SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6297342 | snp | A/G | 0.5 | 0 | intron-variant | Phf2 | Mm_Celera | 13:48812204 | CTCCCTACGCCTCAG[A/G]TTCCCCAATTATCNA | 18676 |
rs6297360 | snp | A/C | 0.5 | 0 | intron-variant | Phf2 | Mm_Celera | 13:48812218 | GNTTCCCCAATTATC[A/C]AGTTAAAGTCTGAAG | 18676 |
rs6297936 | snp | A/G | 0.5 | 0 | intron-variant | Phf2 | Mm_Celera | 13:48812299 | CGTGGAGGGTCTTGC[A/G]GTGGGGGGAGAGGGG | 18676 |
rs6297966 | snp | A/C | 0.5 | 0 | intron-variant | Phf2 | Mm_Celera | 13:48812318 | GGGGGAGAGGGGGGT[A/C]CAGGCTGTGCCCCAT | 18676 |
rs6298006 | snp | G/T | 0.5 | 0 | intron-variant | Phf2 | Mm_Celera | 13:48812336 | GGCTGTGCCCCATCA[G/T]TCACCTATCAGTGCC | 18676 |
rs6298561 | snp | C/T | 0.5 | 0 | intron-variant | Phf2 | Mm_Celera | 13:48812424 | AACCCAAGTCAGCAA[C/T]GCATGAATCTAACTG | 18676 |
rs6351705 | snp | A/G | 0.5 | 0 | intron-variant | Phf2 | Mm_Celera | 13:48853730 | GACTCTAAACACAGG[A/G]GGTGAGCTTAATCTC | 18676 |
rs6352216 | snp | G/T | 0.5 | 0 | intron-variant | Phf2 | Mm_Celera | 13:48853821 | AAGACTTCTTACAAC[G/T]CCAGGAGATCCCCCA | 18676 |
rs6353747 | snp | C/T | 0.5 | 0 | intron-variant | Phf2 | Mm_Celera | 13:48854100 | GTGATTGGCTGGAGC[C/T]GGGGACAGGCNGGAA | 18676 |
rs6353763 | snp | A/C | 0.5 | 0 | intron-variant | Phf2 | Mm_Celera | 13:48854111 | GAGCNGGGGACAGGC[A/C]GGAAGAGGGGTGGAC | 18676 |
rs13470923 | snp | A/G | | | missense | Phf2 | GRCm38.p3 | 13:48807715 | AGATTGGTGGTGGCA[A/G]CAAAGGCACAGGCAA | 18676 |
rs45635301 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48841076 | TCCCTGATGACAGTG[A/C]TCTAAGTCCTCTCTA | 18676 |
rs45641088 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phf2 | Mm_Celera | 13:48837699 | CCGTCCCTGCAGAGT[C/T]CCATCTCACTACAAG | 18676 |
rs45690174 | snp | G/T | 0.375 | 0.216506 | intron-variant | Phf2 | Mm_Celera | 13:48831449 | CTTTCACAATAAACA[G/T]CAGAAACCCACCAAC | 18676 |
rs45698062 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48819254 | CAGATGTGTGGTCAC[C/T]GCGCCAGCTGCCTCC | 18676 |
rs45707365 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Phf2 | Mm_Celera | 13:48857123 | TTGGCCTGTCACTGG[A/G]TGCTGCTGTGCGTGC | 18676 |
rs45715033 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Phf2 | Mm_Celera | 13:48856197 | GCTGTCTCACCTTCC[A/G]GAGTCATAGGACATT | 18676 |
rs45715536 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Phf2 | Mm_Celera | 13:48849254 | CAGAGCCTCACTGGC[A/C]CTCCAGCTTCCACAA | 18676 |
rs45722831 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Phf2 | Mm_Celera | 13:48856023 | AGCACCATGATACCC[A/G]CCAAGTGCCACTGGA | 18676 |
rs45729497 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Phf2 | Mm_Celera | 13:48803118 | CACTGGTCAAGTGAT[A/G]TAAGCCTCGCTCAGG | 18676 |
rs45796003 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48815339 | TCCCTGCTGCCTCGC[C/T]GGCCCACACTGAGGC | 18676 |
rs45797377 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48855615 | CTAACCTCCTGTAGC[A/G]TGACAGTTTCCCACT | 18676 |
rs45797984 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48819051 | AAGCTGGCATCCTGC[A/G]GTCTTTGAGAAGCAG | 18676 |
rs45835497 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Phf2 | Mm_Celera | 13:48859623 | CACACTTGCCTGAAC[A/G]TTGGCCTCTGCCTGG | 18676 |
rs45841781 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Phf2 | Mm_Celera | 13:48814539 | GGTCTTCAGGACATA[C/T]TTTTCTCAACAGGAG | 18676 |
rs45849081 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Phf2 | Mm_Celera | 13:48817049 | GCCTTCTCCTAGTGC[G/T]CTCAAACAGATGCAC | 18676 |
rs45883370 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Phf2 | Mm_Celera | 13:48855926 | ACTGGTAGGACCAGG[C/T]GCTTACAGGGGAGAG | 18676 |
rs45888197 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48818818 | TTGGTGAAGACAGGC[C/T]ATGGACATGATTCCC | 18676 |
rs45890107 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Phf2 | Mm_Celera | 13:48828567 | GCTCAGATGCCCAGC[A/G]CTCATTTAAAATGGA | 18676 |
rs45892834 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Phf2 | Mm_Celera | 13:48821327 | TTGCACCAGTTGAAG[C/T]GTTCCTTAGGAAGAC | 18676 |
rs45894532 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Phf2 | Mm_Celera | 13:48857789 | GCCTGGCTTTGTGTC[A/G]AACGTTGAGAAGGGC | 18676 |
rs45913769 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48821806 | GGATGCTGGTGTGGC[A/G]GGTAGAGCCTACTGG | 18676 |
rs45913877 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48837426 | TTTAGGGCCTTAACC[A/G]AGCTAGACAAGGATT | 18676 |
rs45928821 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Phf2 | Mm_Celera | 13:48815766 | ATGTCACATATACAC[C/T]GCATGCAGACTCAAG | 18676 |
rs45960341 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Phf2 | Mm_Celera | 13:48831432 | TCAGCTGCCCATGTG[A/C]GCTTTCACAATAAAC | 18676 |
rs46057250 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48803949 | ACCTGTGGGTAGCCA[C/T]GCCGCTGAAACTTGA | 18676 |
rs46111349 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Phf2 | Mm_Celera | 13:48850645 | CCAACACTGGCACAA[A/C]CCTATAACTGAGCCT | 18676 |
rs46138327 | snp | C/T | 0.5 | 0 | intron-variant | Phf2 | Mm_Celera | 13:48852142 | GTACAGAGCTGGTGA[C/T]AGGATAGCCCACCGC | 18676 |
rs46169462 | snp | A/T | 0.42 | 0.183303 | intron-variant | Phf2 | Mm_Celera | 13:48856886 | ACGTTGAATGAATGG[A/T]AGTACTCAGCAACCG | 18676 |
rs46184047 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48814898 | ACTTGGGACCTGTCT[C/G]TCCATCACCCACAGT | 18676 |
rs46197815 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf2 | Mm_Celera | 13:48843509 | TGAGTCTTAGTTTGC[C/T]TAGGAAACTTTGACT | 18676 |
rs46212599 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48835515 | ACAGTTGCAGCTCAC[C/T]ACATGGACCCAGTGA | 18676 |
rs46276329 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Phf2 | Mm_Celera | 13:48827411 | CACACAGAAGGAGAT[A/G]TAAGGGACACACAAG | 18676 |
rs46277420 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48844151 | GAAGATCAGGGAACA[C/T]ACGGAATCCTGAGCC | 18676 |
rs46278656 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48824936 | GGCAGTTCAGTCCTG[A/T]GTAGGTGAGTACGCA | 18676 |
rs46302217 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf2 | Mm_Celera | 13:48852128 | CCCCAGATACACAAG[C/T]ACAGAGCTGGTGATA | 18676 |
rs46313743 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Phf2 | Mm_Celera | 13:48806308 | CCTGCATGGCCACTA[C/T]GGAGCTTCCCGGGCT | 18676 |
rs46402429 | snp | G/T | 0.18 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48857730 | AAAGCCTTCAGTCTA[G/T]CTGGCTGGCTCTGCT | 18676 |
rs46477319 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48821308 | AGCTGCTCAGGACTT[G/T]ACATTGCACCAGTTG | 18676 |
rs46496067 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Phf2 | Mm_Celera | 13:48858079 | TCTCTCTGGTCTCCA[A/G]GCAGTCATTTCTCAC | 18676 |
rs46498306 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Phf2 | Mm_Celera | 13:48836165 | TGTCCAGAAGCCACC[A/G]GTGAACACTATGCAG | 18676 |
rs46582411 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48852067 | TCCACACCTGACTGA[C/T]TCGTTCACTACCCTT | 18676 |
rs46591866 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Phf2 | Mm_Celera | 13:48834753 | AGCTCAAAGCCCACT[C/T]AGATGAAACTGCATG | 18676 |
rs46610071 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48820199 | CTTCAAACAGACCAC[A/G]CAAGGGAGAGCCCAG | 18676 |
rs46621185 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Phf2 | Mm_Celera | 13:48810493 | AGAGACATTTCCTGA[A/G]CCCGAGGAGAGGGAA | 18676 |
rs46662289 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Phf2 | Mm_Celera | 13:48840091 | GGATTGGCATTCTGT[C/T]GATGCCCAGTCAGAG | 18676 |
rs46667173 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48821406 | TCCCATGCCAAAGTC[A/G]GCTGGCCACACAGCC | 18676 |
rs46678364 | snp | A/T | 0.5 | 0 | intron-variant | Phf2 | Mm_Celera | 13:48843504 | CCAAGTGAGTCTTAG[A/T]TTGCCTAGGAAACTT | 18676 |
rs46711693 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48827025 | CAGAAGGTTCACAAC[C/T]AAGAGAGGAGGAAAT | 18676 |
rs46716926 | snp | A/G | 0.375 | 0.216506 | intron-variant | Phf2 | Mm_Celera | 13:48848750 | ACACCTGGGCACCCC[A/G]AGAGCTTGCAGCAGG | 18676 |
rs46740973 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48857170 | ATGGCTGAAGGTGTT[C/T]AGTTTATCGCAGCTC | 18676 |
rs46745747 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48840527 | TATTCACACCGGCCA[C/T]TGAGAATTCACACCA | 18676 |
rs46750917 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Phf2 | Mm_Celera | 13:48862189 | AGGATTTCATCACAG[C/G]AGTGAGCACAGCACA | 18676 |
rs46793130 | snp | A/T | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48851376 | ACATAATCCATATGG[A/T]CAGGAAATCGTTCCT | 18676 |
rs46803959 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Phf2 | GRCm38.p3 | 13:48823451 | GAGATGCTTCTCAAC[A/G]GTGCCTTGTGTGCCA | 18676 |
rs46839645 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48803749 | AGCGACAGGAGGAGA[A/G]GATCCCACATGACTC | 18676 |
rs46916694 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Phf2 | Mm_Celera | 13:48818266 | ACATCTCCCTAGCAG[C/G]TTCCCTTGGTCCTAG | 18676 |
rs46986001 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phf2 | Mm_Celera | 13:48824877 | TGCTGGGACCTCTAC[A/G]TGTGGCCTCATAGGT | 18676 |
rs47000636 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Phf2 | Mm_Celera | 13:48841057 | CACTGAGCACATCTC[A/G]GTGTCCCTGATGACA | 18676 |
rs47001222 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48816366 | TGTGACTCCAGGCTC[A/G]CACAGACTTTCCTCG | 18676 |
rs47030390 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48841923 | ATAAAGACAATTCAG[A/G]ACAATGGAACAGCTT | 18676 |
rs47052726 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48824766 | AACCACAGCCTAGTC[C/T]TGTTGGCCCAGTCTG | 18676 |
rs47181062 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Phf2 | Mm_Celera | 13:48829203 | TGCATGCTGGCCACC[A/C]TTTGTACTGCAGCAG | 18676 |
rs47183726 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Phf2 | Mm_Celera | 13:48834954 | AATAGGGCCACACAC[A/G]TATGGGGCTTGCCTG | 18676 |
rs47199339 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48803824 | CCGGGTTTAGAAATC[C/T]CCCATGGACCCAACG | 18676 |
rs47214381 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48815371 | GTACTCTCTATGGTC[C/T]CTGCAGCTCGGACTG | 18676 |
rs47238855 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48842084 | TGTACAAAGATCACT[C/T]GAAGAAATGGTATCT | 18676 |
rs47262772 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48838575 | AATGTACCTCAAATT[C/T]AGGCAAGATTTGTCC | 18676 |
rs47275911 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Phf2 | Mm_Celera | 13:48844161 | GAACATACGGAATCC[C/T]GAGCCCAGCATTTTT | 18676 |
rs47396553 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48820445 | CAGCATAGCAACCCA[C/T]AGGCTGAGCCCAGAA | 18676 |
rs47429283 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Phf2 | Mm_Celera | 13:48830273 | TAAAAGAGCCTGCCA[A/G]CAGGTCTGTTCATAT | 18676 |
rs47469773 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48833668 | CCAGGGCAGTGTGAC[C/T]CTAGCATCTTCCAGA | 18676 |
rs47492983 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Phf2 | Mm_Celera | 13:48819257 | ATGTGTGGTCACCGC[A/G]CCAGCTGCCTCCTGG | 18676 |
rs47500816 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Phf2 | Mm_Celera | 13:48841032 | GTGTTACTCAGCTCC[A/G]CAGCTGTTTCACTGA | 18676 |
rs47669495 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48825151 | TTCCTGAGTGTGAAA[C/T]GTCCCTAAGTGTGTC | 18676 |
rs47682560 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48835762 | AAGCTTCGCTCGCTC[A/G]GGAGACAGCGACTGG | 18676 |
rs47690685 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48818054 | CAAGAAATGTTCACA[A/C]ATCCCTACAGCCCAC | 18676 |
rs47719201 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48823785 | CCTGCTGGTACATGG[A/G]GAAGCACCTATTGGA | 18676 |
rs47757285 | snp | A/C/G | 0.132653 | 0.220748 | intron-variant | Phf2 | GRCm38.p3 | 13:48840834 | CTCACAGGAGCCACG[A/C/G]AGCATTCGTACGGGC | 18676 |
rs47771202 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Phf2 | Mm_Celera | 13:48837770 | CAGGGATCATGTGAC[C/T]GTCACCCACTTCTGA | 18676 |
rs47781588 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48823438 | TTGGCGCTCAGAAGA[A/G]ATGCTTCTCAACGGT | 18676 |
rs47829093 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Phf2 | Mm_Celera | 13:48834104 | CCAGGCCCCAGAAGA[G/T]CCAAGACACAGCAGA | 18676 |
rs47841213 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48803985 | CTGGAGTATAGGTCG[G/T]CGGGATAAGGGAGGC | 18676 |
rs47904723 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48828163 | TCACCAGGGATGGAT[C/G]AAACCATGTTCAGCT | 18676 |
rs47916275 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Phf2 | Mm_Celera | 13:48819667 | TAGTTAGTGTGGTGT[A/C]TGCTTAGCCTGCCCC | 18676 |
rs47916277 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48833376 | TATGCCTTCCCCAGC[A/G]GATAGGTTGTTGACA | 18676 |
rs47968898 | snp | C/G | 0.46281 | 0.131194 | intron-variant | Phf2 | Mm_Celera | 13:48852323 | AAAGTACTCTCGGGG[C/G]TGAGGCCACGGTGGA | 18676 |
rs47992656 | snp | C/G | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48862104 | AGCCTAAAAAATGTG[C/G]CCAAGTCACCACATC | 18676 |
rs47995360 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Phf2 | Mm_Celera | 13:48817521 | CTTCCCTTTCTTCGG[C/T]GGCTCCATCTTGGTC | 18676 |
rs48002150 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Phf2 | Mm_Celera | 13:48835499 | GCAGTGGGAGTCACA[C/G]ACAGTTGCAGCTCAC | 18676 |
rs48031967 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48853413 | CTATCATTCAGCAGC[C/T]GAGGAGTCTTGATTT | 18676 |
rs48065349 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phf2 | Mm_Celera | 13:48835331 | CCTTTATCACTCTCA[C/T]GTTCAGTCTCCTTCA | 18676 |
rs48086649 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Phf2 | Mm_Celera | 13:48824195 | TCTCGCTGCCTCAGG[C/T]CAAACAGGCCTCTCA | 18676 |
rs48115519 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48822071 | GCAGGTAGCAGAGCC[C/T]ACTAGGTGCTGGGGA | 18676 |
rs48175966 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48837388 | TGACCCATACGCCAC[C/T]GGCTTTTGGTGCTAG | 18676 |
rs48201385 | snp | C/T | 0.260355 | 0.249785 | synonymous-codon | Phf2 | GRCm38.p3 | 13:48823093 | GTTTTCCACCCACGA[C/T]AGTTTCTTCACAATG | 18676 |
rs48223866 | snp | C/T | 0.18 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48806776 | CTTGTTGGTTTCTGA[C/T]CTCACATATGACCGC | 18676 |
rs48231477 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Phf2 | Mm_Celera | 13:48852442 | AGAAGAGTGACTTCA[A/T]CACCCATGTCCAGAA | 18676 |
rs48264187 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf2 | Mm_Celera | 13:48815846 | TGTGTGGTACAGGGC[A/G]GTGCACGGCATTTGC | 18676 |
rs48270459 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48815408 | AAACAGAAACAAGGA[C/T]GTTCCACACAACACA | 18676 |
rs48275477 | snp | C/G/T | 0.408163 | 0.193609 | intron-variant | Phf2 | GRCm38.p3 | 13:48832432 | ATAGGAATGCCAAGC[C/G/T]GTCCATGGTACTGAA | 18676 |
rs48321438 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Phf2 | Mm_Celera | 13:48858200 | CAGCTGTGGCTCAGA[A/G]TGGGATAGATAAGGC | 18676 |
rs48371702 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48859319 | GGCTCGCCAAAAGGT[C/T]CCGCTGTCCCACAAC | 18676 |
rs48451514 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phf2 | Mm_Celera | 13:48821031 | CCTCCCAGAGTAACT[A/G]TAAAGATGCCTTAAA | 18676 |
rs48472545 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Phf2 | Mm_Celera | 13:48856343 | CAAGCCCAGCATGGG[C/T]GACAGTGATCAGTGT | 18676 |
rs48496810 | snp | A/G | 0.197531 | 0.244432 | synonymous-codon | Phf2 | Mm_Celera | 13:48814002 | GAAGCTCTGCAAGGC[A/G]CCGAACACACCAGGG | 18676 |
rs48573649 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Phf2 | Mm_Celera | 13:48801356 | CTAGAAACAGGAAGG[C/T]CACGCCCACCTCCAG | 18676 |
rs48609131 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Phf2 | Mm_Celera | 13:48835192 | ACCCTGATGCTCCCC[A/G]TGGGCTGAGGTACTC | 18676 |
rs48621887 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48819795 | CCTACAGGGGAAAGG[C/T]TGACCTCCCGTCTCC | 18676 |
