SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs215239286 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11932946 | ACATTTAGAAAATAA[A/G]TAATTATCTTTAGGT | 75725 |
rs215241343 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12015732 | TAATTTATAGAAAAG[-/T]TATGTTAGTGATTAC | 75725 |
rs215246852 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11932064 | TTCAAAATCTGTTTT[A/C]ATTTCTTACATGAGC | 75725 |
rs215277029 | snp | C/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100101 | TGGTATCATGTGCTA[C/G]TTCTGTGAGGACGGA | 75725 |
rs215296619 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11952530 | ATCCACCCTCAGACT[C/G]TCCACATTCATACCT | 75725 |
rs215314861 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12092680 | AACATTTATTTGTTT[C/T]CTAAGTAGGTTTCCT | 75725 |
rs215334730 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12051765 | AAGTGGCAGCCTAGC[C/T]GGTGTCATTTATATT | 75725 |
rs215366714 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11911029 | CTATAACTCAGTTCT[C/G]TATCACTTGCTTAGT | 75725 |
rs215395547 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12093704 | AACTATAAACCCAGC[A/C]GAGCTAATCAGTGCT | 75725 |
rs215414826 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11985934 | TTTTATTATTTTGTA[C/G]TGCTGGAGTCAAATC | 75725 |
rs215417727 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12042796 | GTAATGAAATTGAAT[A/G]TTCATGCTGAGCTTG | 75725 |
rs215429467 | snp | C/T | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12099990 | GCTTTTGAGGGTTTC[C/T]TCTCCTACATCGGTT | 75725 |
rs215454215 | in-del | -/AAAAG | | | intron-variant | Phf14 | Mm_Celera | 6:11995322 | CCAAAAAAAAAAAAA[-/AAAAG]TACTTTGTATTTATG | 75725 |
rs215471591 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11911649 | CTCACAAGGCTGGAG[G/T]ATGAAGTAGCCAACA | 75725 |
rs215476221 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11961056 | AGATATACCCTTAGG[A/G]ATATCCAACAGCCTT | 75725 |
rs215478414 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12058430 | TTAGTCAAGCTCCTT[C/T]GATGGCCGTTTAGAG | 75725 |
rs215479205 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12092581 | TTGGGACCTCATTCA[C/T]GAGCAACTTCTCTTT | 75725 |
rs215480776 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12004220 | ATCATATTTACTTTT[-/C]GGGTATACTTTCTAA | 75725 |
rs215493782 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12005834 | GTGGTCAGAAAAAAT[G/T]TTAATATAAATGCAT | 75725 |
rs215493783 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12037954 | AATATAAGTCATGCT[-/G]CTTATTGTAGCATCT | 75725 |
rs215497418 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12041925 | GGTTACTTGTTTAAA[A/G]TAATCATTAGCTTAT | 75725 |
rs215498258 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032624 | ACATTTCAAATGTTA[-/T]CCCCTTTCCTGGTTT | 75725 |
rs215541619 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12070561 | GATCTGCATAAGAGT[A/G]ATAATAACCTTGTGA | 75725 |
rs215552477 | in-del | -/TAAG | | | intron-variant | Phf14 | Mm_Celera | 6:11935648 | AATGAGACCTATATT[-/TAAG]TAGTGCCCACATAGA | 75725 |
rs215558564 | in-del | -/CTT | | | intron-variant | Phf14 | Mm_Celera | 6:12095413 | ACCCAATCCAGAAGC[-/CTT]CTTCATTATGTTTCA | 75725 |
rs215574342 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11993650 | AGCTCAGTTGATACA[A/G]TGCTTACCACACAAG | 75725 |
rs215574393 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11979416 | TTAGGAAGAATCATT[G/T]AATTTCTAGGTGAAT | 75725 |
rs215575887 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11961883 | GTCAGCTTCAGGCAT[A/G]AGCTTGCCTCTTCCT | 75725 |
rs215600051 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12050022 | CTGTCCTGATGTAGT[A/C]GTATTGGCACTTACC | 75725 |
rs215600452 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040463 | GCATTAGAATAGATA[A/G]TAAATGCAAGTGTAA | 75725 |
rs215610191 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11981344 | GTTACTTGTTCTCTG[C/T]ATTTCTATTGCTTGT | 75725 |
rs215616068 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916978 | ATGGTACACTTGTCC[C/T]CTTTCCATTGGTTGG | 75725 |
rs215621319 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12035127 | AATAAACAGAATTCC[C/T]TAAAGGAATCCTTAT | 75725 |
rs215622212 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12046093 | GTAAAAAATGCAGAG[-/A]AAAAATGTATTTTAT | 75725 |
rs215627831 | in-del | -/TATATATATA | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032502 | TGTATATACATACAC[-/TATATATATA]TATATATATATATAT | 75725 |
rs215629602 | snp | C/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12040996 | ACATTATATATTATT[C/T]TCTCCCAAGCTTGGT | 75725 |
rs215632427 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052912 | AAATTTTAAAATAAT[A/T]CCAGCCAAAGATATA | 75725 |
rs215652299 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11920318 | AGTCAGAGGCCAAAA[G/T]AGAAGCCTGATCATC | 75725 |
rs215663615 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11909532 | CTGAGTTGAAAACTA[A/G]ACGAAAAGAAGAAAT | 75725 |
rs215676218 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910028 | CTAACAGGTCAAATT[A/G]TCAACACTTAAATTT | 75725 |
rs215686493 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11997327 | AAGTATTTCTATGAA[A/G]TCAGTTTTCTATGTT | 75725 |
rs215697755 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11960384 | TGAAGAGAAGAGGCT[A/G]CACAGATTACATTGA | 75725 |
rs215718467 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11914415 | TAAGCCAGGCAAGAT[A/T]TATGTCACTCTTAAG | 75725 |
rs215721463 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12075811 | TGACTTCACTCCTTC[C/T]TGTGAACATAGATCC | 75725 |
rs215754471 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11944072 | TTGTGATAAGCTTTT[A/G]TAAGGAGATGTAGGG | 75725 |
rs215765430 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11951220 | TAAATTTGTTTCTTC[-/T]TTTTATTTTTTAATT | 75725 |
rs215806998 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12076334 | GTATAACCACTGTAA[A/G]ATTTCCAGAACCAGA | 75725 |
rs215808246 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12069157 | TGTGTATATATACTT[G/T]ATATATAAATACATA | 75725 |
rs215812175 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11941756 | TGTATATATATGTGG[A/T]GTGTGTGTGCGCGCG | 75725 |
rs215821797 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12020819 | TATGTTAAGAGGGAC[A/G]AGTCAGTCACAATCT | 75725 |
rs215846291 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12069881 | TGCAGTCTTACTAGC[A/C]CACTGGTTCCTTCCT | 75725 |
rs215863885 | in-del | -/GC | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021976 | AGCTTGTGTGTGTGT[-/GC]GCATGTTCTACCTAG | 75725 |
rs215873529 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11942506 | TCTAGGGAAATGAAG[A/G]ATAAATAGGTAAATT | 75725 |
rs215875065 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11932114 | TTTGATTATTAGCTG[C/T]GTATATGGGGCTTCT | 75725 |
rs215875742 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057287 | TGTCTGTGCCTGTAG[A/G]TGCTTGTGTATGTAA | 75725 |
rs215878029 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12021723 | CTGTCACAGTAATAC[A/G]TCATAAACTTGGTAC | 75725 |
rs215883922 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925787 | TAGAGAATCTGTGAA[C/T]ATTCTTAAAGTTACT | 75725 |
rs215888647 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12013793 | AAATTTAATGGCACG[A/T]AATTTATTAAAGTTG | 75725 |
rs215915313 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12003401 | GCAGAGCGAGGCCGT[A/G]GGGAAGGTCTGCTTA | 75725 |
rs215921719 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12058039 | GAAACTCACCTCTAA[A/G]TTCACTTGGTGACCC | 75725 |
rs215952643 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918515 | ATGTAATTCAGTGGT[A/G]GAATACACATCTAGC | 75725 |
rs215964127 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052349 | GTTGAGATTTAGAAT[C/T]GATGACCTGTCTGAT | 75725 |
rs215982458 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11996581 | CTATCTTCCCCAAAA[C/G]TCAGCAGATCTTTTG | 75725 |
rs215986308 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12074106 | TAAGGAATTTAAAAT[A/G]TTGAAGTATATTAGC | 75725 |
rs215987586 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11995696 | CCCTTTCTCCTCCCC[C/T]CCAGCTCTCCTCCAA | 75725 |
rs215993396 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947779 | ACCTACACTTCTTCC[G/T]ATTGTTTTGAAATCA | 75725 |
rs216000893 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:11945707 | TGTCATGCTATTTTT[-/C]ACTCTCCAACCACCA | 75725 |
rs216006851 | in-del | -/CA | | | intron-variant | Phf14 | Mm_Celera | 6:11946669 | CTCTATACTTGGGGG[-/CA]GGGGGGGATGGAGTG | 75725 |
rs216028191 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12026747 | TGGAGGAACGGGTCA[A/C]CCCTCAATCAGTCCT | 75725 |
rs216048521 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11939616 | GTGGGTGTTGTGACA[A/T]ATGCCTGTAATCAGA | 75725 |
rs216071771 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11996056 | TTCTTCCAGCTCCAG[C/T]AATCCTATCCCCCAC | 75725 |
rs216074387 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11919292 | TAGACACAGATGTAG[A/G]CAAAACACCCATACA | 75725 |
rs216084665 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12018882 | TGCAAGCATAACAGA[A/G]TATCTTTAATAGTGT | 75725 |
rs216098867 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12020115 | TTCATCTGATTTCTG[A/G]CTCTTTGGTAAGTGG | 75725 |
rs216099571 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12068410 | AATACTTAATAAAAT[C/G]CTCAGGTAAAGAGTA | 75725 |
rs216112142 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924765 | TAGAGTGGTAAACAG[-/T]TTTTCCATATATTTT | 75725 |
rs216145577 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054950 | ACACACACATACACA[C/T]ACTCAGGATGGATAG | 75725 |
rs216158801 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11940522 | TGATTGTTACATATC[A/G]ATATAACAGGACTCT | 75725 |
rs216163672 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036452 | GCAGGATGGAATCTC[A/T]AACCAGTTCTGTTAC | 75725 |
rs216192094 | in-del | -/AAA | | | intron-variant | Phf14 | Mm_Celera | 6:12022465 | AAGAGACTAAAGATC[-/AAA]AAAAAAAAAAAAGTT | 75725 |
rs216195057 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12030382 | TTAACTTCTTTCTTT[C/G]CAATTTGTACCCCTT | 75725 |
rs216206225 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12056829 | TTTGTGGACATGCTC[A/G]CGCTTTCACATAATT | 75725 |
rs216222681 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12002888 | TTATAATAGAACATG[A/C]TATTTTTCTTTGGTC | 75725 |
rs216243486 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12098998 | CTTCTAGAGTCAACT[A/G]AGCATGATGAACTAT | 75725 |
rs216256433 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12049213 | TTTCCAGATCATGTA[C/T]TCACACACTGTACTG | 75725 |
rs216275725 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12082556 | ACCCTCATGTTTATT[A/C]GTGTGTTAAAGCCAT | 75725 |
rs216289345 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12086176 | TTCATAACCTCCAAG[-/A]AATTTGGAAATAAAA | 75725 |
rs216309848 | snp | G/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925444 | TCTGTTTACTGTCTT[G/T]CTTCCCCTGGCTTTC | 75725 |
rs216322863 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11958904 | AACTGATTTATCGCA[C/T]GAGTTTAACTAGACA | 75725 |
rs216323158 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11918033 | ACAAAACAGTGAGTA[G/T]AGTTACTAATAGTGA | 75725 |
rs216324483 | snp | A/G | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099262 | CTTGTTCCTCCTGAT[A/G]TGCTCAGCTTGCTTT | 75725 |
rs216326426 | in-del | -/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008862 | CTAGCTTCTTTCTCT[-/G]GTTTGCCTTATTAAG | 75725 |
rs216329553 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11992839 | CAGTTCAGGATACTG[A/G]TCCTCAGGCTGAGAA | 75725 |
rs216336919 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11959664 | TTCACATTCACCTGC[A/G]TCTAAGTTGCAGATA | 75725 |
rs216337325 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959837 | TATTAATTTAATTTC[C/T]GTGGTCACATAAGAG | 75725 |
rs216339772 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12034514 | GAAGAGCTCTGATCA[A/G]TAGAACAGCTGACAA | 75725 |
rs216339864 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12041833 | GTGATGAAACTCAAA[A/G]ATTTGAGTTCGTAGC | 75725 |
rs216342255 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12097509 | TAACTGAAGAAGTCA[-/TT]TTTTTTTCACTAAAC | 75725 |
rs216345811 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12033865 | GATAGATTACTTTAT[C/T]TTTCTGAAAATTCTC | 75725 |
rs216350269 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917355 | ATCTATTGTAGAACC[C/T]CCTTTACTTTGAGCC | 75725 |
rs216364631 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11994586 | CTAGCTAGAACAATA[A/C]GACAACAAAAAGAGA | 75725 |
rs216376079 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12035031 | TAGTGATTTAAAGTC[A/G]TCAATGGAATTAAAG | 75725 |
rs216379451 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083726 | CTGGAATCCACAATA[G/T]GGTCTGGGTTTGATG | 75725 |
rs216388772 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11939037 | CAAAAAAACAAAAAC[-/A]AAAAAAAAATCAGAC | 75725 |
rs216438476 | in-del | -/TT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062938 | TATAATTTGATACAG[-/TT]TTTTTTTTATTTCAT | 75725 |
rs216460519 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12031902 | AATGTTCTCTTGGTT[-/A]ATTTTTTTTTCTTTC | 75725 |
rs216493501 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12084388 | TCTCAGTCTTTACAT[A/C]ATAGCCACTAATATC | 75725 |
rs216509063 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11950350 | CTGGGAATGGCTTGG[A/C]CTTTGGAAACCTCAG | 75725 |
rs216511422 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12062244 | CAGGGGGATACTTGG[C/T]AAGTTTTCCCATGGG | 75725 |
rs216516097 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12005140 | TGGGGAATTTGAGTA[-/T]TTTTCCCTTTAATAT | 75725 |
rs216522515 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12036050 | TTCTCCTTAGGGCTC[A/G]AGAGAGGCCTGTCTG | 75725 |
rs216538861 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11930931 | GGTAGAATATGTACC[-/A]AAAAATGACTAGTTA | 75725 |
rs216538950 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11950268 | GCAGTAGCTGAGAGA[A/C]TACATGTGATCCGCA | 75725 |
rs216563677 | in-del | -/TTCTCAGACATTATGTTC | | | intron-variant | Phf14 | Mm_Celera | 6:11979683 | GGATAGACCTCTTCA[-/TTCTCAGACATTATGTTC]CTGGGCCTCACTTTT | 75725 |
rs216569453 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12029121 | TTAAGGGTCCTGTAG[A/C]ACGCAGATTGTCACA | 75725 |
rs216570252 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11950949 | TTCAGCTATTTCCAG[A/G]TCGGTCAGTTTCTTA | 75725 |
rs216575163 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061626 | AGCGGACTGGCTGGA[A/G]TAACCTAAAAATTCC | 75725 |
rs216584791 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029921 | TCTGTTTTCAGCGGG[G/T]GATGGGTCTTTTCTC | 75725 |
rs216597486 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11937596 | TCAGGTGCTTTTACC[A/C]ACTGAGCCATCTCAC | 75725 |
rs216661330 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12014539 | TACTGTTGATGTACA[C/T]GGATTGGTTGTTGAC | 75725 |
rs216662753 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083339 | CTGCCTTTGCACCCT[-/G]GCATTCCCCTACACT | 75725 |
rs216673067 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12003517 | GCCAGTCTCATCCAT[A/G]TATGGTAGGTGCAAT | 75725 |
rs216673189 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057322 | TTTTTTTTTTGGTGA[A/G]TTTATGCATGTGAAT | 75725 |
rs216687560 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11951224 | TTTGTTTCTTCTTTT[C/T]ATTTTTTAATTTTAA | 75725 |
rs216750703 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12068554 | TATATATATATATAT[A/G]CAAATATGAGTAGAT | 75725 |
rs216751404 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12091420 | CGTCTCTGTGTACAG[C/T]AGCCATGAACTATCC | 75725 |
rs216761308 | in-del | -/CTAATTT | | | intron-variant | Phf14 | Mm_Celera | 6:12068470 | TTGATTTTCCTTATA[-/CTAATTT]TAAGGTCTTTACTAA | 75725 |
rs216781977 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060998 | CAGGTTCTGTGGTTT[G/T]ATTTCATGTATGTTG | 75725 |
rs216808289 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11931229 | AATAAAATCACAACT[C/T]CGTGATATTTGTAAA | 75725 |
rs216834624 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12012626 | CTTAAGTTTTCACTC[A/C]CTTCAATTTGTTATT | 75725 |
rs216858129 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061500 | AGTTTCATAAAAGTG[A/G]AGCCTCTATTGAAAC | 75725 |
rs216871644 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083243 | GTTTTCCTCTTTCCA[A/G]GTCTCCCCTTCAGAA | 75725 |
rs216876383 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11922828 | TCTACACTACATTAT[C/T]TAGCCCAAAGTATCC | 75725 |
rs216889505 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12001806 | TTGTATCCCTAATTG[C/T]TCCAGGACTTTTATT | 75725 |
rs216894182 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12034449 | AACATCCTTAGTGAT[A/T]AGGGGAAAGCAACTT | 75725 |
rs216904916 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11932040 | ATTGATAATAATTTC[A/T]TTGAGTCATTCAAAA | 75725 |
rs216906765 | in-del | -/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12012235 | TGTGGTGGGAATGAG[-/T]TTTGAGACAGGGTTG | 75725 |
rs216907012 | snp | G/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11923964 | GAGGCCAGATCTCAG[G/T]GTTTGTGCTTGGGAG | 75725 |
rs216924393 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12028186 | GTGGTTCTTCTCAGT[A/T]AACCAGAAAGCTGAA | 75725 |
rs216937445 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11959541 | CATTTCTTGATTTGC[A/G]AATGAGAAGAACGAT | 75725 |
rs216939085 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010340 | AAAGGACTACTTGAG[A/G]CCTGTTAAATTGTGA | 75725 |
rs216960980 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060612 | AGTTATGCAACAGTG[C/T]CGTGATGCTGGGCGG | 75725 |
rs216961716 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924400 | GTGAGGAGAATTGGT[A/G]AAGAGAATTCTGAGT | 75725 |
rs216989514 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12091472 | TTCACACACCGTGTA[A/C]TTGAGCTCTTACATG | 75725 |
rs216993947 | snp | A/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12041094 | GAATGAAGCATTTCT[A/T]TTAATAATATCCTAA | 75725 |
rs216996835 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916877 | AGAGACTATTACAGA[G/T]CTTTGAAGCTTGATA | 75725 |
rs217002761 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11949645 | ATAGAATAGGTTTAC[A/G]GGTAGTTTTTAAGGA | 75725 |
rs217019733 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083280 | TATTCCATCACCCCT[C/T]TCCCTACCTCTGTGA | 75725 |
rs217021195 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12092357 | GTTCACATCTAGGTA[C/T]CACTTTTCTCCTCTG | 75725 |
rs217047624 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11990541 | TTTTGCTTTTGATCT[-/A]GGTAGTGATGAATGG | 75725 |
rs217056510 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12000043 | CATTAAGTGATTAAG[G/T]AAATTGCTGGTGGTT | 75725 |
rs217065535 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11930489 | AATGAATGTTACTTT[C/G]AGAGATCCTGAAATA | 75725 |
rs217075028 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11929269 | AGATGTGAGCAGTTA[C/G]TAATCTTATTATTAA | 75725 |
rs217079971 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12097023 | AATCCATTTAGCAAT[C/T]GGGCCACTTGAACGC | 75725 |
rs217129035 | in-del | -/TT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12064827 | CCCTGGCTCTTTATG[-/TT]TTTTTTTTTTTCTTC | 75725 |
rs217137843 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11986222 | CTTTCTTTTCTTTTC[-/T]TTCCTTCCTTCCTTC | 75725 |
rs217139362 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12098060 | CTGTCTTCCCTCACT[A/T]GGGCCATTCTCTCAC | 75725 |
rs217146632 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12046842 | ATGTTTACTGAATAG[A/G]AATTTTGTGTTGTAC | 75725 |
rs217146962 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12087864 | GAGCAGTGGTCTTGA[A/G]CTGTAATTCTAAGTC | 75725 |
rs217164021 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12062183 | CAGGAAGTATGGCAG[A/G]TAACAGATGTCTCTA | 75725 |
rs217164660 | in-del | -/AT | | | intron-variant | Phf14 | Mm_Celera | 6:12062168 | TGAGGATGACAAGAC[-/AT]AGGAAGTATGGCAGG | 75725 |
rs217165396 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11923130 | TCAATAATCACATGT[C/G]ATAATTTAACTAATT | 75725 |
rs217190831 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11977255 | TGCCAAATAGCAAGG[A/G]TACAGTGGGATGCAT | 75725 |
rs217193579 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12088940 | AGAACTTTGAATGTA[C/T]CTGCTTTCCTGCCTA | 75725 |
rs217204936 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11978301 | CACATTGGTGAAGCT[C/T]TGTTAGAGGTGTGCC | 75725 |
rs217248606 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11957594 | CACATTTTTCTACAT[A/G]CTAACCACCAGTTGA | 75725 |
rs217251456 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11979260 | GGTTATTATATGGAG[A/G]CTGTAGATTAAACTG | 75725 |
rs217251476 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11957649 | GGTCTTTTTTCCATG[A/G]ATGGTTTTAGCTCCT | 75725 |
rs217269310 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12038892 | TTGATAACAAAAGCA[A/G]CACACAGCTACTTTT | 75725 |
rs217278030 | in-del | -/TG | | | intron-variant | Phf14 | Mm_Celera | 6:12021552 | CACGCAAAATTTTTT[-/TG]TTGTTGTTTGAAACT | 75725 |
rs217281099 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12079591 | CATTTAATCCACGAT[-/A]GCCTCTTTACCAAGG | 75725 |
rs217301541 | snp | A/C | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040147 | TATGAAATGAGGGAA[A/C]TACAGAGCTTGTTGG | 75725 |
rs217312619 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12019454 | CCCCAACTTATATAT[G/T]TAGTATGTTCTTCAT | 75725 |
rs217317480 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908671 | GTGGGGAGGAATGTA[C/T]TGATTGGGGAAAAAA | 75725 |
rs217326204 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11958598 | AGCATTGAGATTTAA[A/T]AGGAAATATGTGTAT | 75725 |
rs217344861 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12033518 | CCTGGACTCTGAGGT[G/T]GTTCCAGGTTATATA | 75725 |
rs217349266 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12046007 | CAAAATAGTAGATGA[A/G]TAGTATTTTAACTAC | 75725 |
rs217350160 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036966 | AGTAGTGTCACAAGC[C/T]TTTAATCCCAACACA | 75725 |
rs217378468 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037262 | TCTTTGAACTGGCAA[C/T]TATAGGAATTATCCA | 75725 |
rs217390532 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906493 | GGAGCGGAATCTCTT[C/T]GGGAACTACTGAAAA | 75725 |
rs217418122 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12090511 | TCTAGACTCCAGGTC[A/C]ATATTTGTATTTTTT | 75725 |
rs217431780 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906878 | TATCGAGCTATACTG[G/T]ACGAAAGTGACAGGT | 75725 |
rs217434525 | snp | A/C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11981300 | GGAGTTGTGTTGCAC[A/C/G]TGCATTACTTGGGGC | 75725 |
rs217442749 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12072775 | AATACATGACATGAG[C/T]TTCATTGGTGAAATA | 75725 |
rs217446491 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060962 | GAAATGATAGGAACG[C/T]GGCCCTTACCAATGG | 75725 |
rs217453356 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11989687 | CACCAATATAGCTGG[A/G]ATATTGCAAAGAAGC | 75725 |
rs217490824 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12002615 | CATTATGAAGTTGAG[-/A]AAAATGACTGAATAA | 75725 |
rs217499070 | in-del | -/CCCCAAC | | | intron-variant | Phf14 | Mm_Celera | 6:12029785 | GGGAGATCTATCTGT[-/CCCCAAC]CCCCATCCCCTTAGT | 75725 |
rs217505699 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12065704 | TGCTTCTGCTCCAGC[A/C]CTCAGAAAGAAGTAG | 75725 |
rs217511586 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11938443 | TTTCCCATTGAACCA[C/T]TGTGGCCCACTGTTA | 75725 |
rs217534824 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12076059 | TTCTTTAACTATAGA[A/G]GTGCGGGTGTCTTCA | 75725 |
rs217536522 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055437 | TTCATTTTTCCCCAT[G/T]CTTAAGGTTCAGTTC | 75725 |
rs217558184 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11928424 | TGGTGCATAGGTGAG[A/G]TTTAAAATGAGAAGT | 75725 |
rs217559676 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11938857 | CCATTAACACAGATA[A/G]CACAGGTAGCCTCTT | 75725 |
rs217569624 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11923853 | AGTACTGTGGTTTAT[G/T]TATATGGATGTCTTC | 75725 |
rs217587615 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12001059 | ATGTAGGCAAGAAAT[C/T]GAACTTTTTGAGTAT | 75725 |
rs217645344 | in-del | -/CATA | | | intron-variant | Phf14 | GRCm38.p3 | 6:12019291 | TGTCATACATACATG[-/CATA]CATACATACATACAT | 75725 |
rs217659818 | snp | C/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12081440 | AGAGATGTGGGCCAC[C/T]GTAACAGCCTCTCAA | 75725 |
rs217663759 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11915767 | TAACCTCACCTATTG[C/T]ATTAGGGAAATTGTT | 75725 |
rs217680539 | in-del | -/AC | | | intron-variant | Phf14 | Mm_Celera | 6:12063201 | ATTTTGTGTGGTGCT[-/AC]ACATCATTACTGCTT | 75725 |
rs217708150 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12029836 | CTGTGGGTTTTGTGG[A/G]TTATGTAGCTCAACC | 75725 |
rs217715017 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12017422 | TCCTTCTCACTTACT[A/G]AGATTTCATCAGGAG | 75725 |
rs217731006 | in-del | -/CA | | | intron-variant | Phf14 | Mm_Celera | 6:12093863 | TCTCAAAGCCTCAAT[-/CA]CACACACACACACAC | 75725 |
rs217737551 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12081961 | CCACATGCCTGTGTG[A/G]TTTATGCAGTTACTT | 75725 |
rs217744698 | in-del | -/GAGT | | | intron-variant | Phf14 | Mm_Celera | 6:12034903 | ACCAAAGAATGCAAG[-/GAGT]GAGTAATATTGCCCT | 75725 |
rs217748931 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076550 | TTGAGTTCTTTTATA[G/T]AATACCTGCTGTGTG | 75725 |
rs217750192 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11957386 | CCTTTGTCTTATAGA[A/G]TCTTTGCAATTTTAT | 75725 |
rs217770177 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12017888 | GTTTCTGAAGGAAGA[A/C]AATGGCAGAGATGCA | 75725 |
rs217774267 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12029139 | GCAGATTGTCACACT[A/C]TTATTGCACAAAATG | 75725 |
rs217787573 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12015350 | ATGGAAGTCAACTTT[-/G]GTCACCTTTTCTTAA | 75725 |
rs217803046 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11957784 | GTTCTCATCATACAG[A/C]TCTTTCACTTCCTTA | 75725 |
rs217804574 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947433 | TCTCCTATGTTGCCA[A/G]TCACTTAATTTGCCA | 75725 |
rs217817423 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11948017 | CAGACAAATAAGATG[A/G]TCAAGATAGGTAATA | 75725 |
rs217827369 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12070408 | ACATTCAGAGAGCAT[A/G]ATTGTCAAGGGTTTA | 75725 |
rs217839872 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11943635 | ATTGGTGTGCAGATG[A/C]AGCAAGAGTTATGTA | 75725 |
rs217843251 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12021790 | ACTATAATGGAGAGA[A/C]AAGGGTTTATTTCAC | 75725 |
rs217846411 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12069908 | TCCTGGAATGTAAAT[G/T]ATTTCCTTGTCTACT | 75725 |
rs217887429 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12022303 | ACAAAGAGACCATGG[A/G]TTTCTTTTCATGGCT | 75725 |
rs217917493 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12033072 | TCTCAGGAGACAGCT[A/G/T]TGTCAGGCTCCTGTC | 75725 |
rs217925703 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11934459 | GTTGTTTTAAAAGTT[A/T]GTTATCAGCTGTAGC | 75725 |
rs217950550 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12000390 | TCCTCTCATTAGACA[A/C]GTTGGCAAGGAAAGC | 75725 |
rs217960253 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11942777 | ACACCTTGCACACTC[C/T]GTTCTAGCTTACTAA | 75725 |
rs217972263 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12026993 | TTTACTCAGGAATGT[G/T]CCTCTGGGTAGAGAA | 75725 |
rs217974896 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083507 | GGGAGTTCTGGGGGG[A/G]GTCTGACTTGTTGAC | 75725 |
rs217979297 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11932996 | ATTTGATATAAATCA[A/G]TGGTACTATGTTTAA | 75725 |
rs217984877 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921758 | ATATTAAGCTGATAC[-/T]TTTTTTTAGTACCAT | 75725 |
rs218025501 | in-del | -/GGCTA | | | intron-variant | Phf14 | Mm_Celera | 6:11961316 | CTAAATCTACAGTTT[-/GGCTA]GGCTTCTTGAAAAGT | 75725 |
rs218072938 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060687 | AGATGATCTCCAGGG[C/T]GCTGTGCTTTTGAAC | 75725 |
rs218080431 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:11995414 | AGATCGCAACCCCCT[-/C]CCCTCCTCTCCTCCA | 75725 |
rs218124112 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12059701 | CTTGGGAGGTTATTC[A/G]GGCAGGGGTTTGCAA | 75725 |
rs218150169 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055067 | CAAACTGTTCCTTAA[G/T]AACTCAAGTTTAATA | 75725 |
rs218158268 | snp | A/G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12053782 | CAGAATAAAGTTGGA[A/G/T]TCAGTAAAGAAAATT | 75725 |
rs218159255 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:11945353 | ATCAAGTTTGGCATT[-/C]CCCCCCCACCCTGCC | 75725 |
rs218180045 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11948878 | TTAGCTTGCTTCCAT[G/T]GTGTCTCCAGATCCT | 75725 |
rs218195869 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11940594 | ACTGGAGTTTAACTC[C/T]CAGGTTCATGTTATC | 75725 |
rs218212211 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921182 | ATTTGTTGTTTGAAG[C/T]CCAGAAACATCAAGG | 75725 |
rs218233588 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054304 | AGCCACTCAGTGTTG[G/T]TCCTGGTTGGTAAAC | 75725 |
rs218234791 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11941176 | TAAGGGCCAAAGTCA[A/T]ATGTTAAGCAGGTAG | 75725 |
rs218239336 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12020194 | GAAACACCATGAACA[A/C]AAGCAACTTAAACAG | 75725 |
rs218240304 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11946679 | GGGGGCAGGGGGGGA[C/T]GGAGTGAAGATGCTT | 75725 |
rs218244226 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12087271 | TAGACAAACGGGACT[C/T]ATGAAACTGAAAAGC | 75725 |
rs218259169 | in-del | -/GACTTATGT | | | intron-variant | Phf14 | Mm_Celera | 6:12084062 | TCCTAGCTGTTCTGG[-/GACTTATGT]ATACTAGGCTGGCCT | 75725 |
