[A/G]CATCAAAATGTCAGA | 71007 |
rs33370748 | snp | G/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134477952 | CTGAATTAGCCAACA[G/T]CAGAGAATAGCTCTG | 71007 |
rs33370749 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478005 | AATGGAACCCAGGCA[C/T]CTGTTACTGTTAAGA | 71007 |
rs33370752 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478036 | CAGTGCCTGTGGTCC[C/T]GATTACTGCATGCAG | 71007 |
rs33370764 | snp | G/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134441655 | TTCCTTCCTTGTGAA[G/T]GGAGCCTTTTAACAT | 71007 |
rs33370767 | snp | C/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134441725 | GTCAGAAAATATCAA[C/T]GACACTGGTTACAAA | 71007 |
rs33370769 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134442005 | TCAAGACCATATACC[A/G]AGGATTCAAAAGAAA | 71007 |
rs33370771 | snp | C/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134442103 | CACCTCTTCCCTTTG[C/G]ATAGACTGAGGAGGA | 71007 |
rs33370935 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134482679 | ACTTTCCATGAGATG[A/G]TGGCTATGGCTCTAG | 71007 |
rs33370938 | snp | A/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134482715 | GAATCTGTTTCTTGT[A/T]CCAAGAGGAAATTTT | 71007 |
rs33370941 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134482756 | ATCATTTAGTACCAC[C/T]TCCTGCTTTCCCCAG | 71007 |
rs33371044 | snp | A/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134470136 | AGATGTTAGTCCGGG[A/T]AGAAATAGTCATCTT | 71007 |
rs33371047 | snp | G/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134470264 | CAATTTAACCATAAA[G/T]CTTCAACTATCCGTC | 71007 |
rs33371049 | snp | A/G | 0.336735 | 0.234472 | intron-variant | D7Ertd443e | Mm_Celera | 7:134470367 | GCTATATTCCCTTGA[A/G]TCTTCCTGCCTGGGC | 71007 |
rs33371052 | snp | A/G | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134470530 | CTCAGGAACCCAAGA[A/G]TGAGAAAATGCCAGG | 71007 |
rs33371104 | snp | A/T | 0.48 | 0.0979796 | intron-variant, downstream-variant-500B | D7Ertd443e, Gm35970 | GRCm38.p3 | 7:134415094 | TTAAAATAGAAAAAA[A/T]GAGGTGGCCGGGAAG | 71007 |
rs33371107 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134415499 | GCATTAAGCAATGAC[A/G]ATGTTATTTCTTCCC | 71007 |
rs33371110 | snp | A/C | 0.489796 | 0.070696 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134416041 | GTTTATCAAACTGTG[A/C]GCCCTCTGTCCCAGC | 71007 |
rs33371113 | snp | C/T | 0.336735 | 0.234472 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134416061 | TCTGTCCCAGCAACT[C/T]ACTCTTGCTTATGTG | 71007 |
rs33371125 | snp | A/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134459456 | TTACAAATGTTCAGG[A/T]GAAACTCCGTTGGCT | 71007 |
rs33371128 | snp | C/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134459561 | CATGGAAGGTGGCCT[C/G]GAACCTCAGCAGCAC | 71007 |
rs33371131 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134459614 | AATCCTGAACCAGAC[C/T]GTTCCTTTATACCTT | 71007 |
rs33371133 | snp | G/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134459845 | ATGGATCTTCCCTTG[G/T]TTTCCCACATGTTCT | 71007 |
rs33371345 | snp | C/T | 0.408163 | 0.193609 | intron-variant | D7Ertd443e | Mm_Celera | 7:134428176 | AGTAAGAGTAGGGTA[C/T]CTGAAGTAGGCTCAG | 71007 |
rs33371348 | snp | A/G | 0.489796 | 0.070696 | intron-variant | D7Ertd443e | Mm_Celera | 7:134428182 | AGTAGGGTACCTGAA[A/G]TAGGCTCAGTCTGAG | 71007 |
rs33371351 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134428217 | GAGGAGACCTGACAT[C/T]GTCTTCCAGGACTGA | 71007 |
rs33371496 | snp | C/T | 0.35503 | 0.226867 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134433199 | ACCTGTGCAGGAAGC[C/T]GATCTCTTTATGCTC | 71007 |
rs33371499 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134433401 | AGCTTTGCCAGCTAC[C/T]TTCCAAGTGCTTCAC | 71007 |
rs33371502 | snp | G/T | 0.260355 | 0.249785 | intron-variant | D7Ertd443e | Mm_Celera | 7:134434080 | ATTTGCTGCACACAT[G/T]CCAATGGCCATGGAG | 71007 |
rs33371595 | snp | A/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478037 | AGTGCCTGTGGTCCC[A/G]ATTACTGCATGCAGC | 71007 |
rs33371597 | snp | C/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478045 | TGGTCCCGATTACTG[C/G]ATGCAGCTCATCTAT | 71007 |
rs33371599 | snp | C/G/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134478143 | TAGCAATCTTGAATA[C/G/T]TTTAAGCACACATAG | 71007 |
rs33371602 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478155 | ATACTTTAAGCACAC[A/G]TAGTCTTGCATAGAG | 71007 |
rs33371716 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134443019 | GGAGGACATGTCTAC[A/G]GTTCCAGATGTTGCT | 71007 |
rs33371719 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134444566 | TTAATCTGACTTGAA[A/C]GTAATGTTAATAAAG | 71007 |
rs33371722 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134444648 | CTTCAATTGCTTCTC[C/T]GAGAAACATCTCCCT | 71007 |
rs33371724 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134482966 | AAATCACAGAGGAAG[A/G]TAAGGGCTATTCTAA | 71007 |