rs48654628 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48818186 | AGACTCCAAGCCTGG[A/T]CCTGAGGTTCTCCAT | 18676 |
rs48667551 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Phf2 | Mm_Celera | 13:48816480 | CTTTGTTTGCTCTCG[A/G]ATTTCCAGCCTTTCC | 18676 |
rs48672629 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48856785 | CTCTTCCCAAACGAC[A/G]TTCAGGTGGAGCCTG | 18676 |
rs48673671 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48825272 | TTATGCTGTGTCTTC[A/G]TTTGTCCACAGACAT | 18676 |
rs48688161 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phf2 | Mm_Celera | 13:48837425 | ATTTAGGGCCTTAAC[C/T]GAGCTAGACAAGGAT | 18676 |
rs48711168 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48814970 | CTCCTGCAGGCAACA[A/G]GGATATCTCAGCAGG | 18676 |
rs48717593 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Phf2 | Mm_Celera | 13:48859116 | ACAGGTCTTCACACT[A/G]GAGGAATGTGCATCC | 18676 |
rs48787447 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Phf2 | Mm_Celera | 13:48834847 | GGAAGAAGCACTGGA[C/T]TCACAACAGCAGGCA | 18676 |
rs48788887 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Phf2 | Mm_Celera | 13:48837063 | CATTGTGTCTGTCAT[C/T]CTTCCCTCAAAAAAC | 18676 |
rs48878478 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48818736 | TCAAGGAAATGGTAG[C/T]CATAGGACGGCCCCA | 18676 |
rs48888952 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Phf2 | Mm_Celera | 13:48840825 | CACACCACACTCACA[C/G]GAGCCACGAAGCATT | 18676 |
rs48905591 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phf2 | Mm_Celera | 13:48822306 | AAAAAAATGTAGACT[A/G]CCACCTAACAAGTCC | 18676 |
rs48908759 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48862097 | TCACACAAGCCTAAA[A/G]AATGTGGCCAAGTCA | 18676 |
rs48921118 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48830922 | AATAAAAATATAAAA[A/C]CAAAAACAGAAACAG | 18676 |
rs48989177 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48819112 | GATCTTGGGAAAAGA[C/T]GAGGAAGGAAAGGGG | 18676 |
rs48995746 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phf2 | Mm_Celera | 13:48835566 | GCCTGCCTCAGTGAG[A/G]ACCACTCCCATCATT | 18676 |
rs49061509 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Phf2 | Mm_Celera | 13:48835657 | AAGGACAGAACATTC[C/T]CTCAAAGCCTGGAGA | 18676 |
rs49076150 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48840947 | TATTTATAGAACGGA[C/T]TTGCTTATAGAAAAG | 18676 |
rs49098401 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48815124 | GCTGGTGCCTTCACT[C/T]GCTCCTGAGGTCCTC | 18676 |
rs49260200 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Phf2 | GRCm38.p3 | 13:48837826 | GGAGATCCTCTCTCC[A/G]TCACATTTCTGCCCC | 18676 |
rs49295894 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48826896 | ATATAAGCACCAACA[C/T]GCTGTTCTCACTGAT | 18676 |
rs49298337 | snp | C/G | 0.124444 | 0.216185 | upstream-variant-2KB, nc-transcript-variant | Phf2, LOC102642832 | Mm_Celera | 13:48872184 | GAACCAGGGCAAGCA[C/G]TGTGTAACCTAAGGG | 18676 |
rs49358348 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48836260 | TTAGCACGACTTTTA[A/G]ATTAAATGTGCTCCT | 18676 |
rs49420633 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, nc-transcript-variant | Phf2, LOC102642832 | Mm_Celera | 13:48872277 | CCTGTACACAATGAA[C/T]TCATTTCAAGCTACC | 18676 |
rs49481251 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Phf2 | Mm_Celera | 13:48859821 | CTACTGTCCTGTTAG[C/T]TCCTGTATGGCAGGG | 18676 |
rs49491059 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48828367 | GAAATGTTCCATGTG[C/T]TGGGTGTGTTGGCAG | 18676 |
rs49500943 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48836213 | AAATGCTACAACGCC[A/G]CCAGAAGTTCCCAAA | 18676 |
rs49511803 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Phf2 | Mm_Celera | 13:48816274 | GAAGATGAAAGGCAG[C/T]GGAGGAAGACATGGA | 18676 |
rs49641556 | snp | C/T | 0.132653 | 0.220748 | downstream-variant-500B | Phf2 | Mm_Celera | 13:48801550 | CCACCATCTCCATAG[C/T]GGACGCCTGTCACTC | 18676 |
rs49694899 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48814889 | ACTACATCCACTTGG[A/G]ACCTGTCTCTCCATC | 18676 |
rs49701033 | snp | C/G | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48818415 | CCGTGGGGTCAGTGT[C/G]AACCTGGCCACTGCA | 18676 |
rs49754436 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48819212 | GCAAGAGTCACAACT[A/G]TATCCCTAGTACTTC | 18676 |
rs49765341 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48822920 | ACTGTCACCCTGAGG[A/G]CAAGGATGTGTCTAG | 18676 |
rs49807274 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Phf2 | Mm_Celera | 13:48854586 | CAGTCCATTCAAGCT[A/G]GGCAACCACCAAGGC | 18676 |
rs49897479 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48814212 | AGAGGGACATCCTCT[C/G]ATCCACAGCCTCCTC | 18676 |
rs49937151 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48851348 | AAGCTATTCCAGAGC[C/T]GGGTGCTATGTTACA | 18676 |
rs49950698 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Phf2 | Mm_Celera | 13:48822692 | TGGGAAGTCTTCCCA[G/T]CACCTCTGCACTCTA | 18676 |
rs49963077 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Phf2 | Mm_Celera | 13:48827057 | ACACAGAGTAGACAG[G/T]CAAAGGTGCCCTCTG | 18676 |
rs50002774 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48814864 | TGCGTGGGTTCCAAT[C/T]GGCTGGCTGACTACA | 18676 |
rs50006163 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Phf2 | Mm_Celera | 13:48850384 | TGACCAGTGACAGTC[A/C]GCACCTGAACTAAAC | 18676 |
rs50031087 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Phf2 | Mm_Celera | 13:48858765 | GCTGTGGGTCAGGAA[C/T]CACTGTGCACAATGT | 18676 |
rs50083265 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Phf2 | Mm_Celera | 13:48860340 | ACCAGGCCATCTGAA[C/T]CCACTAAGCTTTAGC | 18676 |
rs50107584 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phf2 | Mm_Celera | 13:48821213 | TCAAAATGTGGTCAA[A/G]TTACGTTAGAAGGAA | 18676 |
rs50184789 | snp | C/G | 0.46875 | 0.121031 | intron-variant | Phf2 | Mm_Celera | 13:48843548 | CAATCAATAGCAGCA[C/G]CAAGTGAGGGACCAA | 18676 |
rs50191618 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Phf2 | Mm_Celera | 13:48826005 | CTCCAGGCTGATGAC[A/C]TTGGCTTTGAGTCGA | 18676 |
rs50228911 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf2 | Mm_Celera | 13:48844260 | AGATGGATCTAAGAG[C/T]CCCAGGCTTGAGTGC | 18676 |
rs50246308 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48815046 | CGTGCCTGGTGGTCA[C/T]TCTTCCCATCCACAA | 18676 |
rs50328982 | snp | G/T | 0.18 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48858538 | CAGACCTTCCAAAAG[G/T]GCACACAGGATGGCA | 18676 |
rs50331418 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Phf2 | Mm_Celera | 13:48835758 | TCAGAAGCTTCGCTC[A/G]CTCGGGAGACAGCGA | 18676 |
rs50400167 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48850974 | GCAGGCAGCCAGCCA[C/T]ACTCAATCTGTTCAC | 18676 |
rs50423684 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Phf2 | Mm_Celera | 13:48814558 | TCTCAACAGGAGGGA[C/G]AGCAAGCTGAACAGA | 18676 |
rs50435850 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Phf2 | Mm_Celera | 13:48855316 | TAAAGAGTATCAGTA[G/T]TCCCTGTGTCCCCAA | 18676 |
rs50473937 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf2 | Mm_Celera | 13:48851290 | GTGCCTCTTACACAG[C/T]GCTGGGTGCCTGGCA | 18676 |
rs50528844 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Phf2 | Mm_Celera | 13:48818940 | TGAAGAGCGAGAGCC[A/G]TAGTAGGAAACAATA | 18676 |
rs50595327 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf2 | Mm_Celera | 13:48859556 | ATTGGGCCAGGGTCT[C/T]TGCTACAGCCTGGCA | 18676 |
rs50659609 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48814280 | ACAGTCACGCACTGT[A/G]GAGAAAGATCTGAAT | 18676 |
rs50707650 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Phf2 | Mm_Celera | 13:48825723 | CTTTGGCTCCTGTTT[C/G]ATCTGAGCTGTTCAG | 18676 |
rs50733213 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48827442 | CCATCCTGTTCAAAC[C/T]CTGAGTCAAACGACC | 18676 |
rs50735776 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB, nc-transcript-variant | Phf2, LOC102642832 | Mm_Celera | 13:48872761 | TCAGAGCCCTCCCGA[A/G]GCTGCTGAGCTATAC | 18676 |
rs50777114 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48816214 | CCCTGGGAAGGCTGC[C/T]CAGCTTCAGGGGATG | 18676 |
rs50778069 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phf2 | Mm_Celera | 13:48823402 | AAAGGTCTCAGAGAG[C/T]CTTAAAGTGGCCCCC | 18676 |
rs50798518 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Phf2 | Mm_Celera | 13:48849333 | CAGAGCACATAGCTT[C/T]GAGTTAACTGCTCCT | 18676 |
rs50828600 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Phf2 | Mm_Celera | 13:48859490 | ACACAGGTCTTCAGT[C/G]TGAATGCTCATCTGC | 18676 |
rs50879357 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48817087 | CTTCAGAGCCTTAGC[C/T]GCAGGGGTGAGTTCT | 18676 |
rs50892272 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48822495 | CAGGACTGGAGCAGG[C/T]ATGTGAGGTCACCGC | 18676 |
rs50900144 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Phf2 | Mm_Celera | 13:48837024 | ACACACGTGACAAAA[C/T]AGAAAATGAACAGAT | 18676 |
rs50903859 | snp | G/T | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48849487 | CCTGGGCTCGACAGG[G/T]TGCTGGGATGTGAAT | 18676 |
rs50909655 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48824718 | CCCAACCAGTGGAGG[A/G]GAACTCTCCATCGTC | 18676 |
rs50915745 | snp | A/G | 0.5 | 0 | intron-variant | Phf2 | Mm_Celera | 13:48856297 | GTGGTGTTAGCAGAA[A/G]GAGAGCCTATGAAGA | 18676 |
rs51061547 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48829255 | CCTCATGGGTCTCTC[A/G]CTTTCTCATGCACCT | 18676 |
rs51067966 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48826399 | ACCCTGTGACATTGT[A/G]AAGTGGTGAATCTCA | 18676 |
rs51078084 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Phf2 | Mm_Celera | 13:48818225 | CCTTATCTCTCCAAG[C/T]CTCGGGCATGATTAC | 18676 |
rs51135289 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Phf2 | Mm_Celera | 13:48825411 | GTGCACTGAGTGTGA[A/G]TGGGTGTGTGCAAAC | 18676 |
rs51136417 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Phf2 | Mm_Celera | 13:48836039 | CACACCAACGCATCC[G/T]TCCAGTGAGCACAGA | 18676 |
rs51196558 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Phf2 | Mm_Celera | 13:48825118 | TCCCAGCCATGCCAG[A/T]GCTGTGTCCTCAGAG | 18676 |
rs51254087 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48824899 | CTCATAGGTTGAGGC[A/C]AGTGATAGGCAGAGC | 18676 |
rs51283835 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Phf2 | Mm_Celera | 13:48828612 | GTGCTGGAACAGCCA[A/C]AGGAGGATGGCTGTG | 18676 |
rs51588106 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48822399 | TTATATGAAGCCCGG[G/T]CCAGGCTCTGCACCG | 18676 |
rs51613619 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Phf2 | Mm_Celera | 13:48855544 | CCTTCAGCGAAGCAC[A/G]ACTCTGTAAGGACCA | 18676 |
rs51641353 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf2 | Mm_Celera | 13:48828228 | ACATAAATCTTAAGA[C/T]GCTGAAAGGGGAAGA | 18676 |
rs51649518 | snp | C/T | 0.375 | 0.216506 | intron-variant | Phf2 | Mm_Celera | 13:48829185 | AGAGCTCTGCCGTGT[C/T]CCTGCATGCTGGCCA | 18676 |
rs51685054 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48815782 | GCATGCAGACTCAAG[A/C]GTGATTTGGAATGTC | 18676 |
rs51698619 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Phf2 | Mm_Celera | 13:48837862 | CCATCCTTCCTCAGA[C/T]GTTCTTACCTTAGAT | 18676 |
rs51725585 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48816183 | GGGAAGCTGTTACCA[C/T]TGCATGCACGACCTA | 18676 |
rs51730508 | snp | A/G | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48815867 | CGGCATTTGCCATGT[A/G]TAGTATGGACTTCGT | 18676 |
rs51749634 | snp | G/T | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48818804 | AGCAGGACCACACAT[G/T]GGTGAAGACAGGCCA | 18676 |
rs51776703 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, nc-transcript-variant | Phf2, LOC102642832 | Mm_Celera | 13:48872660 | GGGTGCCTCCATTTA[C/T]TCTCCTTATCTTCTG | 18676 |
rs51788131 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48836030 | ACTGGAAAACACACC[A/G]ACGCATCCGTCCAGT | 18676 |
rs51803472 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48835633 | CACAGCCCTCTCTAG[A/T]GGTAGATGAAGGACA | 18676 |
rs51835572 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Phf2 | Mm_Celera | 13:48841242 | GCCTTGAAGCAAGCA[A/G]GAGCACGGAGCATGA | 18676 |
rs51890830 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48824824 | GACCCACAGACACAC[C/T]GTCCCGCAGACTCAT | 18676 |
rs51916480 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48804059 | CAGAAGGGCTTAATC[C/T]ACCAGCCTGGCTCAG | 18676 |
rs51969445 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48835922 | TCCAGTCTTGGTTAC[A/T]GGTGACAAAGAGAGG | 18676 |
rs51986990 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48819981 | GGGCTCCTAAAGGGC[C/T]GTAATATCCCTTAGA | 18676 |
rs51990594 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Phf2 | Mm_Celera | 13:48801566 | GGACGCCTGTCACTC[C/T]AGTGAGTTGTCTCAG | 18676 |
rs52006658 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Phf2 | Mm_Celera | 13:48857327 | CAGCAGCACAAAACC[A/G]AGCAGCCCTTGTTTA | 18676 |
rs52045111 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Phf2 | Mm_Celera | 13:48825743 | GAGCTGTTCAGTGTG[C/T]TTTAAGAGAAAGGAG | 18676 |
rs52048650 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48822459 | GGACAGACGCGATGA[C/T]GGCGATGACTCAAAG | 18676 |
rs52181741 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Phf2 | Mm_Celera | 13:48830361 | TGTGAGGCAAAGGGC[C/T]GAGGAAACTCTGTCT | 18676 |
rs52208770 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Phf2 | Mm_Celera | 13:48844302 | CTCGCTGCTTAGTAG[C/T]CTCCTTTTACATTTT | 18676 |
rs52300338 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Phf2 | Mm_Celera | 13:48815486 | TGTCAACCAGGTGTA[C/T]AGTGTGGTATGTATG | 18676 |
rs52358195 | snp | C/T | 0.32 | 0.24 | intron-variant | Phf2 | Mm_Celera | 13:48815565 | ACACGTAGTATGAAG[C/T]ATATATGGAGTGTAG | 18676 |
rs52398201 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Phf2 | Mm_Celera | 13:48825631 | CAGCATGTCATTAGT[A/G]TGCACGAGGAGCACA | 18676 |
rs52505147 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Phf2 | Mm_Celera | 13:48848942 | AAGGACGGTGGAAGC[A/G]TGGGCTCACGGGCAG | 18676 |
rs211706621 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48844604 | CAAGTGTGACCTTGA[A/G]TGTTTGATCCTCCTG | 18676 |
rs211709340 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48856804 | AGGTGGAGCCTGCTG[A/C]TTCTGTGTCATGAGA | 18676 |
rs211747813 | in-del | -/CC | | | intron-variant | Phf2 | Mm_Celera | 13:48806848 | ATGGGAGCAGTGACA[-/CC]CCCCCCCCCCCGCCC | 18676 |
rs211763991 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48868000 | ACAGGAAAAGTACAT[C/T]GAGGAGGGAAACCTG | 18676 |
rs211771740 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48855692 | TCATCCCCTGCCCAA[A/G]CATCTGGTTCAGAGG | 18676 |
rs211832157 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48867175 | TCAATTCTATCCCTT[C/T]TGAATCCAAAATCCA | 18676 |
rs211863428 | in-del | -/GGAT | | | intron-variant | Phf2 | Mm_Celera | 13:48838981 | TTACTGTCTCAAGTA[-/GGAT]GGATCTTTCTTAGGA | 18676 |
rs211907991 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48831259 | GGGGTAGGGTTAAAG[G/T]CTCTGAACTTGACTA | 18676 |
rs211914116 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48838922 | GTATACATGTATGTT[A/G]ATGCCAGGGCAGGAC | 18676 |
rs211915948 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48815336 | GTCTCCCTGCTGCCT[A/C]GCTGGCCCACACTGA | 18676 |
rs211977080 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48838500 | TTACCACAGCAGCAC[A/G]GCTGTGTAAATCAAG | 18676 |
rs211977446 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48807009 | GAGGATCTGTGCATG[A/C]GTGTTTACAGCAGCC | 18676 |
rs212048691 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48808315 | GTCCTACACTGAGAA[A/C]GAGGAGTCCCCACAT | 18676 |
rs212096878 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48829487 | TGACTTCAAAATTTA[A/G]TACAGGAGTCAAGTG | 18676 |
rs212119671 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48837280 | CACTGAATAAAATAA[A/C]AAAAAAGAAAAGTCT | 18676 |