rs218262602 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11915334 | CAGCTTGCACTCTGA[G/T]AGAAGCATCCTTCCA | 75725 |
rs218267562 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921758 | AATATTAAGCTGATA[C/T]TTTTTTTAGTACCAT | 75725 |
rs218278261 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12001129 | CCACTGCTTACTGCT[C/T]AAAGGTAGTGGAATT | 75725 |
rs218312051 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12006637 | ACTATCAAATACGTG[C/T]GTATTTATATAAAAA | 75725 |
rs218322577 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12087911 | AAAGATATAGAAAAA[C/T]CCTGAAGTTTTCATA | 75725 |
rs218326974 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008544 | GGATATATAGATTTT[C/T]ACTGGGTTGTATTAT | 75725 |
rs218340876 | snp | G/T | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099054 | CTAACTTAAGATCTA[G/T]TTTTGCCTCTTCCTG | 75725 |
rs218347774 | in-del | -/TTTTTTT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12068678 | TATAATAATCCCAGC[-/TTTTTTT]TTTTTTTTTGGAAAC | 75725 |
rs218360218 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12049246 | GATTGAAGTGTGCTG[A/G]CTACTCTTGTTACTT | 75725 |
rs218366564 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12023374 | TCCCTCCCCGCCAAT[-/C]CCCCCCTTCCCTTCT | 75725 |
rs218403219 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12005261 | TTTGCCAAATCTTGA[A/G]TGTTTGTATTGCACA | 75725 |
rs218424922 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11998535 | GTAACTCCCTCTTGG[A/C]ATGACCGAGCATATT | 75725 |
rs218427008 | snp | C/T | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099301 | GCCCAGGACCACCAA[C/T]TATGGGGTGGCACAA | 75725 |
rs218457788 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11996791 | GGTTCACAACAGCAT[C/T]GTTACATATGTTCTT | 75725 |
rs218479175 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11999394 | TGTTTCAATGTTAAC[C/T]TTGAAAAAGCTGATA | 75725 |
rs218511534 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12050130 | AAGAATAAGAGGAAA[A/G]GAAAGGGAAGGAAGG | 75725 |
rs218515860 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036693 | CTTGTGGTATGTAAG[A/T]GCTCTAGTCAGAAAT | 75725 |
rs218517606 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917410 | GGTTATTAATGGTAC[C/T]CACTGTTTTCATGGG | 75725 |
rs218531370 | snp | A/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | GRCm38.p3 | 6:12099882 | TTGTCGTCTCCTGGC[A/G]TACTTTCTCATAGCA | 75725 |
rs218533298 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12058138 | GGTCTCATACAGCCA[A/C]GGATGCCTCAAATTG | 75725 |
rs218544151 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11993727 | GATCATGATGCATAC[C/T]TGTAATCTCAGTACT | 75725 |
rs218550982 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12037053 | AGTTCCAGGACAGCC[A/C]GGGCTACACAGAGAA | 75725 |
rs218553225 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12050769 | AGTTTTTAGTTGAGT[A/G]TTGTACTTTGGGGCT | 75725 |
rs218577519 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11926554 | CTAACGTCAGGGGCA[A/G]CCAGGCTCTCTGCAT | 75725 |
rs218587791 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918845 | CTGGCCTGGACTAAC[A/G]CTGTAGTCCAGGCTG | 75725 |
rs218587870 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927388 | ACTTGTATGTTCACA[C/T]AGTTTAAAAGCAGAG | 75725 |
rs218589803 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11910109 | CTGGAGACAATAGTG[C/T]TAACAATTTAGAAAA | 75725 |
rs218593320 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030756 | GTGTTCTTTCTGTTT[C/T]TATTTTATGAAATAA | 75725 |
rs218604011 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031161 | ATTGCTTTTATGTTA[C/T]TGATTTCAGCCCTGA | 75725 |
rs218612235 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917925 | CATCGAGGAAATGGA[C/T]GGCTGTCAGTGATTG | 75725 |
rs218617970 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11980590 | AGATTATTTCCTTTT[C/T]GATTTTGTTTCAAGT | 75725 |
rs218639622 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11919321 | CACTAAAAATAAAGG[C/T]TAATTTTTTGAGGTC | 75725 |
rs218648461 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11994240 | GGTTTGATACAGATA[C/T]CTGCATCTGACTCTT | 75725 |
rs218679476 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054242 | GTGAATACAGATGCC[C/T]GCAGAGGCCAGAAGC | 75725 |
rs218683992 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11999258 | GCATTTGAGTACTGT[A/G]TTTCTAGTCAGTGAA | 75725 |
rs218697367 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12085565 | GCTGAGCCTTCTTCC[C/T]AGTGTCATATGTAAC | 75725 |
rs218710619 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083988 | TGAAGGAGGCAGAGG[C/T]AGGAGGATCACCCCG | 75725 |
rs218716122 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:11952560 | CCTCCCCACCCCCCT[-/G]ACTCCATGTGGATGT | 75725 |
rs218716182 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12085447 | ACTGCAGAGGCCAGA[A/G]GCATCAAATTCTCTA | 75725 |
rs218731568 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12078975 | ACACATTTTTGCTTT[C/T]CTTCTTTATCAGTGT | 75725 |
rs218764095 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11922553 | GCCTCCTTACCAATC[A/G]ATATACTCAATGCTC | 75725 |
rs218776248 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11921563 | CATTCTGTACATCTA[A/C]AGGTAGTCATAAGCA | 75725 |
rs218786858 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12084450 | CTTCACCCGTGATTC[C/T]CTGCATTAACATTTT | 75725 |
rs218795993 | snp | A/G | | | synonymous-codon, missense, nc-transcript-variant | Phf14 | Mm_Celera | 6:12047842 | GTGTGATGAATGCAG[A/G]CTGTGCTACCATTTT | 75725 |
rs218799080 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11960455 | TCCACAGGACGCATA[G/T]GGGAGGTTAGATTAA | 75725 |
rs218803565 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12073301 | AACGCAGCTTTTTTG[-/T]TCCTTTGTGTATTGT | 75725 |
rs218804932 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11915698 | TCTAGAAAAATGATT[A/C]CACCTCACCAAAGTA | 75725 |
rs218816287 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079353 | GTAGAATATGTGGTA[C/G]CAGAACAAAGGCATG | 75725 |
rs218827807 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11953022 | GCATTCTCTTATATG[A/G]CTTTGAGTATATTGA | 75725 |
rs218828621 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11916492 | AAAATCAACCAACCA[A/G]ACCAATAGAACTGCA | 75725 |
rs218838373 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11990983 | CAACTGTGGTTGATT[A/C]TTTGGAAAATATTAG | 75725 |
rs218855231 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11961283 | TGCAGTGAATCTTAA[C/G]TGGAAAGCAATTATG | 75725 |
rs218857660 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950543 | TTGAAGTATTTTCAG[G/T]ATATTTTCCTCTATT | 75725 |
rs218867911 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11951491 | TGTAGATCATTGGCA[A/G]TTTTTGTGTTTTGTT | 75725 |
rs218876959 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11991593 | ATAATTGAAAGCTAT[A/G]TTGACAATGCATTCC | 75725 |
rs218878852 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11954231 | TGAAGGATAACCAAA[A/C]TTAAGGAATTTTCTC | 75725 |
rs218932423 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12064061 | AATCATTTAACTCTA[-/T]TTTTTTGTTTGTGCC | 75725 |
rs218979739 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12081868 | TTACACAACCTGGCC[A/C]CAGCTCCCTAGGAAG | 75725 |
rs219009952 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036109 | CTTGAGTTCCAATCC[G/T]CAGGTCCCATATATA | 75725 |
rs219017602 | in-del | -/GGATA | | | intron-variant | Phf14 | Mm_Celera | 6:12057860 | TCTGTGATAAGTTAT[-/GGATA]AGACATGTGGGATCA | 75725 |
rs219019260 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12004047 | TGATGCTGTAGAGCT[A/C]CTGTGAAGACAGCCT | 75725 |
rs219029536 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12082434 | TTTTAAAAATAGTTA[A/G]TAAGGACCTATGTAT | 75725 |
rs219060440 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12075386 | TGTTACTCACACACA[C/G]ACATATCTATGCATG | 75725 |
rs219064046 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12033020 | AATGGTTGGCTGTGA[G/T]CATCTGTCTCTGTAT | 75725 |
rs219070805 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11993106 | atttatttatttatt[C/T]attcattcattcatt | 75725 |
rs219071103 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997635 | TCACCTGAAAAAAAA[A/T]ATTTTTATTTACATT | 75725 |
rs219073147 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12027464 | ACACTCCTCAGCTAA[A/G]GCAGCACGTAGCCCT | 75725 |
rs219075830 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11988225 | ACGGTCTTTCTAAAG[G/T]GTTAGGTACTAAGTA | 75725 |
rs219106032 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12062388 | ACCATTCTCGTCCTT[C/G]CTGTGTTCAGCTTTA | 75725 |
rs219116339 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12074190 | GTCTCTTGTCTGTCT[A/G]TATTTCTCTCTCGCT | 75725 |
rs219120853 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997946 | TTAAATACATGGTCC[C/T]CAGTTGGTAGAACTA | 75725 |
rs219133226 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12063261 | TTAATTACTAATAAA[A/G]CTTAGGAAACACAAA | 75725 |
rs219145292 | snp | C/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909275 | TCCTGCCTCAGCCTT[C/G]CAAGAGTTGGCATTG | 75725 |
rs219151327 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12042684 | TACAAGTGGATCTTC[A/T]TAGAAAGAAAAATGT | 75725 |
rs219159817 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079306 | GGCACTGACAATGGC[A/G]AGTATTTAATTGGTC | 75725 |
rs219164555 | in-del | -/TGTA | | | intron-variant | Phf14 | Mm_Celera | 6:12022708 | ATTCGTGTGTGTGTG[-/TGTA]TATGTGTGTACATAT | 75725 |
rs219196620 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947938 | TAGCCTCATTAAAGA[C/T]AAGTCTACCTTTTCA | 75725 |
rs219211281 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12057476 | ATCAAGCTGCGTTCC[C/T]TGTCTCCATTCCCTG | 75725 |
rs219214419 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12063726 | TCTTTGTTAAGTTCT[C/T]AAAACAGATTGTTAC | 75725 |
rs219218986 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11954026 | TTCTGGAGGGTCCCC[C/T]CAATCTCCTGTCTCC | 75725 |
rs219221167 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11976890 | TGTGTTAATGCTGGA[A/T]GAACACTGAACATTT | 75725 |
rs219238947 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031139 | CATTGATTCTTTGTA[A/T]TTTTTAATTGCTTTT | 75725 |
rs219246690 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12053146 | CAATGAAGCAAGAAT[A/T]GCAAAAGAGACCTCC | 75725 |
rs219250110 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043896 | TCCCTTTTAAAGTCT[C/T]GCCCCAGAGGCTGCT | 75725 |
rs219263140 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12086762 | TTCAGTCATCATTGG[A/G]AGGCCCAAGAGACTG | 75725 |
rs219268577 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11919799 | GGGACTGAAGAGATG[A/G]CAGTGTTTTTGTTTT | 75725 |
rs219294849 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11932327 | GTTGTATACAAATCC[-/T]TATCTCCCTCTTTTT | 75725 |
rs219305727 | in-del | -/AT | | | intron-variant | Phf14 | Mm_Celera | 6:11985882 | ACATACCCAAGTAAC[-/AT]AACATTTTTATCAAT | 75725 |
rs219315744 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024236 | CTCCACGTGGATGCC[C/T]CCACCCTCCAACCCA | 75725 |
rs219321869 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11913967 | TTTTTTATTTCCTTT[A/G]TGGATTCCTAAGTTC | 75725 |
rs219322963 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12044951 | GACTTCTTTTGAAAA[C/T]TTAAACATTTTATTC | 75725 |
rs219324223 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024587 | GGCAGTCATGCTAGG[C/T]CTACAGCCTCAGTAG | 75725 |
rs219370604 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12017534 | ATCTTAATAGAAGGA[C/T]TTAGGTTGTTCTTAG | 75725 |
rs219391777 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031612 | TCTTTTTTACATCTA[C/T]TGAGACTTGCTTTGT | 75725 |
rs219400538 | in-del | -/GT | | | intron-variant | Phf14 | Mm_Celera | 6:12053283 | GTGTGTGCACAGTGC[-/GT]GTGTATGCGTGCATA | 75725 |
rs219411424 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079429 | GGCAAAAAGAGCATG[A/G]CAGAGATAAGGCTAG | 75725 |
rs219417863 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079751 | CAGATGTCAGTTGAT[A/G]GAAAATAATCTACTC | 75725 |
rs219427147 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11912037 | AGATTTGGGGGAGTT[G/T]GAGATTTAGAGTTTT | 75725 |
rs219432250 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11955694 | GTTTGTGCTTTCAAA[A/C]TGTTTTGCCCATGCT | 75725 |
rs219437227 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947157 | TAGGGGTTCATAGTT[A/T]CAGAGAGTGACTCCA | 75725 |
rs219443132 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079922 | ATTTATAATTTCTCT[A/G]ATTTTCTAATATTAA | 75725 |
rs219444419 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906636 | TGAGTTCCAGGACAG[C/T]CAGGGCTATACAGAG | 75725 |
rs219444670 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12072509 | GGACATTTACGACAT[C/T]TTCACATAATGCAGA | 75725 |
rs219459623 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11951787 | TTGAAAATAGTTAAC[A/G]TATAAGATATGAATT | 75725 |
rs219461227 | in-del | -/CA | | | intron-variant | Phf14 | Mm_Celera | 6:11955092 | TGCCTGGTGTGGGTG[-/CA]TGGGTCTTTAGCAAG | 75725 |
rs219471449 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11946348 | GCTGGGATTAAAGGC[A/G]TGCGCCACCACCACC | 75725 |
rs219483704 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12059577 | ACAAGTCTATATGAC[A/T]GGGCCCAGTCTATAT | 75725 |
rs219488050 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12037809 | AATCTGTTGGTGAAA[-/TT]CTTTGAAAATATGTT | 75725 |
rs219496426 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12070810 | GTCTTCATCCTAACT[C/T]CTACTAGAATGACCC | 75725 |
rs219496684 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12078809 | GATTGAGAACCATCT[A/G]TAGTTGCAGTTTCAG | 75725 |
rs219497223 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907089 | CCCCTCTTGGGACCA[A/G]GTAATCTGAGAGCCA | 75725 |
rs219497637 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024511 | TCAGCTGCTCCTGTC[C/T]ATTGGTTGAGTGCAA | 75725 |
rs219520579 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11954648 | TTCTGTCAATGCAGA[C/G]TCAATATTAAAGCAC | 75725 |
rs219526290 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12071690 | TAAAGAGACCATTGG[C/T]TAAATGATGCATTGT | 75725 |
rs219572077 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11946891 | ACTTGAGCCCACCAA[A/G]AAATACTACCATTGA | 75725 |
rs219597885 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11945235 | ACAATGCAGCCTGCT[A/G]GGTTTGGGGGCATAG | 75725 |
rs219598460 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11946669 | CTCTATACTTGGGGG[C/G]AGGGGGGGATGGAGT | 75725 |
rs219607680 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11936538 | ACACAAAAACAAAAC[C/T]ACACTAAAGATACAG | 75725 |
rs219659397 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11977417 | GTCAAACTTGGAGTT[G/T]AAGTTTCTTCCTGCC | 75725 |
rs219664943 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917492 | AAACTCCTGCACCTT[C/T]ATGCTTTATGCTGCT | 75725 |
rs219671986 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12030062 | TCTAAGTTGTTTCCA[A/G]TGTCGGCTATTATGA | 75725 |
rs219683166 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12030564 | GGTTTTGGGCCTGCT[A/G]TAAATTGTCTTTATT | 75725 |
rs219683180 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12022795 | TAAAGTCCAGAGAGG[G/T]TAATTGAGAAGTTCT | 75725 |
rs219733102 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023477 | TGTACACACTGTTGA[G/T]AAAGAGAGGGTGGCA | 75725 |
rs219755819 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908205 | TAACCTTTTCTACCA[C/T]CCTAAGTCAATGTTC | 75725 |
rs219767957 | in-del | -/AGAT | | | intron-variant | Phf14 | Mm_Celera | 6:11944556 | AGACAGAAGAGATGG[-/AGAT]AGATGGCTTTTGAAA | 75725 |
rs219768053 | in-del | -/TTAAATTT | | | intron-variant | Phf14 | Mm_Celera | 6:11979723 | TCACTTTTTAGGGAG[-/TTAAATTT]AAGAAATCACAACAT | 75725 |
rs219794364 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060039 | TTGTTTGTTCTTGTC[A/G]TCTTGCCATTTCCTA | 75725 |
rs219815118 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12021866 | GAATTCAAACGGCAT[A/G]AATCTGGAAGCATGA | 75725 |
rs219817778 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12074307 | GTTAAGTAAAAAGCA[A/G]ATTGCTTTTACTGTC | 75725 |
rs219829672 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12015384 | CGGTCTACCTTATTT[C/T]TGAAACAGGGTCTAT | 75725 |
rs219837891 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12088262 | CAATACACAAAAGAA[-/C]TACAAATTTTAACAT | 75725 |
rs219886155 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11937228 | AGAGCAAGTATGTAC[-/A]AGTAAATCAAGCACA | 75725 |
rs219886432 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12056894 | TGTGCTAAATCTTCT[C/G]TTGTGTGTTAGAAAT | 75725 |
rs219886842 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907226 | ATCCCAACAACAGAA[G/T]GTAACCCCAAGGAAC | 75725 |
rs219903426 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052427 | TGCAAACATAACAAA[C/T]AGAGTTTCCTGTTTC | 75725 |
rs219915819 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12051053 | TCAAAATATTTTCTA[C/T]GGTTATTCTTTTACA | 75725 |
rs219961510 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11918264 | AGTGTTTTTACTCTG[C/T]CTCAAAATAAACAAA | 75725 |
rs219967221 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11940001 | ATCCTGAAAGTCCCC[C/T]ATACCCCACCCCCCA | 75725 |
rs219984126 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12051873 | TGTATAATTTAAGTA[A/T]TTTAGCATCACACCA | 75725 |
rs219989364 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11942982 | ACCCTTTCCATCCAG[C/G]ATGAGAGGATATAAG | 75725 |
rs219992641 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12084022 | TACACCTTTGTTTTT[A/G]TTTTGAATCAGGGTC | 75725 |
rs219999339 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918720 | TCAGCAGTTCAATGC[A/G]AGCATTGGCTGTATA | 75725 |
rs219999637 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12030981 | TATGACATTATGATT[-/C]TGTGCATTTCCTTAC | 75725 |
rs220057224 | in-del | -/ATATATAT | | | intron-variant | Phf14 | Mm_Celera | 6:12098713 | AGGATAGTATTTAAA[-/ATATATAT]ATATATATATATGAG | 75725 |
rs220063167 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12073869 | AGTTGGAATTCAGTT[A/C]CCCTAAAACTCGCTT | 75725 |
rs220065058 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12002422 | TAACAGATATTATAC[A/C]CCAGTCGGACCTAAG | 75725 |
rs220066006 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12001239 | CAGACAGTCTGTACA[C/T]CAACCCCTCAAATCC | 75725 |
rs220066073 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11992494 | GAGAGAATCTTACTT[C/T]CCTGTCTTATGTTGA | 75725 |
rs220080992 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010864 | TTGATTCTTTAAAAG[C/T]TGAATTTTAGAGATA | 75725 |
rs220096089 | snp | C/T | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100216 | CCAGCACCTCTGGAG[C/T]GGTCCTGGACGCACC | 75725 |
rs220101471 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12066971 | CTCCTAGGCATAAAC[A/C]CAAAAGATACTTCAC | 75725 |
rs220121789 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11930750 | CACATGAAATGTTAA[A/G]TTTGGAAGGCAGCAT | 75725 |
rs220129997 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12018509 | GTCTCTGCAGAATAA[A/G]GTATTTCCTCTCCCA | 75725 |
rs220135424 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11994852 | ATAAAATATATTGGG[A/G]TAACTCTAACCAAAC | 75725 |
rs220198436 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:11920950 | ATGATGTAGATTGTA[-/C]AGACTTACAGTATAT | 75725 |
rs220238901 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12065735 | GTGGATCTTCATATT[C/G]ACCAGGGCTACATAG | 75725 |
rs220244327 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11995764 | GTATATCAAGTTGCA[A/G]CAGAACTAAGTGCAA | 75725 |
rs220249959 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12024567 | GCTTGTTGGGTCTTT[A/C]GGAGGGCAGTCATGC | 75725 |
rs220261210 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12088961 | TCCTGCCTACAATGG[-/T]TTTTTTTAATTGGAT | 75725 |
rs220263405 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12034094 | AGAAGATAGCATAAG[C/T]TGTACCCTAGAAAAT | 75725 |
rs220280361 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12034563 | GGGGAAGGGAACTAT[C/G]ATTCACTGTTTGATC | 75725 |
rs220297605 | snp | A/C | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010290 | AAATGTAAATGAAGA[A/C]AATACCTAATTAAAA | 75725 |
rs220298497 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11986502 | AGGTATGGGAATCAC[A/T]CCTAAATTTATTAGG | 75725 |
rs220306132 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055687 | TGTCCATGTGTGTTG[C/T]GATAATAAAAATACT | 75725 |
rs220316951 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12017506 | ATGTTAACAGTTGCT[C/T]TTTTCCCTAAATATC | 75725 |
rs220317113 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12086648 | AAAACAGCTGGTTGG[-/A]AAAAACAAGCCAGTA | 75725 |
rs220317863 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12027660 | AGCTGAGGGCCAGTG[A/G]CTGCACTGACCACTC | 75725 |
rs220330966 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12028596 | AATTTTTTTTGTAAA[A/T]AAAAAAAATACAGTT | 75725 |
rs220336222 | in-del | -/CACACACA | | | intron-variant | Phf14 | Mm_Celera | 6:12041577 | ATGCACACACACACG[-/CACACACA]CACACACACACACAC | 75725 |
rs220341039 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11923453 | GTTTCCTCCTCTCTG[A/G]ATGTGTGTATTCTTT | 75725 |
rs220350900 | snp | A/C | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924011 | TTCTCGTCCTCTCAT[A/C]GTGTGCAGAGCACCT | 75725 |
rs220358987 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11938552 | CAGAAGTCACTGCTG[A/T]TTTCTTATTCCCAGG | 75725 |
rs220363998 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11944806 | AAAGAATTAAAGGAC[-/A]TTGCATACAATGTTA | 75725 |
rs220414334 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12098486 | CCTGGCTATGTTTCA[A/G]GATTTTCTCATAGGG | 75725 |
rs220419868 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11917052 | AACTTGCCAGCCAGG[C/G]TGGCAGTTACCCATA | 75725 |
rs220428767 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11928592 | AGACATTTCTCTTTC[C/T]GAGGGATGAAATAGT | 75725 |
rs220428951 | in-del | -/TTTA | | | intron-variant | Phf14 | Mm_Celera | 6:11923290 | TGTGCCAATCGGATT[-/TTTA]TTTTCAACATGCTCT | 75725 |
rs220429617 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12013400 | CCATGTTCTTTTTGG[-/T]TTTTTTTTTTTTTTT | 75725 |
rs220431106 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12003490 | CACACCAATCATCAA[-/T]AAAGACAATGGGCCA | 75725 |
rs220475996 | in-del | -/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12079625 | TTTCTATACTGACAC[-/T]TAGTCTCATTAGTAG | 75725 |
rs220485136 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12014897 | AGGAGCTTGCCTGGG[C/G]CTGGTTACACTGCAC | 75725 |
rs220492799 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12051461 | TTAGAAAAGTGCAGT[A/G]GGGTACCCTAGATGG | 75725 |
rs220494824 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12064941 | TTTGGTTAAATACAG[A/G]AAATAGAACATTAGC | 75725 |
rs220495635 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12082977 | AGCTCACACTTAGAA[A/T]GCACCCTCCCTGGGT | 75725 |
rs220504199 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12097120 | ACCAAGAAAACAGTT[A/C]ATTGGGGCTGGTTTT | 75725 |
rs220513040 | in-del | -/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12078312 | ACATCAGTATTTTTA[-/T]TTTTTTTATATGCAT | 75725 |
rs220518991 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083326 | CACCCACCTGCTCCT[A/G]CCTTTGCACCCTGGC | 75725 |
rs220522059 | snp | C/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12047181 | TTCTTAGATTGTGTA[C/T]TTCATATGAGGCAAG | 75725 |
rs220528382 | in-del | -/TG | | | intron-variant | Phf14 | Mm_Celera | 6:11950743 | TCTAGCTAGACTGTC[-/TG]TGTCTTTTCAGTAAG | 75725 |
rs220528514 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12075694 | TTTTTAAAGAAAATA[A/G]AAACCTTTCCAGTCA | 75725 |
rs220535295 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11937582 | CTTCGGAAGAGCAGT[A/C]AGGTGCTTTTACCCA | 75725 |
rs220553084 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11991157 | CATGTATATTTTCCA[A/G]AGATATTGAAAAATC | 75725 |
rs220556779 | in-del | -/ACAC | | | intron-variant | Phf14 | GRCm38.p3 | 6:12041533 | GCTGCATGCAGACCA[-/ACAC]ACACACACACTCACA | 75725 |
rs220561056 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949220 | TTCACTGTGGTGTTT[C/T]CATTTATGCAGAAAT | 75725 |
rs220606982 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12043224 | GATTCCACATTTTAC[A/G]TGGGATTGGATTTGG | 75725 |
rs220637132 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12033309 | CATAGAGTAATATAT[-/C]CCCTAGGGCCTTTTC | 75725 |
rs220670442 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949939 | AGTTCTTGTTTTATA[G/T]TTTGTATTTTGGACT | 75725 |
rs220682247 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11912360 | GTTTTAGGTTCTCCC[A/T]GTGCTGAAGGCACTT | 75725 |
rs220683859 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043781 | TTTCTAGGTGAGAAG[C/T]GCAGTGTTCTGTAGT | 75725 |
rs220685681 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12053936 | AAATATATTTCCTGT[-/C]ATAAGAGTAAGATCA | 75725 |
rs220695815 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11928022 | TGCATTGTGATTTGC[A/T]ACAGAATCTCGTTTA | 75725 |
rs220697254 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12056632 | TTTTAAAATCTTTAG[-/T]TCTGAAGTACAGAAT | 75725 |
rs220701952 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12094177 | GGCATATCAAGAAAG[C/G]GAAAGTCGTAATGAA | 75725 |
rs220711153 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11995985 | TTCAGTCTCTGGGAG[C/G]CCTCGTGGCCCCAGA | 75725 |
rs220711846 | snp | A/T | | | synonymous-codon, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11933536 | CAAAGAGAAAGCAAC[A/T]GTATCTGATAGTGCA | 75725 |
rs220716544 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036641 | TGACTTGAAGCAACA[C/T]AGAACAAATGTGTGT | 75725 |
rs220717610 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12063144 | AGGGTCAACTGAACA[A/G]TTAAGCAGATAGGTT | 75725 |
rs220724206 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11935041 | GTGTAGCAAACTCTC[A/C]GGGATTCCATGCCAG | 75725 |
rs220737638 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:11916848 | ACTGGGAACCATCCA[-/C]CCCCACCTGATCTAG | 75725 |
rs220741507 | snp | C/T | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100226 | TGGAGTGGTCCTGGA[C/T]GCACCGGCCATGGTA | 75725 |
rs220742449 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905887 | GCTCACGAAGCCAGC[C/T]AAGTAAAAGTCAGCA | 75725 |
rs220782995 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11926341 | TTCTCCTTTCAAGTC[A/C]GGCGGTGCTGAGCAG | 75725 |
rs220790965 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11940218 | TGCAGACCCCTTCAG[A/C]TCCTTGGGTGCTTTC | 75725 |
rs220795857 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11994074 | CTCATATCAGCTGAT[A/G]TATGCTGCATGATTG | 75725 |
rs220797903 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11980013 | CCCCCCCCAATTCCA[G/T]TCTTCTAGATACACA | 75725 |
rs220799675 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | GRCm38.p3 | 6:12039507 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 75725 |
rs220813839 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12096543 | GTACTGACTACCAGG[A/C]AGCTAAGATGAGGGT | 75725 |
rs220826890 | in-del | -/TG | | | intron-variant | Phf14 | Mm_Celera | 6:12086131 | TTCCTAGAAACAAAC[-/TG]TGTTATTGTTAGCTT | 75725 |
rs220840929 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12091699 | AAAGTTTTTTGGCCT[A/G]ATAGTGGTTCCAGAT | 75725 |
rs220850626 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11948347 | TGCTCACCTATGACA[C/T]ACCTCCTCCAACAAA | 75725 |
rs220856657 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12095268 | TTTCTGCTGTCTCAT[A/C]CTGCGGTTGTGGAGG | 75725 |
rs220857577 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12094104 | CATCAAACAGCCTCT[A/G]CTCTGAGCTACACTC | 75725 |
rs220870893 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12044808 | TGCTAAATTTATATT[C/T]TCTTCATGGTTAAGG | 75725 |
rs220876617 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11986578 | CATGTGATGGAAATT[G/T]AGGTCCAACATGTAA | 75725 |
rs220877907 | snp | A/G | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:11989030 | TTTGGTTCTTTCATC[A/G]GCTATCTTGTTGGCA | 75725 |
rs220883168 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908681 | ATGTACTGATTGGGG[-/A]AAAAAAATCACCAAA | 75725 |
rs220885921 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037465 | TGTACAGAACAGTTT[G/T]GTAGTGTTTGACAGG | 75725 |
rs220901508 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11990162 | TATAACGGAATAATA[G/T]TATCTACTTTTCAAC | 75725 |
rs220905456 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11980919 | CAGTATAAGGTGACT[A/T]ATATGTATATTGTTT | 75725 |
rs220913334 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12035294 | CTTTCCCTAATTTTT[-/A]TTAAAATGAACCTAA | 75725 |
rs220920928 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11976278 | TCAGTGAACTGACCT[A/G]TGCAGACTCATCTCT | 75725 |
rs220927380 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094476 | TTGCCTGGCAAGATA[C/T]GAGACCTTGGTGGGA | 75725 |
rs220968647 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11960404 | GATTACATTGAGAAA[C/G]TTGCTGCTGGTGGAG | 75725 |
rs220973604 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11914481 | GAGAGTTTATATAAT[A/G]GAAACCTAAGGGCTT | 75725 |
rs220976993 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11961378 | AATTATCTGCTATCA[C/T]TCTCTAGCTATGCTG | 75725 |
rs220985155 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11988021 | GAGTTGGAGTTTAAA[A/G]CTAACACTGCTAACC | 75725 |
rs220987899 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906528 | CCCTTAAAAGTTCTG[C/T]GAGCCAGGCAATGTG | 75725 |
rs221040930 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11962465 | TTGTTATTATTGCTA[A/G]TATATCAGTTTAATT | 75725 |
rs221041654 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12021196 | ACCACCTATCCGTGC[C/T]TCTCAGTGCCAGATC | 75725 |
rs221048749 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12050480 | ATGCAGGTGCTGAGA[A/C]TTAAACCTGGGGCCT | 75725 |
rs221050112 | snp | G/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12040681 | AGCAAATGACATTAC[G/T]TGACTTATAGCAAAG | 75725 |
rs221051799 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11938788 | CTCATATATTTCTCT[C/G]TTAAGCCATTTTCTA | 75725 |