rs33371727 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134483070 | GCTGCTTGAGTGGTG[C/T]TTGCTTGTCTTGGTT | 71007 |
rs33371730 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134483144 | AGCCCTTTTCATACC[C/T]GACTTCAAGTTTTTT | 71007 |
rs33371733 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134483210 | AGGAGGCACAATTTG[A/G]TCCTTAATGGTTTTT | 71007 |
rs33371825 | snp | C/T | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134470583 | GTTGATAGCTAAGTC[C/T]AGAGGTGACTCAATT | 71007 |
rs33371827 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134470644 | TTCCAGCTTTACACG[A/C]AGGCTCCATTGGGTC | 71007 |
rs33371829 | snp | G/T | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134470709 | CCTGCACAAATCTCA[G/T]TTGCTTTCCTGGTGT | 71007 |
rs33371832 | snp | A/G | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | Mm_Celera | 7:134471090 | AAATTCAACATATGC[A/G]ACCTTTGAGCTAAGT | 71007 |
rs33371915 | snp | C/T | 0.375 | 0.216506 | intron-variant | D7Ertd443e | Mm_Celera | 7:134472898 | ACAGACAGTTATCAT[C/T]TCTATATTTGAGCTA | 71007 |
rs33371918 | snp | A/G | 0.375 | 0.216506 | intron-variant | D7Ertd443e | Mm_Celera | 7:134472913 | CTCTATATTTGAGCT[A/G]CACCCACCACATTCT | 71007 |
rs33371921 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134472987 | CTGACTCTGTCCTTA[A/C]CTGACTCTAAACATA | 71007 |
rs33371968 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134416866 | TGCTCCATATAGATA[A/G]CACACTTCAGTTAAG | 71007 |
rs33372076 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134460057 | GGCTTCCTGGGTAGA[C/T]GGGTGCTGGCAAAAA | 71007 |
rs33372078 | snp | A/C | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134460366 | TGGGTGACTGGAAGA[A/C]CCTTGCTATGGTGCA | 71007 |
rs33372081 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134460785 | TCTCTTTCTCATAAA[C/T]AGAATGTATGTCTTG | 71007 |
rs33372194 | snp | G/T | 0.5 | 0 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134428231 | TCGTCTTCCAGGACT[G/T]ATGTGGATGCAACTG | 71007 |
rs33372197 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134428330 | TTAGTAAATGTGAGA[C/T]CCACTGTTCAAATGA | 71007 |
rs33372200 | snp | A/G | 0.336735 | 0.234472 | intron-variant | D7Ertd443e | Mm_Celera | 7:134428459 | ACATACCTCCACACA[A/G]CTCTCATCAGGATTT | 71007 |
rs33372203 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134428976 | GTCACAGGACTCTCA[C/T]AGGGAAACACTATGA | 71007 |
rs33372315 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134510511 | CTCCCCTGTGAGACA[A/C]CAGGCTTCTGATTAA | 71007 |
rs33372318 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134510553 | AAGTTCAGCAGAGCT[C/T]ACCACTCTCCCTGGT | 71007 |
rs33372320 | snp | A/C | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134510666 | ATCTGGAAGGTAAGG[A/C]CAACTGAAAGAATTG | 71007 |
rs33372323 | snp | C/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134510714 | TGTGTGCAGTCACAG[C/G]CTTAGGGCAAGGTCA | 71007 |
rs33372335 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134486423 | TCTAACCTGGCTCAT[C/T]GCCACTCAACAGGCT | 71007 |
rs33372338 | snp | C/G | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134486513 | CCAATGGGCAAAGAA[C/G]AGTGCAGAGAGGCTG | 71007 |
rs33372341 | snp | A/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134486515 | AATGGGCAAAGAACA[A/G]TGCAGAGAGGCTGGT | 71007 |
rs33372385 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134434252 | GATTTATAAAACACC[A/G]TGGGCTCAAATGCAT | 71007 |
rs33372388 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134435039 | AATTGGGCTGTTTCC[C/T]TTAACTTAATCTCCG | 71007 |
rs33372391 | snp | A/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134435412 | GAAAATGATGTTGTC[A/T]TGATGCATAGCCTGG | 71007 |
rs33372424 | snp | C/T | 0.260355 | 0.249785 | intron-variant | D7Ertd443e | Mm_Celera | 7:134496738 | TTCATGGTCAAAGCC[C/T]AGGTTAACAGGAAGG | 71007 |
rs33372427 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134496932 | CTGTAATAGTTCAAC[A/G]GCTTTGGACTATTTT | 71007 |
rs33372430 | snp | A/G | 0.336735 | 0.234472 | intron-variant | D7Ertd443e | Mm_Celera | 7:134496995 | AATGGAAAAGAATCC[A/G]CCTGAGATAAACACA | 71007 |
rs33372433 | snp | A/G | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | Mm_Celera | 7:134497060 | TACCAGCCACAAGCA[A/G]CTATCTTTCCAGAAA | 71007 |
rs33372446 | snp | A/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134503728 | CAAGCATCAGTGTCA[A/G]ACAGTGCCGTGCCCT | 71007 |
rs33372449 | snp | C/G | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | Mm_Celera | 7:134504136 | TGAAACTCTCATTGC[C/G]CTGTTACCCTGACCT | 71007 |
rs33372452 | snp | A/C | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134504470 | GTGCAATGAGGGACT[A/C]TGGTTTGTCTGTAAT | 71007 |
rs33372555 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478159 | TTTAAGCACACATAG[C/T]CTTGCATAGAGGTGA | 71007 |
rs33372558 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478180 | ATAGAGGTGAGATCT[A/G]AGCATTGCCATGTTA | 71007 |