rs212154297 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48822444 | CATTCTCATGCTCCA[A/G]GACAGACGCGATGAC | 18676 |
rs212180543 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48843314 | GATCCTGTCTCAAAT[C/G]GATACTCTCTGACAG | 18676 |
rs212181954 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48836646 | GCCTTTTCTTGACTT[A/C]CTGTATCCCCGCAAA | 18676 |
rs212210504 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48845115 | ACCACATCGGGCCCA[A/G]GCAGTGAACTCAGGC | 18676 |
rs212242779 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48842410 | ACATAGGGGAGGGGC[A/G]AGCATGCCCTTCCAG | 18676 |
rs212274880 | in-del | -/CAT | | | intron-variant | Phf2 | Mm_Celera | 13:48846969 | TGAAAATTCACACAG[-/CAT]TAAAACCTGTGCTAG | 18676 |
rs212462947 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48854073 | CCTCCTGCTGGCCCA[A/G]TTCACAAGAAGGTGA | 18676 |
rs212483151 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48823170 | GGCAGTCAGGAGGAC[A/G]GGGCCCCGGGGCTCC | 18676 |
rs212520008 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48834386 | GCTCTTTCTGCTCAT[A/G]GGTCTTAGTCTACGA | 18676 |
rs212550033 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48827104 | TGCTCAGACCCAAGG[C/T]GGAACCTGTCGGAAC | 18676 |
rs212583886 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48833825 | CAAGTCCTGGTGGAC[A/G]CTCTCCATGTTTGTC | 18676 |
rs212584030 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48840061 | GTCTCACTTAGCTAT[C/G]TATCTATGAGTTACG | 18676 |
rs212602414 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48848467 | GCTCAAAGTGAAAGC[A/G]CTGACCTAGTGTGCA | 18676 |
rs212615333 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48819282 | TCCTGGGACTCTCTC[A/G]GCCCTTTCCAGGTTA | 18676 |
rs212648074 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48839575 | GTGTGTTTGTGTGTG[A/T]GAGAGAGAGAAAGAG | 18676 |
rs212675030 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48811396 | GCACCCAGAACTGGG[C/T]ACCAAGGTGAGGGCC | 18676 |
rs212833618 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48826588 | ATAAAGGCTTGGTCC[C/T]AGCCTGTGCTGCTAT | 18676 |
rs212858182 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48834913 | GGGGTGTTAGGTGGG[A/T]TAAACCAAGCTCCCA | 18676 |
rs212883640 | snp | C/T | | | synonymous-codon | Phf2 | Mm_Celera | 13:48817656 | CAGAGTTTTGGGGGG[C/T]TTGGGGGATTTGGGG | 18676 |
rs212887817 | in-del | -/GAA | | | intron-variant | Phf2 | Mm_Celera | 13:48846661 | CGACAAGCCCCTCAT[-/GAA]GAAGATCTCTTGATG | 18676 |
rs212919038 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf2, LOC102642832 | Mm_Celera | 13:48869989 | TGCCTGAAGCAGAGA[A/G]GAGGGAAATGGGGAG | 18676 |
rs212919675 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48818716 | AACTATCCCAGCTTT[A/G]AGTCTCAAGGAAATG | 18676 |
rs212924300 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48809352 | CCACACCTAGGCCCT[G/T]TCAGGAGAGTCTGAG | 18676 |
rs212986522 | snp | C/T | | | intron-variant | Phf2 | GRCm38.p3 | 13:48809951 | CACAGTACCCTTTCC[C/T]GCACAGTACCCCTCC | 18676 |
rs213081657 | snp | A/G | | | synonymous-codon | Phf2 | Mm_Celera | 13:48832102 | GCCGTGTTTGTGCCA[A/G]GTCCGCTTTTTCTTG | 18676 |
rs213124010 | in-del | -/T | | | intron-variant | Phf2 | Mm_Celera | 13:48823517 | AGACAGCCCAGAGAC[-/T]CCCCCCACCCCCCTC | 18676 |
rs213203092 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48858212 | AGAATGGGATAGATA[A/C]GGCTCAAAAAGAAGA | 18676 |
rs213294533 | in-del | -/CC | | | intron-variant | Phf2 | Mm_Celera | 13:48869061 | AGACTCATTATCTCA[-/CC]CCCCCCCACCCCCTT | 18676 |
rs213311800 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48864315 | TCAAGTGGTAACATC[A/T]CATGAACTGAAATTT | 18676 |
rs213313044 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48804747 | AAGTATGGAGGGGTG[C/T]GGCCCATCAGCTGCC | 18676 |
rs213373771 | snp | A/G | | | synonymous-codon | Phf2 | Mm_Celera | 13:48805847 | GCTGTACGGAGCATC[A/G]TCTGAGCCTTTCCTC | 18676 |
rs213383733 | in-del | -/G | | | intron-variant | Phf2 | Mm_Celera | 13:48820961 | AGGGATTTGTTTCTA[-/G]GTTATCCCAGGGGGA | 18676 |
rs213501571 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48855498 | GTCTGAGGTCTTCTC[C/T]GATGAAAGCTCAATT | 18676 |
rs213523961 | snp | A/G | | | synonymous-codon | Phf2 | Mm_Celera | 13:48828838 | GGCAGGGACAGCTAA[A/G]CCCAGGCCATCTTTC | 18676 |
rs213554827 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48847471 | AGTATTCCTACAGCA[A/C]GATGTGAGGTAAAGA | 18676 |
rs213612693 | snp | C/G/T | | | intron-variant | Phf2 | GRCm38.p3 | 13:48864936 | GAGTCCCACAGGCAT[C/G/T]CAGCACGGCAGCCCT | 18676 |
rs213622948 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48859148 | TTCCTCAGTGTGTTC[C/T]CGAAGACAGACTGGC | 18676 |
rs213672234 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48821329 | GCACCAGTTGAAGTG[C/T]TCCTTAGGAAGACTT | 18676 |
rs213718934 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48816813 | ACACATCCACCCCTC[C/T]GTCCCTCCTTTCTTC | 18676 |
rs213739814 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48813834 | TCGGCCGAGATCCCT[C/T]GGAACCCCCTGCCCA | 18676 |
rs213748849 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48862247 | CTAGAACAATGAAAC[A/G]AATACCTAAAGGTGC | 18676 |
rs213788274 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48814621 | CCATTGCAGCCTCCA[A/G]CAGTCTCAGGAAAGG | 18676 |
rs213809669 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48861301 | GGCTAAATACTTGAT[C/T]CCAAATAGCCAAAAT | 18676 |
rs213887362 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48836445 | ACAAGACGGTGGCAG[A/G]TGCCTACTGTCGCAG | 18676 |
rs213889285 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48811991 | ATCTAAAAACAGCTC[C/T]GGCAGATGAAGGAAC | 18676 |
rs213945599 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48835768 | CGCTCGCTCGGGAGA[C/T]AGCGACTGGCACTGA | 18676 |
rs213945711 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48812566 | AATGAGATCTGAAGA[A/C]AGCTACAGAATACTT | 18676 |
rs213954335 | in-del | -/A | | | intron-variant | Phf2 | Mm_Celera | 13:48852338 | CTGAGGCCACGGTGG[-/A]AAAGGGGCACGGTGT | 18676 |
rs213997313 | snp | A/G | | | utr-variant-3-prime | Phf2 | Mm_Celera | 13:48802739 | CGATGGGTGGACACC[A/G]CCACCTGAGATGGCC | 18676 |
rs214118639 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48857990 | CTGGAGCAGGAGTTA[G/T]AAGTGATCATGAATC | 18676 |
rs214161013 | in-del | -/AT | | | intron-variant | Phf2 | Mm_Celera | 13:48831871 | TCCCCAGTGAAAGAC[-/AT]GTGGGCTGAGTGAAC | 18676 |
rs214170450 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf2, LOC102642832 | Mm_Celera | 13:48869358 | TAGATATTTGGGGGA[A/G]GCAACACAAGATACT | 18676 |
rs214188818 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48822264 | ATTCCATGACACTAC[A/C]AATTCCACATGGGCT | 18676 |
rs214201180 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48824921 | AGGCAGAGCAGCCAC[A/G]GCAGTTCAGTCCTGT | 18676 |
rs214257277 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48840755 | CACAGCAGCCATGCC[A/G]CAGCCTTTACATAAG | 18676 |
rs214263463 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48841546 | AAAAAAGTAGAAAAA[C/T]CACACTTACAGGTTT | 18676 |
rs214318377 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48850115 | CACATACTACAAGCA[G/T]AATATAACACACATG | 18676 |
rs214320958 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48832329 | ACTGCCACCTTCCTG[A/C]CAGGACCTTCCCCGT | 18676 |
rs214357174 | in-del | -/C | | | intron-variant | Phf2 | Mm_Celera | 13:48808588 | TCATCTACACCTACA[-/C]ACCCATCCACGCCTA | 18676 |
rs214421990 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48845297 | GCAAAGTTATAAAGG[A/C]AGGAATCCTTAGATA | 18676 |
rs214489171 | in-del | -/AG | | | intron-variant | Phf2 | Mm_Celera | 13:48862354 | CTGACCTACACACAC[-/AG]ACACACACACACACA | 18676 |
rs214508634 | snp | A/G | | | synonymous-codon | Phf2 | Mm_Celera | 13:48804636 | GGTACCCGTGGAGGC[A/G]GAGGCAGAGGTGGAG | 18676 |
rs214515906 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48823981 | GTACTTCTCCACGGC[C/G]TTTGCTACAGTCCCT | 18676 |
rs214567955 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48842199 | TGTTGCAGATCCTGC[C/T]CCGTAGCTGTCACGG | 18676 |
rs214568578 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48837366 | ACAGATAGGAAAGTA[A/G]CAATCTTGACCCATA | 18676 |
rs214615758 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48868116 | ACTAAGTAACTTAGA[A/T]GTGGAGTGGAAGGTA | 18676 |
rs214663906 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48809096 | GCATCCCAAACTGGG[A/T]TTAGGGAGCAGTGCT | 18676 |
rs214669846 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48839403 | GTCAGTCTCTTCAGT[A/T]CCTTTGATAAGTTGC | 18676 |
rs214721150 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48846099 | CTTCTGGCTGGAGGT[G/T]CAAAGGTGCATGCAC | 18676 |
rs214775433 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48831107 | AGTAAAAGAAGCCAC[C/T]CCTATACTGGGTGAT | 18676 |
rs214782629 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48830390 | CTCAGAAAGAAGAAG[A/G]GGAGGAGGAAGAGGA | 18676 |
rs214829983 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48823386 | TAAAGAGGGGTAAGA[A/G]AAAGGTCTCAGAGAG | 18676 |
rs214842398 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48819424 | AGTGTTAGCAGGCCA[A/G]CTTAGGCCAGCCTGG | 18676 |
rs214845488 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48827890 | GGCTTCCATTTTCCA[A/G]CAGGGGTGGCAGGAT | 18676 |
rs214895056 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48815407 | GAAACAGAAACAAGG[A/C]CGTTCCACACAACAC | 18676 |
rs214907930 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48820243 | CTCAGGTTCCCCCCC[C/G]ACCCCCCGGGCTTGA | 18676 |
rs214942850 | in-del | -/G | | | intron-variant | Phf2 | Mm_Celera | 13:48828148 | AATTGTCACCAATGT[-/G]CACCAGGGATGGATC | 18676 |
rs214961278 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48808447 | CCTATACCTGTGCCC[C/T]GGTCTCACCTCTACC | 18676 |
rs215021976 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48862557 | CAAGTTCTAGGCCAG[A/T]CAGGACCACATGATG | 18676 |
rs215120508 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48839008 | AGGACCTGAACCTTA[C/T]CATGTATACACTAGC | 18676 |
rs215176730 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48827158 | ACCAGGCCCCAGACC[A/G]AGGTGGCATCATTAC | 18676 |
rs215219296 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48859262 | TAGATTCCGAGTCAG[C/T]GTTTGTTCTTTTCCC | 18676 |
rs215263373 | in-del | -/CACACACACA | | | intron-variant | Phf2 | Mm_Celera | 13:48843982 | ATACATGTGCACATT[-/CACACACACA]CACACACACACACTC | 18676 |
rs215346683 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48835008 | TTTATCATCTGAGCC[C/T]CAAGCTCTCACTTAA | 18676 |
rs215367748 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48844299 | CTACTCGCTGCTTAG[C/T]AGCCTCCTTTTACAT | 18676 |
rs215383359 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48816167 | GACCAGATCATGCCC[A/T]GGGAAGCTGTTACCA | 18676 |
rs215418506 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48849911 | CAGACACACACACAC[A/C]CCATATATATACTAC | 18676 |
rs215420723 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48840540 | CATTGAGAATTCACA[C/T]CAGCCATGGAAAAAT | 18676 |
rs215420900 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48812630 | GTGTGGCCAACCGGA[A/G]CGAGCAGGGTTGACC | 18676 |
rs215438678 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48825542 | GCATGGTCTGTGTGT[C/T]ATGAGTGTGTGTCAA | 18676 |
rs215487379 | in-del | -/ACCT | | | intron-variant | Phf2 | Mm_Celera | 13:48820398 | AGCCCAGAGCATGGA[-/ACCT]ACCCCTCTTCCCCTC | 18676 |
rs215500964 | in-del | -/CTCACTGCTGG/CTCCCGGCTGG | | | intron-variant | Phf2 | Mm_Celera | 13:48822633 | GGTGAGCCCCTAACC[-/CTCACTGCTGG/CTCCCGGCTGG]CTCATGTAGCCACCA | 18676 |
rs215541073 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48860038 | AGCTCAGGACTTGGA[A/C]TCCCTGGAAGGTCCT | 18676 |
rs215591642 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48854365 | GGCAGAAAGACAAGG[C/T]CTGATCCCCTGGCCA | 18676 |
rs215640213 | in-del | -/CTCCAGCACAGTACCCC | | | intron-variant | Phf2 | Mm_Celera | 13:48810184 | TAGTACAGTATCCCT[-/CTCCAGCACAGTACCCC]CTCCAGCACAGTATC | 18676 |
rs215777180 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48845077 | GAAACTGGAGAAACC[A/C]TTGCAGGAGTTGGTT | 18676 |
rs215791118 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48811178 | AGGAACTGCCTGCGG[C/G]GGGCTGCGGGAGCTG | 18676 |
rs215820025 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48812068 | GCACAGACAAGTGGA[C/T]GTAGCCCAGCACTCA | 18676 |
rs215841993 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48844511 | AAATTTTGTTTAGCT[C/T]TGCCACTGCCCAGTT | 18676 |
rs215897889 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48855621 | TCCTGTAGCGTGACA[A/G]TTTCCCACTTGCTAC | 18676 |
rs215904892 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48834433 | CTCAGCTTGCACTGA[C/G]CACCAGGGTGAGATT | 18676 |
rs215910994 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48815227 | CCTTCTGGGTGTGCC[C/T]TGCCCTGCCCCACTG | 18676 |
rs216016824 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48852050 | AGGTGGTGCTTAGCG[C/T]ATCCACACCTGACTG | 18676 |
rs216048750 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48828993 | TGTCCCTGACCACAT[A/G]CCTCCCAGGTCCCTA | 18676 |
rs216075641 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48851384 | CATATGGACAGGAAA[A/T]CGTTCCTGTGTGTCA | 18676 |
rs216075642 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48864147 | GGGCCAGAAGGGGAT[A/G]GGGACAGGCAGGAAA | 18676 |
rs216109720 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48829385 | AAACTCACAAGCTGA[C/T]CCTAAAATCCACCGT | 18676 |
rs216184607 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48818500 | GGGATGGGATGGGGG[A/G]AGGGGCAGCTGCCAT | 18676 |
rs216317269 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48865018 | TGGAGACTGAGACGT[C/T]AGAGGGCTCTTGCAG | 18676 |
rs216336068 | in-del | -/C | | | intron-variant | Phf2 | Mm_Celera | 13:48823174 | GTCAGGAGGACGGGG[-/C]CCCGGGGCTCCCATT | 18676 |
rs216355911 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48839556 | ATCATGCAACAGTGT[A/G]TGTGTGTGTTTGTGT | 18676 |
rs216414248 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48847202 | CAGCATGCAAAACTA[C/T]GGTGGCAGGAAAAAG | 18676 |
rs216415576 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48839082 | CCACCGGACACCCTA[C/T]GGAAAAACTAACTGA | 18676 |
rs216425666 | in-del | -/T | | | intron-variant | Phf2 | Mm_Celera | 13:48831944 | CAGGGCTTCAGTGGA[-/T]TGGGCCCATGCCTTG | 18676 |
rs216451857 | in-del | -/G | | | downstream-variant-500B | Phf2 | Mm_Celera | 13:48801386 | GGGCGAGTGACACCA[-/G]GGTGCTTATGGGGCT | 18676 |
rs216470335 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48846201 | ACCAATTAAAAGGCA[A/G]AGACTGTAAAATAGA | 18676 |
rs216478671 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48818147 | AGGCTCAGGAGGCTG[C/T]CTGGGTCTGGTTCCT | 18676 |
rs216499826 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48837881 | CTTACCTTAGATAAA[C/T]GCAAGGAAGAGCCAC | 18676 |
rs216570767 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48818006 | TGTTGCATACTGTCA[A/G]GTGACATGGCTCATC | 18676 |
rs216586923 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48814797 | GTCTCAGGGACACTT[A/C]TACTGAAATGACAGA | 18676 |
rs216597955 | in-del | -/GTAGAGGTCACCAG | | | utr-variant-3-prime | Phf2 | Mm_Celera | 13:48803294 | CTCCTAAGCAGAGCC[-/GTAGAGGTCACCAG]GCTCCAGTGGGGAGC | 18676 |
rs216646426 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48810146 | CCTCCAGCACAGTAC[C/T]CCCTCTAGCACAGTA | 18676 |
rs216661271 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48806148 | CCCCCACCCCAGGCT[A/G]GCTTCAGGAGCCTGT | 18676 |
rs216661610 | in-del | -/CCCTCT | | | intron-variant | Phf2 | Mm_Celera | 13:48854672 | ACCTCCCTCTCAACC[-/CCCTCT]CCCCCCCCCCCCCGA | 18676 |
rs216729186 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48866843 | CAGGTTTAAGGATGT[C/T]GGATGAATTTATGCA | 18676 |
rs216743298 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48842325 | GATCCTGTGGTGCAG[C/T]GCATTATGGTGGGGG | 18676 |
rs216788999 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48816745 | GCCTACCTATCCATC[C/T]CTATCCGTTTACCCA | 18676 |