rs221052772 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021974 | CCTAGCTTGTGTGTG[C/T]GTGCATGTTCTACCT | 75725 |
rs221061259 | in-del | -/TTT | | | intron-variant | Phf14 | Mm_Celera | 6:12075237 | AACTTTTTAAAAAAA[-/TTT]TTTCTTTAAGTAAAT | 75725 |
rs221102870 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12014083 | ACAAAAGTTGGTCTC[C/T]TGATTATCTGTGATC | 75725 |
rs221107500 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947801 | TGAAATCAGGAACTG[-/T]TTTTTTTAAATAAAT | 75725 |
rs221107597 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052397 | AAAGCAATATCAATG[C/T]AAAACACAATTTCCT | 75725 |
rs221117405 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11909855 | ATATAGAAATGCCAT[A/G]ATTCAAAAGAAAGTC | 75725 |
rs221121862 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12046766 | TCTTTATTGTGATCA[-/T]TTTTTTAAGTTACTT | 75725 |
rs221125171 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910258 | CTCACTGCCTCAGTA[A/G]CATCAGCTTTGATCA | 75725 |
rs221149349 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094698 | TTTAGGTTACAAAGT[A/T]TACCATAATTTAAAA | 75725 |
rs221156767 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12074432 | CACAGAGCGATGTCC[C/T]AGGCCTCCATTCACT | 75725 |
rs221166163 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910295 | TTTCTTTAGTAAGAC[A/G]TGGAATGTGAGAATT | 75725 |
rs221172290 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12043832 | TCATCATTGTATAGG[C/G]AATACTGCCTGTTGT | 75725 |
rs221198992 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076232 | TTTAATATTTAAGTG[C/T]TTTTATTTTGAAACA | 75725 |
rs221210456 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11988181 | AATTGAAAAATTTAT[G/T]GTATTTCTTCCTGTC | 75725 |
rs221239966 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12068242 | TTAAGCCAGTGAATT[C/T]CTATTAGGAAAGTGT | 75725 |
rs221240746 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12026878 | TATTGGCTAAACATA[C/T]TGACCTTTAAATCTA | 75725 |
rs221242628 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12069559 | CCTGCAGGCCTAATC[A/G]TCCTTACATGTGCTT | 75725 |
rs221258420 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029458 | GATATTTTCTCTATT[C/T]ACATTTCAAATGCTA | 75725 |
rs221263530 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076980 | AGTCTTTGTCCCAAA[A/T]TAGTGGCACAAGCTA | 75725 |
rs221270295 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11998327 | GACGTGCTAGAGTCA[A/T]GGATATCAGCTATGG | 75725 |
rs221271190 | in-del | -/CTCG | | | intron-variant | Phf14 | Mm_Celera | 6:12004065 | TGAAGACAGCCTGGC[-/CTCG]CTTGCTGCTGAGAGC | 75725 |
rs221275973 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11942112 | AGGTTTATTTGGGAG[G/T]GAATATACAGAGACT | 75725 |
rs221283331 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11962611 | GATAATATTGTTTCA[A/G]AAATACTTTTGCTGT | 75725 |
rs221296000 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12070197 | TGTAGTATGTTGTCA[C/T]AATGTTTCACTTGTT | 75725 |
rs221296377 | snp | A/C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11940117 | CTTCCCAGTGATGGC[A/C/G]GACTAGGCCATCTTC | 75725 |
rs221303768 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11913750 | TTTGAAATACTTTAC[A/G]TGCAAAATTCAATGA | 75725 |
rs221339147 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12070072 | CTATTACCTCCATTC[A/C]CTCATCACAAAACAT | 75725 |
rs221349596 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11930797 | TCATGGAAATAGAAA[G/T]GTTTTTTTCTTTTGC | 75725 |
rs221351908 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11940823 | ATCTTTATTACCAGT[C/T]TGCCCTCGATATTTC | 75725 |
rs221358116 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11931464 | CAAGGGCTTGCCTTT[A/G]AAGTATTTAGTGGAA | 75725 |
rs221365346 | in-del | -/CAT | | | intron-variant | Phf14 | Mm_Celera | 6:12033937 | TGAAAAAGAAAAGAA[-/CAT]CCTGAACAAATGGTA | 75725 |
rs221370881 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11943204 | GGGTGGGTGACTTCT[C/T]CAGTAAAGCACACAC | 75725 |
rs221384367 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12021990 | GTGCATGTTCTACCT[A/G]GCTTGTTGCCCCCAG | 75725 |
rs221385975 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905960 | CTCTGTGACTTCTCC[C/T]GTGACTGGGGCCCCC | 75725 |
rs221389579 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12062315 | TTGCTGTGAGAAGGA[A/G]GTCACAGAAGCGCAC | 75725 |
rs221412472 | snp | C/T | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099107 | ACAAAACAATATCAC[C/T]ATAAGTAACTTAGGA | 75725 |
rs221412743 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11943175 | AGAGGCAAACAGTAG[C/T]AATAATAGGCTGGGG | 75725 |
rs221424367 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11993411 | ATTTCAATGTTTTGT[A/C]GTTTCATGGCATGGC | 75725 |
rs221437963 | snp | C/G | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099477 | CAAAAAACTAGCCAG[C/G]ATACTCCTTTTCTGA | 75725 |
rs221483755 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12072489 | AGGACGATGGTTCTT[C/T]AGAAGGACATTTACG | 75725 |
rs221506770 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12018288 | TTTCCTCATGTTGTG[A/G]TGACCCCAAACCAAA | 75725 |
rs221523560 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024197 | CTGCTCCATATCTCA[C/T]ACCTCCTCCCTACCC | 75725 |
rs221538669 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12019719 | GATTTCTAGGCAAGC[A/G]TGCTCTGTAAAGGGA | 75725 |
rs221542513 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12027544 | ACTTCTAATAATGAA[C/G]TCAATGATTCTTGAA | 75725 |
rs221569775 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12054446 | CAAGAGATTTATTGA[C/G]GGAGGGGGAAACCAG | 75725 |
rs221593123 | snp | A/G | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12047258 | TGAAACACCAAGTAC[A/G]TGGCAGAACTTGACA | 75725 |
rs221605311 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12020386 | GAACTACCAGCTCAT[C/T]GGTGGCCCCACCCAC | 75725 |
rs221610108 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985297 | ATAGACATCATAGCT[G/T]TGTAGAAATTGATTG | 75725 |
rs221634579 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11918136 | AAAAAAAAAGGTAGC[C/T]GAGAGTGGCTAGGTA | 75725 |
rs221643879 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916006 | CATTTGAAACAATCG[C/T]TTTCATGCTCTTTGT | 75725 |
rs221647972 | snp | C/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12048398 | GATATAATCACAGCT[C/T]TGTATGAAAACCTAG | 75725 |
rs221653648 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908269 | AGTTCTTCCTTGGGG[C/T]AGGTTTAATGGGCAC | 75725 |
rs221694763 | snp | A/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908834 | ATATCCATGCCAATT[A/T]CTGAAATAATGGATG | 75725 |
rs221697400 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927884 | ACATGCCTTTAATCC[A/T]AGCAGTGGGGAGGAA | 75725 |
rs221715296 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11920544 | ATGACAGTTACATCA[A/G]GCAATAAAAGATTCT | 75725 |
rs221731134 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11911056 | TAGTGTGTGTAAGAA[G/T]TTTAGTTCCATCCGT | 75725 |
rs221740351 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11962956 | GTCAGTCTTTAGACT[-/A]AGAACACTGGAAAGC | 75725 |
rs221824655 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12078133 | GCTTCCAGACGTATT[C/T]CTGTTACATGTTATA | 75725 |
rs221826061 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12061759 | TTCATTTGAACTCTC[C/T]CCTTAAGAATGCCCA | 75725 |
rs221834953 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11931624 | ATGATTTGTAGAACT[C/T]TTGAGCTGAAAACAA | 75725 |
rs221841410 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12049694 | CATTTGTGCCTCTTT[C/G]GGAACTTGATACAGC | 75725 |
rs221863000 | in-del | -/GTGT | | | intron-variant | Phf14 | Mm_Celera | 6:12053237 | GACAGGAGCCTCGTG[-/GTGT]GTGTGTGTGTGTGTG | 75725 |
rs221873249 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11932174 | TGAACCTTAAATTCC[C/T]AGTTAAATTTACAGG | 75725 |
rs221880853 | snp | C/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925066 | GATAATTTTTGCTAT[C/G]TTTGTCCATTTTCTT | 75725 |
rs221887435 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12086936 | GGAAATGCCATCACA[A/G]AAGAGCCCAGACATG | 75725 |
rs221898784 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12056874 | TTTACATGTTATTCA[A/T]ATGCTGTGCTAAATC | 75725 |
rs221906345 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11975565 | GAGTGGTCTTGGATT[C/T]TGTTAGTAAGATTCT | 75725 |
rs221909775 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12091872 | TGTATTAGTCAGGCC[C/T]ACGGTTTAAATGCAC | 75725 |
rs221916742 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037402 | TTTAATTAATCCCAG[A/T]ATATGTTAAAAGTCC | 75725 |
rs221917055 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12097220 | AGAGAAGGAACTGAG[-/T]TTTGCATCTTGACCT | 75725 |
rs221918197 | snp | A/C | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925519 | ATGGGCTAGGCCCTC[A/C]GTGCTTGATCACTAT | 75725 |
rs221943635 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11938632 | TTGTTCTTCTGCATA[A/T]AACCAGAAAACAGAG | 75725 |
rs221956814 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11939131 | AAGTGATGGCCTACG[C/G]AAACGTTTGGAGTTA | 75725 |
rs221962348 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083562 | GGCTAAAAACCCCCT[C/T]AGCTCCTTCAGTCCC | 75725 |
rs221967730 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12092961 | TATACTTTTCTCAAG[A/G]TACATCATGTGAAAG | 75725 |
rs221974055 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12070646 | TACCTTTAAATTTAG[C/T]CTCAAACAAGTTTTT | 75725 |
rs221982444 | in-del | -/AA | | | intron-variant | Phf14 | Mm_Celera | 6:11917885 | CATATAGGCTCTCAG[-/AA]AAAAAAGAGTTTAAG | 75725 |
rs221983058 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11955062 | TCTGGGGCTGGAGGT[A/T]TAAGCATGTGTGAGC | 75725 |
rs221989377 | in-del | -/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12088349 | GGTCCCATATTCTAA[-/T]TTTTTTTAATTCAAG | 75725 |
rs222008200 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031809 | GTGTTTGAAGGTCAA[C/T]ATGATCTCTAAGCTC | 75725 |
rs222010082 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12049589 | ATTTATTTTGTATGA[-/TT]TTTTTTTTTGCAATG | 75725 |
rs222014034 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11944176 | CAGTTTCTATATAAC[A/T]ATTACCCCCAAATAT | 75725 |
rs222034963 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010586 | ATAAATGAATCACAG[A/G]CACTTAATAAACTCC | 75725 |
rs222058541 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12014949 | AGACCAATGCTTGTT[A/C]TCAGCTTAGTTTCTT | 75725 |
rs222074717 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12097262 | GGAGAAGACTCTCCT[C/T]CCACACTGGGTGGAG | 75725 |
rs222081314 | in-del | -/AAAA | | | intron-variant | Phf14 | Mm_Celera | 6:11920670 | AATGCCTTCTTTATC[-/AAAA]CTTCCAGGAGTAGCT | 75725 |
rs222114662 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11991238 | ACTTTCCTATCATTC[C/T]GTACATCTCCAATAT | 75725 |
rs222153005 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12098247 | CTTTTCCTCTTTTTT[C/T]CCAACCATCTCATGT | 75725 |
rs222153016 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12004439 | TCATAAATTTTGGGA[-/TT]TTTTTTAAAAGATGT | 75725 |
rs222164959 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12062363 | ATGGTATATAAACAC[-/T]ATGACATGTACCATT | 75725 |
rs222165618 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11935522 | GTTTTAATAACCTCT[A/G]CTTGATACTATAGCT | 75725 |
rs222187367 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12033393 | TTCTTCCCTCTCCTC[A/G]GCTAAAGTCTGCTGC | 75725 |
rs222212174 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11977570 | TTATACTGGTTTCTA[A/G]TTGTTATAAACACTT | 75725 |
rs222212926 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11992173 | TTTAGCCTCAACAGT[A/G]CAACCCTGTTGTATC | 75725 |
rs222227115 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11973356 | ggacactgtccctgt[A/G]ccctctagttagtct | 75725 |
rs222230766 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040593 | TACTAGTAATTTATT[A/G]ATTTTATTGCACTAG | 75725 |
rs222242360 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12034037 | AACAAAGCAAAACAA[C/T]GGATGTAAGAACTTA | 75725 |
rs222244237 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032957 | TCCTTCAGTCCTTTC[-/T]TCTAACTCCTTCATT | 75725 |
rs222271030 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11978557 | CTTATTCCATCCCTC[C/T]TCCCCCTGCTTCTAT | 75725 |
rs222279310 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095393 | ATTACCCACGTCTGA[C/T]TATCACCCAATCCAG | 75725 |
rs222304406 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12086301 | TAAATATCAGAAGTA[A/G]GCAGGGATGTTACAC | 75725 |
rs222325841 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12037131 | ATTTTAATGAGCTAG[A/G]GGTAAAGGGAATTAA | 75725 |
rs222343323 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11973917 | GAGGTACCATGTGGC[C/G]CTGAGAGGAAGGTAT | 75725 |
rs222346457 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12063381 | TAATGACCTTTTCTG[C/T]TCTTACAGTAGTATA | 75725 |
rs222360502 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12015098 | GCTTACAGGTGAGAT[G/T]AGGGTTGTAGTTTAT | 75725 |
rs222376255 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11952745 | TTGGGGGTCCAGATT[A/T]ATTGAGGCTGCTGGT | 75725 |
rs222401802 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11954369 | GGCTGACACAGTTTT[C/T]AGGGAGAGCTGCAGC | 75725 |
rs222427476 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031322 | CTCTCTCTCCTCCCC[C/T]ATGTGTCTGTCTGTC | 75725 |
rs222441296 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11975718 | CAGTGGTCAGAGTAC[C/T]CTCTGCAGGCAAGCT | 75725 |
rs222463392 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12001392 | GAGTTACTCCAAGAT[A/C]TATTATTTGAGTCTA | 75725 |
rs222469352 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11935605 | CTTTTTCTTCTTCTA[A/G]TGAAAACATTTACAT | 75725 |
rs222496022 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11955116 | TAGCAAGAGCAGTAA[A/G]AGCAGTGTGTGCTTA | 75725 |
rs222506414 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11926561 | CAGGGGCAGCCAGGC[C/T]CTCTGCATCCAGCGC | 75725 |
rs222506904 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11957046 | TTTCACCACATCTTC[C/T]ACAGCAACTGCTGTC | 75725 |
rs222556177 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11971927 | AGAGGTTCTTTTATT[C/G]TTGAGAATAGTTTTA | 75725 |
rs222558826 | in-del | -/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12069430 | TAGCCCTGATCATCC[-/T]TTTTTTTTTCTTTTT | 75725 |
rs222561594 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12065829 | AAAGAGAAAGAGAGA[A/G]ATTATTCCTAATTAT | 75725 |
rs222565259 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12002342 | TACATCCTGATAGTA[C/G]TAGTCTTCAATACCC | 75725 |
rs222571836 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12062474 | TGTCAAGGCTAGGAT[-/G]TGCTGGCTATTTGAG | 75725 |
rs222578593 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12051957 | TTGGCTATCAGATCA[-/T]TTTTTAGTTTTTGTG | 75725 |
rs222595729 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12017636 | CTACAAATGACATAA[A/G]CACTTCGTTAATAAT | 75725 |
rs222604459 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11961339 | TGAAAAGTAATGCTC[A/T]CTGCAGTCATGCTTC | 75725 |
rs222607263 | in-del | -/AAATGAAAAAGAAAAG | | | intron-variant | Phf14 | Mm_Celera | 6:12033920 | CACACAGAAAAGAAC[-/AAATGAAAAAGAAAAG]AACCTGAACAAATGG | 75725 |
rs222608815 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12018457 | CCCTCTGCTGAGGGT[A/G]GGCAACTCCCATTAT | 75725 |
rs222620577 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12041409 | CCTAGTAATGTAAAA[A/C]ACAGACGAAAGGATC | 75725 |
rs222640867 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12006267 | TGTAAACACCATTAT[C/T]TTATTTCCTTTAAAC | 75725 |
rs222644384 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12058617 | TGGTGGTCCCTGTGC[G/T]TGGACCCTTTTCCTT | 75725 |
rs222656068 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094835 | CCAAGAAACAAACCA[C/T]ATGGGAAGTATTTAA | 75725 |
rs222657835 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11917913 | AAGCTCCTGAAACAT[A/C]GAGGAAATGGATGGC | 75725 |
rs222675905 | snp | C/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009578 | AGGGCAGGGAGATAG[C/G]TAAGTCAGCAGGTTA | 75725 |
rs222731324 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061828 | GAGGAGAGTTGACAC[A/G]TGACTTGGTGTCCTT | 75725 |
rs222732120 | in-del | -/TA | | | intron-variant | Phf14 | GRCm38.p3 | 6:12023834 | GTTGTTGTTTTTATT[-/TA]TTTTTTATTTTTTGT | 75725 |
rs222741706 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11971726 | tttgttgaaaatgct[G/T]tcttttttccactgg | 75725 |
rs222746774 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060651 | TAGCAGCTGCCACTC[A/G]GCCATATCTGTGTGG | 75725 |
rs222749018 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11929722 | AGAAAAACAATTTTG[C/G]TGAGGGAAACATTAA | 75725 |
rs222752353 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12072086 | AAGATTAATGGCCTT[A/C]CTTTGGGGAAAATAG | 75725 |
rs222753151 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11930653 | CTTATGCATAAGATA[A/G]ATTTTCAGAATATAT | 75725 |
rs222753282 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11921947 | CAAAGCAAGTGATTG[A/G]TGAAAGGGCTCATTT | 75725 |
rs222768456 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11932467 | GCCCTAGGTGGGGAT[A/G]GAAACAGCTTGCTAA | 75725 |
rs222773053 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12097306 | AGCCTTCAAAGCCCA[C/T]CCCCTACAACAAGGC | 75725 |
rs222789510 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12013246 | GTTAGAGACCAGTCT[A/G]AGTTACTAGTCCCAT | 75725 |
rs222809834 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12098342 | CCTGTTGGTAAACTT[C/G]TCCCCAGCAGGCTTG | 75725 |
rs222819013 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11923337 | TGTACTTTTAAAAAA[C/T]ATCTCCCTTCACTCT | 75725 |
rs222834447 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12063804 | AGATTTTAAGTTTGC[A/G]GCTATAAATTTCAGT | 75725 |
rs222845016 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072445 | GAGTCCTATCTGTAC[A/G]TCCTGTCTGTGCGTC | 75725 |
rs222848664 | in-del | -/TA | | | intron-variant | Phf14 | Mm_Celera | 6:12064332 | TTGCATATACGTGTG[-/TA]TGTGTGTGTATCTGT | 75725 |
rs222863059 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12015813 | TTACAGACCATCTTG[A/T]CAAAAGTCTGAGTTA | 75725 |
rs222863292 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12058199 | AATTCTCCTGTGCCT[C/T]CCAAGTGTCGAGCTT | 75725 |
rs222863603 | snp | A/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925369 | AAAGGAAGTCATGAC[A/T]GGAACTCAAGCAGGT | 75725 |
rs222882984 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12064752 | TTTAAAGCCAAAATT[A/T]TAACATGCAGCAATA | 75725 |
rs222886970 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11951392 | AATATGGCACAGTTG[A/G]TATAGGTGCTTGCTG | 75725 |
rs222895744 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927473 | AAGTTTCAGTTAAGG[C/T]AACCCGAGAAACAGA | 75725 |
rs222913746 | snp | G/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925241 | GCAAATATCAACGTC[G/T]GAGTGGTGTCTTAGT | 75725 |
rs222922052 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12005305 | GTGTATTAGTTGTAA[A/T]TGAACTATTTATATT | 75725 |
rs222928010 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11978856 | TCCTTTCTCTAGCTC[C/T]TCCATTGGGGACCCT | 75725 |
rs222928501 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11920693 | CAGGAGTAGCTGCAC[-/A]ATGTGACATACAGGC | 75725 |
rs222947767 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12090860 | ATGTTGGTTTTCAGG[A/G]TCTTTAGACACATTT | 75725 |
rs222966037 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11937355 | TGCACATTTTGTAGA[A/G]AAAATTTGCTGTAAG | 75725 |
rs222966506 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927542 | ACCTGAACATTAAGA[C/T]CTTTTTGTATTTCGC | 75725 |
rs223009818 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12093402 | TAGTTGTATGTGTTT[C/G]ATGATCTTCCTTCTA | 75725 |
rs223013720 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12069934 | CTACTGTGTCCATGC[C/G]GTGTAGATCACCCAT | 75725 |
rs223043447 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11958287 | TTTCCAAGACTTTTA[A/T]CATGAACAGGTGTTG | 75725 |
rs223044748 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11979642 | AAGTCAGGTTGTCCC[C/G]TGTCTCAGGTCCTTT | 75725 |
rs223045355 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095483 | ACTACTAACGCGTGT[C/T]TAAGAAAACATACAT | 75725 |
rs223053031 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12062270 | ATGGGGTATGGGTTA[C/G]CTCAGGGTTTCCAGC | 75725 |
rs223082421 | in-del | -/TA | | | intron-variant | Phf14 | Mm_Celera | 6:11988151 | ATATGCTAATTTTTT[-/TA]AAAAAATGTTTTCCA | 75725 |
rs223089474 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12035629 | ATTATATAGTTTCTG[A/G]GATATTAAATTGTAA | 75725 |
rs223091498 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985429 | CTATGGCTGAAATAT[A/T]TGAGACTGTATCTTC | 75725 |
rs223092662 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:11932338 | ATCCTTATCTCCCTC[-/TT]TTTTTTTCCACTTCC | 75725 |
rs223106055 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11958937 | CCTCTATTGTTGTGA[A/G]TTACTATTTCTACAT | 75725 |
rs223125268 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12046225 | GTGACTCCAAACATT[A/C]TGATCAACGTAGAAG | 75725 |
rs223125360 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12037157 | ATTAACAGTAGGATT[A/G]AGGCACATATTTGGG | 75725 |
rs223129661 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12086387 | ACAAAACTTTAATAA[C/G]ACCCTATATGTTAGC | 75725 |
rs223131959 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12096513 | CTGCATCTTCATCAG[A/G]AAGCTTCTAGCAGAG | 75725 |
rs223145080 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11946461 | GGAATTACAGGCATG[A/G]GCTATTTTGCTGCCA | 75725 |
rs223154472 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11955337 | AAAGGACAAATAAAG[C/T]AGAATGCTTACTCTC | 75725 |
rs223165405 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031903 | TGTTCTCTTGGTTAA[-/T]TTTTTTTTTCTTTCA | 75725 |
rs223171005 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11960523 | TTTGTACAACAAAAA[A/T]GATAAAAACTTTAGA | 75725 |
rs223172547 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11933366 | AATGAAGATATTCAA[A/G]TAAAAGAAGAACAGC | 75725 |
rs223182163 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11963390 | TTTACTTTTTATGTG[-/T]TTTTTTTTTTTAATT | 75725 |
rs223208750 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906717 | TAAAGAGCATAACTA[G/T]CGGACAGAAATGCCT | 75725 |
rs223237523 | snp | C/T | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099067 | TATTTTTGCCTCTTC[C/T]TGTCTTAGGGTTTCT | 75725 |
rs223240754 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925563 | TTACAGCTGGATCTC[C/T]TGGAGGCATTTCCTC | 75725 |
rs223277857 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12049279 | CCATCTTTTATCCTT[C/G]TTCAACTTCCTTTTT | 75725 |
rs223280034 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Ndufa4, Phf14 | Mm_Celera | 6:11907967 | TGCGGTTTAAGACTG[C/T]AGCTGCTTCCTGACT | 75725 |
rs223289657 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12090982 | TCTGTATCACTCCAT[C/T]GTCAGACAAACTGGA | 75725 |
rs223301776 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094058 | GTTATAGTCTTCTGC[A/T]CAAATATCAATAATG | 75725 |
rs223338604 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043062 | CTAATCCATTTCTCA[A/T]GCTGGGAAGAGATAC | 75725 |
rs223348153 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12065922 | TGTATCTAGTACTTG[A/T]ACTTACCAACATTTC | 75725 |
rs223374913 | in-del | -/GGGGTTTTTTTG | | | intron-variant | Phf14 | Mm_Celera | 6:12083161 | TTGGTGATAATGGTT[-/GGGGTTTTTTTG]GTTTTGTTTTTGTTT | 75725 |
rs223388565 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11979810 | TTACCTGTCTAAGTT[C/T]TAAGTAGTCTTAAGT | 75725 |
rs223401917 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959099 | GGAAACAAGAAGAGC[C/T]GGAGTTGTCCTCCTT | 75725 |
rs223421302 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11998880 | CAGAGACGTTTCTGG[A/G]ATGCGAACAAATGTC | 75725 |
rs223434683 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11909759 | CAGCGAGGCTGCTAG[C/T]AACAGAATTTCATGA | 75725 |
rs223444475 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12084515 | TTATGAACTGTGTCT[C/T]TATGTGGAGAAGTGT | 75725 |
rs223451276 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12048728 | GTATGCACCTCCAAT[A/G]AGAATATCACAGGTA | 75725 |
rs223454985 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060172 | ACTTCCGTGGGTGCC[A/G]CAGACTGAGGCCAGC | 75725 |
rs223493660 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11991332 | CAAGAAGTGTTAACT[A/G]TGTGAAAATGCTGTT | 75725 |
rs223497395 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11931384 | GAACCTTTCCTTCTT[A/G]TCTGCTGCTTAGCTT | 75725 |
rs223510857 | in-del | -/GTGTGTGTGT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021896 | GCAGATGCACAGACG[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 75725 |
rs223534507 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927230 | CCATATCAGCCCCCT[A/T]GGCATACTTAGGGGA | 75725 |
rs223563999 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12058326 | CAGTCTCAGAACCCA[G/T]TTGTTGAAAAAATTG | 75725 |
rs223582671 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927577 | ATTGATGAACATTTA[C/G]ATAAAGTATAAGATA | 75725 |
rs223640964 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12016868 | ATTTTAACAAATCTG[A/T]AGGACTTTTACAGCT | 75725 |
rs223641017 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12005524 | CCCATCTCCCCTTCC[A/G]CCTGTTTCTATGAGA | 75725 |
rs223641988 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12021077 | GACTCCACTTTCACC[A/G]GTAGCCTATCCTGTG | 75725 |
rs223653980 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053448 | ATAGCACTATCTTCA[A/G]GCCTTTCTACATAGG | 75725 |
rs223665677 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11920165 | CAAGTCACAGAAATG[C/T]TTGACAGAATATGAT | 75725 |
rs223680508 | in-del | -/CA | | | intron-variant | Phf14 | Mm_Celera | 6:11951384 | GAATCAGCAATATGG[-/CA]CAGTTGGTATAGGTG | 75725 |
rs223708168 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12091560 | AGATGCTTCTCAAAT[A/G]GGGATTGAAATGTTG | 75725 |
rs223717480 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11920645 | GCCTGCATCTCCAGT[G/T]ATAGGATGAAATGCC | 75725 |
rs223725901 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12041119 | TCCTAAATGAAGTAC[A/C]ACATTAACTTTTGCC | 75725 |
rs223728614 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11980665 | GAATAAATGCCAGAT[A/G]TTTCTTAATAACTAT | 75725 |
rs223733220 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12006388 | ATTTGAGAATTTAAG[A/T]CTTTGCCTTCTACCG | 75725 |
rs223765209 | in-del | -/GT | | | intron-variant | Phf14 | Mm_Celera | 6:11959745 | AGGAATAGAAATAAC[-/GT]AGTACAGATAATTTT | 75725 |
rs223770483 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12056941 | CTCTTGATGCTAAAA[C/G]TTACACTTTTGTATA | 75725 |
rs223775830 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925612 | TACTCCAGCTTGTGT[C/T]AAGTTGATACACAAA | 75725 |
rs223787808 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11910183 | GCAGTAGGGACTTTG[C/T]GTGTAGTAGATTATA | 75725 |
rs223805481 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079605 | TAGCCTCTTTACCAA[A/G]GGATTTTCTATACTG | 75725 |
rs223806089 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11959718 | ACACACTTAACCATG[C/G]TTCTGAGGTGAAGGA | 75725 |
rs223837975 | in-del | -/TATG | | | intron-variant | Phf14 | Mm_Celera | 6:11962344 | ATTGTATGTATGTAT[-/TATG]TATGTATGTATGTAT | 75725 |
rs223843670 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12045167 | TAGCCAAAATTTACT[A/G]GTTACTAAGTTTTGA | 75725 |
rs223864502 | snp | A/C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11918332 | TTTATTATGGTAATC[A/C/G]CTTCATAGTGTTTAT | 75725 |
rs223897185 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11994977 | TCACAATTTTTCATA[A/T]TTTTGTTTTCCTGGC | 75725 |
rs223901584 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032055 | TATCCATTCTGTTAG[G/T]CAGCGTCTTTTGGGA | 75725 |
rs223910145 | in-del | -/CCATAGTGATACATTT | | | intron-variant | Phf14 | Mm_Celera | 6:12097308 | CTTCAAAGCCCACCC[-/CCATAGTGATACATTT]CCTACAACAAGGCCA | 75725 |
rs223911897 | in-del | -/TAATT | | | intron-variant | Phf14 | Mm_Celera | 6:11996467 | TAAATATCATAAAAA[-/TAATT]TAATATACTACAAAC | 75725 |
rs223918597 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11954564 | TCCTCTATGGCTTTG[A/T]TTACAGTGCCCTGCT | 75725 |
rs223928430 | in-del | -/AAGATAT | | | intron-variant | Phf14 | Mm_Celera | 6:12087373 | ACACAGTGGAAACAC[-/AAGATAT]GTAATTTTTGCCTCA | 75725 |
rs223934902 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12057461 | AACTAGGCTACTTGA[A/C]TCAAGCTGCGTTCCC | 75725 |
rs223961794 | in-del | -/TTTATATATG | | | intron-variant | Phf14 | Mm_Celera | 6:12076142 | ATCTTTCCTATACAT[-/TTTATATATG]TTTATATATGTTATT | 75725 |
rs223963657 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024666 | TAGGTATATGCCCAA[G/T]AGTGGTATAGCTGGG | 75725 |
rs223963692 | in-del | -/GG | | | intron-variant | Phf14 | Mm_Celera | 6:11962376 | TATGTGTGTGTGTGT[-/GG]ATATGTGGATATATG | 75725 |
rs223978156 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12003936 | CATATTTCACCCCAC[G/T]GGTCTCAGAAGTAGT | 75725 |
rs223989530 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11995794 | AACTCTCCTGCTGAG[A/G]CCTGACAAGGCAGCC | 75725 |
rs224011176 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12017505 | AATGTTAACAGTTGC[-/TT]TTTTCCCTAAATATC | 75725 |
rs224021899 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12035848 | TAAAGGCATGTGCCA[C/T]CACTGCCTGGCAAAT | 75725 |
rs224022324 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12084608 | GAAGTGGGTGTGAGG[A/G]ATCAAACCCTTTATC | 75725 |
rs224034478 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052193 | TCTTTTCCCTCTTCC[-/T]CCTCCTCTCTTCCTC | 75725 |
rs224051779 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11918776 | TATGAGAAACTGTCT[C/T]CAAAGGGGGCTGGGG | 75725 |
rs224062208 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029851 | GTTATGTAGCTCAAC[C/T]ATCATCCATTGACTT | 75725 |
rs224099852 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12060205 | GAAACCACGCCTAGC[A/C]GTGCAACTTCAGAGA | 75725 |