rs33372561 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478238 | GCTGCTTTCATTACA[A/G]ACATTCCTGAGTTCT | 71007 |
rs33372576 | snp | C/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134483335 | CCCAGAAGAAAGGGT[C/T]TACCACAACTCCATC | 71007 |
rs33372579 | snp | C/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134483373 | CAAGGAATAGTCATT[C/T]TTAATATTGTTGTTT | 71007 |
rs33372582 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134483398 | TTGTTTGTAACAATG[C/T]CAGCAATAGTGTGGT | 71007 |
rs33372664 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134473091 | GCTTTTCAGAGACTG[C/T]CAGCCTAAAAGCCTG | 71007 |
rs33372667 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134473355 | GAGGTCCAGTCTTTA[C/T]CTGCTCTTGAAAAAG | 71007 |
rs33372669 | snp | A/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134473394 | CCTTCCTGGACAAAG[A/T]CATCTTTGGGAAATG | 71007 |
rs33372671 | snp | A/C | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | Mm_Celera | 7:134473421 | AATGAGAAGAGCCAA[A/C]TGTTCATCGGGAAAA | 71007 |
rs33372672 | snp | C/G | 0.459184 | 0.136902 | intron-variant | D7Ertd443e | Mm_Celera | 7:134473426 | GAAGAGCCAACTGTT[C/G]ATCGGGAAAAGAACA | 71007 |
rs33372804 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134444708 | AAAAACCACTGTGCC[C/T]AATTAGATGCTGCAA | 71007 |
rs33372807 | snp | A/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134444925 | AACTGAGCATCTCAC[A/G]GCAAGACACCTGCAT | 71007 |
rs33372810 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134444970 | TGTGAAGGGATGCTA[C/T]GGAATCCTGCTTGAA | 71007 |
rs33372813 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134445267 | CGCCAGAACAAGACC[C/T]TTTGCTATCAGAGCC | 71007 |
rs33372844 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134460935 | CCACTCATCTGCTCT[A/G]TGGCTCAAAGATTTC | 71007 |
rs33372847 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134460958 | AAGATTTCTTATTGG[C/T]CAAAGCTAATGAGAA | 71007 |
rs33372849 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134460997 | ATGAAGATCACTTTG[C/T]CCTTGATATTCCTGA | 71007 |
rs33372852 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134461028 | GACCTCCAGAGGCCC[A/G]TTCTCTATAGGAAAT | 71007 |
rs33372864 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134471207 | AAGAGATGAGAAATA[A/C]AAAAACCAGCTCATT | 71007 |
rs33372866 | snp | A/G | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134471399 | TCGTTTTTTTCATTA[A/G]AGCCAACTTTGCTTC | 71007 |
rs33372869 | snp | A/G | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134471818 | GACAAGATCATGGTC[A/G]TATCGAAGCAGCAAT | 71007 |
rs33372872 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134471873 | CTCAGCCAGTATCTC[C/T]GGCTGAGTTTCCCAC | 71007 |
rs33373084 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134486592 | AATCACAGTTTTTAC[A/G]AACTTCCTGTAAGCA | 71007 |
rs33373086 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134486668 | CTGTCCCTTGCTCTT[A/G]GCTGCAGGCTGCTTC | 71007 |
rs33373089 | snp | G/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134486842 | ATTCAATTTTTGTGT[G/T]GTCTTCTTGAGACAG | 71007 |
rs33373092 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134487188 | ATCTCTATTCAAGGC[C/T]GATCCGGTGTCAGGA | 71007 |
rs33373176 | snp | C/T | 0.21875 | 0.248039 | intron-variant | D7Ertd443e | Mm_Celera | 7:134510998 | AGTTAAAATTCAAAT[C/T]GGACTGCAGTCCTGT | 71007 |
rs33373179 | snp | C/T | 0.277778 | 0.248452 | intron-variant | D7Ertd443e | Mm_Celera | 7:134511009 | AAATTGGACTGCAGT[C/T]CTGTTTTGAAGTGAA | 71007 |
rs33373181 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134512773 | ATTATGGAAGCCAGG[A/G]AAAAAAAAAAGAATA | 71007 |
rs33373236 | snp | G/T | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | Mm_Celera | 7:134497515 | AGCACATGTGACGTT[G/T]TTTTGTACAATCTCC | 71007 |
rs33373239 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134497859 | GATTGGGCAATGGAT[C/T]AATGAATAAGGACGC | 71007 |
rs33373242 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134497972 | GGAACTGGAAGAAGC[C/T]AGCCTTGAACCCTGC | 71007 |
rs33373304 | snp | C/G | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | Mm_Celera | 7:134504840 | AAGTCAAGTATAGGA[C/G]ACTTCTCATTACCCT | 71007 |
rs33373307 | snp | G/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134505501 | TAAAGTGACTGAAAC[G/T]GCCATTGGTGGCCAT | 71007 |
rs33373310 | snp | C/T | 0.35503 | 0.226867 | intron-variant | D7Ertd443e | Mm_Celera | 7:134505533 | GCTACTCCATGACAC[C/T]AAAGTCACATCAACA | 71007 |
rs33373312 | snp | C/T | 0.375 | 0.216506 | intron-variant | D7Ertd443e | Mm_Celera | 7:134505643 | TGCCTAGAATATGCA[C/T]TGAAGTATTTAAATG | 71007 |
rs33373316 | snp | C/T | 0.165289 | 0.235211 | intron-variant | D7Ertd443e | Mm_Celera | 7:134436119 | TCAAATAGATCTGCC[C/T]ATGCTGGCCAGCAGT | 71007 |
rs33373320 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134436189 | CAGGTCTCGTGGTCA[C/T]CTTACTTGGATCCTT | 71007 |