rs217028570 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48824084 | TTCTCTTGGTCATGG[C/T]GTTTTATCGTAGCGA | 18676 |
rs217050808 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48803709 | AGGTGGGGAGAAATT[A/C]TTTTTTAAAAAGACC | 18676 |
rs217055369 | in-del | -/GAGA | | | intron-variant | Phf2 | Mm_Celera | 13:48842685 | TGTGTGTGTGTGTGT[-/GAGA]GAGATATGTGTGCAC | 18676 |
rs217080389 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48821286 | CCCGGGAGAGGCTGG[C/T]GGCCTCAGCTGCTCA | 18676 |
rs217080496 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48812810 | GCCCGGTTCTCAGCA[A/G]TCAGTGGCTAGGGCC | 18676 |
rs217141310 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48813654 | GTCCTTGCACATCAA[A/G]CACAAGCGCGCTGCA | 18676 |
rs217305312 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48841715 | AGTTCAAGGCCAGCC[A/T]GGTCTATATAGTGAG | 18676 |
rs217310861 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48836572 | CAAAAAACAATTACA[A/G]CTCCTAGGAAATGAT | 18676 |
rs217344386 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48849125 | TTTGTTACACATATT[A/T]ATTTAGGGTATATGC | 18676 |
rs217403879 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48820278 | ACCCAAAGTGACAGC[C/T]ACCATGGGTGGAAGC | 18676 |
rs217489732 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48841477 | AAGATCTGACACCCT[C/T]TTCTGGAGTGTCTGA | 18676 |
rs217493215 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48818617 | GGCCTCCCCTGAGGC[C/T]ACCCCTAGCTAACTG | 18676 |
rs217521079 | snp | A/G | | | synonymous-codon | Phf2 | Mm_Celera | 13:48804399 | GAGAAAGACTCCAGG[A/G]GCCATGGGCTGGGAG | 18676 |
rs217533303 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48837137 | ACCAGGCTTGATAGC[A/G]TGAGATCAATTCCCT | 18676 |
rs217538139 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48840672 | ACTTTACACTGCCAT[A/G]GAGAATCCACACCAG | 18676 |
rs217542221 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48811271 | GGGGCACGGGGCCAC[A/G]GCAGCTCTGGTTTCT | 18676 |
rs217590327 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48850038 | TGCACATACATATCA[C/T]ATAATCCATACGCAA | 18676 |
rs217594606 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48811800 | GAACATGATATTGCA[C/T]TCAAAACAGTAATCT | 18676 |
rs217650680 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48837567 | TAGTATATAAAAATC[C/T]TCAGCAAACTATATC | 18676 |
rs217679699 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48858950 | CTGCAAGGTCAGGGC[A/G]GCATTAGAGGTGGCC | 18676 |
rs217702921 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48843858 | GACACCTGCTGCCAA[A/G]CCTGATGACCAGAGT | 18676 |
rs217708214 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48826375 | GATTCATGGGTGCTG[C/T]TTTTCTGGACCCTGT | 18676 |
rs217758040 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48842892 | GGGTTTCAGGCATTC[A/G]CCTAGCTTTTAAATG | 18676 |
rs217759533 | snp | C/T | | | utr-variant-3-prime | Phf2 | Mm_Celera | 13:48803162 | GGACATTCAATACCC[C/T]ACAGCTCCTTTCTGT | 18676 |
rs217775672 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48825659 | ACATTCATCTGGAAG[G/T]GACTCGTCCATGCTG | 18676 |
rs217834609 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48806204 | TGCTGCAGCAGCGAG[A/T]GAGAGACTGAGGGGA | 18676 |
rs217904571 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48834355 | CACCCCACTGTCTGC[A/G]TCTATTTCCTCTTCA | 18676 |
rs217944411 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48837989 | GTGGGGGAGGGAGAC[A/C]GAGTTTCTCTGTAGC | 18676 |
rs217951857 | in-del | -/A | | | intron-variant | Phf2 | Mm_Celera | 13:48862610 | AAAACCAACAGGAAT[-/A]AAAAAAAACAATAGG | 18676 |
rs218019799 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48813208 | TATGGGTGAGGTCCT[C/T]ATGAGACAGGTGTGG | 18676 |
rs218070391 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48814214 | AGGGACATCCTCTCA[C/T]CCACAGCCTCCTCCT | 18676 |
rs218093258 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48833628 | CTTGGAAATGACTCC[C/G]AGGTGCACCTGTGGC | 18676 |
rs218125633 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48805061 | TGGGTACCATGTGAG[G/T]GAGAGGTGCCTATCT | 18676 |
rs218203217 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48808604 | ACCCATCCACGCCTA[C/T]ACCCCTATCTATACC | 18676 |
rs218257434 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48831178 | CGAGAAAGCAGGACC[A/T]GAAGGAAAAGGTGCC | 18676 |
rs218329469 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48809200 | CTTCCTGGTGGTCTC[C/T]ACAGTCTCCACCAGG | 18676 |
rs218332680 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48838478 | GGGGAAGTTGTGGGA[C/T]GCAAGATTACCACAG | 18676 |
rs218367080 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48809720 | GGAGAAAGCGTCAGA[C/G]CCTCTGAAAAGAAGC | 18676 |
rs218400774 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48858125 | CTGAGTTCTCCAGGT[C/T]TGACACGAGCATACC | 18676 |
rs218411422 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48830424 | GGAAGAGAAAGAGGA[A/G]GGGGAGGGGAGGAAG | 18676 |
rs218420821 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48810426 | GCCCCACTGAGATTG[A/G]ATAGGCAAGCTTGGA | 18676 |
rs218470590 | snp | A/C | | | intron-variant, upstream-variant-2KB | Phf2, LOC102642832 | Mm_Celera | 13:48869655 | CTCCAGCCTGCTACT[A/C]GCTGTTAAAAACTCA | 18676 |
rs218545869 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48868395 | ACCTCCAACTCAATG[C/T]ATAACCAAGGTTGGC | 18676 |
rs218661313 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48832783 | TGTACGGTTTGGGGT[C/T]GAGCCTTAGAACCCA | 18676 |
rs218710359 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48860596 | AGGATACAAGGAAGG[A/G]GGTGGAGAGCTGCTC | 18676 |
rs218744506 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48868752 | GGCTACAGGAGCAGG[A/G]AGAGGCCCCAGCCTT | 18676 |
rs218750462 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48803810 | CAGCTAGGCTGAGCC[C/G]GGGTTTAGAAATCCC | 18676 |
rs218794993 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48867593 | CTTAAGAGATCCTCA[C/T]TCTAATCCTCCCCAA | 18676 |
rs218810346 | in-del | -/A | | | intron-variant | Phf2 | Mm_Celera | 13:48848514 | TATCCAGCACTGAGG[-/A]ACGCAGTGAAAGAAG | 18676 |
rs218876115 | snp | C/T | | | synonymous-codon | Phf2 | Mm_Celera | 13:48804678 | GGCAGTGTTAGGAGC[C/T]GGCTTCCTTTTGGTG | 18676 |
rs218877212 | snp | C/G/T | | | upstream-variant-2KB, nc-transcript-variant | Phf2, LOC102642832 | Mm_Celera | 13:48872256 | GCAGACAGGTTACCC[C/G/T]GTCAACCTGTACACA | 18676 |
rs218882551 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48835735 | GTGTGTCCCTCCCAA[A/G]AGCCTGCTCAGAAGC | 18676 |
rs218929311 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48827271 | CACAAGCAGGTCTTC[A/C]CGCTGGAGCTCTCAA | 18676 |
rs218946165 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48852250 | AAGGCTGGGCAGAGC[C/T]CTAAGCTCCCAGGCC | 18676 |
rs219034820 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48864275 | GAGTGTCACCTTGTG[C/T]GGTGCAGAGGTAAAT | 18676 |
rs219045684 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48862904 | GTGTGTGTGTGCTCG[A/G]CACACACACATGTAA | 18676 |
rs219080990 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48831487 | TCTGCCCAGTGATGC[C/T]ATCCTTCTAACGTAA | 18676 |
rs219081108 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48839213 | AGATATAACACCAAC[A/G]AAAGAGGCGGCAGCA | 18676 |
rs219088345 | snp | A/G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48827946 | TTTTATGTGGGTCCT[A/G/T]GGGATGCAAGGTCAT | 18676 |
rs219110217 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48863254 | AGCATCAGATAGAGG[C/T]GGGGTTGCTAGAACA | 18676 |
rs219131249 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48838851 | TGTGTGTGTGTGTGG[C/G]GGGGTGTGTTTGTGT | 18676 |
rs219153675 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48816292 | AGGAAGACATGGAGA[C/T]GATGGCATGCTTGGT | 18676 |
rs219163051 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48861819 | AGTGAGGGAGTTCCA[C/G]GCCAATGAGAAAGCC | 18676 |
rs219176758 | in-del | -/ACAC | | | intron-variant | Phf2 | Mm_Celera | 13:48847675 | CACACACATACACAA[-/ACAC]ACACACACACATATA | 18676 |
rs219211450 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48808681 | CCTCACCTACACCTA[C/T]ACCCTTATGCCTACA | 18676 |
rs219218939 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48860486 | GAGCACCTGGTGCAG[C/T]TCCAAAACACCACCA | 18676 |
rs219239671 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48861253 | GCAGAAAAGTACCAG[C/T]CAATCCTCCAATTTA | 18676 |
rs219398168 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48828475 | CCCCACCTCCACTCC[C/T]GCCCCCGCCACAACA | 18676 |
rs219405523 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48835104 | TCTGCATGACTGCCT[A/C]GGAGGGCAAGAGTAA | 18676 |
rs219410461 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48834768 | TAGATGAAACTGCAT[A/G]GTATGAGCAGATCCT | 18676 |
rs219427729 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48836716 | GTTTGCCAGCTCTTA[C/T]CTAGGCTCACCAAGA | 18676 |
rs219499113 | snp | C/T | | | downstream-variant-500B | Phf2 | Mm_Celera | 13:48801509 | GACAGGGCTGATACA[C/T]CTTCAGCCTTGCCTA | 18676 |
rs219513215 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48839702 | ATGTTTTTAGATTAC[A/G]TATTAGGTAAGGGTC | 18676 |
rs219554974 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48803899 | ATGGCTAAGAAGTGA[A/G]GCCCCACCCCAGCAA | 18676 |
rs219563432 | in-del | -/A | | | intron-variant | Phf2 | Mm_Celera | 13:48821199 | TCACACTTCAATCTC[-/A]AAAATGTGGTCAAAT | 18676 |
rs219697319 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48835154 | AGCTGGAGGGGCCCC[C/T]ACTACCAGAGCCATG | 18676 |
rs219761808 | in-del | -/CACACACACA/TC | | | intron-variant | Phf2 | Mm_Celera | 13:48829657 | GGAACAAATAGAAAG[-/CACACACACA/TC]ACACACACACACACA | 18676 |
rs219777010 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48830499 | CTCCCAATGCAGGTG[C/T]GCACATGTGCGTACA | 18676 |
rs219778721 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48823735 | ATCTTCTTGACTAGT[C/T]GGCAGCCTGACTCAG | 18676 |
rs219835157 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48824318 | ATCCATCCATCTTAC[A/G]TATGAGCTGGCTTTT | 18676 |
rs219847178 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48823643 | TCTAACTTGACATAA[A/G]CCGGAGTCATCTGAG | 18676 |
rs219858475 | in-del | -/GA | | | intron-variant | Phf2 | Mm_Celera | 13:48850816 | CCGAAGGCCAGGAAC[-/GA]ACACACACACACACA | 18676 |
rs219914581 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48829931 | TGCCATCAAAAAAGT[C/T]ACAAGACAGATGGAT | 18676 |
rs220023353 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48831382 | GAGCTGAAGGAGACG[C/T]TCTCTGCTCAGAGGA | 18676 |
rs220039773 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48830625 | GTCATGAGAGAGACA[C/T]GCAAGTCAAAACATG | 18676 |
rs220059841 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48822754 | CTAATAGTTAATGAG[C/T]TCTCAGGACATTAGA | 18676 |
rs220075882 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48805189 | CAGCCTAAGCTCACA[C/T]AGTGGAGACTTCCTC | 18676 |
rs220189414 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48821778 | CTGCTGAAGTGGACA[A/G]TAATCTGACTGAGGA | 18676 |
rs220197819 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48807165 | AAAGTCACATTATAC[C/G]ATCCATTTAGATGGT | 18676 |
rs220376807 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48865340 | CAGAGATTAGGATGA[A/G]GCTCACACGAAGCTG | 18676 |
rs220498136 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48855907 | ATAAACTGTCATCAT[A/G]GCCACTGGTAGGACC | 18676 |
rs220538803 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48829160 | AGGGACCACAGTGAC[C/G]AGGGACAGCAGAGCT | 18676 |
rs220557653 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48867268 | ACGACTGAATGAGGA[A/G]TCTTGCAGTGGCTTA | 18676 |
rs220559059 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48855023 | ACTCACAGAGCCCCC[A/T]CCTGTCACCCATCAC | 18676 |
rs220576953 | in-del | -/CTT | | | intron-variant | Phf2 | Mm_Celera | 13:48833587 | CCAGCCAGTTTCTAC[-/CTT]CTTCTCTGAGAATCT | 18676 |
rs220586844 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48829109 | GGAAGCAAGACACAC[A/G]GGTCCACTGATAACT | 18676 |
rs220598698 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48829605 | AGAGGTGCCAAGGCC[A/G]TGTAAGCAAAAGGTA | 18676 |
rs220616540 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48865520 | GATGATGTCACAGAA[G/T]TTAAGAACACAGGTT | 18676 |
rs220674201 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48864713 | TAAGCCAATTGTACA[C/T]GCAAGGTACTTCCTC | 18676 |
rs220719058 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48853068 | ACACTAGGGGCGCCA[A/G]GCCCTCATTCAATTT | 18676 |
rs220800721 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48864630 | GCTGTGGACCTCTTG[C/T]TGGGCTTACCACACT | 18676 |
rs220843550 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48858390 | AGTGCTGGGAGACCA[A/C]GGGTCAGTCACACAC | 18676 |
rs220863682 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48848120 | AATACACATAAAATT[A/T]AAAAAAAAATTTAAA | 18676 |
rs220869310 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48828461 | AACTACTTAGAGAGC[C/T]CCACCTCCACTCCTG | 18676 |
rs220870099 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48850324 | ATGACCAGAGTTTGC[A/C]GTTTAATTTCTGTAT | 18676 |
rs220905111 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48826006 | TCCAGGCTGATGACA[C/T]TGGCTTTGAGTCGAA | 18676 |
rs220928766 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48849412 | GGCCTGAAGGATCCT[A/G]AGAACATTCACTCCT | 18676 |
rs220929068 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48861445 | TAAATACCTAGGGAA[C/T]AGAAGTGACGGATCA | 18676 |
rs220935479 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48859589 | CCAGGTGGGGCAGAG[C/T]GGCCCTCATTCAAAT | 18676 |
rs220952329 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48820658 | CTTCTACCTCGCTTC[C/T]GTGCTAGCTTTCACC | 18676 |
rs220958126 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48826716 | GACTTATGATATGAA[C/T]AGTTTGCTCCATCAC | 18676 |
rs220958959 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48868908 | CCCTTTTACTGCCCA[C/G]AGACCCAAATACATG | 18676 |
rs220983129 | in-del | -/TT | | | intron-variant | Phf2 | Mm_Celera | 13:48862994 | GTAAATAGATAAATG[-/TT]TTTTTTTAAATAAAG | 18676 |
rs220983407 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48860760 | TTGTGTACTCAGCAT[A/C]TGGGTGTGCCACACC | 18676 |
rs220990874 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48825232 | CTATCTGTGGGCTGC[C/T]TCAGTGTGTCCTGAG | 18676 |
rs221014731 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48818815 | ACATTGGTGAAGACA[A/G]GCCATGGACATGATT | 18676 |
rs221037469 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48818184 | TCAGACTCCAAGCCT[A/G]GACCTGAGGTTCTCC | 18676 |
rs221067040 | in-del | -/TTGAATTCAAGGCTAGA | | | intron-variant | Phf2 | Mm_Celera | 13:48851475 | GAGACAGGCAGATCT[-/TTGAATTCAAGGCTAGA]CTGGTCTACAGAGAG | 18676 |
rs221076592 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48817220 | CCCTCTGTGCCCTCT[C/T]TCTCCAGGAGCCTCA | 18676 |
rs221086147 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48847642 | ACACATACACCACAT[A/G]CACACAAACATACAT | 18676 |
rs221114949 | in-del | -/CAGGGGGGAA | | | intron-variant | Phf2 | Mm_Celera | 13:48813117 | CAGGGCACTGGGGAG[-/CAGGGGGGAA]CAGGTCCCTTCACGG | 18676 |
rs221115513 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48857568 | CCAGCCCTGGGGTCC[A/G]GGGCCCCTGAAAGCA | 18676 |
rs221136946 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48842506 | CATCTACACTATGGG[C/T]TGGACCAAGCATCCA | 18676 |
rs221195200 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48852729 | CAAGCTGGTGTGCAC[C/T]AACACACTCAGTTTA | 18676 |
rs221196315 | in-del | -/AGA | | | intron-variant | Phf2 | Mm_Celera | 13:48852465 | TCCAGAAACTTCTCT[-/AGA]AGGAGTGGGACAACA | 18676 |
rs221256852 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48851813 | AGGGAGGGACTGGGT[A/G]GCACTTAGAAGAGCC | 18676 |
rs221300750 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48833033 | GTCAGGAAACTCCAT[G/T]GGGACAGAAACCACG | 18676 |
rs221414437 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48843742 | GGCAGGGTATAAACG[A/G]AATGCTTGCTCTCTG | 18676 |