rs224101011 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12054054 | TTAGTTCTATATCCT[C/G]TTACGTGCACTTTTC | 75725 |
rs224105792 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11913446 | TAAATTGAAGACAGA[A/T]TCATATTTTTATTCA | 75725 |
rs224116990 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921460 | AATTGGAGCTGAAAT[A/T]TTGTTTAGAGTATAA | 75725 |
rs224119491 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12030126 | CTATGTGGTAAGGTG[A/C]AGGTTATGTGCCTTT | 75725 |
rs224121348 | in-del | -/TTAC | | | intron-variant | Phf14 | Mm_Celera | 6:12051271 | ATTTTAATATAGATA[-/TTAC]TTCCTAAAGTACTCT | 75725 |
rs224121424 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054571 | AGGGTGGCCTGGGAT[G/T]GAGGGACTATGTGGT | 75725 |
rs224122171 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12078373 | GCCTGGTGTGTGTGG[A/G]TGTGCATGCATGCAC | 75725 |
rs224170856 | in-del | -/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12058704 | CAAATGCTCTTTGTC[-/T]TTTTTTTTTCCTATT | 75725 |
rs224203842 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030150 | TGCCTTTGGCTACTC[G/T]GCTTGGCTAGCATTA | 75725 |
rs224214466 | in-del | -/TG | | | intron-variant | Phf14 | Mm_Celera | 6:11989395 | TAGTTTAAAATATTC[-/TG]TGATAAAAGACATTT | 75725 |
rs224218196 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11951981 | ATGGCAGAAAATATG[A/G]TGACATGGTAGGTCA | 75725 |
rs224220448 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11921984 | TGCTCCCAGACCATA[A/G]TATATCATTGCAAGA | 75725 |
rs224229235 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12078852 | CCTCTTCTGTATTAA[A/G]TAGACACAGAAATGG | 75725 |
rs224263045 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924852 | TTTTTTTCACTAGCA[C/T]CTTAACTTCACCTTC | 75725 |
rs224291841 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12063483 | ATAAATATTTATGCT[G/T]TCTCTGTTTTCAGGA | 75725 |
rs224321849 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917583 | CCAACGTCTACAAGT[C/T]CCCAGAGTTTTACCC | 75725 |
rs224325829 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12005675 | TCTGCTACATATATG[C/G]CTGGAGCCATGGGTC | 75725 |
rs224334759 | in-del | -/CCTTGTTTTTA | | | intron-variant | Phf14 | Mm_Celera | 6:12043129 | TCATGTTCCGGGTTT[-/CCTTGTTTTTA]TTTTGTTTTGTTTTC | 75725 |
rs224338266 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057745 | CCACAAGCTTACACC[A/G]CTTGTTAAAGACAGA | 75725 |
rs224341194 | in-del | -/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12086233 | CAAACAGGAATAGCA[-/T]TTTTTTTTTCTTAAC | 75725 |
rs224363401 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083460 | GCCATGGGTCCCTCC[A/G]TGTGTACTCTTTGGT | 75725 |
rs224374050 | in-del | -/CACACG | | | intron-variant | Phf14 | Mm_Celera | 6:12041571 | GCGCGCATGCACACA[-/CACACG]CACACACACACACAC | 75725 |
rs224381234 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997206 | CACGGTATTTATTCT[C/T]CATTTATTGGTCTCA | 75725 |
rs224391601 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997814 | GGTCTGAGCTCCTTC[C/T]CCTTTGATGCTATTC | 75725 |
rs224391822 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12034738 | ATCATTGAGGAATTT[C/G]CTGCAGTGTCTTGGC | 75725 |
rs224412775 | snp | A/C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083881 | AGCACCCATACTTTG[A/C/G]TCTTTCTTCTTCTTG | 75725 |
rs224430310 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11959862 | TAAGAGTTTTTCAAG[A/G]ATATATTACTACTTC | 75725 |
rs224431806 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12036886 | ATCCATTATTTGTCT[A/G]TCAGGAGTTTAACTT | 75725 |
rs224435050 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12035437 | TTTAATAATTACTGT[A/G]TAATTTTTAGATGTC | 75725 |
rs224436758 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949439 | AAATGTTATTTTTTT[C/T]CATAGCTGAATAGTA | 75725 |
rs224446333 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12076902 | AGGTTTTATTAATTA[A/G]CATCAAGTATTTGAG | 75725 |
rs224481023 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030949 | CTATTCCAGGTTTTT[G/T]GACTAAGGTGTTTAA | 75725 |
rs224485275 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950049 | TACCAGGAATATTTA[C/T]TTTGATGTAACCCCA | 75725 |
rs224487010 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11950491 | CTTACTCAAAGCATC[A/G]CAGACTCTTACCTAG | 75725 |
rs224506072 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029391 | ATTATGTGACAATGT[C/T]TCCCCCATTAATTGG | 75725 |
rs224538773 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12012742 | ATTTTGTGTAATAAA[C/G]TATTTATAATCACTG | 75725 |
rs224543516 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11952466 | TACTTTTATTATGTA[-/T]TTTTTAAATGAATTT | 75725 |
rs224547214 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031466 | TTTTGTTCTTAATTT[C/T]TGTGTTGGCCTGTTT | 75725 |
rs224558854 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12054622 | AGGAGTTGTGGGGTA[-/TT]TTTTTTTTTTAACTT | 75725 |
rs224561734 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11950176 | AGCATTTAATTTTGG[A/G]GTTATAGTTCCAGAC | 75725 |
rs224599708 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032034 | AAAGAATGAATCCTG[-/T]TTTTGTATCCATTCT | 75725 |
rs224615911 | in-del | -/AAA | | | intron-variant | Phf14 | Mm_Celera | 6:12002209 | CATTTCATACTTATC[-/AAA]AAAAAAAAAAATCCA | 75725 |
rs224644701 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083030 | AAGGCTGAGAAAGCA[-/G]GTTCAGCTGCACGGG | 75725 |
rs224679406 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12084218 | CATGTTCTGGGTTAT[A/G]CATACAGTGGTGCCT | 75725 |
rs224703899 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12057951 | TAAGTAAATCCTGAC[-/A]AAAACAGAAAAAATT | 75725 |
rs224708836 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030006 | TAATACTCCATTGTG[C/T]AAATGTACATTATCT | 75725 |
rs224732046 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11958125 | TATATTGAATAGGTA[A/G]GGAGAGAGAGAGTGG | 75725 |
rs224744859 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12002699 | TTTCTGTCTTTATTA[A/T]AATGAAGTGCTTTTA | 75725 |
rs224749242 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12014166 | GTAATGAATTTCGGT[A/C]CATTAAATTCAGTAA | 75725 |
rs224754282 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11960702 | TTTTTCTTATATAAG[G/T]GATGCAAATCTGGTA | 75725 |
rs224757460 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12033150 | TATATGGGATGGATC[C/T]CCATGTCAGGCAATC | 75725 |
rs224761455 | in-del | -/AA | | | intron-variant | Phf14 | Mm_Celera | 6:12057573 | AGGGGAAACATGGTT[-/AA]TTTTTTTCTTTTTAG | 75725 |
rs224766525 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12003230 | TTCTTCTCTCAGCTT[A/G]TCTTAGATGTGTGTT | 75725 |
rs224767485 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950951 | CAGCTATTTCCAGGT[C/T]GGTCAGTTTCTTAAG | 75725 |
rs224767572 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11961409 | GGTTTTTTAGTTAGG[C/T]GTCTTGAGGATTTTT | 75725 |
rs224770118 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060745 | TGCTGCAGTTTTTCA[C/T]TACGGTATGTTTCCT | 75725 |
rs224785185 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949022 | GTATTTTTTGAGAGC[C/T]GGCTACTATTTGACA | 75725 |
rs224802989 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11948114 | CTTTATTCCTGTGAA[C/G]AGACACCATGATAAA | 75725 |
rs224829456 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11952102 | ACCCGTGTTCTAGAT[A/T]ACAGAGGAGGACAGC | 75725 |
rs224876636 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11962798 | GAAGAGGTATGTTTA[-/T]TTCCCTCATTAACGA | 75725 |
rs224961225 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12002171 | CTTCAAAGTAAAACT[A/C]ATCAAAAGATTTGGG | 75725 |
rs224970899 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12056422 | TATTGATGCACAAAA[A/G]TTGCCGGGTGTATAA | 75725 |
rs224972704 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12004523 | GAATCCTTCTTTCTT[A/G]TAGAGAACACTGCTT | 75725 |
rs224981318 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12091125 | ATGTTTGATCACTTT[C/G]TGCTTTTTCATATCT | 75725 |
rs225001617 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11928423 | TGGTGCATAGGTGAG[-/A]GTTTAAAATGAGAAG | 75725 |
rs225002815 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12030786 | ATTTGAGGAGTATTG[A/G]CACTATTTCTTTCTC | 75725 |
rs225044082 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12061155 | TCTTAATAAGAATAG[C/T]TTTTAATGCAGCAAA | 75725 |
rs225054350 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11928683 | TCCAGAAGGGATGTT[G/T]AAGATGTTGAAGGGA | 75725 |
rs225079535 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008887 | ATTAAGACAGAGGAG[C/T]ATAAACCATCTGTAA | 75725 |
rs225085377 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055783 | CCTCAGCTCTGGTAG[A/T]GGAGTCGCATGGTAG | 75725 |
rs225088115 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011759 | AGAATTTCTTCATTA[C/T]TGGCTTTTTATAAAC | 75725 |
rs225107874 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12061508 | AAAAGTGAAGCCTCT[A/C]TTGAAACTCTTTACT | 75725 |
rs225114019 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11921261 | CTAGAGAGAGAATAG[A/C]TTTGTTTACTACTTC | 75725 |
rs225129599 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12042389 | ATTTTCAAACTTTAA[A/G]CACACACACATACAC | 75725 |
rs225130646 | snp | A/C | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924050 | GCCATTAGGGATGGA[A/C]CTTCTAGTTGAGCAC | 75725 |
rs225131312 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12023721 | TGACTTTTGCTGGAT[C/G]CTGGAGATTTGAACA | 75725 |
rs225143231 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061954 | GAACTAATTGTCACA[C/G]TCTGGTCAATTCCCT | 75725 |
rs225143662 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11998577 | TACGTTGGAAACTTA[C/T]AGTTTGTATTTTGAT | 75725 |
rs225165527 | in-del | -/TCTCGC | | | intron-variant | Phf14 | Mm_Celera | 6:11950518 | CTAGAAAAATCATGG[-/TCTCGC]TATATTGAAGTATTT | 75725 |
rs225177195 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12001362 | TTTGTCACAAGTCTT[G/T]TACTTGTTTGTTTAG | 75725 |
rs225196463 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12046438 | ATTTAAAATTTTAAT[A/T]TATTTTTGGATCAGT | 75725 |
rs225201815 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11960819 | AATTAAAACCAACAA[-/T]TTTTTTTTCAGTATG | 75725 |
rs225219106 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12016925 | CCTGTTTCCTGTGGC[A/G]CAGGGAGTGCCCTGT | 75725 |
rs225221001 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11931515 | CCATTATTATAAAAA[-/T]TGTAGAAATTATTGC | 75725 |
rs225253509 | snp | A/C | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925378 | CATGACAGGAACTCA[A/C]GCAGGTCAGGAACTT | 75725 |
rs225258259 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12088017 | TAGTATGAGGGGATG[A/G]AAACATGTTCACTCC | 75725 |
rs225259827 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12057097 | TCTTCTAGTTGGATG[C/T]AAGACTAAACCTCCT | 75725 |
rs225273938 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12052837 | TACTTTAAAGACATT[A/G]TTTCCTTCTAATTTA | 75725 |
rs225282559 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12038400 | GTTTGCAGCTCTTGC[C/T]ATTGCTTCTCGTGTG | 75725 |
rs225302699 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032689 | CCCTCCTTCTAAGAC[G/T]GTGTTCCTTCCACCC | 75725 |
rs225320169 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12092410 | GCACCATAAAAACTA[A/G]CCAGTGGGAATGAAG | 75725 |
rs225323264 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11942214 | ACAGTGGGAATGTAT[G/T]TGGCAGTTAGTTAGT | 75725 |
rs225327273 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950649 | ATGCCTATTTGTATC[C/T]TGTCTTTCAGCAGCA | 75725 |
rs225340403 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12045247 | TAATCTTCTATACTC[-/T]TATGTTTTTAAGAAA | 75725 |
rs225345225 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12060139 | CTGAACCGAAGCAGG[A/C]AGGTTCCTGTGAGTC | 75725 |
rs225367550 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12093633 | TTCTCGCTGTACCTC[A/C]TGTACTCACTGCTTT | 75725 |
rs225367606 | snp | A/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925684 | GGAGACTCAGCTTCG[A/T]GAGGAACCTGTACTC | 75725 |
rs225367675 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11917947 | CAGTGATTGAAGGGT[C/G]GGTAGAATGGGAGAT | 75725 |
rs225379235 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11957441 | TCTTATATCACGAGG[C/T]ATTGGTGTTCTGTTC | 75725 |
rs225385030 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11929465 | TTAACCTGATCAAAT[A/G]ATATTCATTAGCATT | 75725 |
rs225397419 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11943316 | TCTCCACCTCAGGAG[A/G]TGGAGACAGAATGTT | 75725 |
rs225403676 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11912762 | ATATCCCTTTGTCTA[C/T]GGTCACCATTTATGT | 75725 |
rs225415264 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11956053 | CCTCTCCGGCTCCCC[-/A]ACCCACCCACTCCAG | 75725 |
rs225415694 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009477 | TTATTCATTTACTTA[A/G]TTAATTTGCAATCTT | 75725 |
rs225425118 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11999670 | CTGCTAGTTCAGCAA[A/G]TGGGTCATTCAGTGG | 75725 |
rs225454693 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12078682 | GTTTGTTTGCCATGA[C/G]TTAAAGGATATGAAT | 75725 |
rs225465445 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949742 | TACTTTTTAAAAATT[G/T]CTATTTTAACTGGAG | 75725 |
rs225470801 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12069376 | TCCGTCTTTAGAAAA[G/T]AAGCATTTGTTTGTT | 75725 |
rs225483389 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12028465 | GTCATTACATTTTAA[A/T]TATGTTTACAAGTCT | 75725 |
rs225495586 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12021038 | ACTGGGATCTCCAGA[C/G]TATTGCCTGGCTTGC | 75725 |
rs225526282 | in-del | -/TTCTGACA | | | intron-variant | Phf14 | Mm_Celera | 6:11946116 | ACCATGGATATCAAT[-/TTCTGACA]TTCTGATGCTAGGAT | 75725 |
rs225549310 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055823 | TAGAGGCAGAGACTC[A/T]CTGGAAGGGAAATCT | 75725 |
rs225565467 | snp | A/G | | | intron-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100356 | TTTCAGTCATGTTCC[A/G]CCAACTTCAACATTC | 75725 |
rs225571764 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11941838 | ACTGGACCACAGAAT[C/T]GTCCCCTGAGTCCTA | 75725 |
rs225576788 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11944842 | GGTGGGTTCCAACAC[A/G]AAGCAGAGATGGAGC | 75725 |
rs225581091 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12072302 | ACTTTGGAGAGAAGA[A/C]AGTGTCTGGTGCTGT | 75725 |
rs225587682 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11945652 | GTACCTGTGCCCCTT[A/T]AGTCTTGTGTCATGT | 75725 |
rs225603432 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12089386 | GAAGTCAAGCACTTA[A/G]AGCAACAGTATGAAA | 75725 |
rs225605997 | in-del | -/CTCAGC | | | intron-variant | Phf14 | Mm_Celera | 6:11922096 | GCTGCATATAACTTG[-/CTCAGC]CTCCTGTCTTACAGA | 75725 |
rs225633196 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12039096 | AGGGTGAGGATTTCT[A/C]TCTCTTTGTTATTTG | 75725 |
rs225692331 | snp | A/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100164 | GAGGACTGGCAAAGC[A/G]ACTGCAGCTCTGCTG | 75725 |
rs225701878 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11996097 | GACACCCTGAGCTCC[A/G]CCTAATATTTGGCTG | 75725 |
rs225703803 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985866 | TTATGTAAGTATACA[A/T]ACATACCCAAGTAAC | 75725 |
rs225708378 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12051008 | ATATGCTTCATTTTC[A/C]TAGGAATTCTTTATT | 75725 |
rs225715126 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11986835 | GCTGTTATTAAGTGT[G/T]GATTCATTTATTGCA | 75725 |
rs225722144 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12091465 | CCTTGTATTCACACA[-/C]CGTGTACTTGAGCTC | 75725 |
rs225728177 | in-del | -/AA | | | intron-variant | Phf14 | Mm_Celera | 6:12029422 | CAATTTCATTTTTTT[-/AA]ATTTAAGGCATTTTT | 75725 |
rs225731263 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949099 | TGTATAATTAATTAA[C/T]TGGTCATATGTGTGA | 75725 |
rs225736567 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11994782 | TTATACAAAGGATAA[A/G]CAAGCTGAGAGAGAA | 75725 |
rs225761380 | in-del | -/TG | | | intron-variant | Phf14 | Mm_Celera | 6:12088936 | AGCAAGAACTTTGAA[-/TG]TACCTGCTTTCCTGC | 75725 |
rs225762739 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997264 | CAGATAAAAGGTTTA[G/T]AGCATAAACATACAC | 75725 |
rs225768644 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11937640 | GAGAATCTTAAGAGC[A/T]AAACTTTCAAATAAA | 75725 |
rs225783656 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12054484 | GCTGCCTCTGCTCAC[A/G]GTAGAAGCAGCAGAG | 75725 |
rs225813956 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11939709 | ATCAAGAACATCTTG[A/G]GATCTTTGGATCTTG | 75725 |
rs225815026 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11940907 | TTTTTTCTGTTGTAG[A/C]TGATGTGTTCAGGCT | 75725 |
rs225824065 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12021569 | TGTTGTTTGAAACTT[A/C]AGAAGCCAGGAGTCT | 75725 |
rs225824115 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029518 | CCCTGCTTCCCAACC[C/T]ACCCACTCCCACTTC | 75725 |
rs225829422 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:11943735 | AATATGGTATCCATA[-/G]GTGCCAAATTAAATC | 75725 |
rs225835689 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12020427 | AACCTCCCGCAATCA[A/T]TCACTTGCAGGCAGC | 75725 |
rs225843989 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12050006 | TGTAAAATACCACTT[C/T]CTGTCCTGATGTAGT | 75725 |
rs225851364 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11999833 | ATCTCAGCCTGAAAA[A/G]CACTAGAGAGTGGAT | 75725 |
rs225863461 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917321 | TAATAGTTGAAGAAC[A/T]GTTCACATTGCAGCC | 75725 |
rs225890630 | in-del | -/AATTAAATGG | | | intron-variant | Phf14 | Mm_Celera | 6:12002968 | ACAGGACAGAGACTC[-/AATTAAATGG]AATTAAATGGGTTGA | 75725 |
rs225894688 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12022162 | TTTGAAAAAATAGTT[A/T]TCTCTTAACGATAGC | 75725 |
rs225915274 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12085733 | AACACAAGAAGTTTA[-/TT]TTTTTTTTCAGTTAA | 75725 |
rs225916290 | in-del | -/ATTTAGTCTT | | | intron-variant | Phf14 | Mm_Celera | 6:11950094 | TTTTAGAGGGATTGG[-/ATTTAGTCTT]ATTTAGTCTTAGTTA | 75725 |
rs225932876 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11909951 | TTGACAACCAGGTGA[A/C]GCCTTTTGAAATATC | 75725 |
rs225940251 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11991281 | AGTTTTAAGCCCTTG[A/G]TGCTCATTTTCTTAG | 75725 |
rs225956192 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917780 | GACAGCAACCAAAAG[C/T]TACAGAGATCACACA | 75725 |
rs225962193 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057247 | TTAGAATCTGATATT[A/G]CATATCAGTAATTGT | 75725 |
rs225968405 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11910330 | CTGTCACACAGAACT[G/T]TTGGCTCCCATGTGT | 75725 |
rs225989059 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12056509 | ATTCAGCAAATATAA[A/G]AATCATGTATTTTTA | 75725 |
rs226019411 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076306 | CTATCCAGGTGACCG[C/T]GGTTTCCATCTTGTA | 75725 |
rs226031829 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11992986 | TCCCAGGTGATTCTA[C/G]ATTCTCTCAAGTTGA | 75725 |
rs226045112 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12051662 | CTCCTAACATGGCAT[A/C]TGACATACTGATGCT | 75725 |
rs226047043 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12057547 | ATTTAATATATTTTG[C/T]TATGTGGGGGAGGGG | 75725 |
rs226050096 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12082125 | AATGCTGATGCGTTC[A/G]CTCTTCACATGATAC | 75725 |
rs226052764 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11918457 | CCATTCTGGTCTTCA[A/T]AGTGACACCTTGTCT | 75725 |
rs226068328 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12077196 | TGTCAGAGTAAAAAA[-/T]AAAAGGAAGCTCGTG | 75725 |
rs226074001 | snp | C/T | | | nc-transcript-variant, intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099653 | TGAAAATGAAGACTC[C/T]TGATTTTAAGTAGGT | 75725 |
rs226084975 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052140 | AATTTCCTGACCGTC[C/T]GTGCATCTCCCCAAT | 75725 |
rs226091741 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12050592 | CTAACTACTCCAGGT[A/T]GTTTGTTTTTAACGT | 75725 |
rs226097174 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950243 | GGTAGCAAGTAGGTA[C/T]GGCTCTGGAGCAGTA | 75725 |
rs226112855 | in-del | -/AT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12098731 | TATATATATGAGTGA[-/AT]ATATATATATATATA | 75725 |
rs226122739 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916998 | CCATTGGTTGGGTCA[C/T]TCCACTCTGGCAGGC | 75725 |
rs226133048 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11909680 | ATGGTAATGAGTATG[C/G]TTATATTAAAAATCA | 75725 |
rs226143051 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12027186 | TCCTGTCCTCAGGGT[C/G]TCATATTGTTGGTGC | 75725 |
rs226148143 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12074830 | CACGCTTTACACTTT[A/C]TTTAATGACCCAAGT | 75725 |
rs226158799 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11994115 | GACTGAGAGATCTCA[A/G]GAGTCCAGGTTAATT | 75725 |
rs226163952 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032874 | TGGTTGGTGAGTTAG[C/T]CCCTGTGAGCTCTGG | 75725 |
rs226172719 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11981024 | CACAGAAGACTATTT[C/T]TCCTGCTCTCGGCAT | 75725 |
rs226226080 | in-del | -/TTT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12057684 | GTCCAAATGCTTTAA[-/TTT]TTTTTTTACTGATAA | 75725 |
rs226226109 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12033402 | CTCCTCGGCTAAAGT[C/T]TGCTGCTCCAGTTTT | 75725 |
rs226232649 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:11948259 | GAGCTGAGAGTTGTA[-/C]ATCTTGATCAGAAGA | 75725 |
rs226276000 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11914819 | CTGACCTCGTAAGCT[A/G]CATAGTTGTGTGGTT | 75725 |
rs226279553 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12084827 | GAAGAGCTTTGTCCA[-/T]TTTTTTAAAGACAAG | 75725 |
rs226292623 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12001423 | TTGTGAAAGGTGTTA[C/T]TTCTTTATATAGTAG | 75725 |
rs226312200 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12029169 | CAAAACAACCCAAAT[-/C]CCCCTACTTCACTAT | 75725 |
rs226312268 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12054968 | TCAGGATGGATAGGT[A/G]TCATATAACAAGTTG | 75725 |
rs226344614 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12027247 | TCTTTTCTGAAGGCT[A/G]TAAACTTATTCAGTA | 75725 |
rs226350944 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11993600 | TTATAGGGATTTATA[C/T]ATATTTGTAAAGTGA | 75725 |
rs226352242 | in-del | -/ACAGGTATGTA | | | intron-variant | Phf14 | Mm_Celera | 6:12058214 | CCAAGTGTCGAGCTT[-/ACAGGTATGTA]ACAGGTATGTAACAC | 75725 |
rs226358045 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11994137 | AGGTTAATTGAGACT[A/G]CTGGTCCTCCTACAG | 75725 |
rs226370167 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031932 | CATGAGTATGTACTG[C/T]CTTACCCTCTCTTTT | 75725 |
rs226373894 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12080092 | CACTAAGCAAAAATT[C/G]AACTATTATGTGATT | 75725 |
rs226382130 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12000235 | TGAAGTTTCTCATTC[C/T]TCATTCCTTTATAAT | 75725 |
rs226396314 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11992437 | TTTCATTAGCCCATT[A/G]TTTGGAAATCCAGAA | 75725 |
rs226425870 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12048560 | GTACTAAGAGGATCA[C/T]AGATTGAATTACATT | 75725 |
rs226444540 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12073108 | ATAAAACAGAAAGAA[A/G]CCTTAGGCGGTTCTC | 75725 |
rs226450561 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055394 | CTTTCCATCTCTGTC[C/T]TTGTTTTTATATCAG | 75725 |
rs226495236 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916779 | CAGCTGAGAAGATTT[C/T]ACTTTAGTCAGCTGC | 75725 |
rs226515683 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11946905 | AGAAATACTACCATT[G/T]AAAATTCAGAAGGAA | 75725 |
rs226532890 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12050723 | TCCCCACGGGGAGGG[A/G]GTTGGGAATGTATAA | 75725 |
rs226536982 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12024602 | TCTACAGCCTCAGTA[A/G]TAGTGTCAGGCCTTG | 75725 |
rs226564731 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12041748 | TTTTGAGACTCAGTT[A/G]ACTACCATCTTCTCC | 75725 |
rs226569932 | snp | G/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909014 | CAGTAGGACATAGAG[G/T]GAGAAAAGACTCAGG | 75725 |
rs226589677 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11938717 | GACAGATTACTGATT[C/T]AGTTTCTACTTCAAG | 75725 |
rs226598170 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910442 | TGTTTGGAAAGAGCC[A/G]TCGTGTGTCTATGAT | 75725 |
rs226599490 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12082918 | AGGGCAAACAAGAAG[C/T]TTACTGAAGGGTAGC | 75725 |
rs226609743 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11995590 | TAGTCTCACATTCCC[C/T]TTCTCCTCCCCTCCA | 75725 |
rs226630788 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916438 | ATGGTTTAGCATGTG[C/T]TTGATCTCTCCCAGG | 75725 |
rs226650890 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12075665 | TCTGATTAGTCAAAG[A/G]CACTATATTAAAATT | 75725 |
rs226651374 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12042598 | ATAAAGACATATCAA[A/G]ACATGAAAACAGAGT | 75725 |
rs226664278 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11979609 | TCTTTGTCTTTAGTG[-/T]AAGTTAACGAAAGGA | 75725 |
rs226666730 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12089843 | TTCATGGTGTTCAAG[-/C]CACAGATTAGCAGAA | 75725 |
rs226670376 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12001598 | GACTTCTTTCTTTCC[A/G]ATTTGTATCTCCTTG | 75725 |
rs226689394 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12082282 | GCTTACCGCTTATAG[A/G]AGACTGGAGTTTGGC | 75725 |
rs226691249 | in-del | -/GAAGT | | | intron-variant | Phf14 | Mm_Celera | 6:11947258 | TCTTATCTACCGTGG[-/GAAGT]AGACAGACAGACAGA | 75725 |
rs226691252 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12074070 | ATTCACAATTGTCTG[C/G]CTCCCATAGATAACA | 75725 |
rs226707623 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11911271 | CACTTTGAGCACAGA[G/T]AGTGGAGACCTGAGT | 75725 |
rs226714861 | in-del | -/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008614 | ATTTCAAGAAGATTA[-/T]TTTTTTTCTAGGGTA | 75725 |
rs226723357 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11976752 | ATAAGTAATCTAATG[-/A]AAAAAATTACAAAAA | 75725 |
rs226735399 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11995310 | ATGACTGCATCAGCC[-/A]AAAAAAAAAAAATAC | 75725 |
rs226743014 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921064 | GGTAATAAGGCCACA[C/T]TGGAGTAGGGTGAGT | 75725 |
rs226744714 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11952872 | ATTCTTTAAATTTAT[A/G]ATTTTGTATTACAAA | 75725 |
rs226764491 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12030627 | TCCCAGGGCTTTTAT[C/G]ATGAAGGGCTGTTGG | 75725 |
rs226774570 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12074938 | TAGTCTGAAGGATGC[A/G]GTGTGCTCATTTTGG | 75725 |
rs226779773 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11948562 | TTATGTATTGCTAGG[A/C]GAAAATACATGACAA | 75725 |
rs226793107 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12070377 | GTTAAGATGTTTATC[A/G]AAGTTTTCATAAGAA | 75725 |
rs226803826 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11945376 | ACCCTGCCTCCCACC[A/C]CGGAATGATGGCATC | 75725 |
rs226822633 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11915272 | TTGACTGGCATGATG[A/G]GCCCAGATTGAACAG | 75725 |
rs226825599 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11981071 | TTGTTCTTTGTTGAG[A/G]GTTGAGGTCCCATGA | 75725 |
rs226841604 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023571 | GCCTACTGATGGTGG[C/T]CAGAATTGTGGCAAT | 75725 |
rs226853232 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11940439 | TGGGGTATTCTGGAT[A/T]GTCCATCCTTTCCTC | 75725 |
rs226865986 | in-del | -/TTC | | | intron-variant | Phf14 | Mm_Celera | 6:12085543 | GTACAGCAATTTAAG[-/TTC]TTAAGTGCTGAGCCT | 75725 |
rs226958719 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12020157 | ACATTAGGAAACTGA[A/G]AACACAAGTGAATCC | 75725 |
rs226973653 | in-del | -/GAAA | | | intron-variant | Phf14 | Mm_Celera | 6:12002208 | CATTTCATACTTATC[-/GAAA]AAAAAAAAAAAAAAT | 75725 |
rs226976395 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11940943 | TGAGTAGTTGGGTAA[A/C]TCTGGACCTTGTATA | 75725 |
rs226986857 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12073751 | GTAAAAAATGTGCTA[C/T]CACACTTTTGTTCAT | 75725 |
rs226991653 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11930869 | TTGTGGTTATTCATC[C/T]GTGATTATGAATAAA | 75725 |
rs227021555 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11946168 | AATTGCTGCTATTTT[A/C]TTATTAGTTTTTTTG | 75725 |
rs227024631 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947364 | CTACCAACTGAGGGC[C/T]AAGTAGTCAAACATT | 75725 |
rs227034198 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12058633 | TGGACCCTTTTCCTT[G/T]TCCTTCGAAGGCTAT | 75725 |
rs227045984 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12025774 | TATATGTAATTTCCC[G/T]TTTATCTAAGTACTA | 75725 |
rs227062522 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12092189 | GATTAGGACAATAGC[A/G]TTGCCTTAATAGCTC | 75725 |
rs227069042 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12020583 | ACTGTTAAGCCACAA[A/C]CTTTCCTTCCTTGGT | 75725 |
rs227075485 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11957437 | TTGATCTTATATCAC[A/G]AGGCATTGGTGTTCT | 75725 |
rs227077598 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053343 | TATTAAGCAAAAACA[A/G]TTTTTTGAAAGATAA | 75725 |
rs227094961 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12093565 | CTGCTGCTTCATGCA[A/G]CTAAGGAAAAGACTT | 75725 |
rs227112945 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11920565 | AAAAGATTCTTTAGC[A/C]TGGCTCAGAGAGCAC | 75725 |
rs227114210 | in-del | -/TGT | | | intron-variant | Phf14 | Mm_Celera | 6:11946671 | TATACTTGGGGGCAG[-/TGT]GGGGGGATGGAGTGA | 75725 |
rs227120290 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11921367 | TTTATAGTATTCTTA[A/G]AAAGCTAGTGTACAT | 75725 |
rs227120320 | in-del | -/TCTT | | | intron-variant | Phf14 | Mm_Celera | 6:12070964 | TAGAATCAATGTCTG[-/TCTT]AGGTGTCTGTGGTTA | 75725 |