rs33373354 | snp | A/C | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478263 | AGTTCTGTTTTAACT[A/C]TGTAAGATATACAAT | 71007 |
rs33373357 | snp | C/G | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478543 | TAGTTAGAAGCCCTA[C/G]TTCTTGAAACTGTTA | 71007 |
rs33373359 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478610 | CCTTTCATTTCTCAG[A/G]TTCTAAGTAATTTTC | 71007 |
rs33373362 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478691 | TCAGGCCTACTAACA[C/T]GAAGTCAGAAGCAAC | 71007 |
rs33373414 | snp | C/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134483521 | ACTTGAAGGCATCAT[C/G]CTGAAAATCTATAGT | 71007 |
rs33373417 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134483974 | TGTCCTCAAGGGCTA[C/T]ATCCTGTCTTTGGCT | 71007 |
rs33373420 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134483982 | AGGGCTATATCCTGT[C/T]TTTGGCTTCTGTTAA | 71007 |
rs33373423 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134484033 | GGTGTCCTTATGTGA[A/G]TCTCTGCTCTGCTAT | 71007 |
rs33373556 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134445304 | CTTTCTTTCTCTGGT[C/T]GCCTCCCGCAGATAA | 71007 |
rs33373559 | snp | A/C | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134445313 | TCTGGTTGCCTCCCG[A/C]AGATAAGACTTAGCA | 71007 |
rs33373562 | snp | C/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134445329 | AGATAAGACTTAGCA[C/G]ATTGATTTGCTTCTC | 71007 |
rs33373657 | snp | A/G | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | Mm_Celera | 7:134461244 | CTTTGTAGGTTCTTT[A/G]TTTGTGAAAAATTTT | 71007 |
rs33373660 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134461276 | GGAATCCTGCTGAGG[C/T]CCCTCTCTGTATTCT | 71007 |
rs33373663 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134461380 | GATACTTCCCACTGG[C/T]TTAGCCTTTTACCAG | 71007 |
rs33373694 | snp | G/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134471974 | CCGACTTGGCTTCTC[G/T]GGAGCAGCATCCTCT | 71007 |
rs33373697 | snp | A/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134471991 | GAGCAGCATCCTCTA[A/T]GGAAAGCCTAATTAG | 71007 |
rs33373699 | snp | C/T | 0.260355 | 0.249785 | intron-variant | D7Ertd443e | Mm_Celera | 7:134472040 | ATTTCTGAGATATAG[C/T]ACCGCGTGTGCACAC | 71007 |
rs33373701 | snp | A/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134472082 | AGGGTGATTGCTCTC[A/G]CCGACACCATGGCTG | 71007 |
rs33373703 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134472343 | GATTAAGTATGAAGG[C/T]TTCCCTCTAATAACA | 71007 |
rs33373814 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134473457 | GAAACTTTTCCAGTT[C/T]TATTTTTTCTTGCCT | 71007 |
rs33373817 | snp | A/C | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134474051 | ATACATTCTTTTACA[A/C]ACTAGAACCATCTCT | 71007 |
rs33373819 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134474125 | AATGCATCTCCAGTA[C/T]CTCTCAAGTCAGTAC | 71007 |
rs33373820 | snp | A/C | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134474167 | TAAAGCATGGTTCTA[A/C]TGACTTCAAAGTGCC | 71007 |
rs33373823 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134474270 | CTGGGTGGGTATTTT[C/T]AGTAGATCAAAGAAC | 71007 |
rs33373875 | snp | A/G | 0.165289 | 0.235211 | intron-variant | D7Ertd443e | Mm_Celera | 7:134487249 | GAAGCCCTTCCTCAT[A/G]AGGATCACAAGTGGA | 71007 |
rs33373877 | snp | C/T | 0.165289 | 0.235211 | intron-variant | D7Ertd443e | Mm_Celera | 7:134488395 | GCCAGGATCTCCTTA[C/T]ACCTTTCTTCCCCTT | 71007 |
rs33373880 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134488634 | ACCCAGTAAAGTTTC[C/T]AGTCCACTTCCTTTT | 71007 |
rs33373883 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134488814 | CATGTTTGCTAGTTC[C/T]ACCATTTCAATGAAC | 71007 |
rs33374004 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134512784 | CAGGAAAAAAAAAAA[A/G]AATACAGGTCCATGC | 71007 |
rs33374006 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134512928 | TGTTGCATTGTGGTT[A/G]TCATGAAACTTACAT | 71007 |
rs33374007 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134513012 | TCTCCCATGTTGAAT[A/G]ACAAGAGAAAGATAA | 71007 |
rs33374015 | snp | C/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134497998 | CCTGCAAAACCTGTT[C/T]CTCCCAGTCAGGCTG | 71007 |
rs33374018 | snp | A/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134498091 | GGCTTTCCTAATAAC[A/T]GCACCAACATTCAAA | 71007 |
rs33374021 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134498120 | AACACTCACCTTATT[A/G]TAAAGCATTAGCAAT | 71007 |
rs33374175 | snp | C/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478754 | TGCACTCTAGGACCC[C/G]AACTTCCCTTTCTGT | 71007 |
rs33374178 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478792 | ATACTATGTCCACAG[A/G]TGTGTGATGTATGTT | 71007 |
rs33374181 | snp | C/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134478858 | CAAACATCAAGCCAA[C/G]AATTTGGACACTGAA | 71007 |