rs221435399 | in-del | -/C | | | intron-variant | Phf2 | Mm_Celera | 13:48808523 | TCATCTGTATTTACA[-/C]CCCCACATCTACATG | 18676 |
rs221481796 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48828382 | CTGGGTGTGTTGGCA[A/G]GGGCAGACAGAGCTC | 18676 |
rs221523333 | snp | A/T | | | synonymous-codon | Phf2 | Mm_Celera | 13:48820567 | GTGGAGGAAATGTCC[A/T]GCGAAGGCCAGGCAG | 18676 |
rs221538025 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48845428 | CAGTAACTGTGCTGC[A/T]GTGATAAGATGCTGT | 18676 |
rs221641038 | in-del | -/AG | | | intron-variant | Phf2 | Mm_Celera | 13:48849897 | AACAGACAGACAGAC[-/AG]ACACACACACACCCC | 18676 |
rs221722220 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48850673 | CCTGCCCTGGTAAAG[A/T]GCAGAGACTGGATTA | 18676 |
rs221728515 | in-del | -/CCTGCATGGAGCACCTGCATGGAGCA | | | intron-variant | Phf2 | Mm_Celera | 13:48860424 | TGAAGCCACACACTG[-/CCTGCATGGAGCACCTGCATGGAGCA]CCTGCATGGAGCACC | 18676 |
rs221745113 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48816405 | GGGACAGGCAGATGC[A/G]CCCTGGCACAGGCCC | 18676 |
rs221746112 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48825033 | GTGAGTGTCACGTGT[A/G]CTGAGAGTTTCCGTG | 18676 |
rs221941310 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48820431 | CAATACACAGATGTC[A/T]GCATAGCAACCCATA | 18676 |
rs221952912 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48824407 | TCCACACCCTCAATA[C/T]GACACACACAAGCTC | 18676 |
rs221992842 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48842470 | TGCTAGCTTTCACTT[C/T]CTCAAGGTTCTGCCA | 18676 |
rs221997144 | in-del | -/ACATTCT | | | intron-variant | Phf2 | Mm_Celera | 13:48823231 | TGCGAGGCTCCTTCC[-/ACATTCT]ACCTTGTAAATCTGC | 18676 |
rs222017766 | snp | A/G | | | synonymous-codon | Phf2 | Mm_Celera | 13:48813064 | CTCGTCAGAGGAGTC[A/G]TCGCTCTGCGGAGCC | 18676 |
rs222021592 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48846640 | TTTTAAAGTGGGCCC[C/T]AGGCCTCGACAAGCC | 18676 |
rs222086872 | in-del | -/T | | | intron-variant | Phf2 | Mm_Celera | 13:48867695 | TTTGTTTTTGTTTTG[-/T]TTTTGTTTCGTTTTT | 18676 |
rs222200691 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48851634 | TCATATTTCAGCCTC[C/T]GGTCACCTTGTTTCC | 18676 |
rs222204729 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48826931 | TGGCAACTACTCAGG[A/G]AATATTTATTTTGCC | 18676 |
rs222541926 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48841994 | CACTTGCAAATGAGT[A/C]ACAGGCACCTAAGAG | 18676 |
rs222675085 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48840276 | AAGTCTAACATACAG[G/T]GCCAATATTGCAGAA | 18676 |
rs222729259 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48839655 | ACAGAGAACGCCGTT[A/G]AGAAAGAAAAGTCTG | 18676 |
rs222764119 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48819726 | CCCAGACCACTCGCC[C/T]AACTGCCAACGGTTC | 18676 |
rs222781134 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48838171 | AAAAATAGAAGATAC[C/T]TTCCTCAACAAGATA | 18676 |
rs222792441 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48847980 | AGGACCTTGGTGTGA[G/T]CCCCAACACCCACAT | 18676 |
rs222859921 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48846923 | CTGTGTGATTCCACA[C/G]ATGCTCTCCCTGGTA | 18676 |
rs222863615 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48844761 | TTATTTCAAGGAAAT[A/G]TTAAATAAAGTTCTT | 18676 |
rs222867074 | in-del | -/GT | | | intron-variant | Phf2 | Mm_Celera | 13:48862881 | GACAAATACATGATA[-/GT]GTGTGTGTGTGTGTG | 18676 |
rs222901317 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48816381 | ACACAGACTTTCCTC[A/G]CAGCTCTGGGGACAG | 18676 |
rs222921559 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48845411 | GAAGCAGCTAGCTGA[A/G]TCAGTAACTGTGCTG | 18676 |
rs222927091 | in-del | -/G | | | intron-variant | Phf2 | Mm_Celera | 13:48810375 | GGTTCTAGAGAAGAC[-/G]CTGGTGGGGTGGGGC | 18676 |
rs222953864 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48822549 | TGGAGAAGTGTAGTT[C/T]GCAGCTGGCAGAGCC | 18676 |
rs222958595 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48810373 | AGGGTTCTAGAGAAG[A/G]CGCTGGTGGGGTGGG | 18676 |
rs222987831 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48844846 | ACTATTAAAAAGTAA[C/T]GCCGGGCGTGGTGGT | 18676 |
rs222987916 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48857288 | GCCAGGCCCCACCCC[C/T]GAACAGTCTGCAGTC | 18676 |
rs222993454 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48838612 | GAAGCAAGGGTAAAA[A/G]CTGACTTTACACTCA | 18676 |
rs223023620 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48815097 | CCATGCTGAGGCTCA[C/T]GTGGCTCCTAAGCTG | 18676 |
rs223081355 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48815435 | CACAGTGGTGGTGAG[C/T]GAGATCACTGTCTCA | 18676 |
rs223085969 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48840172 | CAGGTGGACAGATCA[A/G]CAACATGTGCTCACG | 18676 |
rs223280670 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48836431 | TTCCCAGAACGGATA[C/T]AAGACGGTGGCAGGT | 18676 |
rs223299917 | in-del | -/T | | | intron-variant | Phf2 | Mm_Celera | 13:48839438 | TCCCCAGTAACCCCC[-/T]CACTCATGCTTGTCC | 18676 |
rs223321372 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48841801 | GCCAGGTCAGGGGTG[G/T]CTGTGTGTCCCTAAA | 18676 |
rs223347955 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48818906 | GTCCCTCAAGTAGCA[A/G]GAGGGCACGTGTCCG | 18676 |
rs223363032 | in-del | -/A | | | intron-variant | Phf2 | Mm_Celera | 13:48814417 | ACACTTATTTTTGGG[-/A]AAAACATAAAACAAT | 18676 |
rs223389187 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48864877 | ACCTAGCAGACTACC[C/T]TCCACTCGCAGTTTG | 18676 |
rs223403843 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48811520 | TCCAGGGTACTAAGG[A/G]TCTCTGAGACTCTGA | 18676 |
rs223404414 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48819653 | AGGACACAATAAGTT[A/C]GTTAGTGTGGTGTCT | 18676 |
rs223448978 | in-del | -/ACACACACAGAC | | | intron-variant | Phf2 | Mm_Celera | 13:48862346 | GTTGTCCTCTGACCT[-/ACACACACAGAC]ACACACACACACACA | 18676 |
rs223454607 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48812181 | GGGCCATGGGACAGC[C/T]GTCTAAGCTCCCTAC | 18676 |
rs223538839 | in-del | -/CTGCCCCCTCGTTCCCAGCC | | | intron-variant | Phf2 | Mm_Celera | 13:48837834 | CTCTCCATCACATTT[-/CTGCCCCCTCGTTCCCAGCC]CTGCCCCAGCCGCCA | 18676 |
rs223558373 | in-del | -/T | | | intron-variant | Phf2 | Mm_Celera | 13:48858741 | GGCCTGTGCAGATGC[-/T]TGTGTGCAGCTGTGG | 18676 |
rs223608072 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48804200 | GACCAGCAGCAAGCA[C/T]TCATAGGAAGGGCAG | 18676 |
rs223628907 | in-del | -/A | | | intron-variant | Phf2 | Mm_Celera | 13:48863001 | GATAAATGTTTTTTT[-/A]AAATAAAGAGTTGAA | 18676 |
rs223636282 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48822463 | AGACGCGATGACGGC[A/G]ATGACTCAAAGCCTC | 18676 |
rs223679312 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48842180 | GAACTGGCAGCTAAC[A/G]GGATGTTGCAGATCC | 18676 |
rs223712075 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48844113 | AAGCATCGAGAGTAC[A/G]TGGCAAACTATTTAA | 18676 |
rs223741701 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48841532 | TAATAAATAAAAAAA[A/T]AAAAGTAGAAAAATC | 18676 |
rs223794939 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48821864 | GAGCCTACTGGATGC[G/T]GAGGACTCTGGGGCA | 18676 |
rs223805256 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48811902 | ATCTCCCGTCATCTA[C/T]GAGGAGGCCTGACCT | 18676 |
rs223808104 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48819972 | TCATGATCAGGGCTC[A/C]TAAAGGGCTGTAATA | 18676 |
rs223885532 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48811438 | TCCTGTCTGCCCTCA[C/T]CCTGGGTGGTACTAG | 18676 |
rs223889414 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48812509 | GCTCTTGACTCCAGG[A/G]TTCAAATCCCAGCAA | 18676 |
rs223994084 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48840313 | ACAGATGAAAAGTCT[A/G]TAACAAGTAAGTCTG | 18676 |
rs224042736 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48805739 | AGCCAGGGCCCTGTG[C/G]GGAGCCGACCCATCT | 18676 |
rs224042765 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48815152 | CTCAGCACCCAAATC[C/T]ACACATCCCTCCCCA | 18676 |
rs224110361 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48818229 | ATCTCTCCAAGTCTC[A/G]GGCATGATTACTAAT | 18676 |
rs224169300 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48839369 | GAACTCACTGATGGT[C/T]ACTGCTTAGGGAGGC | 18676 |
rs224195274 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48810528 | ATGGCTCCACAGCCC[C/T]CTCTGAAGGCTGCCT | 18676 |
rs224241214 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48838942 | CAGGGCAGGACATTG[G/T]GTGTCTTCTTCTGTG | 18676 |
rs224243279 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48846767 | ATAGCATGATCGCAA[A/G]GATGGCCAAGACGAA | 18676 |
rs224290279 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48808322 | ACTGAGAACGAGGAG[G/T]CCCCACATCTCTCCC | 18676 |
rs224316240 | in-del | -/A | | | intron-variant | Phf2 | Mm_Celera | 13:48865288 | TGCCTGTTGCCAGCC[-/A]AAAAGTTACAGCTTG | 18676 |
rs224361353 | snp | A/C | | | intron-variant, upstream-variant-2KB | Phf2, LOC102642832 | GRCm38.p3 | 13:48870419 | GGCTCCTGGCCTCCG[A/C]GGCCACTGCGGCCCC | 18676 |
rs224369304 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48809049 | GCCCTCATCTCCCCC[A/T]GGGTACACTGGTGCC | 18676 |
rs224433607 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48833979 | GTCTGGGAGGTCTGG[A/G]AGGTGCCTCAGAGCC | 18676 |
rs224446344 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48816899 | AAAATGTGGGAGAGC[A/T]CTGTACTCATCCTGG | 18676 |
rs224460280 | in-del | -/ATGGG | | | intron-variant | Phf2 | Mm_Celera | 13:48840239 | CAGCAACACAGATGA[-/ATGGG]AAACACATTAGTGAG | 18676 |
rs224494097 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48839627 | CAATTTAATTAAAAA[A/C]CAGGTTTGTACAACA | 18676 |
rs224509359 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48809403 | CCAATGGCTGCACAA[C/T]GCCCAGGTAGAGAGC | 18676 |
rs224518498 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48808762 | TACCCTCATGTACAC[C/T]TGTACTCAGCCCTGC | 18676 |
rs224636192 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48866102 | CCCCTGCCTCACATC[C/T]ACCCCAACAGCAGCC | 18676 |
rs224651169 | snp | G/T | | | intron-variant | Phf2 | GRCm38.p3 | 13:48839317 | ACAGGTCGTCCTGGA[G/T]AGGGGCGGGGCTCAT | 18676 |
rs224669903 | snp | A/C | | | intron-variant, upstream-variant-2KB | Phf2, LOC102642832 | Mm_Celera | 13:48869221 | AGAGGCCTCCGGGCT[A/C]TCACCCACTGTGATC | 18676 |
rs224729620 | in-del | -/ACACACACACACACAA | | | intron-variant | Phf2 | Mm_Celera | 13:48808831 | CACACACACACACAC[-/ACACACACACACACAA]TCTCTATCTGTATCT | 18676 |
rs224730169 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48868001 | CAGGAAAAGTACATT[A/G]AGGAGGGAAACCTGG | 18676 |
rs224805963 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48863584 | TCCAACCCTGGGGGA[C/T]GGGGGCCTTGAGTAG | 18676 |
rs224842990 | in-del | -/TTGT | | | upstream-variant-2KB, nc-transcript-variant | Phf2, LOC102642832 | Mm_Celera | 13:48871821 | TGGTTGGTTGGTTGG[-/TTGT]TTGGTTGGTTGGTGA | 18676 |
rs224884017 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48864454 | TTTCTGTTTTTGAAA[C/T]TCAGTGCCTTGGTGT | 18676 |
rs224943862 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48829812 | GAAGATAAATCTTCA[C/T]GACCTTGGATTTGGT | 18676 |
rs224947144 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48836817 | AAGGACAAAAACTTC[A/G]AGGGAACACTGTGAA | 18676 |
rs225003592 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48837838 | TCCATCACATTTCTG[C/G]CCCAGCCGCCATCCT | 18676 |
rs225018135 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48814176 | AGCCCTGAGTTTCCA[C/T]TGCGGGAAGTCTGCT | 18676 |
rs225055125 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48830348 | AAAATATTTAAAGTG[C/T]GAGGCAAAGGGCCGA | 18676 |
rs225077675 | snp | A/G | | | synonymous-codon | Phf2 | Mm_Celera | 13:48835259 | GCAGTGGTAAATGTC[A/G]ATGTCTGGTGCCTCT | 18676 |
rs225087088 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48861110 | AAGACACACATGAGT[A/G]GAGAGAGATGCAGTG | 18676 |
rs225101685 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48804978 | CTTTCTGCCTATGGG[A/T]ATCACTTAAAAGTGC | 18676 |
rs225161190 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48813105 | CAGCAGGTCAGGGCA[A/G]GGCACTGGGGAGCAG | 18676 |
rs225222792 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48806586 | TAAACCTCTGGCTAT[C/T]AGGAAGGCCCTGGAC | 18676 |
rs225261936 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48830988 | TCAGAAGGATACACA[A/C]AGCAACCGGTCCAGC | 18676 |
rs225323800 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48838342 | TAGACAGCAAGACTG[A/G]ATTACAAGTCTTCAA | 18676 |
rs225411394 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48834204 | TGTCCCCGGAATCTT[A/G]GATAAGACTTGGCCC | 18676 |
rs225440198 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48827110 | GACCCAAGGCGGAAC[C/T]TGTCGGAACATCTGT | 18676 |
rs225480036 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48833345 | GCCCAGGGGCAGGGT[C/T]TGGTGATGCAGTGCA | 18676 |
rs225506158 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48827748 | AACACATGTGTGGAG[A/G]TCAGAAGACAACTTT | 18676 |
rs225608956 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48860022 | GAACCAAGACTAGTT[C/T]AGCTCAGGACTTGGA | 18676 |
rs225656377 | in-del | -/TCTGGGGTAGC | | | intron-variant | Phf2 | Mm_Celera | 13:48824270 | CACCTGACCAGGCTG[-/TCTGGGGTAGC]TCCGTATAACCTGAT | 18676 |
rs225834616 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48865553 | TCTTGCAGAGGACTA[A/G]GTTCAATTCCCAGCA | 18676 |
rs225913019 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48810872 | AACTTCCCACTCACG[C/T]CATCTGGGTGACCCC | 18676 |
rs225929200 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48838777 | TAGCTAGAAACAGAC[C/T]AGCGGAATAGAATTA | 18676 |
rs225949216 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48809525 | CACTACTAGTACCAG[A/G]GACACCTGCTACATG | 18676 |
rs225964605 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48829343 | CTTCTACCACATCTT[A/G]TGGAATCCCAGGTAA | 18676 |
rs225965053 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48855550 | GCGAAGCACGACTCT[G/T]TAAGGACCACTAAGC | 18676 |
rs225968621 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48867704 | TGTTTTGTTTTGTTT[C/T]GTTTTTATTTCAAGA | 18676 |
rs225978980 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48811603 | TTCCCACCACCAGAG[A/G]CTGTGTGACACCCTG | 18676 |
rs226027312 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48830050 | TGCCTACAATTCCAG[C/T]GCCAGGGGAGGTAAT | 18676 |
rs226027367 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48866540 | GAGACATGACACTCA[A/C]TCCCCTCCCCCAAGG | 18676 |
rs226029502 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48838244 | GATGAAAAGCCAAAA[C/T]CTTTCCCCAGAAGAC | 18676 |
rs226032181 | in-del | -/TCGA | | | utr-variant-3-prime | Phf2 | Mm_Celera | 13:48803429 | CCATGCTCCGCTCGC[-/TCGA]TCGCTCGCTCCACCT | 18676 |
rs226054315 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Phf2, LOC102642832 | Mm_Celera | 13:48871758 | CCCCTGCAGTCTTGC[C/T]CTGAACTGGCTCCCT | 18676 |
rs226068943 | in-del | -/ACACA | | | intron-variant | Phf2 | Mm_Celera | 13:48806849 | TGGGAGCAGTGACAC[-/ACACA]CCCCCCCCCCGCCCC | 18676 |
rs226088756 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48822842 | TGTCCCACAACTGGC[C/T]ATCCCAGTGGCTCCC | 18676 |
rs226209009 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48806487 | TCTATTTAAGCAGAG[C/T]ACACTCACCAAGGGG | 18676 |
rs226249583 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48861672 | CTGAGTTCTGATCCC[A/C]GGTGCCCATGTTGAT | 18676 |
rs226251016 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48807432 | GCCCAGAGCGCAGAA[C/T]AGAGAATCACCTTGC | 18676 |
rs226272856 | snp | A/G | | | downstream-variant-500B | Phf2 | Mm_Celera | 13:48801470 | CTTGTAGTTGTCCAT[A/G]GGGTGTCATCAGCTT | 18676 |
rs226379177 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48836458 | AGGTGCCTACTGTCG[A/C]AGCTCTGGAGAGGTC | 18676 |