rs227122742 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11981278 | CTGTCTGTGAGCCTA[A/C]GGTACAGGAGTTGTG | 75725 |
rs227134142 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985564 | ACCCTTTGGCTAGCA[C/T]TGTGTTTCCATGTGA | 75725 |
rs227136101 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12013434 | AATGTTTTTGTTTTG[G/T]TTTTGATGACTTTTT | 75725 |
rs227140414 | in-del | -/AG | | | intron-variant | Phf14 | Mm_Celera | 6:11975933 | AGAGCCCTCCCAGGC[-/AG]ACATCTCTCCCTTGG | 75725 |
rs227142715 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11997725 | CCCCTGCTTCTATGA[A/G]GGTGCTCCCCTATGT | 75725 |
rs227144308 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030498 | ACAACATTATCTTGC[C/T]CCTAATTTTAGTGGA | 75725 |
rs227174743 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11939180 | ATAGTGCTCATTTGG[A/G]CTTGTCACTTACCTC | 75725 |
rs227176867 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:11959462 | TGGGAACATTAGACT[-/C]CTTAAACGTCACCAC | 75725 |
rs227186457 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12050060 | TAGTAGTTTATTGAA[A/G]TGCTCTTCACTAATC | 75725 |
rs227190426 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11960535 | AAATGATAAAAACTT[A/T]AGACTTTTTCTGAAT | 75725 |
rs227196583 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031005 | CCTTACTGTCTGTTG[-/T]TTCGCCCCCTTTCTT | 75725 |
rs227229543 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11938797 | TTCTCTCTTAAGCCA[C/T]TTTCTAAGGCTTAGA | 75725 |
rs227239166 | in-del | -/AAT | | | intron-variant | Phf14 | Mm_Celera | 6:12075976 | GCAATAAAATAAAAC[-/AAT]AATATCACTTAGCCA | 75725 |
rs227253109 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12024299 | TCTTAAGGGTTAAGT[A/G]CATCATGAATGAACA | 75725 |
rs227253406 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12067130 | CCCTGGCCTTTCTGA[A/T]GCTCATGCACACAGA | 75725 |
rs227256114 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12065322 | CTTTCTTCCTGGCTT[A/G]CAGTTTCTTCTCAGT | 75725 |
rs227283028 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11939263 | GTGTTTCTGTTATGA[A/G]CCATGTACAGGAAGT | 75725 |
rs227286694 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12022286 | GTGTGCCCTAATTTA[A/T]TACAAAGAGACCATG | 75725 |
rs227296524 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11938053 | TATAAATATATTTCC[A/C]TGTGTAATCTCACCT | 75725 |
rs227318918 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024151 | AGATTAATTATTGGC[A/T]TAATTCCCCGTGCCC | 75725 |
rs227345284 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12016963 | CTCATGTGGCCACGT[A/G]TAAGTAGAGCAGTGA | 75725 |
rs227380848 | in-del | -/TAC | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12099879 | TTTTGTCGTCTCCTG[-/TAC]GCGTACTTTCTCATA | 75725 |
rs227384956 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11930052 | CAAGAGTTGTCCTTA[C/T]TAGAGAAGCTCTAGT | 75725 |
rs227385288 | snp | A/C | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909253 | GCAGGCCTCTGACTC[A/C]AGATCCTCCTGCCTC | 75725 |
rs227390775 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12097723 | TCCTTTTATACTCTC[A/C]TCTCATCCACGCACC | 75725 |
rs227401722 | in-del | -/TTTTTT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12069252 | GTTATATATGATGTC[-/TTTTTT]TTTTTTTTTTTTTTT | 75725 |
rs227406684 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11946023 | CTCCATTTACTTCTC[A/G]CTATTTCATTGTCAC | 75725 |
rs227437773 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11988035 | AACTAACACTGCTAA[C/T]CTCATTTCTTATTCT | 75725 |
rs227439995 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12075263 | AGTAAATGGCATTGC[A/G]GCACTATCTTATTTC | 75725 |
rs227469094 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12098622 | CTCTGTTTTCTCTTT[A/G]TCCCTCAGTCTTTAA | 75725 |
rs227474584 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11991559 | AAAAGCTGAACTAAT[A/G]CTAAATGAATTTTAA | 75725 |
rs227481109 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12075715 | TTTCCAGTCACCACT[C/T]ATCTGCAGCCCAGTT | 75725 |
rs227482933 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12068532 | CAAATGAGTCTTGAC[A/G]ATTATATATATATAT | 75725 |
rs227512448 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12096866 | AAATAAGTCACCTTG[A/G]TCATAGGGTTTTTTC | 75725 |
rs227527950 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11929912 | TCTGTGTAGTATAGT[A/G]TGGTGTTTATAGCAT | 75725 |
rs227534935 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11978168 | CATACTTTTATAGAG[C/T]TACTTTATGAAGATA | 75725 |
rs227535269 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11992522 | TGAAGTTGTTATGTC[A/G]TTGAGGATAACTTTC | 75725 |
rs227537991 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12046498 | TTTTATTCACTCCTG[A/C]AACTGGGATTACAGT | 75725 |
rs227543675 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009727 | GCCCATTGACCTGCT[A/G]CTATGGCTTTATCAG | 75725 |
rs227551367 | in-del | -/TGTCT | | | intron-variant | Phf14 | Mm_Celera | 6:11917084 | ACTTCTCTGTCTGTC[-/TGTCT]TGTCTTGTCTCTTTC | 75725 |
rs227555295 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11979148 | GATTTTAATACATAT[A/T]TTTATTACTCTATTG | 75725 |
rs227565145 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12052032 | CCATCCCTGTTGGGT[A/C]CTGAGCCCTCTTGCT | 75725 |
rs227570211 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11940536 | CAATATAACAGGACT[C/T]TTTGTTTTGTTTCTT | 75725 |
rs227578600 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12069028 | GACAAACAAAGCAAA[A/C]AAAGCCAAACAATAC | 75725 |
rs227584115 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11941122 | TGTGTATAGAGCTGA[A/T]AATTACTTGAGGATT | 75725 |
rs227601743 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11990728 | ATAGCATTTTCTCTA[A/G]ATAAAAAAGACCTCA | 75725 |
rs227602379 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905801 | CCAACCTTCAAAATG[-/TT]TAAGAGTTGGTATTA | 75725 |
rs227625307 | in-del | -/GAAAAAA | | | intron-variant | Phf14 | Mm_Celera | 6:12077190 | TCATACTGTCAGAGT[-/GAAAAAA]AAAAAAAAAAGGAAG | 75725 |
rs227625897 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11998505 | TTGGGGCCAATCCTT[C/T]CTCACTGTGGCCTTG | 75725 |
rs227628745 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11994117 | CTGAGAGATCTCAGG[A/G]GTCCAGGTTAATTGA | 75725 |
rs227635390 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053519 | CACTGTGCCCTTGGT[A/G]AAATCAGAATAGGAA | 75725 |
rs227655154 | in-del | -/TATCAGAGGTT | | | intron-variant | Phf14 | Mm_Celera | 6:11914078 | ACTTATGTGTGTATG[-/TATCAGAGGTT]CGTGTCTGGTGTGGT | 75725 |
rs227672308 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12045966 | AACCCTGAAGACCTG[A/G]AAAAATTGAACATAA | 75725 |
rs227711464 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12073125 | CTTAGGCGGTTCTCT[A/G]AAGTAAACGTTTGTG | 75725 |
rs227731618 | snp | C/T | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099282 | CAGCTTGCTTTCTTA[C/T]AGAGCCCAGGACCAC | 75725 |
rs227753336 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12046413 | ATCCCAGAGAAACAG[A/T]TATTTGAACATTTAA | 75725 |
rs227756900 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11932626 | GAAGGCTAACATGAC[A/C]CATGACACAAGCAGT | 75725 |
rs227759424 | snp | G/T | | | nc-transcript-variant, missense | Gm6578, Phf14 | Mm_Celera | 6:12099831 | GAAGAGCTTCGAAAG[G/T]ACCTCCTTCTTGAGC | 75725 |
rs227761075 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079686 | AATTTTTAATAGGTT[A/G]TAACTAAAATGTAAT | 75725 |
rs227782956 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12052677 | GTGGTCCTATGGATT[A/G]CACAGCAGGTCAAAA | 75725 |
rs227798712 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906875 | CTCTATCGAGCTATA[C/T]TGGACGAAAGTGACA | 75725 |
rs227798856 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11915476 | GTTCTAGGACAGCCA[C/G]AGCTACACAGAGAAA | 75725 |
rs227802109 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12017875 | ACAGACAACTGAGGT[C/T]TCTGAAGGAAGAAAA | 75725 |
rs227805404 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12026456 | GCCTGGAAGTCCAGT[C/T]CTTTGTCTTTACTCA | 75725 |
rs227816926 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12017823 | TTCCTTGTAGTAATG[A/G]TACTTAAACAGTGGT | 75725 |
rs227819496 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12066052 | TAAAATAAGCTCAGG[A/C]AGTTTCCTTCTCTCT | 75725 |
rs227851426 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907405 | CGCAGAGAGAAGATT[A/G]GGACACACGCTAAGC | 75725 |
rs227862059 | in-del | -/GTA | | | intron-variant | Phf14 | Mm_Celera | 6:12035956 | GACTTACTTTCCATT[-/GTA]GTATATTTATATTAT | 75725 |
rs227863441 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12073144 | TAAACGTTTGTGTTC[A/G]CTAGATGTTGCCAGT | 75725 |
rs227878549 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12095060 | CACCACGTCAAGTGC[A/G]TGGAACACGGATCAT | 75725 |
rs227882432 | in-del | -/TC | | | intron-variant | Phf14 | Mm_Celera | 6:12018495 | CCCTAGCACATCAAG[-/TC]TCTGCAGAATAAAGT | 75725 |
rs227891551 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009004 | GTGTTTTGTTTTAAT[A/G]TTTATTTTTTTTATA | 75725 |
rs227900102 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11988641 | TGAATGTTACAATAA[A/G]TGGAAAATAAATGTG | 75725 |
rs227908188 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12044305 | GGTTGAGAACCACTG[G/T]TCTAGCACCTTGACT | 75725 |
rs227922804 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11938773 | TTTAATCGTAGAATT[C/G]TCATATATTTCTCTC | 75725 |
rs227937585 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11928832 | CTAAGATTTCAGGTC[A/G]TAAGTTTACTTTTGT | 75725 |
rs227939930 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11938732 | AGTTTCTACTTCAAG[-/A]AATTCAGTTTCTTCC | 75725 |
rs227940262 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947087 | TGTCTTGGTTACTTT[C/T]GATTGCTATTATAAG | 75725 |
rs227944132 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12073894 | TCGCTTTCAGTCTGA[G/T]GTAGTTTTTGCAGTG | 75725 |
rs227959928 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11930185 | TAACCAGCAAACTAG[G/T]GGTGTCTGTCTTATT | 75725 |
rs227976781 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11963248 | ATACCAATATAAAAT[A/T]TGCATTTCTAAGTTC | 75725 |
rs227987039 | in-del | -/AGCGAGAG | | | intron-variant | Phf14 | Mm_Celera | 6:11916130 | GCACAATATTAAACA[-/AGCGAGAG]AGTGTGTGTGCGCGC | 75725 |
rs227997582 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12047796 | AGTAGTTTCAACATT[C/T]AGATCCACTCTGACT | 75725 |
rs228003293 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11916485 | AAGTACTAAAATCAA[A/C]CAACCAAACCAATAG | 75725 |
rs228009697 | snp | A/C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11914209 | GAATCCTCCTTACCT[A/C/G]GTTTCCTCTTGTTCG | 75725 |
rs228021152 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11922616 | CAAGATCACTGGCTG[A/T]TGGCATTGCTCAATG | 75725 |
rs228022289 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906312 | TGATCTCTGTAAAAA[A/G]ACATCAGGATGGTGT | 75725 |
rs228032019 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12038769 | CAAAGAAGAAAGTTA[A/G]CAAATACTATCAGCC | 75725 |
rs228063349 | snp | G/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908604 | GAAGAATGGAGTAGA[G/T]AAAAGGGCTATTGTA | 75725 |
rs228108775 | in-del | -/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12028721 | GTGCAGACTGAATAA[-/T]TTTTTTTTTCAAAAA | 75725 |
rs228115869 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12097349 | AGCAAGGACATACCC[G/T]CTAATAGTGCTACAA | 75725 |
rs228138651 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095802 | CCCTCAATCCAGACA[C/T]GCTGAGAGGTTTCCA | 75725 |
rs228155392 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997938 | TCATATGTTTAAATA[C/T]ATGGTCCTCAGTTGG | 75725 |
rs228162175 | in-del | -/A | | | intron-variant | Phf14 | GRCm38.p3 | 6:12022815 | TGAGAAGTTCTGAGG[-/A]AAGACAGGTGGCAAA | 75725 |
rs228162237 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11923733 | TCAACATGTATTTGT[A/G]GAATAAATAAATGAG | 75725 |
rs228162293 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12090376 | CAAGAAAGAGTACGA[C/T]AAATTCTTGGGTACT | 75725 |
rs228162450 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12057641 | CTGGTACTTACGTGG[-/T]TTAAAAAATTAGAAG | 75725 |
rs228164406 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12047756 | AAGTCGCTATGTAAC[A/T]CTGTGTTCTTTTGTC | 75725 |
rs228187557 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12096645 | GGCCAAGCATATACA[A/C]ACCATCACAGTTGGT | 75725 |
rs228190914 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12088497 | AGTCTGATTTCCACT[C/T]CAGAGGGCAGTGACT | 75725 |
rs228191782 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11989645 | AGTTTAGTCCAATAC[A/G]ATAATTTCTCTAATT | 75725 |
rs228201322 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11990356 | AATGAATTTTCATAA[A/G]CTCCAACGAACAAAG | 75725 |
rs228204690 | in-del | -/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12050315 | GTTCTGTGCATGATA[-/G]TTCTGTACAGAAAGA | 75725 |
rs228218658 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11936706 | TGGCTTTTGCCTTTG[G/T]AGTTTGTAAATTAGT | 75725 |
rs228232086 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12042653 | ATTTGTAAGGAATGC[A/G]AACAAAGACGGGATT | 75725 |
rs228237391 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11976512 | CTAAAAGTATGACTC[A/T]TAAATTTTTTGGCAT | 75725 |
rs228240976 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924090 | GTTCAATAATATAAG[C/T]AGTGTCTTCAGCAGT | 75725 |
rs228264062 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12082450 | TAAGGACCTATGTAT[C/T]TGTCCATACAAACTT | 75725 |
rs228267830 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12052331 | GCTTGTTTTGTAGCA[C/G]CGGTTGAGATTTAGA | 75725 |
rs228275324 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12091255 | AAGAAATCGCTCTTC[C/T]CTATTCTAGAACCTA | 75725 |
rs228294952 | in-del | -/GG | | | intron-variant | Phf14 | Mm_Celera | 6:12033561 | ATTTGTATCCAATAA[-/GG]GGCAATGGCATTTGT | 75725 |
rs228309690 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12063041 | CAAACTCCTAGTATA[-/TT]TTCTTCAAGTCAGCC | 75725 |
rs228313125 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11911463 | TGGTCAATGAAGCAT[A/G]CACCATTAAAAATAA | 75725 |
rs228314165 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083098 | TTTTTCCTACGTGGA[G/T]CTATTTCAGAAAACC | 75725 |
rs228324530 | in-del | -/ACCTATATAG | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12081393 | TGTGGACCTAAAGGT[-/ACCTATATAG]ACCATGTTGTCCACA | 75725 |
rs228345412 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985709 | GTTAAGAACATCTCA[C/T]TTACTTATGATGGCT | 75725 |
rs228346405 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11954059 | GGTTGCCTGTTTTGA[-/T]TTTTTTTGTTGACCC | 75725 |
rs228386706 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11959396 | GTAAAGGGGCTCTTT[C/G]ATCTCAGAGGGGTCA | 75725 |
rs228387913 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011032 | AAAGAGTCTAGAAAA[C/T]TCTTATCTGTGAATT | 75725 |
rs228394868 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12000782 | TGAGAGAAAGTACTT[C/G]TAATTTAGAATGTGC | 75725 |
rs228400664 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11958786 | AAGACCAAGAGAGAG[-/A]AAAAAGCAATAAAAC | 75725 |
rs228442995 | in-del | -/A | | | intron-variant | Phf14 | GRCm38.p3 | 6:12026735 | AGGGAGAAGGGTTGG[-/A]GGAACGGGTCAACCC | 75725 |
rs228448678 | snp | C/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040215 | TGTGTCTTCCCAGAG[C/G]TTCACAGAGTTTACA | 75725 |
rs228481708 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12033526 | CTGAGGTGGTTCCAG[C/G]TTATATATGTTTATC | 75725 |
rs228498273 | snp | C/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12040818 | TTAATGGGTATTTTT[C/T]TATTTTAGGGTTTCT | 75725 |
rs228502912 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095753 | TGATGAGTGAACTTT[C/T]AGCTCTCCAGTTATG | 75725 |
rs228506281 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12078552 | TTTCTACAGCCCTTT[C/T]GCATTTGTATGTTGA | 75725 |
rs228519709 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12034322 | AATAATAATAGTAAT[A/T]AAACATATGCAAAGA | 75725 |
rs228548801 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12045409 | ACAGATTTAATGCAA[A/T]TTTTCTACATGAAAA | 75725 |
rs228570293 | snp | A/C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12071047 | ATAGTTCCAGAGGTA[A/C/T]GAGTTCTTTTTCATC | 75725 |
rs228571705 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11989619 | AGAGAATTTCATCTG[C/T]TTTTTTACGGAGTTT | 75725 |
rs228579804 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12037640 | GAAATGAAGGAGTGT[A/G]ATCAAAGTGGCTACT | 75725 |
rs228585169 | in-del | -/TA | | | intron-variant | Phf14 | Mm_Celera | 6:11963385 | TTTATATTTACTTTT[-/TA]TGTGTTTTTTTTTTT | 75725 |
rs228592966 | in-del | -/ATTC | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12047566 | TATGCTTACATATAT[-/ATTC]ATTCATTCATTCATA | 75725 |
rs228595558 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12087416 | TTACTCAGCAGAGTG[A/G]TTTTGAAATGGTCTG | 75725 |
rs228626021 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Ndufa4, Phf14 | Mm_Celera | 6:11907615 | TTTTTGAGTTCATGA[C/T]CCATCAGTTCTCCAC | 75725 |
rs228634790 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11914879 | ATGGCCTGTGGAAAA[A/C]AACTTCCAGTGCTAC | 75725 |
rs228657611 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12023115 | TGTCCAGGTAGATGG[A/G]AAGTCATCAAAGGCA | 75725 |
rs228666920 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11955785 | TTCATAACCTCATGA[C/T]TATACCTTAGTTTGG | 75725 |
rs228668469 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12037188 | GTTTGGTGCTGAATT[C/G]TGGTATCTAGAAAAT | 75725 |
rs228679188 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12038453 | TAGCCTTGCTTCCCC[A/G]TGATTGTTTTCCGTG | 75725 |
rs228685738 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12002979 | GACTCAATTAAATGG[A/G]TTGATAATCCCATTA | 75725 |
rs228702568 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11944650 | TTTAAACCAAAGCTA[A/G]ATATAGGAGGGGCCA | 75725 |
rs228706631 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906751 | AAAAGCACTAGTTTT[A/T]GGAATGAACTCTGAA | 75725 |
rs228711608 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12079052 | AATGACAATATGCCC[-/T]TTTTAAAGTGTGTAT | 75725 |
rs228713487 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11974101 | TGTGTGGTGCAATGT[G/T]TACTTTGAGCTTCAT | 75725 |
rs228725787 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11957504 | GCTCTTCCCCACTTT[A/C]TCCTCCATAAGTCTC | 75725 |
rs228738010 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12032864 | GTGTACTCTTTGGTT[A/G]GTGAGTTAGCCCCTG | 75725 |
rs228773890 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11935962 | ATGTTTAGATTTTCT[A/G]TTTATATAGCTCTTG | 75725 |
rs228810786 | in-del | -/GATT | | | intron-variant | Phf14 | Mm_Celera | 6:12068621 | TTGTCTTCAAAATAA[-/GATT]AAGTAACAGCACCCT | 75725 |
rs228824961 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12076293 | TTCCTAGCTCCTTCT[A/G]TCCAGGTGACCGTGG | 75725 |
rs228839968 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060494 | AATTTCCACTGTGAT[C/G]AATCAGTTTATAACA | 75725 |
rs228845564 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12068283 | AGACATCTGTAGAAA[A/G]CAGTTGTAGTTTATC | 75725 |
rs228846488 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11910617 | CAAAGGAACTCTTAG[A/C]TTTGGGTTTTAAAAA | 75725 |
rs228849664 | in-del | -/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062939 | TATAATTTGATACAG[-/T]TTTTTTTATTTCATT | 75725 |
rs228870604 | in-del | -/AAC | | | intron-variant | Phf14 | Mm_Celera | 6:12042172 | TTTGTATGAGATGAA[-/AAC]AATATTTAGCCTTAG | 75725 |
rs228890013 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924836 | CCACCCCCATTAGAC[-/T]TTTTTTTCACTAGCA | 75725 |
rs228895990 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12043360 | CAGTAGCATTCACAA[A/G]ATAGGTTCATCATTT | 75725 |
rs228909543 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12077355 | TTAAGAGCATGCCTA[C/T]GTGCATTCCAGTACC | 75725 |
rs228919979 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906246 | CTACAATGGGAATAA[C/T]GGTTGAACTTGGATT | 75725 |
rs228931051 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11912627 | GAAGGCTGGGGAGAT[C/G]TCACAGTAAACGATG | 75725 |
rs228933345 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12028768 | CCATGTATCTAAAAA[A/T]TTAATAGGAAAAGAT | 75725 |
rs228948597 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12021345 | TGCTCTTAGGAAACC[A/G]CTTCCCGGAAGATTT | 75725 |
rs228960931 | in-del | -/CCAGTGA | | | intron-variant | Phf14 | Mm_Celera | 6:12015435 | AGTAGGTGTGGCTGG[-/CCAGTGA]CCACAAAGAATCACT | 75725 |
rs228986312 | in-del | -/GACAAGAAT | | | intron-variant | Phf14 | Mm_Celera | 6:11994521 | TAAAATTGGGGACAA[-/GACAAGAAT]GCCCTCTCTTCCCAT | 75725 |
rs228987292 | in-del | -/GT | | | intron-variant | Phf14 | Mm_Celera | 6:11951569 | ATTACCAATAAGATC[-/GT]CAAGCCTCAAAGGGT | 75725 |
rs228994821 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12016488 | TTATGTAAAAGGATG[A/T]GCGCGCACTGAGTGA | 75725 |
rs228996230 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12064467 | TGCCATGGGATGCTG[A/G]GAATTGAACACTGGG | 75725 |
rs229014781 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12070424 | ATTGTCAAGGGTTTA[G/T]ATATAAACCTTAATG | 75725 |
rs229029927 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12065206 | AACTTCCTCTCATCA[A/C]ACTCAGTATTTATAC | 75725 |
rs229039591 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11915153 | AGGTCATGCATTCTA[G/T]ATATACTACTCTTTA | 75725 |
rs229046836 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11943699 | ATAGCCATGGGGTTT[A/G]TTTCTTAAGCAAGAT | 75725 |
rs229049937 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12022780 | TAAAGTCTAAAAATT[-/A]AAAGTCCAGAGAGGT | 75725 |
rs229058582 | in-del | -/TA | | | intron-variant | Phf14 | Mm_Celera | 6:11941106 | CTTAGACTCTGAAAG[-/TA]TGTGTATAGAGCTGA | 75725 |
rs229066036 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12022312 | CCATGGATTTCTTTT[A/C]ATGGCTCAATTTGAC | 75725 |
rs229076850 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11942204 | ACTCCTGGCAACAGT[A/G]GGAATGTATTTGGCA | 75725 |
rs229083359 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11937870 | CATTTTTAGGCAACT[A/G]TGTATTTATTAATTT | 75725 |
rs229098299 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12016935 | GTGGCACAGGGAGTG[C/T]CCTGTGTGTGCTCTC | 75725 |
rs229099134 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12033477 | CGAAAGTTCCACTAT[-/G]CCCCCCAAAAGGTCC | 75725 |
rs229107827 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12059162 | AGCAGGGTTTTTTTT[C/G]CTGTGGGTAACACTA | 75725 |
rs229123799 | in-del | -/ATA | | | intron-variant, cds-indel | Phf14 | Mm_Celera | 6:12011480 | TAAATTTCCTGGATC[-/ATA]ATTGAGTTTTTCTCT | 75725 |
rs229140487 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12059783 | ACCTGAACTGAGAAG[A/G]AGGTTTCAGCCTTTC | 75725 |
rs229156160 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12007318 | AGATATAAATAACAG[C/T]GAGTATGGATCTTGA | 75725 |
rs229157449 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023687 | CTTCTAACTCCGGCT[A/T]ATAGATACACACTTT | 75725 |
rs229157544 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072247 | GGCATAGGTTATGTT[A/G]GGATGAGAAAGAAAT | 75725 |
rs229166427 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008940 | TACACAATTGAATGT[C/T]TCCATTAATATTTGC | 75725 |
rs229203821 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095927 | GAAGTTGAGAGATCA[C/T]ATCTCAAACTGAAAG | 75725 |
rs229225648 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12046046 | GCCACAGAGATGTAG[C/T]TCCAGCTGTCATTTA | 75725 |
rs229225936 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12035457 | TTTTAGATGTCCAGG[-/A]AAGCTAAACCTTTAA | 75725 |
rs229233443 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12096729 | CTGGATCCATTCTCA[C/T]TGTCCTCTCTATCTC | 75725 |
rs229235231 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11928779 | AACATATAATCCCCA[G/T]TCGTCTACTGCCCTG | 75725 |
rs229247761 | in-del | -/TG | | | intron-variant | Phf14 | Mm_Celera | 6:11939934 | AATTTTGCTTTTGAC[-/TG]TGGCTAGCTTTTTTT | 75725 |
rs229260993 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11945482 | TAAGTTTCTTTGGTG[A/T]CTATAAAATCTGGTC | 75725 |
rs229264023 | snp | A/C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11934401 | GCGTACATTAGAAGA[A/C/T]GGTAACATCAAGCTC | 75725 |
rs229273589 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12014505 | TCATTCTCTAACTGA[A/G]TCGTAGGTGTGTTGT | 75725 |
rs229276480 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12022967 | TGTGAATGACATAGC[A/T]ACCTTGTCAACTAAT | 75725 |
rs229284259 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12063400 | TACAGTAGTATACAT[A/G]GCCATTATTCAATAT | 75725 |
rs229292884 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12069109 | CACAAGTTCCTATAT[A/G]AATACATATTTATAT | 75725 |
rs229299825 | snp | A/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100265 | AGCAGCAACGAAGGA[A/G]CCATGATCCTGAAAA | 75725 |
rs229302698 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11911746 | CACCTGACTGCCATT[-/A]TGCATGTCTTCACAA | 75725 |
rs229302980 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918374 | TAGCATATTCAGTAG[A/G]ACATGGTGGTTCGTT | 75725 |
rs229312017 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11935788 | CATAGACTGACCTAC[A/G]GAAGGCTGATTTCTC | 75725 |
rs229319539 | snp | A/C | | | intron-variant, upstream-variant-2KB | Phf14 | GRCm38.p3 | 6:11925788 | AGAGAATCTGTGAAT[A/C]TTCTTAAAGTTACTG | 75725 |
rs229327683 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11995134 | AATACCTTTAGTTGT[G/T]CTAGGAACATACCTG | 75725 |
rs229334433 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:11921281 | TTTACTACTTCATCT[-/C]CACACTGCTGACCTC | 75725 |
rs229334733 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12015184 | AATTAATTTGAGGTT[C/G]AATCATGATAGTCTG | 75725 |
rs229350335 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12001593 | ACTTTGACTTCTTTC[-/T]TTCCGATTTGTATCT | 75725 |
rs229381856 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036422 | ATACATTCAGAGAGA[G/T]AAATATTTAAGCATG | 75725 |
rs229406273 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11961795 | GAGGAGCTCTTAGCA[C/T]GAGGTCATTTATTAG | 75725 |
rs229463030 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11932947 | CATTTAGAAAATAAG[C/T]AATTATCTTTAGGTC | 75725 |
rs229471852 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043594 | ATTTATTCTACATAT[C/T]AAGACATTTAATTGA | 75725 |
rs229494177 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094990 | AGGCAATAAGGAACC[C/T]GTGAGGAATTTTAAT | 75725 |
rs229499193 | snp | G/T | | | synonymous-codon, nc-transcript-variant | Phf14 | Mm_Celera | 6:11987054 | CAAGGCAGAGCTGGC[G/T]CGATCTACCAGACCA | 75725 |
rs229499649 | in-del | -/CG | | | intron-variant | Phf14 | Mm_Celera | 6:12021389 | TGGTGATCTAAATCA[-/CG]GCTAATTTCTTAGCT | 75725 |
rs229505517 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12044273 | GGGGGGGGGGGCTGT[A/G]GGGGTCGCGACCCAC | 75725 |
rs229506025 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11932055 | TTTGAGTCATTCAAA[A/G]TCTGTTTTCATTTCT | 75725 |
rs229519217 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11944304 | TGAATGGTTCTAGTG[C/T]AGGGTCTTTGAAGCT | 75725 |
rs229522430 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12085778 | TCTAGATCAAAACAC[A/G]GTAGGATTTACTTTC | 75725 |
rs229554876 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11961903 | TGCCTCTTCCTCAGT[A/T]CTGAGATTATATAAA | 75725 |
rs229565088 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11962934 | GGAATAGTAAATGCC[C/T]GAGTCTGGTCAGTCT | 75725 |
rs229567403 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11952238 | CTGAGCTAAACATGT[G/T]AACTGCTGTGATTTG | 75725 |
rs229575767 | snp | A/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12099898 | TACTTTCTCATAGCA[A/G]TAGTCACAAAGGACA | 75725 |
rs229583676 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036873 | AACATCATATTTTAT[C/T]CATTATTTGTCTATC | 75725 |
rs229602402 | snp | G/T | | | missense, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11933922 | CTAGCGAAGCAGGTG[G/T]CAAGAAGAAGAGGAG | 75725 |
rs229605887 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12050793 | TGGGGCTGCTAGTAA[C/T]GTATCATTTATGTTT | 75725 |
rs229607211 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11981374 | TGGTTTTCTGTAATG[A/G]TCTGTGGTCTAATCT | 75725 |
rs229646076 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12058559 | GAGATTAAGGTTGAA[A/G]TATATATAGATGAAT | 75725 |
rs229652383 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12017284 | GTATCTTCTTTTCTG[-/A]AAACAGTATATCAGA | 75725 |
rs229653607 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11961696 | TAACTAAAATTCAGG[-/T]TTTTTTGTTTGTTTG | 75725 |
rs229671650 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11994281 | GTTGGGTCTTTCAGA[A/G]GGCAGTCATGATAGA | 75725 |
rs229687074 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11981302 | AGTTGTGTTGCACGT[A/G]CATTACTTGGGGCTC | 75725 |
rs229691212 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12006153 | AAAACCTAAGTGGCA[C/G]CTTGTGTCTTATCTA | 75725 |
rs229700111 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12041843 | TCAAAGATTTGAGTT[C/T]GTAGCAGGTTTCAAG | 75725 |
rs229704188 | snp | A/C | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12007781 | CTAAAAGAAGAAACT[A/C]CTCAAAGTGATCGGG | 75725 |
rs229709158 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12064434 | GAAAGTGGGATTGCA[A/G]GGCTACAGGTTGTGA | 75725 |
rs229709267 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997475 | CAGCAAGTTTACCTG[C/T]CGAGGTTGCCTTTCA | 75725 |
rs229729830 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12059282 | TTTTAAAGACATTTT[A/G]TATTTTTCATGACAT | 75725 |
rs229750769 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053594 | GATAACTATGTAGAA[A/G]TAAATATATTTGCAG | 75725 |
rs229758191 | in-del | -/CCTATCTGTACGTC | | | intron-variant | Phf14 | Mm_Celera | 6:12072434 | TTTAGTCGATGGAGT[-/CCTATCTGTACGTC]CTGTCTGTGCGTCAC | 75725 |
rs229764593 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11920461 | CTAGGCCTAGATATG[A/C]TTCTACAGAGGCTAG | 75725 |
rs229766814 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11998134 | TGCCTAAGAGTGATT[A/G]CTGATAGTCATGTGA | 75725 |