rs33374195 | snp | C/T | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | Mm_Celera | 7:134505981 | CGGAACATCCTTCAA[C/T]GAAAACAGATGTGTG | 71007 |
rs33374197 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134506297 | TGAGCTGAGTGATTG[C/T]CTCAATGAAATGGAA | 71007 |
rs33374200 | snp | G/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134506738 | GGCATTGTTCAGTAG[G/T]TGTAGTAAATAAAAG | 71007 |
rs33374203 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134506813 | GATGTTTCTGAGGCT[C/T]CTAAGGCTCCAGAAG | 71007 |
rs33374206 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134484054 | GCTCTGCTATGCCCT[C/T]TCCATGATCAACCAA | 71007 |
rs33374209 | snp | C/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134484140 | GCATTTTGTCATGGT[C/G]ATGATAAAACGAACA | 71007 |
rs33374211 | snp | A/C | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134484146 | TGTCATGGTGATGAT[A/C]AAACGAACATACTTG | 71007 |
rs33374285 | snp | A/C | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134445487 | GAGAGAGAGAGAGAG[A/C]GCTGAGATCATCACT | 71007 |
rs33374288 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134445979 | TGTGAAAACTCTGAA[C/T]TATTGACACTGGCCA | 71007 |
rs33374291 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134446098 | AGAAATTCTTCCTCT[C/T]ACCCAGCCATATTGT | 71007 |
rs33374355 | snp | A/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134436757 | GACAGCTTACTTAGG[A/T]GGATCAGACATATTT | 71007 |
rs33374556 | snp | C/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134461494 | CTGCAGTCATGATGT[C/G]CACATGCTCCTAGAG | 71007 |
rs33374559 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134462184 | ACTGGAAGGCAGAAC[A/G]GCCTTCAAAAGTAGC | 71007 |
rs33374561 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134462298 | TTGTAAAAGGTGAAA[C/T]TTTTATGGCAATAGC | 71007 |
rs33374656 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134472491 | AGACAGATATGGTAT[A/G]TAACAAACACACCTA | 71007 |
rs33374659 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134472550 | ACACATACCTACTTT[A/G]CATCTACAGCTATTC | 71007 |
rs33374661 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134472604 | ATTAAAATGAGGATT[C/T]AAAACCATAATTTGC | 71007 |
rs33374666 | snp | A/C | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134488852 | TTAACCAGCATTTAT[A/C]TTGATCATGAGTCAG | 71007 |
rs33374669 | snp | A/T | 0.297521 | 0.245442 | intron-variant | D7Ertd443e | Mm_Celera | 7:134490881 | TATGCTAAAGCTGTG[A/T]GAGCTGTCTAGAATT | 71007 |
rs33374671 | snp | A/G | 0.297521 | 0.245442 | intron-variant | D7Ertd443e | Mm_Celera | 7:134491093 | TTCCCTTCACTTCCT[A/G]TGCTCACTGCAGGAG | 71007 |
rs33374814 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134498400 | CTAAAGCTCATGTTT[A/C]AAAAGAATAAGAGAC | 71007 |
rs33374817 | snp | A/G | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134498413 | TTAAAAAGAATAAGA[A/G]ACTGTTCTGCAATCT | 71007 |
rs33374820 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134498520 | AGAGACAGCTAAGTG[C/T]AAACTCGCAGGGCTA | 71007 |
rs33374823 | snp | C/G | 0.260355 | 0.249785 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134499389 | GACACGTTTCATTCT[C/G]GCTTGTTTTCTACTT | 71007 |
rs33374836 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134474315 | GGATGGATGCTAAAC[C/T]TGAACATTCAATACA | 71007 |
rs33374838 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134474456 | TCACACTGATTTTCT[C/T]CTCCAGGAGCAAATG | 71007 |
rs33374841 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134474484 | ATGGTTGAAATATTG[C/T]GAGTCTTTGTGAAAA | 71007 |
rs33374984 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134479169 | GACAGGGATGAGACT[A/G]TGTAGGAAGAACAGC | 71007 |
rs33374987 | snp | C/T | 0.489796 | 0.070696 | intron-variant | D7Ertd443e | Mm_Celera | 7:134479226 | CCTGCACACAAACGT[C/T]GGCGGGTAGGAAGCC | 71007 |
rs33374990 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134479419 | TCATAGACAAGCTTG[C/T]TGCAGCCTTCTCACC | 71007 |
rs33374993 | snp | G/T | 0.244898 | 0.249948 | intron-variant | D7Ertd443e | Mm_Celera | 7:134479517 | AGGCGGTGGGTGGAC[G/T]AGGGCACAAAGGAGA | 71007 |
rs33375078 | snp | C/T | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134507769 | CCTCCCTCTCCCTTC[C/T]GTGCTTTGGCCATGC | 71007 |
rs33375081 | snp | G/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134508002 | CTGAAATACAATACG[G/T]TTCAGCAAAACCCCT | 71007 |
rs33375104 | snp | A/C | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134485253 | TTTTAAAAGTTATTA[A/C]GATTCCCCATGATGG | 71007 |
rs33375106 | snp | A/G | 0.489796 | 0.070696 | intron-variant | D7Ertd443e | Mm_Celera | 7:134485268 | AGATTCCCCATGATG[A/G]CATTCAGCCATTATT | 71007 |
rs33375109 | snp | A/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134486224 | TATATATCATTTTGC[A/G]AAAGTGTCAAAAAAA | 71007 |
rs33375112 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134486302 | GAACCTTCCCATCTG[A/C]ACTCCTGAATCCCTA | 71007 |