rs226408817 | snp | C/T | | | utr-variant-3-prime | Phf2 | Mm_Celera | 13:48802773 | ACTCATGACGCCACC[C/T]AGGGGCTCAGACAAG | 18676 |
rs226459030 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48804274 | CCCTGATGACCTGAG[A/G]CCAGAATCCTCTTTG | 18676 |
rs226640155 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48864042 | CATGGCACTGTGTGA[A/G]TGAGCCTTAAAAATT | 18676 |
rs226645463 | in-del | -/G | | | utr-variant-3-prime | Phf2 | Mm_Celera | 13:48802489 | GAAAGAAAAGGGGGT[-/G]GGGGGGCCAGAACCC | 18676 |
rs226665961 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48850568 | GCACATGAGAATTCA[A/G]AGTGAGACTAGCTAT | 18676 |
rs226697855 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48862457 | TGTAAAAGCCAAACA[C/T]GGAGGTGCATGCCTT | 18676 |
rs226702070 | in-del | -/T | | | intron-variant | Phf2 | Mm_Celera | 13:48824207 | GGCCAAACAGGCCTC[-/T]TCATGCCTCTACACT | 18676 |
rs226703109 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48867556 | GGAAGCACCAACACT[C/T]CACCACTCCAAGCAT | 18676 |
rs226718129 | in-del | -/T | | | intron-variant | Phf2 | Mm_Celera | 13:48854995 | TCCCATGGGAATGCA[-/T]TACCAGAGTGGTACT | 18676 |
rs226787140 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48861037 | CCCTCAAAATATTTA[A/G]AAACAAACTGAGGGA | 18676 |
rs226810635 | in-del | -/GTCGTCC | | | intron-variant | Phf2 | Mm_Celera | 13:48857193 | CGCAGCTCGAGGTGT[-/GTCGTCC]CCCCGCCCCCCCCCC | 18676 |
rs226905424 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48859427 | CAAAAAACTGCCTAA[C/T]GGGATTTCCTAAGGG | 18676 |
rs226930672 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48853635 | AATTAAAGCCTTCTC[C/T]CTGGATGAAACCCTC | 18676 |
rs227023092 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48851453 | TTACTACCAGCACTT[A/G]GGGAGCAGAGACAGG | 18676 |
rs227028888 | in-del | -/C | | | intron-variant | Phf2 | Mm_Celera | 13:48815247 | CTGCCCCACTGGCCA[-/C]CGGGCTCAGAGGCGC | 18676 |
rs227035056 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48856477 | AAGGGCCTGCCTGTG[G/T]CTCAGCTGGCTGAGA | 18676 |
rs227054229 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48858878 | GCTATGATTCAGGGG[A/G]CCTGATTGGCTGGTT | 18676 |
rs227077849 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48834690 | CCGTCCCTGTGTTCC[C/T]ACTGGCTACATCTCT | 18676 |
rs227108041 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48858062 | TCTCAACCACTGAGT[A/G]ATCTCTCTGGTCTCC | 18676 |
rs227255937 | in-del | -/GT | | | intron-variant | Phf2 | Mm_Celera | 13:48855977 | CTCAGCAGATCAGGG[-/GT]GTGTGTGTACCTGTC | 18676 |
rs227291390 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48842096 | ACTTGAAGAAATGGT[A/G]TCTGCCTGACCGGTG | 18676 |
rs227305614 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48848265 | AGGGTGATGTGTAGG[A/G]TAGGGGAGGCAGACA | 18676 |
rs227333426 | snp | A/G | | | synonymous-codon | Phf2 | Mm_Celera | 13:48826072 | GTCTGAGAACTCGAG[A/G]TTGGTCACGTTGAGA | 18676 |
rs227359087 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48847132 | CTTGAACATACACCG[A/C]AAAGTGAAAGCTGCC | 18676 |
rs227368658 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48831140 | TCTTTCTAGGAACAA[A/G]CCCCGGGAAGCAGAG | 18676 |
rs227405018 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48851069 | ACCTGAGCTTATATA[C/T]GCAGTACAAACATAA | 18676 |
rs227418261 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48824019 | GGTTCCCTCCCTGAC[C/T]TCACAGCATGATGAA | 18676 |
rs227426474 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48858491 | CCAAATAACACTGGT[A/G]GGTTCAAGGCAGGAA | 18676 |
rs227456955 | in-del | -/TG | | | intron-variant | Phf2 | Mm_Celera | 13:48812704 | AGGCTCACACCCATC[-/TG]TACAGCTACAGTGTA | 18676 |
rs227492532 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48824777 | AGTCCTGTTGGCCCA[A/G]TCTGAAGATAGGATA | 18676 |
rs227562164 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48825342 | TAAGACAGGCATCCA[C/T]GAGTGCACTGAGTGT | 18676 |
rs227621775 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48834133 | GAGAGCCCAGGAGTC[A/G]GGAGCACCCACCCCA | 18676 |
rs227722149 | snp | A/G | | | utr-variant-3-prime | Phf2 | Mm_Celera | 13:48801943 | AGAGAGAGAGAGAGA[A/G]AGAGAACAGCTTGAT | 18676 |
rs227731183 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48831567 | GTAGGTGACTCAGAA[A/C]AGCTTCCCTAAACTG | 18676 |
rs227732808 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48822216 | GAAGGTTCTAGGTGT[A/G]TGGGCCTGGTCAGGA | 18676 |
rs227823458 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48826248 | TATGGCCTCCCTGGA[A/G]GACATGGTGGGGTGG | 18676 |
rs227827068 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48828532 | AGCCTTGGGTAAAGC[A/C]CAGAATTTACATATT | 18676 |
rs227827610 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48849933 | ATATACTACAATAAG[C/T]AAATATATACACCAC | 18676 |
rs227872299 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48826965 | TCTGTGTCTGGTCGG[A/G]AAAAGTTGAGGCTCG | 18676 |
rs227872328 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48818592 | CTGCTAGTGGAAAAC[A/G]CATCAAGATGGCCTC | 18676 |
rs227878125 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48861206 | GTCAAAATCCAGCTG[C/T]CTCTTTTCCTTTTTC | 18676 |
rs227923069 | in-del | -/C | | | intron-variant | Phf2 | Mm_Celera | 13:48856943 | TCAAACGTTCAACTG[-/C]CCAGGATATAGGAAA | 18676 |
rs227932494 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48822061 | GGGCACAGAGGCAGG[C/T]AGCAGAGCCCACTAG | 18676 |
rs227945018 | snp | C/T | | | synonymous-codon | Phf2 | Mm_Celera | 13:48807771 | GCCACCCTTGGCCTG[C/T]CCCGTGCCCCATGTG | 18676 |
rs228101983 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48827901 | TCCAGCAGGGGTGGC[A/G]GGATTATAACGCACA | 18676 |
rs228114368 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48851166 | GGGTTCGCTGGCCAG[A/T]CGGTAGAGCAGAATG | 18676 |
rs228184264 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48845873 | AGTCACGTGTCACAC[A/G]ATGTGATGATCTCAG | 18676 |
rs228191009 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48829286 | CTCCCCACCCCCCAC[C/T]CCCCCACACACATTT | 18676 |
rs228210007 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48862140 | ACTCAAAAACCAGGA[A/G]CCAAAACCTTTTCTT | 18676 |
rs228248333 | snp | C/T | | | synonymous-codon | Phf2 | Mm_Celera | 13:48823090 | GTAGTTTTCCACCCA[C/T]GATAGTTTCTTCACA | 18676 |
rs228266414 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48845101 | GTTGGTTCTCTCCCA[C/T]CACATCGGGCCCAAG | 18676 |
rs228327158 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48815244 | GCCCTGCCCCACTGG[C/T]CACCGGGCTCAGAGG | 18676 |
rs228330510 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48823772 | AACTTTGAAACTGCC[A/T]GCTGGTACATGGGGA | 18676 |
rs228363360 | in-del | -/A | | | intron-variant | Phf2 | Mm_Celera | 13:48824567 | CTTCCTCCTACAAAC[-/A]AATCAATTAAAACCC | 18676 |
rs228593445 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48853856 | AAGAGGGTGAGCTCT[A/T]TGACTCATCTTGCTG | 18676 |
rs228602896 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48824485 | ACTTTCCTGACTCCC[A/G]CATCTGGTGTGCATG | 18676 |
rs228617671 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48827660 | GGAGATAAAACCCAG[A/G]ACTTTTATCATGTAA | 18676 |
rs228629250 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48847059 | AGGAACTGAATGGAT[A/G]GGTCACTAAACCATG | 18676 |
rs228634916 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48851947 | CCTTGGCAAGTGTAG[C/G]TTCCCCTCTCAAAGT | 18676 |
rs228671424 | in-del | -/AG | | | utr-variant-3-prime | Phf2 | Mm_Celera | 13:48801920 | ATAATAAAATTAAAA[-/AG]AGAAAGAGAGAGAGA | 18676 |
rs228674282 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48816596 | AAGGTAGACAGACAC[A/G]GAAGGGGAGTGAGCT | 18676 |
rs228700503 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48858593 | CTCTCTGCTACTGGG[G/T]CATTATTGCTCTCCC | 18676 |
rs228708199 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48863699 | CCCGTGAGGATGGTT[A/G]TAATAAAAAGACTGG | 18676 |
rs228752562 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48814448 | AGCACTTCAGCTATG[G/T]GCTATTAGATACTGT | 18676 |
rs228780938 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48844901 | GGAGGCAGAGGCAGG[C/T]GGATTTCTGAGTTCG | 18676 |
rs228840408 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48844178 | AGCCCAGCATTTTTA[A/G]GCTTTGCATGTGCAT | 18676 |
rs228861561 | in-del | -/TC | | | intron-variant | Phf2 | Mm_Celera | 13:48824699 | TCTCCAGGCTTGCTG[-/TC]TCTCCCAACCAGTGG | 18676 |
rs228894857 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48843220 | TTTGAGTGTGGTGGC[A/G]CACACCTTTGATCCC | 18676 |
rs228895146 | snp | G/T | | | intron-variant | Phf2 | GRCm38.p3 | 13:48840001 | CACAGGAAAAAAAAA[G/T]TGATTTCCTCAGAAA | 18676 |
rs228898805 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48849538 | CTGCTTCTGAAAACA[A/T]GACAGAAATTTGATC | 18676 |
rs228952768 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48848444 | CAACTAAGAGAGCTG[A/G]GGACGTCGCTCAAAG | 18676 |
rs228956001 | in-del | -/C | | | intron-variant | Phf2 | Mm_Celera | 13:48828612 | GTGCTGGAACAGCCA[-/C]AGGAGGATGGCTGTG | 18676 |
rs229081498 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48816103 | GTTGTCCCTGAAGCC[A/C]CTGGGGTGAGGGCTA | 18676 |
rs229108083 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48810684 | AACAGCTGTCCTGGC[A/G]CTGTCCAGCTGCGCT | 18676 |
rs229176619 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48845953 | AATCCCAACACTGGG[C/T]GGTAGAGACAGGAAG | 18676 |
rs229192841 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48840385 | GGGATGTGGGTTTGC[A/G]GGTTGATTTGAAGTG | 18676 |
rs229256308 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48857966 | TTCCAGAAGATGGTG[C/T]TGGATGTCCTGGAGC | 18676 |
rs229276732 | in-del | -/T | | | intron-variant | Phf2 | Mm_Celera | 13:48851051 | CCTGTCAGGCAAATG[-/T]GAACCTGAGCTTATA | 18676 |
rs229319645 | snp | C/T | | | intron-variant | Phf2 | GRCm38.p3 | 13:48839350 | AGCCCCACCCCTTCC[C/T]GAGGAACTCACTGAT | 18676 |
rs229344164 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48844216 | TCAGAGGGGCTTGCA[G/T]AGGTTCTCACTTTCC | 18676 |
rs229351882 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48817483 | AGTGCCCCAGCATAT[A/G]AGGGAGGGGCTCAGG | 18676 |
rs229372760 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48838916 | GCATGTGTATACATG[C/T]ATGTTGATGCCAGGG | 18676 |
rs229407428 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48809861 | GCCAGCACAGTACCC[A/C]CTCCAGCACAGTATC | 18676 |
rs229425459 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48855385 | TCAAAACCAGGCTAC[C/T]TGCAAGGTCCCCAGC | 18676 |
rs229447879 | in-del | -/G | | | intron-variant | Phf2 | Mm_Celera | 13:48834618 | AGGAGCCCTGAGGAC[-/G]GGAATGGGGTCTCAC | 18676 |
rs229469121 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48840519 | CCACAGAGTATTCAC[A/C]CCGGCCATTGAGAAT | 18676 |
rs229494954 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48823846 | GGGTGACTTGAGCCT[A/G]CAACCCTGGTCTAAG | 18676 |
rs229556160 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48849575 | ACAACATGCAGGGTG[C/T]CACATTCTTCTTCCA | 18676 |
rs229636617 | snp | C/T | | | synonymous-codon | Phf2 | Mm_Celera | 13:48820066 | TTCCAATAGGTGCTT[C/T]CCCATGTACCAGCAG | 18676 |
rs229668779 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48813663 | CATCAAGCACAAGCG[C/T]GCTGCAGGCCGGGCT | 18676 |
rs229724109 | snp | C/T | | | synonymous-codon | Phf2 | Mm_Celera | 13:48804717 | CTTCCTGTTTTTCTG[C/T]TCCTCCTAAGAACAA | 18676 |
rs229746624 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48841111 | ACTCAGGGTCAGCTG[G/T]TCCCCTCCCATCCAG | 18676 |
rs229893579 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48812887 | TGTTCTGCGAGTGCT[G/T]AGGGACACAGCCAGG | 18676 |
rs229906821 | in-del | -/C | | | intron-variant | Phf2 | Mm_Celera | 13:48813387 | CTCAGGGGACTGGTA[-/C]CTTCCTGGGCTTCCC | 18676 |
rs229991130 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48848497 | ACAAGGCCCAAGGCC[C/T]AATATCCAGCACTGA | 18676 |
rs230045051 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48818489 | CCCCGGGGGGTGGGA[G/T]GGGATGGGGGGAGGG | 18676 |
rs230140450 | in-del | -/G | | | intron-variant | Phf2 | Mm_Celera | 13:48828957 | AGCACTATGGAGAGA[-/G]GGGAGGGTGGGAGGC | 18676 |
rs230244334 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48811288 | CAGCTCTGGTTTCTC[A/G]TTAGCAGACAGCCCC | 18676 |
rs230263718 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48835105 | CTGCATGACTGCCTA[G/T]GAGGGCAAGAGTAAA | 18676 |
rs230319659 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48840690 | GAATCCACACCAGCC[A/T]TGGAGCATCCATACC | 18676 |
rs230329564 | in-del | -/C | | | intron-variant | Phf2 | Mm_Celera | 13:48823363 | AGGGGATTGACTCTA[-/C]CCCCCAATAAAGAGG | 18676 |
rs230370944 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48840201 | CGCACAGAAAACAGT[A/G]TTTGTCTTAAAGTTT | 18676 |
rs230426937 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48867254 | GACATGGCCAAGACA[C/G]GACTGAATGAGGAGT | 18676 |
rs230480873 | in-del | -/GGGCCCCA | | | intron-variant | Phf2 | Mm_Celera | 13:48814888 | ACTACATCCACTTGG[-/GGGCCCCA]GACCTGTCTCTCCAT | 18676 |
rs230539778 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48826230 | AACATGCCGGGAAAG[C/T]GCTATGGCCTCCCTG | 18676 |
rs230561188 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48832177 | CACCCAACTTTGGAA[A/G]CCCTTACTCCTACAA | 18676 |
rs230594728 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48807120 | AGGAAGGAAATCCTG[G/T]CATGTGCCACAGCAT | 18676 |
rs230614329 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48831287 | CTAATGAAGAGGCAC[A/G]CATCTGTGAACGTAT | 18676 |
rs230624141 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48825483 | GTGTGGAAACCCTAA[C/T]TAAGACAGGCATCCA | 18676 |
rs230679419 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48838531 | AAAGGGATGACACAC[A/G]CATCAGGAAGGATTA | 18676 |
rs230689578 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48837727 | AAGGAAGGGGTGTGC[C/T]CTGTGCCCCCTGGAG | 18676 |
rs230707812 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48808065 | ATGATATGGGCTGGA[A/C]ACTTAACAGTGGAGA | 18676 |
rs230709901 | snp | C/T | | | synonymous-codon | Phf2 | Mm_Celera | 13:48817665 | GGGGGGCTTGGGGGA[C/T]TTGGGGGGCTTGGGA | 18676 |
rs230738114 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48837304 | AAAGTCTAGGAACAG[C/T]ACTAGTGAATTCTAT | 18676 |
rs230739139 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48838009 | TTCTCTGTAGCTTTG[A/G]CTGTCCTAGAACTCA | 18676 |
rs230776268 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48815173 | TCCCTCCCCATGGCA[C/T]CCATCAGTTAAGGCC | 18676 |
rs230833069 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48843398 | ACCTTTCAGAGAAAG[C/T]GGCTTGAGAAGAATG | 18676 |
rs230835518 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48836658 | CTTCCTGTATCCCCG[A/C]AAACGTCACCAGTAA | 18676 |
rs230844912 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48822273 | CACTACAAATTCCAC[A/G]TGGGCTCAGGAGTAA | 18676 |
rs230854072 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48806743 | ATGGTGCCTGTACCC[A/G]TTACAGAAGGCCAGA | 18676 |
rs230902023 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48814700 | ACACTTGTATACACA[C/G]AGCTCTAGTGCCTCA | 18676 |
rs230904549 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48806281 | GACTGGGAGGAGGTG[C/T]CTGCCCAGCAGCCTG | 18676 |
rs230918796 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48842411 | CATAGGGGAGGGGCG[A/G]GCATGCCCTTCCAGG | 18676 |
rs230986725 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48865354 | AGGCTCACACGAAGC[C/T]GCTTCCTTCCAGACA | 18676 |
rs231126963 | in-del | -/TAAA | | | intron-variant | Phf2 | Mm_Celera | 13:48844763 | ATTTCAAGGAAATGT[-/TAAA]TAAAGTTCTTCAAAG | 18676 |
rs231164433 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48812618 | GGGCCTGAACGAGTG[G/T]GGCCAACCGGAGCGA | 18676 |
rs231246104 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48842244 | AAAATCAGCTTTAAA[A/G]GCAGAAAGACTTATT | 18676 |
rs231296441 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48834398 | CATAGGTCTTAGTCT[A/T]CGAAGCCAGGGGACA | 18676 |
rs231306772 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48852017 | TCTGGGAGCCACAGC[A/G]GAGCCGTCTCTGGGT | 18676 |