rs229783501 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11920952 | GATGTAGATTGTACA[A/G]ACTTACAGTATATGG | 75725 |
rs229790250 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12086195 | TTGGAAATAAAACAT[C/T]CTTTTATTAGTCTGT | 75725 |
rs229801033 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11914674 | ATGAGAAACTATATT[A/G]AAGGATTGGCCCATT | 75725 |
rs229812807 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12086885 | TTCCACTGGAAGTTG[C/T]TACCTCTGAGGAAGA | 75725 |
rs229827276 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12016168 | TTTAATAGAATTTAA[A/C]GATGACTATAGGTCT | 75725 |
rs229849263 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12005770 | GTTGTTCTTCCTGTG[C/G]TGTTGCAAGTCCCTG | 75725 |
rs229863239 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12058385 | TGCCTCAGTGGTCAG[C/G]CTAAAATGAAGACAG | 75725 |
rs229869068 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12079863 | TGAACTAAAGTCTCA[C/T]CTGATATCTCATTCA | 75725 |
rs229876121 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11954970 | ATTATTTGAAAATAA[A/G]TATATGTATTTATGT | 75725 |
rs229881959 | snp | A/C | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906157 | ATCACATCCCTTGAT[A/C]TTGTCCAAATAAGGG | 75725 |
rs229892048 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12080886 | TAATTAAACAGTAAG[A/G]ATTTTATAATTATAG | 75725 |
rs229948001 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927676 | TCACAGGCTCTGCTG[C/T]TAGACCACACTTGCA | 75725 |
rs229992647 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11953249 | AGAGTTTAAAAAATA[A/C]ACCGTGTTAAATCAT | 75725 |
rs229998735 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12031754 | TGTCAGTTAGCTCCG[A/G]CATTTCTGTTTACTT | 75725 |
rs230018689 | in-del | -/AGA | | | intron-variant | Phf14 | Mm_Celera | 6:12077276 | ACACCACATCTGATG[-/AGA]AGAAGTACGAGGTCA | 75725 |
rs230019787 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11918608 | ACCTGCACCTTATAG[G/T]TTGTTAACCTAAATA | 75725 |
rs230033457 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12070341 | AGGAAGACCACTATT[C/T]TTGGGAAAACTACAA | 75725 |
rs230053501 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12036536 | TTTTTTAAATTTAGA[A/G]ATTCCAAAACAAAAC | 75725 |
rs230068939 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030008 | ATACTCCATTGTGTA[A/T]ATGTACATTATCTTT | 75725 |
rs230073180 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12084461 | ATTCTCTGCATTAAC[A/C]TTTTAGTGTTTTTAT | 75725 |
rs230101887 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11992786 | TTAAAACATCCTGAC[-/A]AAAAACGGCATAAGG | 75725 |
rs230105972 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11995449 | TAGTCTCCCATTCCC[-/T]TTCTCCTCCCCTCCA | 75725 |
rs230107624 | snp | C/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975693 | AGGAGTCTAGCTCTC[C/G/T]CCTGAGTTTCAGTGG | 75725 |
rs230129781 | in-del | -/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011566 | CTATTTTCAAAGATA[-/T]TTTTTTCCTGTTCTA | 75725 |
rs230146506 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12078140 | GACGTATTTCTGTTA[C/T]ATGTTATACACTAAA | 75725 |
rs230148386 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12085405 | TCTGTGTGTTCTATG[C/T]GGGGACTTGTGTTCC | 75725 |
rs230150361 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12065157 | GTCTTGATTACTTAC[C/T]GACTCACTGAAATAG | 75725 |
rs230157059 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11951611 | GCTACATAGCCAAAA[A/G]GTAGAAAAATATACA | 75725 |
rs230164151 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12017686 | GGTGCTGAGCAAGTA[-/T]TGTCGGAAGGCCATC | 75725 |
rs230183236 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12058995 | AAGCTAATTTATGGC[A/T]TACATAATTTTCAGC | 75725 |
rs230186295 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12078798 | ACCTACATGGGGATT[A/G]AGAACCATCTATAGT | 75725 |
rs230195414 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:11955939 | AGCCTAGTTGGTAAC[-/TT]TTTTTTTTATTGATT | 75725 |
rs230215649 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11952640 | TTAGTCTCTTATGTT[C/T]ATTTGTGATTGAACA | 75725 |
rs230228614 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12003393 | GAGATAATGCAGAGC[A/G]AGGCCGTGGGGAAGG | 75725 |
rs230239828 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11934246 | GAAAATATGTAGAGA[G/T]ACATTTTTCTATCTG | 75725 |
rs230253968 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12058153 | CGGATGCCTCAAATT[G/T]GTTATGTAACCAAAG | 75725 |
rs230275162 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949743 | ACTTTTTAAAAATTG[C/T]TATTTTAACTGGAGC | 75725 |
rs230276609 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11960370 | AATACATCACTGCAT[A/G]AAGAGAAGAGGCTAC | 75725 |
rs230282639 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12062013 | TGTATTTGGATTCAA[A/C]CCAAACTTAAAGGAC | 75725 |
rs230282658 | in-del | -/CT | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909133 | GCATGGTTTGTTTTC[-/CT]TCTCTCTCTCTCTCT | 75725 |
rs230321138 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11932810 | GACAGTTTTACAGGG[C/T]TAACATTGTTTTGCT | 75725 |
rs230321435 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11945151 | GAAGTATAGCGATTG[C/T]TTTTCTTATTGGTTT | 75725 |
rs230323444 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11953654 | TGCACTTATCATCCC[A/T]GTTACTGGGAAGAAG | 75725 |
rs230327332 | snp | C/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925771 | GGCAGATGGATGGAA[C/G]TAGAGAATCTGTGAA | 75725 |
rs230363452 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12013716 | AGTCAATGAGTATAA[A/T]TACATTGTACTTATA | 75725 |
rs230375901 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950384 | CTACCTCCAATGATA[G/T]AGCTCCTTCAACAAG | 75725 |
rs230377708 | in-del | -/GTC | | | intron-variant | Phf14 | Mm_Celera | 6:12078501 | GGAGAATTGACCCTA[-/GTC]GTCTGAAAGGACAGT | 75725 |
rs230381332 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12035034 | TGATTTAAAGTCGTC[A/G]ATGGAATTAAAGTTA | 75725 |
rs230429046 | in-del | -/AGAGAG | | | intron-variant | Phf14 | Mm_Celera | 6:12055364 | GAGAGATGGAGGGAC[-/AGAGAG]AGAGAGAGAGATGTC | 75725 |
rs230508609 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12043402 | GTGAAATAAGACTTA[A/G]AACAAGTTTTGAATT | 75725 |
rs230523626 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12005806 | CTTCAGTCCTTCCCC[-/T]AACTCCTCCGTTGTG | 75725 |
rs230527236 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12003025 | TATTGGTCAATCTCT[A/T]GCCCAGCTTGTTCAA | 75725 |
rs230535917 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12084871 | TTCTGTATGTTGCCA[C/T]CTGCTCTACTGTTGC | 75725 |
rs230538581 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12003538 | TAGGTGCAATTCTTT[A/T]CTATTTTACATTCTT | 75725 |
rs230542537 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11926602 | AACTTTTCCCACCAA[G/T]CTCAGTGTGGAGAAG | 75725 |
rs230544344 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12093680 | TACTCTCTGCAACTT[C/G]ACAACCTGAACTATA | 75725 |
rs230548512 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12062254 | CTTGGCAAGTTTTCC[C/T]ATGGGGTATGGGTTA | 75725 |
rs230580229 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12004096 | CGTAATGGTGCCATT[C/T]TCTCTGCACTGTTTT | 75725 |
rs230581487 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12063019 | CTTGAAAGGAAAAAT[A/C]AAAATTCAAACTCCT | 75725 |
rs230587326 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11995745 | TGGGTACCAATCTGG[G/T]CTGGTATATCAAGTT | 75725 |
rs230631363 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11931847 | TAGAATAGTACCTTA[G/T]AGGCGTAAAATGTGA | 75725 |
rs230636141 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11930686 | ATAATTGACACTATT[C/T]ATTTTCCTTCTTTCT | 75725 |
rs230639151 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924260 | TAGTTGAGGCATTGT[C/T]TCCCCCAGTATATGG | 75725 |
rs230643625 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12060999 | AGGTTCTGTGGTTTG[A/C]TTTCATGTATGTTGT | 75725 |
rs230661943 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057358 | TGTACATGTGTAGAA[A/G]CCAGAGACAGCCTCA | 75725 |
rs230674400 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11945851 | GTAGTTAAAATTCTC[A/T]AAAGCAGATGTAGAG | 75725 |
rs230683489 | snp | C/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925531 | CTCAGTGCTTGATCA[C/G]TATTTGAGAAAATAC | 75725 |
rs230686946 | snp | G/T | | | nc-transcript-variant, intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099777 | CCCTGATCCTTTTCT[G/T]ATGGTTTCTCTCCTG | 75725 |
rs230712720 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12092101 | AGCTGACTTTCTCAG[A/G]GTGGTGCATCCGGTG | 75725 |
rs230722139 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12023811 | ACCTTTGTAAGGTTT[-/G]TTGTTGTTGTTGTTG | 75725 |
rs230742690 | snp | C/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11925914 | CTGTATCCGGGTCGC[C/T]GTTCTCCCTATTGTC | 75725 |
rs230742743 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918204 | TTGTCCTGAGTTTGA[A/G]TTTAGCTTAGACTAC | 75725 |
rs230747278 | in-del | -/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:12018394 | ATCTCAAATGCCACT[-/C]CCCCCCCCCTTTCCT | 75725 |
rs230755604 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11981133 | AGTTGTGGTCATTGT[G/T]GTTTAGGTCTTATTT | 75725 |
rs230772179 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11923802 | ATAAGATTTGCCATA[C/T]TTGTATTATGTTCTT | 75725 |
rs230777125 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010706 | TATCTAGTAGGTGTG[C/T]TTTAAAAGTTTAAAA | 75725 |
rs230782115 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12085252 | TAAATTTCCCTTCAG[-/A]AAAAAAAATCTGATG | 75725 |
rs230782956 | snp | G/T | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099189 | ACAGGAGTTTAAACT[G/T]GGCAGGAACCTAGAG | 75725 |
rs230821783 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12034806 | ATCAGACATGCAGTG[C/T]CTGAGTGCACCATCG | 75725 |
rs230834137 | snp | A/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011498 | ATTGAGTTTTTCTCT[A/T]TGAGATTTGATTGGA | 75725 |
rs230840145 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11931256 | TAAAGTTTACCAGGT[A/G]TTACAACGTTGAGTT | 75725 |
rs230842072 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12001230 | TTAGAACATCAGACA[A/G]TCTGTACATCAACCC | 75725 |
rs230852127 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11930450 | TTAATTCTGTAACTG[-/A]AAAAAAAATTCCTTA | 75725 |
rs230863565 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12056116 | CTTCTTTTGTGAGGC[C/T]GTTCATCTTGGTATT | 75725 |
rs230893048 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12091365 | CTGAGGTGTGCACAG[A/G]TCTTGTGCATGCTTT | 75725 |
rs230894087 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12001823 | CCAGGACTTTTATTA[G/T]GAAGGAGTGTTGAAC | 75725 |
rs230919066 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11923980 | GTTTGTGCTTGGGAG[A/G]TGCTGATGATTACGT | 75725 |
rs230920317 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11980367 | TTTTAGGTTAAGTGT[A/T]TATAGGTTAAATGCA | 75725 |
rs230928239 | snp | A/G | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12040928 | AGCCCTTCTACAGTG[A/G]TTACTATTAGAACAG | 75725 |
rs230940873 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924494 | CTTGCTTTTGGACTG[C/T]TTCGTGCTCCTCCCA | 75725 |
rs230948653 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12090861 | TGTTGGTTTTCAGGG[G/T]CTTTAGACACATTTC | 75725 |
rs230977293 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12034393 | GACAGTTCACAGAAG[A/G]AAGAAATAAAAATGG | 75725 |
rs230993648 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12091525 | AGTCTCTAGGCCTTG[A/G]GAGGAGGAGGAACTG | 75725 |
rs230997514 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11959438 | CTGAGAGCCACTGCA[A/G]GAGAAGGATGGGAAC | 75725 |
rs231014762 | snp | A/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12039828 | CTGCAAGTCTGTATC[A/T]CCTCACTTACTGCGA | 75725 |
rs231042541 | in-del | -/TTGTTTGTTTGTTTGTTTGTTTGT | | | intron-variant | Phf14 | Mm_Celera | 6:12087103 | ATTCCCTGATTTATC[-/TTGTTTGTTTGTTTGTTTGTTTGT]TTGTTTGTTTGTTTA | 75725 |
rs231046306 | snp | C/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909198 | ACTTTTGCTAAGTAC[C/G]TACTCTGTACCATAT | 75725 |
rs231057376 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11978958 | AACAGCCATATCAGG[C/T]TCCTTTCAGCAAGCA | 75725 |
rs231059151 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12034549 | TGATGGAGATGTGAG[A/G]GGAAGGGAACTATGA | 75725 |
rs231080717 | in-del | -/TA | | | intron-variant | Phf14 | Mm_Celera | 6:12085613 | ATAACTATGTGACTG[-/TA]TCACTAATCACTTTA | 75725 |
rs231116101 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11958391 | ATATTGAAAGTTTGA[A/G]AACTCCATCTTTGTG | 75725 |
rs231122840 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11946494 | TTGGCATTTGGAAGC[-/T]TTTTAAAAGAAGCTC | 75725 |
rs231124522 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029894 | CCACATATAAGTGAA[C/T]ACATACCATATTCTG | 75725 |
rs231135143 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083281 | ATTCCATCACCCCTC[C/T]CCCTACCTCTGTGAG | 75725 |
rs231142409 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959681 | CTAAGTTGCAGATAA[C/T]CTGTGATGTTCTTTA | 75725 |
rs231186310 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083767 | ATGGATCCCCAGGTG[A/G]GGCAGTCTCTGGACG | 75725 |
rs231210874 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12038617 | CTAGTAGTTAAATTT[A/T]AAAAATGAACATTTT | 75725 |
rs231218107 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11943034 | ACTATAAAATAAGAG[G/T]AGAGAAAATGGGTAC | 75725 |
rs231223005 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12020514 | TATTCCTGTGTCAAG[C/T]TGACATAAAGCTAGC | 75725 |
rs231230101 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11978080 | TATTTCCTTCTGCTT[C/T]AGTTTTACGTTCTCT | 75725 |
rs231236989 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12068925 | CTGCCTGAATTTTTT[A/T]AAATACTTCATGCCA | 75725 |
rs231271603 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12061443 | TTTTGAGAAAGATAT[C/T]TCTAAAACAAAGTTT | 75725 |
rs231276790 | snp | A/C | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908539 | TATGTTCAGGACTTT[A/C]AGAAGTTCACCAATA | 75725 |
rs231281318 | snp | A/G | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12012180 | TTTATACTTATGACC[A/G]CATAGTAACTTTATG | 75725 |
rs231296558 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12070522 | TTTTATTTCATTTTA[C/T]CCCAGCTGTTCTTTT | 75725 |
rs231298158 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12051922 | TTTCACAACTTGTTG[A/T]ACCTTAAGGTTATAT | 75725 |
rs231331119 | in-del | -/GGGG | | | intron-variant | Phf14 | GRCm38.p3 | 6:12044254 | ATAGGCAAGTCCTGT[-/GGGG]GGGGGGGGGGGCTGT | 75725 |
rs231356003 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032581 | TAGAGACACTTTTTT[A/T]AAAATTTATTAGATA | 75725 |
rs231360237 | in-del | -/AAATA | | | intron-variant | Phf14 | Mm_Celera | 6:12071974 | TAAATTTTTTGACAT[-/AAATA]AAATATCTTCTTTAT | 75725 |
rs231362879 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11957566 | TCCACTTAGACTTGA[C/G]CTTTGTACAGTTCAC | 75725 |
rs231374578 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052342 | AGCAGCGGTTGAGAT[G/T]TAGAATTGATGACCT | 75725 |
rs231377887 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11943949 | TCCTAAAACAAGGAA[A/C]ACTACCATTGGACTT | 75725 |
rs231383929 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11994163 | TACAGGGCCGCCCTC[C/T]TCCTCAGCTTCTTCC | 75725 |
rs231406912 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12043757 | CAGTCGGTTCTCCAG[A/G]TGCTCATGTTTCTAG | 75725 |
rs231409773 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036809 | GTTTAGTATTAGAAC[C/T]CAAATACATAGTTTT | 75725 |
rs231451963 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12048632 | TTGGCAGTTCCTTAG[-/T]TTTTTTTAACTTTCA | 75725 |
rs231472980 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11934973 | CAAAGTAGTAACTGT[C/G]TATTTTAATTAAGCT | 75725 |
rs231477685 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036821 | AACCCAAATACATAG[-/T]TTTTTTTTATTTTAT | 75725 |
rs231481247 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12068368 | AAGGTGGCAGTCCCT[A/C]TTTAATCAGGTCATT | 75725 |
rs231485916 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12084108 | AGAGAGATCCTCCTG[C/T]GTCTGGAGTGTTGAC | 75725 |
rs231494068 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11936153 | GTTGAGAAACCTGTA[A/G]GTCTACTCTAGAGTA | 75725 |
rs231520203 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12077287 | GATGAGAAGAAGTAC[A/G]AGGTCAGTTGGAATC | 75725 |
rs231520936 | snp | C/T | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099410 | TCTTAGGAAGAGATT[C/T]TTCTCAGTTGAGACT | 75725 |
rs231535402 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11993934 | TTTACACACACACAC[A/C]CCCAACCCCTACTCC | 75725 |
rs231554701 | snp | C/T | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100019 | TTAACTTCGATGGTG[C/T]GTCTGTTTTGGGGAG | 75725 |
rs231592627 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11994424 | CTATTTTTGTCTTTG[C/T]AGTTCTTTCCTACAG | 75725 |
rs231598086 | in-del | -/CTTA | | | intron-variant | Phf14 | Mm_Celera | 6:11962516 | TATTAGAAAGCCTGG[-/CTTA]CTTGCAGTTATTTGC | 75725 |
rs231607356 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11950817 | TAGGTCTTCATGCTT[A/G]CTCAGCATGGGCTTA | 75725 |
rs231619845 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11995787 | AAGTGCAAACTCTCC[G/T]GCTGAGACCTGACAA | 75725 |
rs231640813 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11996526 | AATCCTTTTAAATTA[C/T]ATTTTATTAAGGATT | 75725 |
rs231649464 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11931013 | ACTAAGATGTTACAT[C/T]CTGTGACTAAAACGT | 75725 |
rs231691416 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12012639 | CCCTTCAATTTGTTA[-/T]TTTTTTTTTTGAAAC | 75725 |
rs231714013 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11987845 | CTCACTGCGTGCATT[C/T]TTACACCAGGCACAG | 75725 |
rs231731534 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11917369 | CCCCTTTACTTTGAG[A/C]CCTTCCCCAAACTAG | 75725 |
rs231740063 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12083072 | AGCAGTTTCAAAATC[A/C]CTGAGACATTTTTTT | 75725 |
rs231765665 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12034162 | ATTCACTCCGAATTA[A/C]GGCAACAACTCCCAA | 75725 |
rs231779270 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029262 | TACATGTGTTGACTT[C/T]TTGAGAAACCTATAA | 75725 |
rs231800075 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959303 | AAAAATTATTTTCAT[G/T]GCTACTTTATAACTT | 75725 |
rs231805598 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11934869 | AAATTTGCTTCACCA[-/T]TTTTTTTTTTACATA | 75725 |
rs231808227 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083652 | GCCTCTGTATTTGTC[A/G]GGCTCTGGCAGAGCC | 75725 |
rs231814450 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947083 | CTATGTCTTGGTTAC[-/T]TTTCGATTGCTATTA | 75725 |
rs231838950 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12049186 | AGACACATGTCCTTT[A/C]AAGTGGCTTCTTTTC | 75725 |
rs231844770 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11949231 | GTTTTCATTTATGCA[A/G]AAATACTTATTGATT | 75725 |
rs231847743 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916967 | AACAGCCCTCTATGG[C/T]ACACTTGTCCCCTTT | 75725 |
rs231877044 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12007820 | GCATGGATGGAAAGC[A/G]AAAGGTGCTCATTTA | 75725 |
rs231895187 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12024897 | GCATTTTGAACATTT[-/C]TTTAGGTGCTTCTCA | 75725 |
rs231912886 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076338 | AACCACTGTAAAATT[A/T]CCAGAACCAGAAAGG | 75725 |
rs231925855 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12074316 | AAAGCAGATTGCTTT[C/T]ACTGTCTTTTGTTTG | 75725 |
rs231937833 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12056803 | ACGAGTGTTTGAGTA[G/T]TTACTTTGTCTTTGT | 75725 |
rs231960770 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12075500 | CTTTCATCTCTGAGA[A/G]GCCAATCCTCCTCCT | 75725 |
rs231967697 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061900 | ATAACCTTACATGTG[A/G]CCCCATGAAAGAACA | 75725 |
rs231987610 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11948977 | AGGAGGGTAAGAAAG[C/T]GTGTGATGCTCATGG | 75725 |
rs231997549 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905762 | GCAAACAAACAACAA[-/C]AACAAAAAAAACCTC | 75725 |
rs232017511 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917564 | CAAAAAATACAGAAT[C/T]ACTCCAACGTCTACA | 75725 |
rs232040337 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12075794 | ATGAAAGTAAAAGCC[A/G]CTGACTTCACTCCTT | 75725 |
rs232041875 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947559 | ATGTTTGCTTGTTGA[A/T]TTATTGATTGATTAT | 75725 |
rs232074734 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060015 | ATTGGCATGGTTATT[A/T]TGTTTGTTTTGTTTG | 75725 |
rs232090779 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11940784 | TACTAAGGCTTTTAT[C/T]GTTTATATTGATAGT | 75725 |
rs232098148 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11929185 | TAGCTTAGATAAATA[G/T]TTTATTTGATTTGTG | 75725 |
rs232098605 | in-del | -/AAG | | | intron-variant | Phf14 | Mm_Celera | 6:11998729 | GAGGAAAAAAAAAAA[-/AAG]GAAAGAAAAATTCTG | 75725 |
rs232104527 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11917987 | AGGCAGCAAAGTGCC[A/G]GCCACACAGGCAGAA | 75725 |
rs232104626 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11910203 | AGTAGATTATATCAT[G/T]TACAAATTCCTCATG | 75725 |
rs232118384 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11910831 | AACAGCATGTCAATG[C/T]CTGTATACAGTCCTC | 75725 |
rs232122503 | snp | C/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009049 | CTGTCTTCACACACA[C/G]CAGAAGAGGGCATCA | 75725 |
rs232147372 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11941634 | TCTTATTCAAAGGAA[C/G]TTTAAATTGTTTCCC | 75725 |
rs232191453 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11958521 | AGACTGTCTTTGGTG[A/C]TATTATACTCTGAAA | 75725 |
rs232197270 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12024571 | GTTGGGTCTTTCGGA[A/G]GGCAGTCATGCTAGG | 75725 |
rs232197320 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032376 | TCATATTTTGTATAT[G/T]AATCTAAAATTATCC | 75725 |
rs232206093 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12025433 | AGAAATGAGCATTTT[C/G]TTCTGACTTTTCATG | 75725 |
rs232213707 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12033428 | GTTTTTGCCGTGTTC[A/C]CCATCACAGTCCTTG | 75725 |
rs232228419 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12027394 | ACTTGGCTAGCCCTT[C/T]TCTCACCTTGGCCAT | 75725 |
rs232258286 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055153 | AGACAGGTAAAGAAT[C/T]TGAATAAAACAGGTT | 75725 |
rs232259713 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11923639 | AAGAGTTTCCTCCTC[A/G]TTGCATTCGGTGATT | 75725 |
rs232275023 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12088842 | GGGCCTCTCCTCCCA[C/T]TGATGACCAACTAGG | 75725 |
rs232282028 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12042539 | GGTTTTCTGAAATTA[-/T]TTTTTAACTATTCAA | 75725 |
rs232283727 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12000532 | ACCTAAAGCTCTCAC[A/T]CAATCAGCTCTTCTG | 75725 |
rs232311278 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12069939 | GTGTCCATGCGGTGT[A/T]GATCACCCATTCTTA | 75725 |
rs232311394 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12077576 | TAGAAAGAAATGCTG[G/T]GCCGCAGCCTCCTTC | 75725 |
rs232319906 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11916904 | GATAACCATGAACAT[C/G]TGTGCCAGGTTTCAG | 75725 |
rs232320912 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11948781 | ATCTTGTGGAATGTT[A/G]CTTACCACTTTTAGT | 75725 |
rs232324910 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060074 | CGTCACACCCTAAGC[A/T]CTATAAACTGAGTGT | 75725 |
rs232351679 | in-del | -/GG | | | intron-variant | Phf14 | Mm_Celera | 6:12061658 | CAAACATTGAACTGA[-/GG]GTTTTTTTTTTTTTA | 75725 |
rs232420522 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12033103 | AGCAAGCACTTCTTG[G/T]CATCCATAATAGTGT | 75725 |
rs232442434 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11920291 | ACAGAGACAAGTTAA[A/G]CAGAACAATTTAGTC | 75725 |
rs232443350 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054944 | AGACACACACACACA[C/T]ACACATACTCAGGAT | 75725 |
rs232450081 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11992817 | TTGAAGAGTTAATAT[A/T]TGCTTACAGTTCAGG | 75725 |
rs232497929 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11922725 | GGCAAAAACTTTTTA[A/G]ATATCACAACTTGAA | 75725 |
rs232545663 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12055964 | TAAAGACCTTAAACT[A/G]TAATTATACTGATAT | 75725 |
rs232545930 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12086588 | ACAGAGCTAAAGATG[A/G]GGAGATTTTATAGAT | 75725 |
rs232555573 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11909539 | GAAAACTAGACGAAA[A/T]GAAGAAATTACCAAG | 75725 |
rs232563725 | snp | G/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12041022 | TTGGTAAAACACCCA[G/T]GTTACATGTTGTCAC | 75725 |
rs232567041 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037236 | GCACAAAGGAGTATT[A/T]CTTCCAAGTATCTTT | 75725 |
rs232567249 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11910088 | CTAGCTGCATTTTAA[G/T]TAGGGCTGGAGACAA | 75725 |
rs232579499 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12075651 | GTAACTATTCCTTCT[C/G]TGATTAGTCAAAGAC | 75725 |
rs232598156 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11993657 | TTGATACAATGCTTA[C/G]CACACAAGCATGATG | 75725 |
rs232611029 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11954598 | CTGATGGCAGAATCA[C/T]ACTCACTGTAAATGA | 75725 |
rs232616759 | snp | G/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924340 | AAGAGCCTCTATGCT[G/T]GTAGATTTCTGTTGT | 75725 |
rs232620797 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12004130 | GTGGAGAGAATCTTC[-/T]TCCTTTTAGGCCTAG | 75725 |
rs232626883 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12031550 | TTGAAATCCAGGATT[A/C]ATCTGCTTTTGTCTG | 75725 |
rs232630125 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12027503 | CAGGGAAAGTTAAGT[C/T]TAATCCCCTCCTATT | 75725 |
rs232645569 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12078460 | AACTGGCGTTCCAGA[-/T]GGTTGTGAGCCTCCA | 75725 |
rs232693417 | snp | C/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12069226 | ATTGCATCAAAAATG[C/G/T]ACATTAATTCGGTTA | 75725 |
rs232709746 | in-del | -/AG | | | intron-variant | Phf14 | Mm_Celera | 6:11941972 | AGTTTGCTGTGTAGT[-/AG]AGAGGATGACCTAGG | 75725 |
rs232719962 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11941764 | TATGTGGAGTGTGTG[C/T]GCGCGCGTGCACACA | 75725 |
rs232726243 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12069886 | TCTTACTAGCACACT[C/G]GTTCCTTCCTGGAAT | 75725 |
rs232726554 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12061662 | ACATTGAACTGAGTT[G/T]TTTTTTTTTTAAGTT | 75725 |
rs232746439 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12020739 | AAAATCCAAGTCTTT[A/T]AAAAATTCAGTGTCT | 75725 |
rs232760241 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009919 | CAGTACTTCCATTTT[C/T]CCATCTTTTATTATG | 75725 |
rs232782716 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11940399 | TGTCTGTGTTTAGTG[A/G]CTGATTATGGGATGG | 75725 |
rs232784317 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060226 | ACTTCAGAGAAGACT[A/G]TTCCCTTAAGAAATG | 75725 |
rs232810543 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054797 | TTGTTGTTATTTGGG[G/T]ATTTTTGTTTGGTTG | 75725 |
rs232816848 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076093 | TTTGGTGTTTTGTTT[G/T]GTTTTGCTTTGCTTT | 75725 |
rs232820872 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11932144 | TTAGGTGATTTAGAT[A/G]TACTAATTAATTTTT | 75725 |
rs232827548 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12054652 | TGCAGGTCAGGGACT[A/G]GCCATTGGTGCTGGG | 75725 |
rs232831732 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11999918 | TGCTTAGCACAGGAG[G/T]GGTCCCCTAGACAGT | 75725 |
rs232858213 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11999995 | ATGATGATATTCTTA[C/T]CCATACTTCCAAGCT | 75725 |
rs232887977 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11946759 | TCTGTGATAGGTTCT[C/T]AAGTAGTGTAGCCTA | 75725 |
rs232897334 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11955915 | CTTAAGGGAGCCATT[C/T]GTGGAGACAGCCTAG | 75725 |
rs232910132 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12018362 | CTTTGAATGCTTTTT[A/T]AAATTTATTTATTTA | 75725 |
rs232910532 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12026762 | ACCCTCAATCAGTCC[C/T]TCTAGGTGAGTGACA | 75725 |
rs232919478 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11922408 | TCTGCAGTCCCATTT[C/T]CAAGAGACTCTGAGA | 75725 |
rs232921964 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12019020 | GGCAAATTTGGGGTT[A/G]AAAGTATTGTGGATG | 75725 |
rs232941875 | snp | A/G | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099136 | GACAGGGTTTGTTAG[A/G]CTTGTGGGCCCATAG | 75725 |
rs232959426 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12049983 | TGCTGAAAGAGAAAT[A/C]ATTTTCATGTAAAAT | 75725 |
rs232988720 | in-del | -/TG | | | intron-variant | Phf14 | Mm_Celera | 6:11944096 | GTAGGGAGATGTAAC[-/TG]TAGCTGATAGGGCTA | 75725 |
rs233004545 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12050335 | GTACAGAAAGAATCT[C/G]TGATGGAATGTAGAT | 75725 |
rs233006874 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023832 | GTTGTTGTTGTTTTT[A/T]TTTTTTTTATTTTTT | 75725 |
rs233010374 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917167 | AACTTTATTTGACAT[G/T]GATTCAGAATGGAAA | 75725 |
rs233010815 | in-del | -/GTGGGG | | | intron-variant | Phf14 | GRCm38.p3 | 6:12044252 | TCATAGGCAAGTCCT[-/GTGGGG]GGGGGGGGGGGCTGT | 75725 |
rs233011208 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12042482 | AAAAATTCAGAAGAA[C/T]TCTGCAACAGATTAC | 75725 |
rs233012729 | in-del | -/ATA | | | intron-variant | Phf14 | Mm_Celera | 6:12044855 | TGATGTGCTATTGGT[-/ATA]ATAATGTTTTTCTTA | 75725 |
rs233038859 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947194 | TCATGGTGTGAGCAT[A/G]GCAGCAGGCAAGCAA | 75725 |