rs33375134 | snp | A/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134446162 | GTGTTCTTCAATGTA[A/G]GCTAACCCTCCTTCC | 71007 |
rs33375137 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134446393 | CCACCTTCTCGCCTG[C/T]CTGCTTTAGGCTCAC | 71007 |
rs33375140 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134448361 | GGCTTATTCTTGTTA[C/T]AGAGTAGAAGAGAAG | 71007 |
rs33375142 | snp | C/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134449167 | CCTTATCACTAGATC[C/G]CAACCACCAACTCTG | 71007 |
rs33375158 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134513980 | ATCCTCCCTCTTCTC[A/G]TGTAACTCAGTTTAA | 71007 |
rs33375161 | snp | G/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134514073 | AAAAACATAGAGTAA[G/T]TTATTTTCTATGGTA | 71007 |
rs33375404 | snp | C/T | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | Mm_Celera | 7:134491889 | GATCATCTTGAGTTG[C/T]TTGACCTGGATTGCT | 71007 |
rs33375407 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134492281 | AGCCCATAGTAAAGG[C/T]ACCGGGGAGAGGGTT | 71007 |
rs33375410 | snp | A/C | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134493113 | GAAAGAACTCATATT[A/C]CCACCAGTAGGCAGG | 71007 |
rs33375413 | snp | A/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134493742 | CCTTTTTGGCCCTTA[A/T]CTGGAAAGTATGTCC | 71007 |
rs33375434 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134462346 | AGTCTTTTGGTGAGG[A/G]AACAAGAAGCCCAGC | 71007 |
rs33375436 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134462543 | AAGAAAATGCCTGCA[C/T]AGAGCCAAACGGCAG | 71007 |
rs33375441 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134462751 | GTGCTGAGATGGGCT[A/G]GCAAGTGCTATGGCG | 71007 |
rs33375454 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134472846 | GTTTTTACAATGTGG[C/T]GACTGTGAGTTTAAG | 71007 |
rs33375526 | snp | C/T | 0.277778 | 0.248452 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | D7Ertd443e | Mm_Celera | 7:134499752 | CCCATCCAGATACAA[C/T]CAGGGAAGTCCTCTC | 71007 |
rs33375529 | snp | A/G | 0.260355 | 0.249785 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134499894 | AGAGCTGCAGGTGCC[A/G]AGGCTGAGGCACACA | 71007 |
rs33375531 | snp | A/C | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134499952 | GCTCAAATTCTTCGG[A/C]ACAGTTCTCTCTCCA | 71007 |
rs33375674 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134474527 | GTGACATTGTGGACC[C/T]TGCTTATGATGACAG | 71007 |
rs33375676 | snp | C/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134474954 | ACAAACATACGTGAA[C/G]ATGTACCCACAGACA | 71007 |
rs33375678 | snp | A/C | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134475082 | GCTCCAGATTATCTC[A/C]TACAGATGACTGTGC | 71007 |
rs33375680 | snp | C/T | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134475261 | TAGATCAACTCAATA[C/T]AAGTTTGGCTTCAGC | 71007 |
rs33375682 | snp | C/T | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134475471 | CTCCCTACTTAGTCT[C/T]TTTGCCAGCCACCAA | 71007 |
rs33375884 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134514633 | TCAGGACACTGACGT[C/T]GCCTGAGTCCTGTCA | 71007 |
rs33375887 | snp | A/T | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134514893 | CACAAGCATCCATCA[A/T]CCTGGTCTTTCCTCC | 71007 |
rs33375890 | snp | A/C | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134514979 | CTGTTCGTGAAAGAC[A/C]TCCAGAGAAGGCGTC | 71007 |
rs33376065 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134486334 | GACAGTGGTATACAC[A/G]AGAAAGCCATCGGAG | 71007 |
rs33376096 | snp | A/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134508025 | AAACCCCTAGGGGCA[A/T]TTTAAGCTTAGCCTC | 71007 |
rs33376099 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134508120 | CTCACATAACAGGTC[A/G]GAATAACTGACCTGA | 71007 |
rs33376102 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134508277 | CACACCCCATGCCAG[A/C]AAGTCTTCTCATGGT | 71007 |
rs33376116 | snp | G/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134493807 | ATTTTAGACTGGTGT[G/T]ATCTCCATTGTTAGA | 71007 |
rs33376119 | snp | A/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134493945 | TACAAAGTTGGAATG[A/G]TGGCATGCTCTTAAA | 71007 |
rs33376122 | snp | A/G | 0.165289 | 0.235211 | intron-variant | D7Ertd443e | Mm_Celera | 7:134494266 | CACATTGACACGTGT[A/G]TACACAGCATGCACA | 71007 |
rs33376334 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134500146 | AGCCAAGGTCCTGTG[C/T]AAAACAAAGCAAGAC | 71007 |
rs33376337 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134500423 | GAATGTTAGAACTGA[A/G]AATTGGAGCCCGGGA | 71007 |
rs33376340 | snp | C/G | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134500575 | TTTCCAAAAGATGTG[C/G]ATAAGAACAGAACTC | 71007 |
rs33376343 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134500623 | TTATTCACACTATAA[C/T]TCCCCAGGGATCTTG | 71007 |
rs33376514 | snp | A/G | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134463638 | TTTTCACTGTGTGAT[A/G]CAATGGCACCAATGG | 71007 |