rs231370889 | in-del | -/G | | | intron-variant | Phf2 | Mm_Celera | 13:48840346 | AGACGGGTGGCAAGT[-/G]GGGTGCTAGTGGTGG | 18676 |
rs231385274 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48833886 | CGAGCTTAACAAGGT[A/G]CTAGAGAGCAAGAAC | 18676 |
rs231419996 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | Phf2, LOC102642832 | Mm_Celera | 13:48872464 | GGTGGTGCAGTTGTC[A/C]TTCAGCAGAAGTGAA | 18676 |
rs231446446 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48837085 | TCAAAAAACTGCAGA[A/G]ACCCGCAAGATGGCT | 18676 |
rs231483609 | snp | A/T | | | intron-variant, upstream-variant-2KB | Phf2, LOC102642832 | Mm_Celera | 13:48870140 | ACGCGGGGTCCCCGG[A/T]GGGGTCCTGCCCGCC | 18676 |
rs231493417 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48820789 | CATAGGCTATTGAAC[A/G]CTCGAGTACCATACA | 18676 |
rs231501286 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48834244 | GAGTGTGGGCACTCC[C/T]ACTGCCAATGTCCCC | 18676 |
rs231521616 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48843104 | CTACTGAGTTACACC[C/T]TTTGCCCTTAAAGAT | 18676 |
rs231527691 | in-del | -/GT | | | intron-variant | Phf2 | Mm_Celera | 13:48838847 | CCTGTGTGTGTGTGT[-/GT]GGGGGGGTGTGTTTG | 18676 |
rs231531603 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48817440 | TTATCCCAGCTGTCC[C/T]TCTGGTCTGGCCCAA | 18676 |
rs231555945 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48839871 | TCAGGCCATCAGAGG[A/G]GTGCAAGTCAGACCC | 18676 |
rs231556281 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48860610 | GAGGTGGAGAGCTGC[A/T]CAAGAGGGCAGTACA | 18676 |
rs231567363 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48813249 | TTTCCTAGGGTCCTC[A/G]AAACCACGAAGGTTG | 18676 |
rs231585829 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48809806 | GCAGTGGCAGCACAT[A/G]GCATTGCAGCCAGAG | 18676 |
rs231606142 | in-del | -/GGGGAGCAGG | | | intron-variant | Phf2 | Mm_Celera | 13:48813111 | TCAGGGCAGGGCACT[-/GGGGAGCAGG]GGGGAGCAGGTCCCT | 18676 |
rs231651156 | in-del | -/TCA | | | intron-variant | Phf2 | Mm_Celera | 13:48814820 | ATGACAGAAGCAAAC[-/TCA]TCATATCAAGATAGC | 18676 |
rs231674319 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48825823 | CCATGCAGAGTAGGG[C/T]TGCAAGCCAGGCTTT | 18676 |
rs231681001 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48838859 | TGTGTGGGGGGGTGT[A/G]TTTGTGTGATATACT | 18676 |
rs231713610 | in-del | -/T | | | intron-variant | Phf2 | Mm_Celera | 13:48863170 | TGCACCAGTGGATGG[-/T]TATCAAGAACATGCC | 18676 |
rs231727703 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48859150 | CCTCAGTGTGTTCTC[A/G]AAGACAGACTGGCTC | 18676 |
rs231741787 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48845508 | AGGGACAGTCCATAA[C/T]GTCAGGGAGAAGCTA | 18676 |
rs231752209 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48826670 | GGTCCCTGGAGGGGA[C/T]TGTAGAACCCTGGCC | 18676 |
rs231782880 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48858311 | CACAATGCCAAGGCC[C/T]GATCACAACCCCCAA | 18676 |
rs231831710 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48810062 | TTTCCAGCACAGTAC[C/T]CCCTTCAGCACAGTA | 18676 |
rs231844305 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48864332 | ATGAACTGAAATTTA[C/T]CTCTGTCTTTTCAAA | 18676 |
rs231851879 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48844310 | TTAGTAGCCTCCTTT[C/T]ACATTTTAACTCATT | 18676 |
rs231889856 | in-del | -/C | | | intron-variant | Phf2 | Mm_Celera | 13:48826307 | CATGGCCGTACCACA[-/C]CCCCCAGGACAAATA | 18676 |
rs231900041 | snp | C/G | | | intron-variant, upstream-variant-2KB | Phf2, LOC102642832 | Mm_Celera | 13:48869593 | AGAAGGGTCTTCTCT[C/G]TAGAAGGAAGGTCAG | 18676 |
rs231968888 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48809110 | GATTAGGGAGCAGTG[C/T]TCATCATCATTCCAC | 18676 |
rs232077021 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48839443 | AGTAACCCCCTCACT[C/T]ATGCTTGTCCAGAAA | 18676 |
rs232082723 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48854118 | GGACAGGCCGGAAGA[A/G]GGGTGGACTTCTCTA | 18676 |
rs232106920 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48835703 | CCAACCACTTGCCCT[A/G]ATCAGGGCAGTGACC | 18676 |
rs232142433 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48852483 | GAGTGGGACAACACA[C/T]CCCAAGCTGACTTCC | 18676 |
rs232143767 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48864973 | ACTGACTGTCTCACG[A/G]CCCAGCTGATAGACT | 18676 |
rs232159918 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48841405 | ACCCGACTGCTCTTC[C/T]GAAAGTCTGAAGTTC | 18676 |
rs232195750 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48813496 | CTGATGGGGAGCCAC[C/T]CCCTGCTATTCCTAT | 18676 |
rs232254019 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48838430 | TCACATGGAAACCAC[A/G]TATATAAAACATGCT | 18676 |
rs232264505 | in-del | -/T | | | intron-variant | Phf2 | Mm_Celera | 13:48848117 | CCAATACACATAAAA[-/T]TTAAAAAAAAAATTT | 18676 |
rs232311277 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48809376 | GTCTGAGTTGGGGAG[C/T]GGCACAGGATCCCAA | 18676 |
rs232323280 | snp | A/G | | | synonymous-codon | Phf2 | Mm_Celera | 13:48828937 | CACACGGGACACCAC[A/G]TCTTCAGCACTATGG | 18676 |
rs232329640 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48844988 | CCTGTCTTGGAAAAA[C/T]AGTCTTTAAAACTTT | 18676 |
rs232383127 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48816683 | TCCATTCCCTCATCC[A/G]CCCACCCATCCGTTC | 18676 |
rs232396120 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48806094 | CGTAGCAAGAGTGTC[A/C]ACTTGAGGCAGGACA | 18676 |
rs232442312 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48811691 | TCCCCCATGTGTTCA[C/T]CAAAACTCTCACTCT | 18676 |
rs232452402 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48835856 | AACACCAAAAGGCGT[C/G]TAACAACCACACCAG | 18676 |
rs232512477 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48835179 | GCCATGGGCTGTGAC[C/T]CTGATGCTCCCCGTG | 18676 |
rs232599495 | in-del | -/A | | | intron-variant | Phf2 | Mm_Celera | 13:48815671 | TGTGTGTAATGGTGT[-/A]ATGGGGGATGCATGT | 18676 |
rs232664002 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48836330 | ATGATAAACTTCATA[C/G]CTATTAAAAAATTAG | 18676 |
rs232691338 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48825612 | AAATGTCAGTGTGCC[A/G]TCCCAGCATGTCATT | 18676 |
rs232723566 | in-del | -/C | | | intron-variant | Phf2 | Mm_Celera | 13:48868783 | TCCCTCCCTGCCTGA[-/C]CTCAGGCCCCAACCC | 18676 |
rs232841659 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48804766 | CCATCAGCTGCCCCA[A/G]GTACATCAGAGTCTG | 18676 |
rs232866366 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48808917 | CAGGTTTCCCTCTCT[G/T]GGTCCCTCCATGAAG | 18676 |
rs232867069 | in-del | -/AGA | | | intron-variant | Phf2 | Mm_Celera | 13:48839920 | GGCTACAGCTTTTAT[-/AGA]GAAGATGTGGAGAGA | 18676 |
rs232872275 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48831426 | CTAAGCTCAGCTGCC[C/T]ATGTGAGCTTTCACA | 18676 |
rs232901151 | in-del | -/C | | | intron-variant | Phf2 | Mm_Celera | 13:48813812 | AAGTGGAGACCTTCA[-/C]GGGGGGTCGGCCGAG | 18676 |
rs232985741 | in-del | -/CA | | | intron-variant | Phf2 | Mm_Celera | 13:48852892 | CCTAAACTCTCCAGC[-/CA]TGGGCTGCGCTTCCC | 18676 |
rs233005267 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48830773 | CGCCTTGCAAAGCAG[C/T]CTGGCAGTTCTCAGA | 18676 |
rs233016836 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48857930 | TGTGTGGGCATGTAC[A/G]TGAGCACAGATGCCC | 18676 |
rs233030480 | in-del | -/AAA | | | intron-variant | Phf2 | Mm_Celera | 13:48856295 | GGGTGGTGTTAGCAG[-/AAA]GAGAGCCTATGAAGA | 18676 |
rs233074586 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48869111 | CAGCTGACAGGTAAC[C/T]AGAGGTGCTATAGGT | 18676 |
rs233115523 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48861418 | AAACCCATGTGGCAC[A/G]GTCTAAAGATCTAAA | 18676 |
rs233171107 | in-del | -/AGTG | | | intron-variant | Phf2 | Mm_Celera | 13:48825017 | GCTGTGTGTGACGTT[-/AGTG]AGTGTCACGTGTGCT | 18676 |
rs233310125 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48834845 | TAGGAAGAAGCACTG[A/G]ATTCACAACAGCAGG | 18676 |
rs233310792 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48864215 | TGAAGGATGAAGATG[C/T]TGGAGAACTAGACAG | 18676 |
rs233336875 | snp | C/T | | | downstream-variant-500B | Phf2 | Mm_Celera | 13:48801634 | GGGGGCTAAGAAATG[C/T]CCCCTACCCAAGGAT | 18676 |
rs233363245 | snp | A/G | | | synonymous-codon | Phf2 | Mm_Celera | 13:48804462 | GGCTGCTGTATATTC[A/G]TGGTCAGCCAGGCTA | 18676 |
rs233430791 | in-del | -/AA | | | intron-variant | Phf2 | Mm_Celera | 13:48812746 | AATAAATAAATCTTT[-/AA]AAAAAAAAAAAAAAG | 18676 |
rs233454829 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48837230 | TGCCTGGGCATCAGC[A/G]TGCACACACTCGCAT | 18676 |
rs233479147 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48846125 | TGCACATCTATATGT[A/G]CACATCTATATGTGC | 18676 |
rs233580122 | in-del | -/CCTACAACCCATCCACG | | | intron-variant | Phf2 | Mm_Celera | 13:48808583 | ACACCCTCATCTACA[-/CCTACAACCCATCCACG]CCTACACCCCTATCT | 18676 |
rs233630440 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48859947 | GGTCTGGTCAGGTAG[C/T]TCCTTCCCTATCCTC | 18676 |
rs233637425 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48859347 | AACAGGGCCTTGTAG[C/T]CAACCTGCATTCCCA | 18676 |
rs233662586 | in-del | -/TCCATATACCCT | | | intron-variant | Phf2 | Mm_Celera | 13:48857823 | ATCTGGCCCAGGCAG[-/TCCATATACCCT]TCCTTCTGTCTTTCT | 18676 |
rs233663783 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48808134 | AGGGAGGGAATGAGG[C/G]CTTGGGTGGAATAAG | 18676 |
rs233664192 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48857220 | CCCCCCCCCCCCCCC[C/G]GCCCCGGCATCTGCA | 18676 |
rs233766658 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48834877 | ACTGTGGAAAAACCA[C/G]GCCCTCAAAGACTTC | 18676 |
rs233904758 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48833164 | TCCTGCTATTTAAGC[C/T]GCACAGCCTGTGGCA | 18676 |
rs233935631 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48860162 | CTAGGCTTTGCCTAG[C/T]TCTGACTCCTGGCAC | 18676 |
rs233937210 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48847877 | CACACACAGATTTTT[A/T]TAAAAAATAGGATAT | 18676 |
rs233941110 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48825421 | TGTGAATGGGTGTGT[A/G]CAAACCCTAAGACAG | 18676 |
rs233995166 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48854410 | AGGGACTGCCTTGAC[A/T]GATTCTCTCAATAAG | 18676 |
rs234022162 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48856644 | AGACCCAGTCTTAGC[A/G]AGAGAAAGGTGGAAA | 18676 |
rs234099788 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48867911 | ATGCTCCATTTCGGA[A/G]AATGATACAAAGTTT | 18676 |
rs234128300 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48838480 | GGAAGTTGTGGGATG[A/C]AAGATTACCACAGCA | 18676 |
rs234178689 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48814831 | AAACTCATCATATCA[A/G]GATAGCAAGACCAGG | 18676 |
rs234192500 | in-del | -/CAGTGC | | | intron-variant | Phf2 | Mm_Celera | 13:48845666 | CATACAGTCCACAAA[-/CAGTGC]CACCAACTGGGGGCC | 18676 |
rs234255269 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48864785 | GGCTCGCAGTACAAC[G/T]GCTAGGGTCAGGAAA | 18676 |
rs234256853 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48844550 | GTTTTGATATAGGGT[C/T]TTACATAGCCCATTC | 18676 |
rs234274971 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48829611 | GCCAAGGCCATGTAA[C/G]CAAAAGGTAGCCTTT | 18676 |
rs234318546 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48867322 | ACAGAATGGAGAGGA[G/T]CCTTCCCCATGATCC | 18676 |
rs234327233 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48855638 | TTCCCACTTGCTACA[A/C]GTGAAGCTTGGACCA | 18676 |
rs234327309 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48843842 | GTTGCTCAGTGACTA[A/G]GACACCTGCTGCCAA | 18676 |
rs234339805 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48830091 | GTACTACACAAGCAC[C/T]TGTATTTATGAGCGT | 18676 |
rs234342457 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48830410 | GAGGAAGAGGAGGGG[A/G]AAGAGAAAGAGGAGG | 18676 |
rs234411427 | snp | C/T | | | synonymous-codon | Phf2 | Mm_Celera | 13:48817794 | CGGTTCTTCCTTCTC[C/T]CGGTCTCCATCACAG | 18676 |
rs234417618 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48837749 | CCCCTGGAGGTTACA[G/T]GGGAGCAGGGATCAT | 18676 |
rs234432660 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48805358 | GTGGAAGAGACCAGG[A/G]AAAGGCCAATGAATC | 18676 |
rs234451855 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48820264 | CCGGGCTTGATGTCA[C/T]CCAAAGTGACAGCTA | 18676 |
rs234510588 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48821524 | TGTACCTGTGCAGCA[C/T]ACTCACCTGAGGGGA | 18676 |
rs234559254 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48819662 | TAAGTTAGTTAGTGT[A/G]GTGTCTGCTTAGCCT | 18676 |
rs234575651 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48822312 | ATGTAGACTACCACC[C/T]AACAAGTCCCTGCTC | 18676 |
rs234577716 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48814196 | GGAAGTCTGCTTATG[A/G]AGAGGGACATCCTCT | 18676 |
rs234619412 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48851502 | AGAGAGTTCTAGGAC[A/G]GTCAGGGCTACACAG | 18676 |
rs234664727 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48826729 | AATAGTTTGCTCCAT[C/T]ACACACAATCTTACC | 18676 |
rs234679036 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48862946 | ACATGTATGTGACAG[C/T]ATATATGTGCTCATG | 18676 |
rs234730301 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48827200 | AGGGACTGTAGGTGT[C/T]CTCAAAGATGGAGGA | 18676 |
rs234758390 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48849162 | CTGGAGAAAATAATC[C/T]ACCTTTTCTTTTCTC | 18676 |
rs234769328 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48859077 | GTCCACTCTGAGGCA[G/T]AGACAGCAGAGGCAC | 18676 |
rs234793138 | snp | A/T | | | missense | Phf2 | Mm_Celera | 13:48819620 | GCAGCTGTTTCCCAG[A/T]CTTGTGAGAACCTGG | 18676 |
rs234803076 | in-del | -/AAG | | | intron-variant | Phf2 | Mm_Celera | 13:48813595 | TGCCAGGGACTGAGC[-/AAG]AAGACCATGTCCCTC | 18676 |
rs234819638 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48860585 | GATGAGGGGAAAGGA[A/T]ACAAGGAAGGAGGTG | 18676 |
rs234897655 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48827272 | ACAAGCAGGTCTTCC[A/C]GCTGGAGCTCTCAAG | 18676 |
rs234926170 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48818156 | AGGCTGCCTGGGTCT[A/G]GTTCCTCCAGGCTCA | 18676 |
rs234947609 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48834364 | GTCTGCGTCTATTTC[A/C]TCTTCAGCTCTTTCT | 18676 |
rs234996633 | snp | A/C/G | | | intron-variant | Phf2 | GRCm38.p3 | 13:48810375 | GGTTCTAGAGAAGAC[A/C/G]CTGGTGGGGTGGGGC | 18676 |
rs234996651 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48818700 | GTGGGAAGGACCCCT[A/G]AACTATCCCAGCTTT | 18676 |
rs235076887 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48831980 | CAGCGCCTGGACCCC[A/G]CCCACCTTGGAAGGT | 18676 |
rs235144345 | in-del | -/AG | | | intron-variant | Phf2 | Mm_Celera | 13:48805676 | ACATGACAAAGTTCT[-/AG]AGAGAGGGTCTAGGC | 18676 |
rs235168183 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48856850 | GGTAGGATGCCACAG[C/G]TCTGGGGAAGAAGGA | 18676 |
rs235466330 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48845186 | TCACAGGGCCCTATT[C/T]CTTATATCCTTCATT | 18676 |
rs235507124 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Phf2, LOC102642832 | Mm_Celera | 13:48872782 | TGAGCTATACAGCAG[C/T]ACAGACCCTACCCCA | 18676 |
rs235565720 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48823311 | GGCTGCAGAGGGTGG[A/G]GTGAGCCCAGCCACA | 18676 |
rs235610087 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48842399 | CAGACTGAGAGACAT[A/G]GGGGAGGGGCGAGCA | 18676 |
rs235614213 | in-del | -/A | | | intron-variant | Phf2 | Mm_Celera | 13:48855182 | GTGAGGGGAATCCAG[-/A]ACAGACTGGGGGCTT | 18676 |
rs235666377 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48841742 | TGAGTTTTGGGAAAG[C/T]CAGAGTTAACTGGTA | 18676 |
rs235737573 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48851386 | TATGGACAGGAAATC[A/G]TTCCTGTGTGTCACT | 18676 |