rs233058929 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12090061 | AACTTCTTCAGGACG[C/T]TCAGACCTCAGGACA | 75725 |
rs233068120 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11909913 | AAAATAATCTTATTA[C/G]CCTAGTTCCTAGACA | 75725 |
rs233085624 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11980232 | CCCAATTGGTGATCA[G/T]TAGGACCCATGAAAA | 75725 |
rs233089497 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12048515 | TTCGTTCCAGTGTTC[C/T]GTCTCAGTAATGCCC | 75725 |
rs233106653 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12082396 | CTCATGCATACACAT[A/G]CACTCATGCACGCAC | 75725 |
rs233166587 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12049233 | ACACTGTACTGCAGA[G/T]TGAAGTGTGCTGGCT | 75725 |
rs233185380 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11928148 | AGTGGGTCCGACTAC[A/G]CTAAAAGTGGATTGA | 75725 |
rs233201993 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040559 | TAAAGTTAAACATGT[A/G]TGAAATAATGTATAA | 75725 |
rs233202182 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12014688 | GAGACTTATCTGAAA[A/T]CATCTAATAACTAGG | 75725 |
rs233203356 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11920744 | TTAAATAAATGTAAG[C/T]TAATAAAGAGAACAC | 75725 |
rs233224209 | in-del | -/AC | | | intron-variant | Phf14 | Mm_Celera | 6:12065103 | TTCACCCACACACAT[-/AC]ACACACACACACACA | 75725 |
rs233234201 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12080770 | TCTGGTTCCCCTACG[A/G]CAGAGAGCACTGTTC | 75725 |
rs233256186 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032347 | AGTAGTTGTGAGTCA[C/T]GATTTTTACTTATTC | 75725 |
rs233262516 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11999415 | AAAGCTGATATTAAC[A/G]AAGAAAAGAAGGGGA | 75725 |
rs233281464 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12000021 | AAGCTGTGCTTATTA[C/T]GTAAGACATTAAGTG | 75725 |
rs233292089 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12096322 | GATTATTTAGGATTT[A/T]GATGATGTCTTAGGG | 75725 |
rs233314047 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12073383 | TGCATACCAGGCTGG[C/T]CTTGAACTCACAGAG | 75725 |
rs233330893 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11989883 | AAGTAGTTAAGATTA[G/T]CACTCTGTTTTCTTT | 75725 |
rs233344253 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947163 | TTCATAGTTTCAGAG[A/G]GTGACTCCATGACCA | 75725 |
rs233350886 | snp | A/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908396 | TAGCATTAGCCCAGT[A/T]CAGGCTTCAGGTGGC | 75725 |
rs233357233 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12087324 | TCTTCAGTAACCCTA[A/C]CTTCTTGTTGAAGTT | 75725 |
rs233358405 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12025311 | CTACATATAGACAGC[A/C]AGTACAATTCTAAAA | 75725 |
rs233369752 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12096993 | GCTTGCCTTGAGCTA[C/T]AGACGCTCTGCAACA | 75725 |
rs233388358 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11990968 | AACACATAGTTTTCC[A/C]AACTGTGGTTGATTC | 75725 |
rs233390722 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037516 | TTCCCACTCACTGTG[C/T]TCCTGTCACGTTTTT | 75725 |
rs233395542 | in-del | -/AAAAA | | | intron-variant | Phf14 | GRCm38.p3 | 6:12063551 | ATAATTCATTGCTTG[-/AAAAA]AAAAAAAAAAAAAAC | 75725 |
rs233448299 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032167 | TGTCATTTTGTTGTT[G/T]CTGTTGTTATTTTTG | 75725 |
rs233485293 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11976954 | AAGCATAGGCCTAGG[A/T]GGATTATCAAAACCA | 75725 |
rs233506441 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11980442 | TATTTTTTAGGTTTT[A/G]TGTCTATATAAATTG | 75725 |
rs233525841 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11953554 | ACACATTCTTCCCAT[A/C]TTCTTGACATAGAGG | 75725 |
rs233543056 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11974385 | TGTGTTTCCTGTAAG[C/T]AACAAAATGTTGGTC | 75725 |
rs233545455 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11955587 | AAGTAAAAAATAGTA[A/G]GTACTTTGATATATA | 75725 |
rs233548315 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030822 | CTTTCTTGGGAGACT[G/T]TTAGTGGCTGCTTCT | 75725 |
rs233555108 | snp | C/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925509 | ACTACCCATGATGGG[C/G]TAGGCCCTCAGTGCT | 75725 |
rs233559634 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023841 | GTTTTTATTTTTTTT[A/T]TTTTTTGTTTTTTTT | 75725 |
rs233574435 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11976102 | ACGCAAGATGGCTCC[C/T]TCACCTGCTCTGGCA | 75725 |
rs233577046 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12025676 | TATTTTGTATAGCAT[G/T]TTTGCTTCTGAAAGT | 75725 |
rs233593978 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959595 | GACCCTTTCATTTTT[A/T]TTGTAGCAAATGTTA | 75725 |
rs233612232 | in-del | -/GATGTAAA | | | intron-variant | Phf14 | Mm_Celera | 6:11944786 | GGAGCATTGATAGCT[-/GATGTAAA]GAATTAAAGGACATT | 75725 |
rs233632265 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11936395 | CACAATACCTAGAGG[A/G]GTGCTTCTAAAACAT | 75725 |
rs233633732 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11913375 | ACAATAAAGAAATAG[C/G]TTCTTTTGAAAAATA | 75725 |
rs233635844 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12044546 | TCTACATCTTCCTGA[A/G]TCAACGTAGAGTGCT | 75725 |
rs233640208 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11914267 | CTGGTTTCGTATGGG[C/T]GTTAGAGATTGACTC | 75725 |
rs233640424 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11945743 | AATCATGAGCTAGCC[G/T]TTCATGTTGTACATT | 75725 |
rs233645480 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905859 | ACAACTTGGGGAGGC[A/G]AGATTGAGATGAGCT | 75725 |
rs233695451 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:11930597 | TTATTTTTATATGTT[-/G]AAAAAATTTCATTGT | 75725 |
rs233696801 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906458 | CTGGAAGTAACGAGA[A/T]ATACTTCCCTGGTAG | 75725 |
rs233707610 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055255 | GAAGCAAGCTGGGAG[A/T]GTGAGGCCAACCTGG | 75725 |
rs233709279 | in-del | -/TGTGAATATC | | | intron-variant | Phf14 | GRCm38.p3 | 6:12044202 | GGTTATGAATTGTAA[-/TGTGAATATC]TGTGAATATCTGTGT | 75725 |
rs233709750 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11945030 | GAAATTTGGATGTGA[-/T]TTCTGTCTCCAGAAG | 75725 |
rs233724462 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079226 | CTTGACAAATGTGGT[A/G]CTACCTAACAAAATG | 75725 |
rs233742519 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12021025 | GTCATCTCAGGGTAC[G/T]GGGATCTCCAGAGTA | 75725 |
rs233759729 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072430 | CTTGTTTAGTCGATG[A/G]AGTCCTATCTGTACG | 75725 |
rs233768657 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12053537 | ATCAGAATAGGAAAT[C/T]CTGTTCTAGTATATT | 75725 |
rs233795473 | in-del | -/TCACCTA | | | intron-variant | Phf14 | Mm_Celera | 6:11917017 | ACTCTGGCAGGCAAC[-/TCACCTA]TCATTCATGTTTCAA | 75725 |
rs233795890 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12098653 | ACTCCCTGTATTTCT[A/G]TTCTGTGGTTTGACT | 75725 |
rs233798778 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11997971 | GAACTATTTGGGAAC[A/G]ATTAAGAGGTGTGGT | 75725 |
rs233813304 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12077764 | ATCAAGCTGCAATGA[-/T]TTTTTTTTAAGGTAA | 75725 |
rs233816320 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12049069 | GTGTTCTTAAAACGT[A/T]TTTCTTAGGCCTTCC | 75725 |
rs233816555 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11992628 | GTAATGACTCAAACT[A/G]TAGAGTTTGTTGTGT | 75725 |
rs233827108 | in-del | -/GACAGACA | | | intron-variant | Phf14 | Mm_Celera | 6:11926379 | GGGTGGGTCCTGCAG[-/GACAGACA]GACAGACAGACAGAC | 75725 |
rs233829193 | in-del | -/GA | | | intron-variant | Phf14 | Mm_Celera | 6:11915353 | GCATCCTTCCAAAAC[-/GA]TGTCTTCTGAACAGG | 75725 |
rs233833863 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12072756 | AAACTATCAGAACTA[A/C]AAAAATACATGACAT | 75725 |
rs233864331 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11989703 | ATATTGCAAAGAAGC[A/G]CACTGGTATTTTTTT | 75725 |
rs233873869 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12031309 | TCTCTCTCTCTCTCT[C/T]TCTCTCCTCCCCCAT | 75725 |
rs233879258 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11920845 | TCAGCTCTCTCAAAC[G/T]ATGAGGCCCTAGTAA | 75725 |
rs233884604 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11937304 | TGAAGAAGTGTGTGT[A/G]CTTGGGATGTCTGAC | 75725 |
rs233884757 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11946578 | CCCTGCAGTCTTCAA[A/T]TTACCTTGACCACTT | 75725 |
rs233904324 | in-del | -/GATGGATA | | | intron-variant | Phf14 | Mm_Celera | 6:11929631 | ATTGAGAAATAGATG[-/GATGGATA]GATAGATAGATAGAT | 75725 |
rs233910640 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916956 | ACGTCCTTAGGAACA[G/T]CCCTCTATGGTACAC | 75725 |
rs233928083 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909318 | TCCATGAACAACATT[C/T]AGCTTCTAGGGATTT | 75725 |
rs233938877 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11938220 | AATTTCTATTTTTGT[A/G]TAAAGCTTCATTAAT | 75725 |
rs233955510 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921668 | AAGAAGGGTCATCCT[C/T]CTTATAAATGCCAGA | 75725 |
rs233962838 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12097096 | TCATTGCTGTGAAGA[A/G]ACTCCAGGACCAAGA | 75725 |
rs233978626 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11939158 | GTTACCACTGGGATG[A/G]TGAATTATAGTGCTC | 75725 |
rs233994769 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12004359 | ACCTGTCCCTTTCTC[A/G]TCGTGCATTCCCTCA | 75725 |
rs233995072 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12087868 | AGTGGTCTTGAACTG[C/T]AATTCTAAGTCTAAA | 75725 |
rs234034954 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11922998 | ATATTTATTTATTAT[-/A]ATTTAAATATACATA | 75725 |
rs234043401 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11977279 | GATGCATGATTTGGA[A/G]ACTGCTTCTCCTTAT | 75725 |
rs234049330 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11996160 | GATGAAGCCTCTCAT[A/G]TGATAGTTACGCTAG | 75725 |
rs234084374 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12088996 | ACAACTCATACAAAG[A/G]ACACTCTCTCTTACA | 75725 |
rs234100493 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11978485 | GTTTTCTTTTTATTG[G/T]ATATTTTCTTTATTT | 75725 |
rs234100626 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11957053 | ACATCTTCCACAGCA[A/T]CTGCTGTCACCTGAA | 75725 |
rs234106958 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12081948 | CTCACAGGTACAGCC[A/C]CATGCCTGTGTGGTT | 75725 |
rs234110006 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12046456 | TTTTTGGATCAGTGG[A/T]ATAATATATGGCATT | 75725 |
rs234122131 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11919071 | TGTTGTTATGCCACG[G/T]ACTGTTTTGATTATT | 75725 |
rs234133368 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11939652 | TGAGAAGTAGAGACG[G/T]GAGGACTAGAAGTTC | 75725 |
rs234135991 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11912910 | AAATGAATTGGGATA[C/T]CTTTTACCATTTCAC | 75725 |
rs234140192 | in-del | -/CTTATAA | | | intron-variant | Phf14 | Mm_Celera | 6:11951806 | AGATATGAATTTATG[-/CTTATAA]CTTTTTAAAATTTAA | 75725 |
rs234160760 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921359 | GAAGTAATTTTATAG[C/T]ATTCTTAGAAAGCTA | 75725 |
rs234176200 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11915499 | CAGAGAAACCCTGTC[C/T]AAAACAAACATAAAC | 75725 |
rs234201046 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11990623 | TCTCCTTGCTTAGCT[A/G]CAATTATTTCATTTC | 75725 |
rs234206242 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11930501 | TTTGAGAGATCCTGA[A/T]ATACTGTGTGCTTTG | 75725 |
rs234210205 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11931027 | TTCTGTGACTAAAAC[A/G]TTGGGCTAGTATTTG | 75725 |
rs234210778 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11957739 | CCATTGATCTACCTG[A/T]CTGTCACTGTACCAG | 75725 |
rs234232777 | snp | A/C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12098316 | ACAGTGGCTTCTATG[A/C/T]GTGCAGAGCACCTGT | 75725 |
rs234266691 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12099005 | AGTCAACTAAGCATG[A/T]TGAACTATCTACTAA | 75725 |
rs234267035 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12079019 | CAAGATTGCTGGAAA[C/T]ATGTCTGCTGAATAA | 75725 |
rs234279784 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927415 | AGAGAGGGAACATTA[C/G]AGGTTTTCTTTGTGC | 75725 |
rs234301495 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11992345 | CAAGAGCTTTCTGTG[A/C]TGTGTTTATAATTTT | 75725 |
rs234311045 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11992862 | GCTGAGAAGTCAACA[C/T]AGAAGAATCCTTATC | 75725 |
rs234314355 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12042325 | TCACATTTGTTAACT[A/T]ACTTACTTTCCTGTT | 75725 |
rs234331183 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11993368 | GGGAATATGGGCAGT[-/A]AAAAAAAACTATGAA | 75725 |
rs234338923 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037268 | AACTGGCAACTATAG[G/T]AATTATCCAATTAGA | 75725 |
rs234344086 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12081728 | GTTCCTATGGTAAAC[A/G/T]CCATAAGTAAAAGCA | 75725 |
rs234360416 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12090596 | TCAGCCTCCAGAGTA[C/T]TGTTGAACTGAACTA | 75725 |
rs234380550 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11979563 | ATAGAGAATGGAAGC[C/T]CTGATAAGATCACTT | 75725 |
rs234384899 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12073968 | TCTGAATTGAGATTA[G/T]TTAGGAATTTTTAAA | 75725 |
rs234390533 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11952633 | GGGGCCTTTAGTCTC[-/T]TATGTTTATTTGTGA | 75725 |
rs234391279 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906504 | TCTTCGGGAACTACT[G/T]AAAAGTGGCCCTTAA | 75725 |
rs234395197 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12095272 | TGCTGTCTCATACTG[C/G]GGTTGTGGAGGGGGA | 75725 |
rs234396841 | snp | A/C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12091462 | TCACCTTGTATTCAC[A/C/T]CACCGTGTACTTGAG | 75725 |
rs234411438 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12026690 | CTTCCCAAGGCAAAA[A/G]CAAGAGGTTTATTTT | 75725 |
rs234434132 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053659 | TAATAATTCAAAACC[C/G]CAAGAATATTTAAAA | 75725 |
rs234435635 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906880 | TCGAGCTATACTGGA[C/T]GAAAGTGACAGGTCA | 75725 |
rs234462629 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947663 | AATCCTCTGCTTCCT[C/T]TCCTGAGATGTGGGA | 75725 |
rs234476830 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11928333 | TTCAAAGAAGGAAAA[A/C]AAGGAAAGGGAAAGG | 75725 |
rs234506725 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12019255 | TGGTGTCCCACCCAG[-/T]TTTTTTCATTTCTGC | 75725 |
rs234527643 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12054100 | TCAGTTTGTTATACA[A/G]CAAATGTCCTTAAGA | 75725 |
rs234527748 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12046156 | CTTTATAACATTTCC[A/G]TGAAGGATTAGTGAC | 75725 |
rs234534153 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11939331 | TGAGGACCTTTAGTG[C/T]TTTATGGAGTCTTAC | 75725 |
rs234542660 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12037090 | TCTCAACAAAACCAA[A/C]AAAACAAAACAAAAC | 75725 |
rs234562450 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12046733 | AAGAAATTTTGACTA[A/G]AAATATAGATAATTG | 75725 |
rs234572946 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079487 | TAACACACTTCTTAC[A/G]GTATCACACTCGCCA | 75725 |
rs234575911 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12065708 | TCTGCTCCAGCCCTC[A/C]GAAAGAAGTAGGTGG | 75725 |
rs234585492 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11971935 | TTTTATTGTTGAGAA[G/T]AGTTTTAATATCCTA | 75725 |
rs234596386 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12031406 | TGTCCCAATAATTTG[A/G]ATATGCTGTATATTC | 75725 |
rs234621431 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12059659 | CAGACAGTGCCCAGT[C/G]TATATGGCAAGGTAG | 75725 |
rs234645011 | snp | A/C | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907143 | TTACCTTTCTCCCTG[A/C]TCTCTGCCACCTTCT | 75725 |
rs234646540 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11915646 | TGTTTTTGGTAAGTA[G/T]CAGTAGACACTCTTT | 75725 |
rs234647182 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12087531 | TAAAATAGTAGAAAT[A/G]CAAATAGTCAAAAAG | 75725 |
rs234658084 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | Ndufa4, Phf14 | Mm_Celera | 6:11907797 | TTAGCGGCGCCTCCC[C/G]GCCAGGGCCGCGCGT | 75725 |
rs234669182 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12037763 | GCAACCAAGCACAGC[A/C]GATACTTAGTAGTAA | 75725 |
rs234678391 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12024265 | CACCTGACCTCTAAA[C/G]TCCCAGAGGCCTCCA | 75725 |
rs234678625 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12072580 | GTATAGGAGACATTT[G/T]GAAATACCTGATTCA | 75725 |
rs234679025 | in-del | -/AAAAAAAACAAGACAA | | | intron-variant | Phf14 | Mm_Celera | 6:12037087 | TGTCTCAACAAAACC[-/AAAAAAAACAAGACAA]AACAAAACAAAACAA | 75725 |
rs234686223 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12072904 | CGAGAAGGAGTGGCC[C/T]TGAGTATTATTTAAC | 75725 |
rs234691040 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11954492 | AGAACTGAACACGTG[A/G]CTCTTCTATAGTAAT | 75725 |
rs234706168 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12073608 | CCATCAGTTGCCATG[A/G]TGCTTATGAGGTTTT | 75725 |
rs234714550 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060059 | GCCATTTCCTATCAT[C/T]GTCACACCCTAAGCA | 75725 |
rs234729519 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11928458 | TACCGTTTAAAAGAT[A/C]GGAATCAATGAAACA | 75725 |
rs234744854 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12043039 | ACGAGTTTCAGGCAC[A/G]GAAATGTCTAATCCA | 75725 |
rs234746213 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11960199 | GACTTACATTGGTGT[C/T]CTCGTAAATAACTGA | 75725 |
rs234779597 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11946367 | GCCACCACCACCACC[A/G]GCTTTTGAGACAGGA | 75725 |
rs234784243 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985987 | AGTGTTGTGTGGATG[C/T]GCTATACATCCAACT | 75725 |
rs234793112 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11921146 | CAGAGGAGACCAAGT[A/C]AAGAGAGAAGCAGAG | 75725 |
rs234794762 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11929281 | TTAGTAATCTTATTA[A/T]TAATATAAACTTGGG | 75725 |
rs234836202 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12014907 | CTGGGGCTGGTTACA[C/T]TGCACCTGTGGTTAG | 75725 |
rs234836742 | in-del | -/ATG | | | intron-variant | Phf14 | Mm_Celera | 6:12021101 | TCCTGTGCTCTGGTT[-/ATG]GTGATAAGCCTTGGC | 75725 |
rs234849771 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11961286 | AGTGAATCTTAAGTG[A/G]AAAGCAATTATGGTT | 75725 |
rs234852859 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12015458 | CACAAAGAATCACTT[A/C]TCTGACTTCCCCAGC | 75725 |
rs234879496 | in-del | -/CA | | | intron-variant | Phf14 | Mm_Celera | 6:12054943 | AGACACACACACACA[-/CA]TACACATACTCAGGA | 75725 |
rs234883527 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12042786 | TACTTAGGATGTAAT[A/G]AAATTGAATGTTCAT | 75725 |
rs234889945 | snp | G/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:11988838 | TTTCTTTTCAGTTGC[G/T]TGCTTCAATTCTTGC | 75725 |
rs234918166 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12005052 | ATAAATTATAGTTAC[C/T]TGCCTACCCCCTCCC | 75725 |
rs234961781 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12023416 | TTACTACCCAACTTC[A/G]TTTGTTATTTTAAGT | 75725 |
rs234970855 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12071652 | CTGAGAAGTACATTA[C/T]ATCAATAGAATCATT | 75725 |
rs234974749 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053896 | CCAACCTGGGGTTGT[A/G]CCACTAAACAATCAA | 75725 |
rs234980307 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11998823 | AGGAGCTGCAGGCTC[A/G]AGGCTCGGGGCTGAC | 75725 |
rs235003947 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12063761 | TTTAACACAGGAGTA[C/T]GATTACCTAATGACC | 75725 |
rs235013478 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12015770 | AATATTCTTAACCTA[A/T]GTTTTTCTCATTTTG | 75725 |
rs235019046 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11944396 | CCAAACTTAGCTATG[C/T]TAGTCCTCAACTGTT | 75725 |
rs235041483 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12006061 | CCACTCTCATTTTGA[A/T]ATAAATGTTTTCTTG | 75725 |
rs235047353 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12057296 | CTGTAGGTGCTTGTG[A/T]ATGTAAAAGGTTTTT | 75725 |
rs235061016 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043810 | GTTCCAGAGACAGTT[C/T]CCTTATTCATCATTG | 75725 |
rs235075561 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024505 | CAGGAGTCAGCTGCT[C/T]CTGTCCATTGGTTGA | 75725 |
rs235089909 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12003408 | GAGGCCGTGGGGAAG[G/T]TCTGCTTACTGGCTT | 75725 |
rs235098092 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12044737 | TTTATTAAATATTTT[A/G]AATATACTTCTTCAG | 75725 |
rs235099484 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12057372 | AGCCAGAGACAGCCT[-/C]AGATGTCCATTCCTG | 75725 |
rs235136629 | in-del | -/TTAT | | | intron-variant | Phf14 | Mm_Celera | 6:12068535 | TGAGTCTTGACAATT[-/TTAT]ATATATATATATATA | 75725 |
rs235164602 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12041492 | GAGAGGCCATATATC[-/A]AAAAAATGTGGTGGA | 75725 |
rs235185396 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12036977 | AAGCCTTTAATCCCA[A/G]CACATGGATGGCAGA | 75725 |
rs235188881 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12076660 | GCTAAGTATACTTTA[C/G]GGGTAATGTTGATCT | 75725 |
rs235206134 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11935301 | GCGTATTTATGGATA[C/T]TTGTTAATATTTAGA | 75725 |
rs235215237 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12069931 | TGTCTACTGTGTCCA[C/T]GCGGTGTAGATCACC | 75725 |
rs235223678 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925475 | TTATAGAATCAAAGA[A/G]TACTAGCCCAGGGAT | 75725 |
rs235236359 | snp | A/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100114 | TACTTCTGTGAGGAC[A/G]GATGGACTCTGGACT | 75725 |
rs235237060 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12021860 | GGGCAAGAATTCAAA[C/T]GGCATAAATCTGGAA | 75725 |
rs235274987 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11942800 | CTTACTAACTTCTGT[A/G]CAACTATACAAACAC | 75725 |
rs235276242 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12092698 | AAGTAGGTTTCCTAA[A/G]TCTTTCCCAAAGGTC | 75725 |
rs235287545 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917494 | ACTCCTGCACCTTTA[G/T]GCTTTATGCTGCTCA | 75725 |
rs235288458 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12038193 | GTAATTCCAAAATCC[A/G]TTTCAGTTTTCTGTT | 75725 |
rs235309494 | in-del | -/CACACACA | | | intron-variant | Phf14 | Mm_Celera | 6:11922942 | CTCATCACTCACACT[-/CACACACA]CACACACACACACAC | 75725 |
rs235313169 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11985158 | CAGGTTTCTAGTACC[A/G]GACATGAGTTTCCTC | 75725 |
rs235341218 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12013915 | GTTCTTCTGCCTTAG[A/G]AAAAGTGCATCACTG | 75725 |
rs235346613 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12093799 | TTTTTACTTGGAGTT[G/T]TCTCTATGTCTACAG | 75725 |
rs235356362 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11993772 | TGTAGATTTTTATTT[-/A]TTTTTCTGAGCTTTT | 75725 |
rs235359028 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12038961 | AGCCCTTCTCTCATA[A/G]AATAGATCTATTTTG | 75725 |
rs235361804 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11960416 | AAAGTTGCTGCTGGT[C/G]GAGATGCTATCTTTA | 75725 |
rs235363339 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11985941 | ATTTTGTAGTGCTGG[A/G]GTCAAATCCAGGTCT | 75725 |
rs235373807 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032549 | GTGTGTGAGTGTGTA[G/T]TTGTATTACTAGAAT | 75725 |
rs235378788 | in-del | -/TGTTGTACTGACTAGTGA | | | intron-variant | Phf14 | Mm_Celera | 6:11945905 | AGTACTGACTAGGTT[-/TGTTGTACTGACTAGTGA]TGTTGGTGTTGTGAT | 75725 |
rs235379296 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052541 | CAACAATAGGTATCA[A/T]TACACAATAAACAAA | 75725 |
rs235419569 | in-del | -/GGG | | | intron-variant | Phf14 | Mm_Celera | 6:12043722 | TCAAGACTAATTGAA[-/GGG]AAAGCCAGAAGAGCC | 75725 |
rs235427648 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11919987 | ACATCTGTCATACAG[C/T]AGTTTTCTTTTCACT | 75725 |
rs235427829 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12033052 | TGTCAGGTTCTGTCA[C/G]AGTCTCTCAGGAGAC | 75725 |
rs235435080 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12051853 | GTTTACTCTAGTTTA[C/T]TAAATGTATAATTTA | 75725 |
rs235454089 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11961272 | TAAGACCAAAGTGCA[C/G]TGAATCTTAAGTGGA | 75725 |
rs235472821 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12067978 | ATCATTTGAGCTATA[C/G]ACACAAACATAAACA | 75725 |
rs235475217 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11916900 | GCTTGATAACCATGA[A/C]CATGTGTGCCAGGTT | 75725 |
rs235486254 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11940605 | ACTCCCAGGTTCATG[C/T]TATCCTTCGGCCTAC | 75725 |
rs235500164 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12020215 | ACTTAAACAGGAAAG[A/G]TTTTATTTCACTCAC | 75725 |
rs235529137 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11923399 | AACTTTTTGTGTATG[A/G]GTATAAATATAAATT | 75725 |
rs235548977 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12060661 | CACTCGGCCATATCT[A/G/T]TGTGGGCCACAGATG | 75725 |
rs235569088 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12085015 | TTTAAACAAGTTTTC[C/G]GTGCGCCAGCAAGAT | 75725 |
rs235581067 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11909784 | CATGACAGGAGGACC[-/T]TTTGCTGAAAATTTT | 75725 |
rs235609646 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11996926 | GTATTTGAGTATGTC[C/T]GTATTCATGTATGAA | 75725 |
rs235622379 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11975123 | TCTCATTGTGTACTA[A/G]ATTTCCTGGATGTTT | 75725 |
rs235623869 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11954028 | CTGGAGGGTCCCCTC[A/G]ATCTCCTGTCTCCTG | 75725 |
rs235637207 | snp | C/G | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099362 | ATTAATCACTAATTA[C/G]GAAGATGCCCTACAG | 75725 |
rs235639261 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11996843 | TTGCTTTTTATAATA[C/T]AGCCATGGTAGTCAT | 75725 |
rs235649871 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11996063 | AGCTCCAGTAATCCT[A/G]TCCCCCACTAGTTTC | 75725 |
rs235658833 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036374 | CCATATTTATGTGCA[C/T]ACACATATACATACA | 75725 |
rs235682884 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11954663 | CTCAATATTAAAGCA[C/G]GGATGTGAGGCTGCG | 75725 |
rs235683369 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12081839 | CTTGACTAGCTCATA[C/G]TGACCTAGCTTTCTT | 75725 |
rs235700674 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12041115 | AATATCCTAAATGAA[A/G]TACAACATTAACTTT | 75725 |
rs235707329 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11993852 | ATTTTATCCCCCTCT[C/T]GGGCCACCCTCTGAT | 75725 |
rs235733827 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12030766 | TGTTTCTATTTTATG[A/G]AATAATTTGAGGAGT | 75725 |
rs235740381 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12017684 | TAGGTGCTGAGCAAG[-/A]TATGTCGGAAGGCCA | 75725 |
rs235764289 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023313 | AAATTTTTAAAGGTT[G/T]TTGATAGTTCCTGTA | 75725 |
rs235771238 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031204 | CTTGCTGTTTATTCC[C/T]CTTGGGTGTGCTTCA | 75725 |
rs235785876 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11980599 | CCTTTTTGATTTTGT[C/T]TCAAGTCTTCCTGCC | 75725 |
rs235806639 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12017463 | TTTCTAAGAACTCCT[A/G]GAAGAATTAGATTAC | 75725 |
rs235807434 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11937172 | AATTTTAAGTAGGAA[A/G]ATATTAACCCTTTCT | 75725 |
rs235820913 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11989966 | TTTAGTGGCAAGTGG[A/G]GGAAATACTGCTTTG | 75725 |
rs235830850 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910111 | GGAGACAATAGTGCT[A/G]ACAATTTAGAAAAGC | 75725 |
rs235840768 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12016733 | TAATAATATTTAAAA[A/G]TGTGTACTTCTTTTT | 75725 |
rs235858562 | in-del | -/GTTTGTTTGTTT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12043970 | AACCAGTGTTTTGGG[-/GTTTGTTTGTTT]GTTTGTTTGTTTGTT | 75725 |
rs235861353 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024206 | ATCTCATACCTCCTC[C/T]CTACCCTACCCCATC | 75725 |
rs235880384 | in-del | -/GAAGGTCT | | | intron-variant | Phf14 | Mm_Celera | 6:12003404 | GAGCGAGGCCGTGGG[-/GAAGGTCT]GCTTACTGGCTTGCT | 75725 |
rs235885154 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008461 | AATTACCCAAGTTTT[C/T]ATGCTGCTGACCCTC | 75725 |
rs235891397 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927863 | CATCAGCCAGGTACT[C/G]CTGGCACATGCCTTT | 75725 |
rs235917522 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083989 | GAAGGAGGCAGAGGC[A/G]GGAGGATCACCCCGA | 75725 |
rs235920747 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12063121 | ATATTTAAATAGCAG[A/C]AATGTCAAGGGTCAA | 75725 |
rs235928232 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066116 | TCTCTCTCTCTCTCT[C/T]TCTTTCTTTTTCTCA | 75725 |
rs235931199 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12014796 | CCTGAGAAAAGCAGT[C/T]TGAGAAAGGAATGAT | 75725 |
rs235936610 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12056232 | TATCCTCTCAAAGAC[-/A]AAAGGGCCAGGTGTT | 75725 |
rs235954074 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12038616 | CTAGTAGTTAAATTT[-/A]AAAAAATGAACATTT | 75725 |
rs235976182 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950218 | TCATGCCCATTAGGC[C/T]AGAAAGCATGGTAGC | 75725 |
rs235980149 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11960478 | TAGATTAAAATGTTC[C/T]ATCACGAAAATTTCA | 75725 |
rs236012668 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12057458 | GCAAACTAGGCTACT[C/T]GAATCAAGCTGCGTT | 75725 |
rs236014173 | snp | C/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11926157 | CCACCCCCGGGGTCG[C/T]CCCTGCTCGGTCGGC | 75725 |
rs236032703 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950561 | ATTTTCCTCTATTAG[G/T]CTTTAGTTCTGGGTC | 75725 |