rs33376725 | snp | A/G | 0.48 | 0.0979796 | intron-variant | D7Ertd443e | Mm_Celera | 7:134475582 | TGAATTCTCAGAATT[A/G]TTAGAAAGGTGTTGG | 71007 |
rs33376728 | snp | C/T | 0.336735 | 0.234472 | intron-variant | D7Ertd443e | Mm_Celera | 7:134475636 | AAGCCAAAGCATCAG[C/T]AAAATAATAGACTAA | 71007 |
rs33376730 | snp | A/C | 0.459184 | 0.136902 | intron-variant | D7Ertd443e | Mm_Celera | 7:134475660 | AGACTAAAGTCATGC[A/C]ACTAGGATGTGAAAG | 71007 |
rs33376733 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134476018 | ACTCAGTGTAGACAT[A/G]TCACAGGAAATGCAG | 71007 |
rs33376737 | snp | C/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134516952 | TGATTAGAAGGCTTC[C/G]AGTAGAAGATTTTCA | 71007 |
rs33376742 | snp | A/G | 0.459184 | 0.136902 | intron-variant | D7Ertd443e | Mm_Celera | 7:134517491 | TTATGTATTGCACTC[A/G]TACTAGGAAGGCCCT | 71007 |
rs33376825 | snp | C/T | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | Mm_Celera | 7:134494351 | CGAATCACTGGCATC[C/T]TCCTCCAAGCTTGTC | 71007 |
rs33376828 | snp | A/G | 0.165289 | 0.235211 | intron-variant | D7Ertd443e | Mm_Celera | 7:134494659 | AAATAAATGGGAAAA[A/G]CAAGAGAGAGGTGGA | 71007 |
rs33376831 | snp | A/C/G | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134494722 | GTTGGAGTTTGCTTC[A/C/G]TGTACTTGGGAAGAT | 71007 |
rs33376985 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134509135 | CAGGGTTGCGAGTAT[A/G]GAATATGCCATGAAA | 71007 |
rs33376988 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134509616 | GGGACTTGCCAATCA[C/T]TCTGCTATCCGGATG | 71007 |
rs33376991 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134509650 | GCTTCTCTGCCCATA[C/T]TCTTGGTTGGTCCCA | 71007 |
rs33377146 | snp | A/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134500719 | ATATAAGACCTCAAC[A/T]AAGAAAGGAATCTGC | 71007 |
rs33377149 | snp | C/G | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134501280 | GGAAACCAGCTGTCA[C/G]AGGCATCACCAAAGC | 71007 |
rs33377152 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134501487 | AGAGCAGGGATGTTA[A/G]ATGAAAGGTCAAAGG | 71007 |
rs33377696 | snp | G/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134476036 | ACAGGAAATGCAGGC[G/T]AGCAAACGAATGTTT | 71007 |
rs33377699 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134476208 | TTAGAGCTGCTTCTC[C/T]CTTGTGAGGCTCTTT | 71007 |
rs33377702 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134476332 | ACAGGTATCACCATC[A/G]TTATTTGTTTACTTT | 71007 |
rs33377714 | snp | C/T | 0.260355 | 0.249785 | intron-variant | D7Ertd443e | Mm_Celera | 7:134494874 | GAGGGATGTTTAGAC[C/T]TCACCATGATCCTTC | 71007 |
rs33377716 | snp | A/C | 0.18 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134495552 | CCTCACCTGAGGGGT[A/C]CCTGCACTCTGCTTG | 71007 |
rs33377719 | snp | A/G | 0.152778 | 0.230321 | intron-variant | D7Ertd443e | Mm_Celera | 7:134495846 | GCCACCTATGTATCA[A/G]TTTCTCCATCTGCTG | 71007 |
rs33377722 | snp | C/T | 0.142012 | 0.225474 | intron-variant | D7Ertd443e | Mm_Celera | 7:134496180 | GGCTTGGTTAATTTT[C/T]TGAACCCTACAGGAT | 71007 |
rs33377765 | snp | A/G | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134518395 | ACAGCTTTCAAGGAA[A/G]TCTGGCTTCTGGCCT | 71007 |
rs33377767 | snp | C/T | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134518712 | AGCCTCCTTCTTTCA[C/T]ACTATTCCACACCCT | 71007 |
rs33377773 | snp | A/T | 0.244898 | 0.249948 | upstream-variant-2KB | D7Ertd443e | Mm_Celera | 7:134521082 | CCCCTAGTTGCAGGC[A/T]GCCTGTGATAACTGA | 71007 |
rs33377804 | snp | A/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134509712 | TGGGTTTTCTGAATG[A/T]TAGTTAGTTCTTACC | 71007 |
rs33377807 | snp | G/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134509750 | GTATATTCATGGCTG[G/T]TTTCTAGTGTCTCAC | 71007 |
rs33377810 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134509895 | GTATCAAGAACACAG[A/G]TACTGCAAGTGGTGT | 71007 |
rs33377813 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134509950 | ATTTAGACAGTCTTG[A/G]TCATGTTGGGAAATG | 71007 |
rs33377965 | snp | A/G | 0.391111 | 0.206368 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134501812 | CACTGTCCTACATAA[A/G]GTACAGGCATCTTCT | 71007 |
rs33377968 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134502021 | TTAGGTAATCCCAGA[A/G]TTCTTGACTTCCACA | 71007 |
rs33377971 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134502105 | AGAGATTGTTATATG[A/G]ACTGAAGCACTAGGT | 71007 |
rs33378475 | snp | A/C | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134476514 | CTACTTCTCCAAAGT[A/C]GCTCTGGTCACTGGG | 71007 |
rs33378478 | snp | G/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134476626 | CTGGAAAGTCTTAGC[G/T]TTGGCCCTGCTTTCT | 71007 |
rs33378480 | snp | A/C | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134476728 | GGTCCTGAGTATCTG[A/C]TCCTGATCATCTCAG | 71007 |