rs235768953 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48829132 | TGATAACTGTAACGG[A/G]AACACGAAGGTCAGG | 18676 |
rs235786574 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48824848 | GACTCATGCCAATGA[C/T]AACACCTGAGACCTG | 18676 |
rs235806640 | in-del | -/G | | | intron-variant | Phf2 | Mm_Celera | 13:48816648 | CCAGGCACTCCTGCT[-/G]GTCCACACACAGCAA | 18676 |
rs235806903 | in-del | -/TTGGTTGGTTGT | | | upstream-variant-2KB, cds-indel | Phf2, LOC102642832 | Mm_Celera | 13:48871813 | TTTTTTGTTGGTTGG[-/TTGGTTGGTTGT]TTGGTTGGTTGGTGA | 18676 |
rs235812178 | in-del | -/TGTGTG | | | intron-variant | Phf2 | Mm_Celera | 13:48815722 | GAGGATATGATGTAA[-/TGTGTG]TGTGTGTGTGTGTGT | 18676 |
rs235933970 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48811400 | CCAGAACTGGGCACC[A/G]AGGTGAGGGCCTAGG | 18676 |
rs235950305 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48839661 | AACGCCGTTAAGAAA[G/T]AAAAGTCTGCTTATA | 18676 |
rs235961878 | in-del | -/T | | | intron-variant | Phf2 | Mm_Celera | 13:48835654 | ATGAAGGACAGAACA[-/T]TCTCTCAAAGCCTGG | 18676 |
rs236008653 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48839586 | TGTGTGAGAGAGAGA[A/G]AGAGAGAAAGAGGGA | 18676 |
rs236016621 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48839358 | CCCTTCCTGAGGAAC[C/T]CACTGATGGTTACTG | 18676 |
rs236016639 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48848069 | TCCATGGGCACCAGA[C/T]ACATAGTACACAGAC | 18676 |
rs236067609 | in-del | -/C | | | downstream-variant-500B | Phf2 | Mm_Celera | 13:48801488 | TGTCATCAGCTTCTT[-/C]CCCCAGACAGGGCTG | 18676 |
rs236072839 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48852276 | AGGCCCTGGTGGGGG[C/T]AGGGGGCTGGTGACA | 18676 |
rs236075801 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48839566 | AGTGTATGTGTGTGT[G/T]TGTGTGTGTGAGAGA | 18676 |
rs236077545 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48846939 | ATGCTCTCCCTGGTA[C/T]CTGCCCAGGGAGAGC | 18676 |
rs236078683 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48827947 | TTTATGTGGGTCCTA[G/T]GGATGCAAGGTCATC | 18676 |
rs236131209 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48847259 | GTGAAAGGGGGAATT[A/G]ATGAACCACAGAGAC | 18676 |
rs236132529 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48839115 | ACAAACTGATAAGCC[C/T]ACTCTAAGATCTAAA | 18676 |
rs236155641 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48864290 | CGGTGCAGAGGTAAA[C/T]TGTCTACCTTCAAGT | 18676 |
rs236162867 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48820356 | ACAACAGCCTTCATG[A/G]TCCCAAACCACTGCT | 18676 |
rs236195965 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48846346 | AGACTCAGACACACT[A/G]AAACAGAAAGCCAGA | 18676 |
rs236236226 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48834692 | GTCCCTGTGTTCCTA[C/T]TGGCTACATCTCTGC | 18676 |
rs236310010 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48830015 | AAAGAGGGGCTGGAG[A/G]GGGTTCAACAGCTGA | 18676 |
rs236351372 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48861276 | CCAATTTAAACATTA[A/G]ATTGCAAGGGGCTAA | 18676 |
rs236362942 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48837606 | CAGCAGCATACCAAG[A/G]GGGCTGTATTCCACG | 18676 |
rs236374374 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48830533 | ATGCAGTGTATGAGG[A/T]AAAAGAGCTCAATAG | 18676 |
rs236426973 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48837044 | AATGAACAGATCTGT[A/T]AGACATTGTGTCTGT | 18676 |
rs236462086 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48816751 | CTATCCATCTCTATC[C/T]GTTTACCCACTGTCC | 18676 |
rs236470964 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48824885 | CCTCTACATGTGGCC[C/T]CATAGGTTGAGGCCA | 18676 |
rs236472968 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48847622 | ATATGTGAACATACA[C/T]ATATACACATACACC | 18676 |
rs236530669 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48816814 | CACATCCACCCCTCT[A/G]TCCCTCCTTTCTTCC | 18676 |
rs236532083 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48809201 | TTCCTGGTGGTCTCC[A/T]CAGTCTCCACCAGGC | 18676 |
rs236742410 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48824093 | TCATGGCGTTTTATC[A/G]TAGCGATAGATAGTA | 18676 |
rs236771424 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48850040 | CACATACATATCACA[C/T]AATCCATACGCAAAG | 18676 |
rs236776617 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48814272 | CAGGATACACAGTCA[C/T]GCACTGTAGAGAAAG | 18676 |
rs236778161 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48804210 | AAGCACTCATAGGAA[A/G]GGCAGGGGCCATGCA | 18676 |
rs236804145 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48816277 | GATGAAAGGCAGCGG[A/G]GGAAGACATGGAGAC | 18676 |
rs236840512 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48805063 | GGTACCATGTGAGGG[A/G]GAGGTGCCTATCTGG | 18676 |
rs236852379 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48844705 | AGGGAAAATAAACTC[C/T]ATTTTAGACAAAATT | 18676 |
rs236876149 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48813074 | GAGTCATCGCTCTGC[A/G]GAGCCAGGGACAGAG | 18676 |
rs236935479 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48855712 | TGGTTCAGAGGGTGC[A/C]GGCTTTAGGTCCTGT | 18676 |
rs236945110 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48842502 | CTCCCATCTACACTA[C/T]GGGCTGGACCAAGCA | 18676 |
rs236999752 | in-del | -/A | | | intron-variant | Phf2 | Mm_Celera | 13:48843681 | GCTTCCAGAAAAATC[-/A]AGAGAATAGGCAAGC | 18676 |
rs237004536 | in-del | -/ACACAA | | | intron-variant | Phf2 | Mm_Celera | 13:48847669 | ACATACCACACACAT[-/ACACAA]ACACACACACACACA | 18676 |
rs237036474 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48824258 | CTTTATCTCATTCAC[C/T]TGACCAGGCTGTCTG | 18676 |
rs237074669 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48841852 | CATATAGACACTGAG[A/G]GGACACTCCCTCCCA | 18676 |
rs237076694 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48811552 | GTCAGCCATTGAAGT[A/G]TTAGCTAGCACATAT | 18676 |
rs237123984 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48813209 | ATGGGTGAGGTCCTC[A/G]TGAGACAGGTGTGGG | 18676 |
rs237142552 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48850195 | ATGCATACATTACAC[G/T]CCAGGGCTCTGCCCT | 18676 |
rs237143335 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48812196 | TGTCTAAGCTCCCTA[A/C]GCCTCAGGTTCCCCA | 18676 |
rs237207125 | snp | C/T | | | downstream-variant-500B | Phf2 | Mm_Celera | 13:48801492 | CATCAGCTTCTTCCC[C/T]AGACAGGGCTGATAC | 18676 |
rs237345761 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48822454 | CTCCAGGACAGACGC[C/G]ATGACGGCGATGACT | 18676 |
rs237368339 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48818472 | AGCCAGGGCCAGGGC[C/T]ACCCCGGGGGGTGGG | 18676 |
rs237453632 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48818908 | CCCTCAAGTAGCAGG[A/C]GGGCACGTGTCCGCT | 18676 |
rs237493308 | in-del | -/AGACCTCCA | | | intron-variant | Phf2 | Mm_Celera | 13:48868996 | AACAGTAAGGTGACT[-/AGACCTCCA]AAACCAAAGCAAACA | 18676 |
rs237518872 | in-del | -/CT | | | intron-variant | Phf2 | Mm_Celera | 13:48854673 | CCTCCCTCTCAACCC[-/CT]CCCCCCCCCCCCGAA | 18676 |
rs237575176 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48829492 | TCAAAATTTAATACA[A/G]GAGTCAAGTGTAGTC | 18676 |
rs237597633 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48809734 | AGCCTCTGAAAAGAA[A/G]CTGTGTTAGGAGATA | 18676 |
rs237718211 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48868803 | GGCCCCAACCCTTGA[C/T]CCTGCACAAAGCTAG | 18676 |
rs237743134 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48819362 | AGTGACCCCAGGCTG[A/G]CCCAGGCAATCTACA | 18676 |
rs237755656 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48840068 | TTAGCTATCTATCTA[A/T]GAGTTACGGATTGGC | 18676 |
rs237784014 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48867623 | AAACAAGGCTTGCTG[G/T]AAATGTGTAATGTGA | 18676 |
rs237819218 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48812013 | TGAAGGAACAGGAAC[C/T]CTGGACGGGCCCGTG | 18676 |
rs237839847 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48832376 | CACCTCCCAGTCACC[A/G]TGCCCATGAACTGAC | 18676 |
rs237905354 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48839065 | CTCTCTATTCCTAAT[A/G]CCCACCGGACACCCT | 18676 |
rs238039445 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48837864 | ATCCTTCCTCAGACG[C/T]TCTTACCTTAGATAA | 18676 |
rs238058810 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48851649 | CGGTCACCTTGTTTC[C/G]AGGTGGAGTAGCTAC | 18676 |
rs238080610 | in-del | -/A | | | intron-variant | Phf2 | Mm_Celera | 13:48812747 | AATAAATAAATCTTT[-/A]AAAAAAAAAAAAAGA | 18676 |
rs238085521 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48808589 | TCATCTACACCTACA[A/C]CCCATCCACGCCTAC | 18676 |
rs238118373 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48851019 | TAGGCTGGTGAGATG[A/G]CTCCATAGGTAAAGT | 18676 |
rs238118640 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48863498 | ACACAGCCCAACACA[A/C]ATGATAAATAGTAAA | 18676 |
rs238150371 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48868224 | GGAGGGAGCTCATGC[C/T]ATGGTGTACATGGGT | 18676 |
rs238183751 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48861830 | TCCACGCCAATGAGA[A/G]AGCCTGTCTGAAAAA | 18676 |
rs238267425 | in-del | -/CC | | | intron-variant | Phf2 | Mm_Celera | 13:48849910 | ACAGACACACACACA[-/CC]CCATATATATACTAC | 18676 |
rs238282960 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48836210 | AGCAAATGCTACAAC[A/G]CCGCCAGAAGTTCCC | 18676 |
rs238357724 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48812123 | GGGCCCCTGTGTGAG[A/G]TCAGCCCAGAGCCTG | 18676 |
rs238397414 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48826941 | TCAGGAAATATTTAT[C/T]TTGCCCTTTCTGTGT | 18676 |
rs238404284 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48864701 | CTGTTCAAACCTTAA[A/G]CCAATTGTACATGCA | 18676 |
rs238418529 | snp | A/C | | | downstream-variant-500B | Phf2 | Mm_Celera | 13:48801449 | GGCCAGTGGGCAGGG[A/C]CACTTCTTGTAGTTG | 18676 |
rs238452091 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48834816 | TAGCACCTGCTGCAT[A/G]GCAGGGCCCAGGGTA | 18676 |
rs238458825 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48827419 | AGGAGATATAAGGGA[C/T]ACACAAGCCATCCTG | 18676 |
rs238463308 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48864027 | CAATAAACACCAACA[C/T]ATGGCACTGTGTGAG | 18676 |
rs238503271 | snp | A/T | | | intron-variant | Phf2 | Mm_Celera | 13:48834490 | CTAGATGGGAGCAGG[A/T]CACATTCCCCTGTGA | 18676 |
rs238518795 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Phf2, LOC102642832 | Mm_Celera | 13:48872266 | TACCCCGTCAACCTG[C/T]ACACAATGAATTCAT | 18676 |
rs238523732 | snp | C/G/T | | | intron-variant | Phf2 | GRCm38.p3 | 13:48834219 | GGATAAGACTTGGCC[C/G/T]GCTGAACAGGAGTGT | 18676 |
rs238536128 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48846641 | TTTAAAGTGGGCCCC[A/G]GGCCTCGACAAGCCC | 18676 |
rs238624426 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48861603 | ACAGCAAGACTGGCT[C/T]AAAACACCAGGACAG | 18676 |
rs238669415 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48832829 | ATCAAGAGAAAGCAT[G/T]TGGGAGAGCCTGCCT | 18676 |
rs238679331 | in-del | -/CTT | | | intron-variant | Phf2 | Mm_Celera | 13:48832582 | CTTTGCACATATGAG[-/CTT]CTTCTGTGCTGTGAC | 18676 |
rs238759085 | in-del | -/CA/CACA/CACACACACACACACA | | | intron-variant | Phf2 | Mm_Celera | 13:48808464 | TCTCACCTCTACCTG[-/CA/CACA/CACACACACACACACA]CACACACACACACAC | 18676 |
rs238814046 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48823740 | CTTGACTAGTCGGCA[A/G]CCTGACTCAGTTTCC | 18676 |
rs238860007 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48858754 | GCTTGTGTGCAGCTG[G/T]GGGTCAGGAACCACT | 18676 |
rs238880228 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48824382 | CTCAACCTCTAGTCC[C/T]TAAACTCCTTCCACA | 18676 |
rs238919640 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48821349 | TAGGAAGACTTCTGA[A/G]CGACCACCCTTTTCC | 18676 |
rs238956799 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48813845 | CCCTCGGAACCCCCT[G/T]CCCACACCCACCAGA | 18676 |
rs238970361 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48840151 | TCCACCATCCACCAT[C/G]CAAGACAGGTGGACA | 18676 |
rs239029252 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48810152 | GCACAGTACTCCCTC[C/T]AGCACAGTAGCCCCT | 18676 |
rs239127937 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48830051 | GCCTACAATTCCAGC[A/G]CCAGGGGAGGTAATG | 18676 |
rs239156143 | in-del | -/G | | | intron-variant | Phf2 | Mm_Celera | 13:48835596 | ACCCTGGGTGGGTAT[-/G]GGCGGATCTAGAAGG | 18676 |
rs239167404 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48866977 | AATACATGATACAGA[C/T]ACAAGGAAGGACTAT | 18676 |
rs239187474 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48839246 | ATCTACAAATGATAA[A/G]CTGGGCTTTATCAAA | 18676 |
rs239189344 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48831495 | GTGATGCTATCCTTC[C/T]AACGTAAGAGAGAAA | 18676 |
rs239189525 | snp | C/T | | | synonymous-codon | Phf2 | Mm_Celera | 13:48807789 | CGTGCCCCATGTGGT[C/T]TGCAGGCAAGAGTCA | 18676 |
rs239191284 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48830678 | TGGCCAGATTCAGAA[A/G]CACCACACTAATGAG | 18676 |
rs239252237 | in-del | -/CCCACG | | | intron-variant | Phf2 | Mm_Celera | 13:48809029 | GCCCCTGTCTACTGC[-/CCCACG]CCCTCATCTCCCCCA | 18676 |
rs239253746 | snp | A/T | | | intron-variant | Phf2 | GRCm38.p3 | 13:48838856 | GTGTGTGTGGGGGGG[A/T]GTGTTTGTGTGATAT | 18676 |
rs239253790 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48808740 | CAGCTCTGTGTACAC[C/T]TGCACATACCCTCAT | 18676 |
rs239473420 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48828477 | CCACCTCCACTCCTG[C/T]CCCCGCCACAACAAA | 18676 |
rs239490644 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48806907 | GCTGCATGGACATCT[A/G]TCAGGTCAGCCCTTG | 18676 |
rs239498932 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48841593 | GTTGGGAAGAAGTTA[G/T]CAAGGCCCACACACT | 18676 |
rs239580991 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48838754 | ACAGGGTGCCACTGG[C/T]ACCTAGCTAGCTAGA | 18676 |
rs239643926 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48829451 | AAAATGAAGAGCTTA[C/T]AATTCAAGACTTACA | 18676 |
rs239656582 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48845365 | TGTGAGAGGGGACTT[G/T]GAGTAGTACTAAATG | 18676 |
rs239744432 | snp | A/G | | | intron-variant | Phf2 | Mm_Celera | 13:48816994 | TCTCCCTGTCCACAG[A/G]GGTTCAGGCCCTTAT | 18676 |
rs239825214 | in-del | -/CTTAT | | | upstream-variant-2KB, nc-transcript-variant | Phf2, LOC102642832 | Mm_Celera | 13:48872665 | CCTCCATTTACTCTC[-/CTTAT]CTTCTGACATTCTCT | 18676 |
rs239843955 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48833479 | GTAACCTGCTCAAAC[C/T]CACACCACACCTTTG | 18676 |
rs239845025 | in-del | -/TCCCT | | | intron-variant | Phf2 | Mm_Celera | 13:48817386 | GCCCTATAGCAGGCC[-/TCCCT]TCCCTTCCCAGTAAC | 18676 |
rs240108644 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48846878 | GTGTTGCTGCTTTGC[C/T]GTTTCTCAGGAAAAA | 18676 |
rs240141143 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48807214 | CGGAGACCTGAAGTA[C/T]GTGACAAGTGGCCAA | 18676 |
rs240173494 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48858395 | TGGGAGACCACGGGT[C/T]AGTCACACACAGGCT | 18676 |
rs240173508 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48845601 | TACAAACTCAAAGCC[C/T]GCCCTCAGTGACATT | 18676 |
rs240234050 | snp | A/C | | | intron-variant | Phf2 | Mm_Celera | 13:48857898 | TTTAAAATTAAACTT[A/C]TATGTGCCTGTCTCT | 18676 |
rs240423783 | in-del | -/ACATACAT | | | intron-variant | Phf2 | Mm_Celera | 13:48830141 | TTATTATACACACAC[-/ACATACAT]ACATACATACATACA | 18676 |
rs240481432 | snp | C/G | | | intron-variant | Phf2 | Mm_Celera | 13:48831188 | GGACCTGAAGGAAAA[C/G]GTGCCGTGGTTTCTC | 18676 |
rs240514616 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48842748 | GAATACATATGTAAG[C/T]ATACATGTAGAGGCC | 18676 |
rs240577089 | snp | C/T | | | intron-variant | Phf2 | Mm_Celera | 13:48852875 | GCACACCCCAACCCT[C/T]ACCCTAAACTCTCCA | 18676 |
rs240578204 | snp | G/T | | | intron-variant | Phf2 | Mm_Celera | 13:48842150 | AAAAGTCCACCACAG[G/T]AGGAAATGCCCACTG | 18676 |