rs33378482 | snp | A/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134476832 | TTCATGTACTTGTGA[A/G]TTTAATATGCTTTCT | 71007 |
rs33378626 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134509996 | ATCTAGTCACTGTGG[C/T]AGCCGTTGGGTGTGT | 71007 |
rs33378629 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134510050 | GCCATTCTCTTCAAA[C/T]CAATTTCCCACCTGC | 71007 |
rs33378632 | snp | C/T | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134510072 | CCCACCTGCTCTGTA[C/T]AGGTATTGATTGTCT | 71007 |
rs33378645 | snp | C/T | 0.260355 | 0.249785 | intron-variant | D7Ertd443e | Mm_Celera | 7:134496333 | TCCTCTGTTTCCTCA[C/T]CTGGCAACTTCTCAG | 71007 |
rs33378648 | snp | A/G | 0.260355 | 0.249785 | intron-variant | D7Ertd443e | Mm_Celera | 7:134496347 | ACCTGGCAACTTCTC[A/G]GGACAGGTTCTGCTC | 71007 |
rs33378650 | snp | A/T | 0.35503 | 0.226867 | intron-variant | D7Ertd443e | Mm_Celera | 7:134496479 | TTCTCTAAGCATTAG[A/T]GAAGTGCAGGACTAC | 71007 |
rs33378653 | snp | A/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134496496 | AAGTGCAGGACTACA[A/G]TGATAGCTTTAAGAG | 71007 |
rs33378794 | snp | C/T | 0.277778 | 0.248452 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134502116 | TATGAACTGAAGCAC[C/T]AGGTTAATAGAGAGA | 71007 |
rs33378797 | snp | C/T | 0.260355 | 0.249785 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134502577 | TATTCCTAGAAAAAT[C/T]GTAGGTTTATATCTA | 71007 |
rs33378800 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134502704 | CTGTGTAGGCAACTT[C/T]GTAGCAAATTTTGTT | 71007 |
rs33378803 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB, intron-variant | D7Ertd443e | Mm_Celera | 7:134503000 | CACACTTGAGAAGGA[C/T]AGCTGCTAAAGAGAC | 71007 |
rs33379375 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134510129 | GTTTAATGGCTCACA[A/G]AGCATAGGTCTGAGT | 71007 |
rs33379378 | snp | A/G | 0.124444 | 0.216185 | intron-variant | D7Ertd443e | Mm_Celera | 7:134510176 | GGTAGAAGAGCTTGC[A/G]GATGGCATGTTAGTA | 71007 |
rs33379381 | snp | C/T | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134510209 | TCTTGAAGTGACTCT[C/T]TATTGCTCTCCTGCC | 71007 |
rs33379386 | snp | A/C | 0.444444 | 0.157135 | intron-variant | D7Ertd443e | Mm_Celera | 7:134496687 | GATTGAGAGTTCATC[A/C]CAGCAACCTTGCTCA | 71007 |
rs33379554 | snp | C/G | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134476907 | TATCTCCCGATATTA[C/G]CTTCAAAATCAGGTA | 71007 |
rs33379596 | snp | A/C | 0.231111 | 0.249285 | intron-variant | D7Ertd443e | Mm_Celera | 7:134503368 | ACTTTTTAAGAAGAA[A/C]AGCAGGAACCCATTA | 71007 |
rs33379598 | snp | A/G | 0.132653 | 0.220748 | intron-variant | D7Ertd443e | Mm_Celera | 7:134503400 | AGTTCCAGGACTCTT[A/G]GCCTATAGTGGTGAC | 71007 |
rs33379601 | snp | A/G | 0.391111 | 0.206368 | intron-variant | D7Ertd443e | Mm_Celera | 7:134503566 | AGAAAGCCGACTGGG[A/G]TAAAATCTGTTTGGG | 71007 |
rs33380244 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134510312 | CTGAAGCTGTTGAGC[A/G]TTCTCCAGAGTACTT | 71007 |
rs33380247 | snp | A/G | 0.32 | 0.24 | intron-variant | D7Ertd443e | Mm_Celera | 7:134510442 | ACTGGGAGCCAAACC[A/G]TCAGTACATGGGCAT | 71007 |
rs45655806 | snp | A/G | | | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134402465 | AGAACCCAGGCAGAC[A/G]GATGTGCACTGTGGC | 71007 |
rs45667772 | snp | C/T | | | intron-variant, utr-variant-5-prime | D7Ertd443e | Mm_Celera | 7:134342537 | AAGATAAGAGGCAGC[C/T]CTAGAGTCAATGGTG | 71007 |
rs45703527 | snp | C/T | | | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134402540 | ACTGGCCAACAAGTC[C/T]ACCCAAAGGAGCAAG | 71007 |
rs45712402 | snp | A/C | | | intron-variant | D7Ertd443e | Mm_Celera | 7:134428446 | TAACACAGCACCCAC[A/C]TACCTCCACACAACT | 71007 |
rs45723494 | snp | G/T | | | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134426909 | CAAACAAACAAACAG[G/T]TCTGGCAATTGAATC | 71007 |
rs45724263 | snp | C/T | | | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134400164 | CCTGGCTACATGCCA[C/T]ATTCCCTCTCCAATT | 71007 |
rs45725959 | snp | C/T | | | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134401555 | AGGTGTTTATAACCA[C/T]TGTGTCCCCACAGGT | 71007 |
rs45808320 | snp | A/C | | | intron-variant | D7Ertd443e | Mm_Celera | 7:134440114 | CAAAAACAAAGCGAG[A/C]CTGTCATTTTCAAGA | 71007 |
rs45809443 | snp | A/G | | | intron-variant | D7Ertd443e | Mm_Celera | 7:134415452 | AAGGAGACTGAAAGC[A/G]TTCTCTCTGAGCTCA | 71007 |
rs45911185 | snp | A/G | | | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134400685 | ACTTCAGCATCATGT[A/G]TATCACATCTATGAC | 71007 |
rs45968504 | snp | A/G | | | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134426460 | ACTGTAAAAGCCAGA[A/G]GCATCGAAAACACCA | 71007 |
rs46008846 | snp | C/T | | | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134507114 | TTGGTTCTGTCATCA[C/T]GTGGGGTGACTAAAT | 71007 |
rs46034457 | snp | G/T | | | intron-variant | D7Ertd443e | GRCm38.p3 | 7:134401312 | TGCCATCTGTTCTCT[G/T]ACCCATCACAGACCC | 71007 |