rs236038011 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12096203 | CTTTTACTTCATAGT[A/G]TTGCGTATGAGTTTC | 75725 |
rs236057565 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12046071 | CATTTAGCCTGATGA[C/T]CCTAATGTAAAAAAT | 75725 |
rs236104605 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12037296 | AGATTTTGGTCCCAG[A/C]CTCTGCCCTCTACAT | 75725 |
rs236106560 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11918754 | AATTCAAAGTGTACC[A/G/T]TGGATATATGAGAAA | 75725 |
rs236107079 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11989821 | TTCATGAAGTTTAAT[A/G]TATTTCTGAGAACTA | 75725 |
rs236139302 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11936267 | TTACAGAGAAATGAT[A/G]TACATCGTCTATAGG | 75725 |
rs236150330 | in-del | -/TG | | | intron-variant | Phf14 | Mm_Celera | 6:11909882 | AGTCTAGAAATTTGC[-/TG]TTTTGTTGATTTTTA | 75725 |
rs236153060 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12070103 | TGTACTGTTTCATGT[-/C]ACCATGAGGAAATGA | 75725 |
rs236160722 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12003275 | AGACACTGTGACCAC[A/G]GCCAGGTTAGGAAGG | 75725 |
rs236185644 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094372 | GAAACAAACTGACAA[G/T]AGATAAAGGCAAAGT | 75725 |
rs236188950 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975492 | CAGGTCTAGCTTTTC[A/G]GGTGTGTTGGGGTGC | 75725 |
rs236206760 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927367 | AGTGATGTGAAGAGG[G/T]GGTGAACTTGTATGT | 75725 |
rs236221607 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927762 | CGTCCCATCAGGCAG[C/T]CTGAGAGTTTGGAAC | 75725 |
rs236226778 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12004081 | CTTGCTGCTGAGAGC[C/T]GTAATGGTGCCATTC | 75725 |
rs236232927 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094509 | AGCTTCCGGTTTTGT[C/T]AAGGACTTTGCATTT | 75725 |
rs236234972 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12041894 | AAGGACATTACTTTG[-/A]AAAAAATTCATACAC | 75725 |
rs236238874 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906977 | TCCCTTGCACTTCTG[A/T]AGGTTTGGTGGTGCA | 75725 |
rs236243162 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11932073 | TGTTTTCATTTCTTA[C/T]ATGAGCTAACTAACA | 75725 |
rs236256386 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11937824 | ACATAAAATATGTTT[A/T]AGAGTGCAGGGAGAT | 75725 |
rs236265355 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12053035 | TCTAAACCCAGACAC[-/TT]TGTGTGAATCTGTAA | 75725 |
rs236270089 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12095245 | GGTATTAAGTCCACT[A/C]GTGTGTGTTTCTGCT | 75725 |
rs236295212 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924714 | CATGAGAACTTAGTC[C/T]ACCTTCTTTTTAGGT | 75725 |
rs236321733 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12002055 | TAAAAACACACCTCA[A/G]CATTCAAATAGACTC | 75725 |
rs236335796 | in-del | -/AT | | | intron-variant | Phf14 | Mm_Celera | 6:11990852 | TATGCTATAAGTAAC[-/AT]AAAAATCATATGCAC | 75725 |
rs236346410 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12086034 | TGTTAAGTACCACAG[C/T]GCTGAGGCAGCCTGA | 75725 |
rs236347930 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12094292 | TAACCCTTGAGCCTG[A/G]CTTTGAAGGCACGTG | 75725 |
rs236375186 | in-del | -/TAAA | | | intron-variant | Phf14 | Mm_Celera | 6:12013318 | AAATAAATAAATAAA[-/TAAA]TAAATAAGTAAAGCT | 75725 |
rs236376179 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11970980 | CAACTTCTCTGTATA[C/T]GACCAGAAGAGGTAT | 75725 |
rs236378592 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12061427 | CTTTGTAATTTATAT[A/C]TTTTGAGAAAGATAT | 75725 |
rs236390860 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043729 | TAATTGAAGGGAAAG[C/T]CAGAAGAGCCAGCAG | 75725 |
rs236413497 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12055892 | CAATCTTTTCATTAG[A/G]ATTAGGCAGGATCAG | 75725 |
rs236415490 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061778 | TAAGAATGCCCACTT[C/G]TCAGTGTACACTCAT | 75725 |
rs236436577 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12092582 | TGGGACCTCATTCAC[A/G]AGCAACTTCTCTTTG | 75725 |
rs236460498 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12041960 | TGTGGACTAATAATG[C/G]GTGTGGGTTTAATGC | 75725 |
rs236468102 | in-del | -/CA | | | intron-variant | Phf14 | Mm_Celera | 6:11980005 | CTCTTTCTCCCCCCC[-/CA]ATTCCAGTCTTCTAG | 75725 |
rs236471112 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083828 | GTCTCCATATTTCCT[C/G]CAGTGAGTATTTTAT | 75725 |
rs236472074 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11987340 | ATGACAGAATGGGAT[A/G]TGCAATTAGTGTTTT | 75725 |
rs236486263 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11962115 | ACTTTAATTTTAAAA[A/T]GGATTTTATTAAGAT | 75725 |
rs236486832 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12042004 | TTCCATTCCTCAAAA[C/G]ATTTGTTTTTAGACA | 75725 |
rs236494629 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11971891 | gtagtacagcttaat[A/G]tcaggcatggtgatt | 75725 |
rs236496831 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12035130 | AAACAGAATTCCTTA[A/G]AGGAATCCTTATACT | 75725 |
rs236509546 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12056553 | TCTACCTAGTATATT[C/T]AGCATGTCTGTTAAT | 75725 |
rs236511578 | in-del | -/TG | | | intron-variant | Phf14 | Mm_Celera | 6:11954847 | AATTTTCCCCAATCT[-/TG]TGTGTTTTGATGATT | 75725 |
rs236515612 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917168 | ACTTTATTTGACATT[G/T]ATTCAGAATGGAAAT | 75725 |
rs236516756 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11913143 | ATGAGTGTGAGGCCA[A/G]ACTAGGCTACAAAAG | 75725 |
rs236517522 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925102 | TTTCATTTTTCTTAA[C/T]AGCTGAATAATATTC | 75725 |
rs236572650 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11950446 | GACTGTGGATCAAGA[A/C]CTCAAATATATGAAG | 75725 |
rs236580832 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12035457 | TTTTAGATGTCCAGG[A/G]AAGCTAAACCTTTAA | 75725 |
rs236587239 | in-del | -/AAACAAACAAAC | | | intron-variant | Phf14 | Mm_Celera | 6:11913170 | AAGAGCATGTCTTCA[-/AAACAAACAAAC]AAACAAACAAACAAA | 75725 |
rs236589556 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905669 | TCCGGCACTAGAGAG[G/T]CCAACCTGATTTACA | 75725 |
rs236608654 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12091873 | GTATTAGTCAGGCCC[A/G]CGGTTTAAATGCACA | 75725 |
rs236612252 | in-del | -/TCTG | | | intron-variant | Phf14 | Mm_Celera | 6:12087489 | ATCACAGTCTGTCCA[-/TCTG]TCTGGTGACTGACAT | 75725 |
rs236619182 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12036057 | TAGGGCTCGAGAGAG[A/G]CCTGTCTGTGAAATG | 75725 |
rs236630358 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12098872 | TCATAAGGAAGATTT[G/T]GTATGTGTGTGTAAA | 75725 |
rs236651748 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083598 | CAACTCCTCCATCTG[C/G]GACCCCATGCTCAGT | 75725 |
rs236663101 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12072394 | ATCAAAATATATTCC[A/C]GACTCTTGCAGAATA | 75725 |
rs236677920 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023922 | AGACCAGGCTGGCCT[C/T]GAACTCAGAAATCCG | 75725 |
rs236690165 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11959878 | ATATATTACTACTTC[A/G]TTGTTGCCTGATTAT | 75725 |
rs236696064 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040340 | CTGCTGAAAATGAAA[C/T]GCACATATACATGTA | 75725 |
rs236719374 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12070591 | ACAGAGTCAATATTA[G/T]GCTGGTCGCGAAAGC | 75725 |
rs236725480 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11911363 | TGTTTTATATTGGCC[-/T]TTTGTTCACATATTT | 75725 |
rs236730611 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11909493 | GCTAGAGTGGGCAAG[A/G]AAAGATGCCCCTGGG | 75725 |
rs236741264 | in-del | -/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12042359 | GCAACAGTGAACTAC[-/T]TTTTAAACACTCAGA | 75725 |
rs236751095 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11999851 | CTAGAGAGTGGATAA[A/G]ATATAGGGGTAAAAG | 75725 |
rs236775606 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12064509 | AGCAACCTTTACTGG[C/T]AACCACTGAGCCATC | 75725 |
rs236777519 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11958796 | AGAGAGAAAAAGCAA[C/T]AAAACATGGACAGTT | 75725 |
rs236799577 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12033841 | AGGAGTAGTATATGC[A/G]ACTCATATGATAGAT | 75725 |
rs236806108 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12063152 | CTGAACAGTTAAGCA[A/G]ATAGGTTTGCTGGCT | 75725 |
rs236810518 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12071435 | ATCCATTGTTTCAAC[A/T]GATTTTAAGCCTCAT | 75725 |
rs236815013 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12000307 | TGGTATCTTGTCATG[A/G]ATAATATGTTTATTT | 75725 |
rs236819115 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925282 | ATTCGTACACAAAAC[A/G]TCATGGCCAAGAAGC | 75725 |
rs236823876 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918875 | GGTCCCAATCTACTC[A/G]AAATCCTCCAACCTC | 75725 |
rs236824154 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12051388 | GTGGGCCTGATGAGA[-/T]TCTGTACCATGCTGT | 75725 |
rs236838643 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12038460 | GCTTCCCCGTGATTG[A/T]TTTCCGTGTGATGTT | 75725 |
rs236854063 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12021058 | GCCTGGCTTGCTACA[A/G]TTGGACTCCACTTTC | 75725 |
rs236871865 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12069449 | TTTTTTCTTTTTTTT[A/T]ATTCGATATTTTCTT | 75725 |
rs236877076 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12039712 | TATTTGGACTGAAAA[C/T]TAAAGAAAGCCAGTG | 75725 |
rs236885685 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11919370 | CTGTTTTTTGAGCTT[C/T]CTGTCACTGTGACTA | 75725 |
rs236900202 | in-del | -/TCCCAT | | | intron-variant | Phf14 | Mm_Celera | 6:12002987 | TAAATGGGTTGATAA[-/TCCCAT]TAAATGGGGATATAT | 75725 |
rs236931024 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12033395 | CTTCCCTCTCCTCGG[A/C]TAAAGTCTGCTGCTC | 75725 |
rs236934913 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12069138 | ATGTAAATAGATATG[C/T]ATATGTGTATATATA | 75725 |
rs236941875 | in-del | -/TTTT | | | intron-variant | Phf14 | Mm_Celera | 6:12019819 | TTTAGGGGCTGAGGC[-/TTTT]TTTTTTTTTCAATTA | 75725 |
rs236950515 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12085569 | AGCCTTCTTCCCAGT[A/G]TCATATGTAACTCTC | 75725 |
rs237013878 | in-del | -/ATAATGGAA | | | intron-variant | Phf14 | Mm_Celera | 6:12046279 | ATCCCAGGATTTAGT[-/ATAATGGAA]ATTTTAGTTACTGAA | 75725 |
rs237023658 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12061583 | AAAAACTGTAGAAAA[A/C]ATTCCAAATATCTTC | 75725 |
rs237041595 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12078976 | CACATTTTTGCTTTC[C/T]TTCTTTATCAGTGTT | 75725 |
rs237071758 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Ndufa4, Phf14 | Mm_Celera | 6:11907731 | CGGCATGCGTATAGA[C/T]CAGGGTCATCCGGCG | 75725 |
rs237078476 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079372 | AACAAAGGCATGGTG[C/G]CTGGAAGAGCTGAGA | 75725 |
rs237081136 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12017519 | CTTTTTTCCCTAAAT[A/G]TCTTAATAGAAGGAC | 75725 |
rs237096991 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12065752 | CCAGGGCTACATAGT[A/G]AGACACTGTCTCAAA | 75725 |
rs237105542 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11953042 | GAGTATATTGAAATG[G/T]GCTATTATAGTACTC | 75725 |
rs237142603 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12035132 | ACAGAATTCCTTAAA[-/G]GAATCCTTATACTTA | 75725 |
rs237157141 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11945518 | GGCAGAAGTAACCAT[C/G]ACTGTGGGTTCACCT | 75725 |
rs237163350 | snp | C/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100168 | ACTGGCAAAGCAACT[C/G]CAGCTCTGCTGCACT | 75725 |
rs237166344 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11954327 | TTTTCTGCTTTATCT[G/T]CCAGTCTTTGGATCT | 75725 |
rs237171842 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11946172 | GCTGCTATTTTCTTA[C/T]TAGTTTTTTTGAGAC | 75725 |
rs237175997 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12014545 | TGATGTACACGGATT[G/T]GTTGTTGACTAGTGC | 75725 |
rs237187938 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11994815 | TACCGAAACAGCTCC[C/T]TTCACAATAGCTACA | 75725 |
rs237190073 | in-del | -/GCT | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924936 | TGTTTCTGAGGCTTA[-/GCT]CTTACTTACTGGAGT | 75725 |
rs237199851 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12051016 | CATTTTCCTAGGAAT[A/T]CTTTATTAAATAATA | 75725 |
rs237221420 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12067711 | GTTTGTTTGTTTTTG[G/T]TTTTGTTTTTTGTTT | 75725 |
rs237227374 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11939530 | GATTTGTTTTACAGC[G/T]GTAGTAATTTTAGAT | 75725 |
rs237243727 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12050668 | CTTCCTATTGATGGG[C/G]CTTTTGATGCTAAGC | 75725 |
rs237257064 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12018840 | TGGGTAGAGCCTCTC[C/T]GAGGACAAGCATGCT | 75725 |
rs237258905 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12035570 | TTTTAAAAATCTAGA[C/T]GCTTATATATGGTTT | 75725 |
rs237283550 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029497 | GCCCCCTATACCCTC[A/T]CCCCACCCTGCTTCC | 75725 |
rs237295295 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11930321 | TAAATTGTACTGATT[A/G]TATTTATTTTTTATC | 75725 |
rs237329769 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12097131 | AGTTCATTGGGGCTG[A/G]TTTTACAGTTTCAGA | 75725 |
rs237332922 | snp | A/C | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010204 | AGGGAAACGCCAGGG[A/C]CAAGAAGTAAGAGTG | 75725 |
rs237343592 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12051252 | AAATACAAAATAGTT[A/G]AAATATTTTAATATA | 75725 |
rs237364344 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12006216 | TAAGTCTTCAGCAGC[-/T]GTGCTATGTGAGCTA | 75725 |
rs237371178 | snp | A/G | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12047226 | TCTGCTGAGTGCTAA[A/G]TATCCTCAGAAGTAC | 75725 |
rs237391223 | snp | C/T | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099060 | TAAGATCTATTTTTG[C/T]CTCTTCCTGTCTTAG | 75725 |
rs237394570 | in-del | -/AG | | | intron-variant | Phf14 | Mm_Celera | 6:12033560 | GATTTGTATCCAATA[-/AG]AGGCAATGGCATTTG | 75725 |
rs237412015 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12049250 | GAAGTGTGCTGGCTA[C/T]TCTTGTTACTTTTCC | 75725 |
rs237420138 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11993020 | TTAACAATAACCATC[A/G]GAGAGGTCTATAATG | 75725 |
rs237438264 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11911221 | GAGTTAGGAATACCG[A/G]CAGATGGAGTTTTAG | 75725 |
rs237447075 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11917046 | TGTTTCAACTTGCCA[A/G]CCAGGGTGGCAGTTA | 75725 |
rs237488631 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11909696 | TTATATTAAAAATCA[A/G]TACAGAAAGTACTCA | 75725 |
rs237514640 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12006425 | GTGGTTACTTAGGGA[-/TT]TTTTTTTTTTTTTTT | 75725 |
rs237516478 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12043070 | TTTCTCATGCTGGGA[A/G]GAGATACTTGACCTT | 75725 |
rs237525691 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917426 | ACTGTTTTCATGGGA[-/T]TTAAAAAAATGTAGG | 75725 |
rs237546772 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12077222 | TCGTGAACCACATTT[A/G]GTCATTAGGTGTTAT | 75725 |
rs237556799 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057153 | TAACCTGAATCCCAT[A/G]AAAAAAAGATTTCTT | 75725 |
rs237561823 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12076062 | TTTAACTATAGAAGT[A/G]CGGGTGTCTTCATAT | 75725 |
rs237586628 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11912123 | GCATGGTGAGAGATC[C/T]TCTGAAAACATTAAA | 75725 |
rs237587888 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12078263 | ATAGACACTTCCTAG[A/T]CCTTAGACTTCCCAG | 75725 |
rs237589138 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12034462 | ATTAGGGGAAAGCAA[C/T]TTAAAACTTCTTTGA | 75725 |
rs237592890 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12057488 | TCCCTGTCTCCATTC[C/T]CTGGCAGGGATTGCA | 75725 |
rs237612241 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11951081 | TAGTAATTCTGTTCA[C/T]TGTCAAAAAAATTGA | 75725 |
rs237618700 | snp | A/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925700 | GAGGAACCTGTACTC[A/T]GATTTCCATAGTAGC | 75725 |
rs237633600 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12001322 | GCAACTATTGCTCTG[A/T]TTTCTTTTTCAAATA | 75725 |
rs237633662 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11992497 | AGAATCTTACTTTCC[A/T]GTCTTATGTTGAAGT | 75725 |
rs237662152 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11949663 | TAGTTTTTAAGGACC[A/C]TCCATATCAACAGTG | 75725 |
rs237676349 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12028242 | TATACTTCACTTCAT[C/G]ATAATGTAGCTTAAA | 75725 |
rs237695428 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11993209 | GCGCCAGATCTCGTT[A/T]CGGATGGTGTGAACT | 75725 |
rs237718604 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12016932 | CCTGTGGCACAGGGA[A/G]TGCCCTGTGTGTGCT | 75725 |
rs237750784 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083260 | TCTCCCCTTCAGAAA[C/T]CCCCTATTCCATCAC | 75725 |
rs237808431 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12013218 | TTTGTGGGTCAGGGC[C/T]AGGAGAATAATTGTT | 75725 |
rs237812577 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12001399 | TCCAAGATATATTAT[C/T]TGAGTCTATTGTGAA | 75725 |
rs237873916 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12020524 | TCAAGCTGACATAAA[A/G]CTAGCACAACTGACT | 75725 |
rs237874345 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12015402 | AAACAGGGTCTATTA[C/T]TGGCCTGGAGTTTGC | 75725 |
rs237886734 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057912 | GAAGGAAACACAGCA[A/G]CATCAGATGGAGTAC | 75725 |
rs237918251 | in-del | -/TCCTCCA | | | intron-variant | Phf14 | Mm_Celera | 6:12065397 | CCTGGTTCTTGGACC[-/TCCTCCA]TCCCCCATCTATTCG | 75725 |
rs237920882 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927345 | TGAGTGCTTGCTTAT[A/T]CCAGTTAGTGATGTG | 75725 |
rs237921322 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12002374 | TTTCTCATCAATAGA[C/T]AGGTCATCCAGACAA | 75725 |
rs237930610 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947849 | ACAGATTTCTATAAG[A/G]ATACCATGTTAGTTC | 75725 |
rs237955343 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12004893 | TTAGGAAAATGCCTA[G/T]TAAAACAACTATAAT | 75725 |
rs237961789 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909340 | AGGGATTTAGTATTG[-/A]AGGGGAAAAAAAAAT | 75725 |
rs237968062 | in-del | -/GT | | | intron-variant | Phf14 | Mm_Celera | 6:12022696 | TTTATATGTGGATTC[-/GT]GTGTGTGTGTGTGTA | 75725 |
rs238027759 | snp | C/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12081459 | ACAGCCTCTCAAATG[C/T]TTTTTTAAAAGAAAG | 75725 |
rs238046910 | in-del | -/TATGAATAGCAAT | | | intron-variant | Phf14 | Mm_Celera | 6:12021513 | CCACATATTCTCAAC[-/TATGAATAGCAAT]ATACCTGTCAGAGTC | 75725 |
rs238048347 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11998050 | ACCTTGGCTTTTATG[G/T]TTTTTTTTCTCTTCA | 75725 |
rs238070155 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11919239 | GACATACTACATATA[G/T]TCCTCTTTATTTTTA | 75725 |
rs238070182 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12073870 | GTTGGAATTCAGTTC[C/T]CCTAAAACTCGCTTT | 75725 |
rs238084814 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947026 | TTCAGTAGTGCTCTG[A/G]TCCCTGTTTACTTAA | 75725 |
rs238102362 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12060966 | TGATAGGAACGTGGC[A/C]CTTACCAATGGCCTT | 75725 |
rs238110274 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921956 | TGATTGATGAAAGGG[C/T]TCATTTGGCTTCTGC | 75725 |
rs238140335 | in-del | -/AT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12093887 | CACACACACACACAC[-/AT]ACACACACACACACA | 75725 |
rs238161255 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11948067 | GAAGGTTAAAGCTTC[A/T]TAATAGCGTTTCACG | 75725 |
rs238171012 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11923925 | TACTGCACCAGCATA[C/T]CTTGGAGGCAGGTTG | 75725 |
rs238191734 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12001071 | AATCGAACTTTTTGA[C/G]TATCCTGCTTTAAGT | 75725 |
rs238197933 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11993110 | atttatttattcatt[C/T]attcattcattcatt | 75725 |
rs238218056 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12089659 | AGAAGATGTCATTAG[A/G]CTCATAATATCACAG | 75725 |
rs238223730 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11923340 | ACTTTTAAAAAACAT[C/T]TCCCTTCACTCTTGA | 75725 |
rs238226786 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11940113 | CTCTCTTCCCAGTGA[G/T]GGCAGACTAGGCCAT | 75725 |
rs238234491 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905977 | GACTGGGGCCCCCAG[-/C]CCAGATGATTAGCCA | 75725 |
rs238236576 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12002836 | CTTTTTAATTAATGT[C/T]CAGATAATAAAGAAA | 75725 |
rs238261436 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11999894 | AACTCCTAGGAAGTA[G/T]TAAGTGCTTGCTTAG | 75725 |
rs238261745 | in-del | -/TAT | | | intron-variant | Phf14 | Mm_Celera | 6:11962342 | ATGATTGTATGTATG[-/TAT]TATGTATGTATGTAT | 75725 |
rs238274195 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12091578 | GATTGAAATGTTGAC[C/T]TATGGGTATCACAGT | 75725 |
rs238280100 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11916979 | TGGTACACTTGTCCC[C/G]TTTCCATTGGTTGGG | 75725 |
rs238309029 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12041193 | CTGTGAAAACATTCT[A/C]AGTAATTTATATCTT | 75725 |
rs238316146 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12082238 | ATTTTCAGTAAGGGG[A/G]CTAGAGAGATGACTC | 75725 |
rs238316576 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12000438 | AATTAGGTAATATTT[A/C]ACCTCAAAGTGGAGA | 75725 |
rs238328885 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12044909 | ATAAAGTGTTGTGTT[-/A]ATATCACAGTACTTT | 75725 |
rs238337279 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925385 | GGAACTCAAGCAGGT[C/T]AGGAACTTGGAGGCT | 75725 |
rs238370523 | in-del | -/TTTTTA | | | upstream-variant-2KB, cds-indel | Ndufa4, Phf14 | Mm_Celera | 6:11907656 | TTTGATAGGTTTATT[-/TTTTTA]TTTTTTGCATAGCAG | 75725 |
rs238379826 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11958372 | TGGTGACTTTTAATT[C/T]CGAATATTGAAAGTT | 75725 |
rs238392977 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12025058 | TAGTGTTAGTGACGA[-/T]TTTTTCCCCCAATCT | 75725 |
rs238394935 | in-del | -/AACC | | | intron-variant | Phf14 | Mm_Celera | 6:11988286 | GTTCCAAAAAAAAAA[-/AACC]CCTACCCATTTAAAG | 75725 |
rs238406793 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11999184 | TATAGCCATGAGACT[A/G]TGTGGGTCTAAGAAT | 75725 |
rs238437924 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11948488 | GTAGTGTCTGATGAC[A/G]GTGCAAGTTTCAACT | 75725 |
rs238441766 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959026 | TTACTTCCTAAATGA[C/T]TTTTTTAACAAAGTA | 75725 |
rs238446384 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12087028 | CTCAGTTCCAATCTA[C/T]AGAGCATTTCCACTC | 75725 |
rs238450100 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11949115 | TGGTCATATGTGTGA[A/G]CATCCTAATTCAATA | 75725 |
rs238463867 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037416 | GTATATGTTAAAAGT[C/T]CCGGTGTGAATTGCT | 75725 |
rs238478435 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921559 | AACACATTCTGTACA[C/T]CTAAAGGTAGTCATA | 75725 |
rs238500796 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12059727 | TGCAAAATGAGTGTC[G/T]TTCTCAGATGTAAGC | 75725 |
rs238504519 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053458 | CTTCAGGCCTTTCTA[C/G]ATAGGTTAGCATTGC | 75725 |
rs238564046 | in-del | -/TTAAG | | | intron-variant | Phf14 | Mm_Celera | 6:11976438 | ATTTGCTTAATACGT[-/TTAAG]TTAAGTTGGGAAGTA | 75725 |
rs238566064 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12084311 | AGAAGTAAATGAACA[A/C]AAGCTGTGTACTTTG | 75725 |
rs238573812 | snp | C/T | | | nc-transcript-variant, synonymous-codon | Gm6578, Phf14 | Mm_Celera | 6:12099823 | TCTCAACGGAAGAGC[C/T]TCGAAAGGACCTCCT | 75725 |
rs238582023 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11960886 | TGCAGACTTTACACA[A/G]TGTAGTTGTATGTGG | 75725 |
rs238590682 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11994155 | GGTCCTCCTACAGGG[C/T]CGCCCTCCTCCTCAG | 75725 |
rs238593394 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11920650 | CATCTCCAGTTATAG[C/G]ATGAAATGCCTTCTT | 75725 |
rs238598895 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029604 | TCATATACATCTAGA[-/T]TTTTAGAAACCTTTT | 75725 |
rs238600540 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12053801 | GTAAAGAAAATTTCA[C/T]AAAGCCATTCACAGT | 75725 |
rs238609222 | snp | A/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100217 | CAGCACCTCTGGAGT[A/G]GTCCTGGACGCACCG | 75725 |
rs238612077 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921192 | TGAAGCCCAGAAACA[C/T]CAAGGGCCACTAGGA | 75725 |
rs238612612 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12081865 | TTCTTACACAACCTG[A/G]CCACAGCTCCCTAGG | 75725 |
rs238656257 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12089348 | AATGCAATGTGGAAT[C/T]CGTGACTTTGATATC | 75725 |
rs238659645 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11957599 | TTTTCTACATGCTAA[C/T]CACCAGTTGAGCCAG | 75725 |
rs238672864 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11915374 | TCTGAACAGGGTGGT[A/G]GTGGCACACATCTTT | 75725 |
rs238684288 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12032901 | CTGGGTAGTCTTGGT[C/G]GATATTGTTGTTCTT | 75725 |
rs238690685 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12039019 | AGAGGAGGCAGCTCA[A/G]TGTTCAAAAAGTAAA | 75725 |
rs238699780 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908752 | GTTGGATGGTTATGG[A/G]TGAATGAGTGAAAAA | 75725 |
rs238734676 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11978540 | CCTGCCCCCTGAAGT[C/T]TCTTATTCCATCCCT | 75725 |
rs238744212 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12080243 | TTTTAGGACTAGTGC[A/C]TATTTCAGTTAATAA | 75725 |
rs238748034 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12036590 | TGGAAATTCATATCT[A/G]ACCATTCATTTAGGA | 75725 |
rs238762883 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12030588 | CTTTATTATGTCTGC[A/G]TATGCTGCTTGTATC | 75725 |
rs238763472 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:11963084 | TTTCTTAAGGCAATA[-/TT]GTAGACTTTGGGTAT | 75725 |
rs238769284 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11985431 | ATGGCTGAAATATAT[A/G]AGACTGTATCTTCAG | 75725 |
rs238776498 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11962320 | CACCTTTCTTCAACA[C/T]AGTAAAATGATTGTA | 75725 |
rs238785013 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11986515 | ACACCTAAATTTATT[A/G]GGTTTTTTTGTTGTT | 75725 |
rs238786969 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11915792 | ATTGTTTACAGTACC[A/G]TACAGTAAGGCAATC | 75725 |
rs238818085 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11958061 | TTTCCAATTTGTATG[C/T]CCTTGACCTCTTTTG | 75725 |
rs238829044 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12022151 | GGCATATCCCATTTG[-/A]AAAAATAGTTATCTC | 75725 |
rs238832085 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11952760 | TATTGAGGCTGCTGG[C/T]CCTCCTACAGGGTCA | 75725 |
rs238850166 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12076736 | ACTTATTATGTAAAG[-/A]AAAAAAAAGGGAATT | 75725 |
rs238878065 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12029583 | AGCAATTTCATTTAG[A/C]TAGACTTCATATACA | 75725 |
rs238884317 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12068267 | AAGTGTAATCTTGAC[A/G]AGACATCTGTAGAAA | 75725 |
rs238898513 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916891 | AGCTTTGAAGCTTGA[A/T]AACCATGAACATGTG | 75725 |
rs238918692 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12020364 | GCTTGCTTGCTTATA[C/G]AACCAAGAACTACCA | 75725 |
rs238928901 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12068634 | AAGATTAAGTAACAG[C/T]ACCCTGTTTACTGCA | 75725 |
rs238951689 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061113 | TCAGCTTAGTATCCA[A/G]GAAAAACTTATGTTA | 75725 |
rs238956159 | snp | C/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011607 | AGCTATAATCCTGGC[C/G]CTATAAACATGGTCA | 75725 |
rs238983102 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12064616 | TGTTTTATTCTAATT[C/T]ATAGCATTTTACTGT | 75725 |
rs238985052 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909201 | TTTGCTAAGTACCTA[C/T]TCTGTACCATATCTT | 75725 |
rs238987423 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11917058 | CCAGCCAGGGTGGCA[A/G]TTACCCATATACTTC | 75725 |
rs239002725 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11931409 | TAGCTTTCTTGATTT[C/T]GGTGTTGCTTGTGTT | 75725 |
rs239009053 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11940831 | TACCAGTTTGCCCTC[A/G]ATATTTCTTGACATA | 75725 |
rs239009127 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11930798 | CATGGAAATAGAAAT[G/T]TTTTTTTCTTTTGCA | 75725 |
rs239024216 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12058620 | TGGTCCCTGTGCGTG[A/G]ACCCTTTTCCTTGTC | 75725 |
rs239042316 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11948847 | TAGCCTAGATAGTCC[-/T]TTCATGCACAGGAGG | 75725 |
rs239067763 | in-del | -/CT | | | intron-variant | Phf14 | Mm_Celera | 6:12080236 | AGTAATGTTTTAGGA[-/CT]AGTGCCTATTTCAGT | 75725 |
rs239068469 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083014 | TGGACTGGGCCAAAG[C/G]AAAGGCTGAGAAAGC | 75725 |
rs239077568 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11931491 | GGAATCTGCTTATTT[C/T]TCAGAAGACCATTAT | 75725 |
rs239099346 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12073477 | CATGTGCATTTTTCG[A/C]ATATGTTCTTATGAG | 75725 |
rs239102107 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927885 | CATGCCTTTAATCCT[A/G]GCAGTGGGGAGGAAC | 75725 |
rs239107311 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12075698 | TAAAGAAAATAGAAA[C/T]CTTTCCAGTCACCAC | 75725 |
rs239107369 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11909799 | CTTTGCTGAAAATTT[C/T]ATTTGGAATGATAAA | 75725 |
rs239153367 | snp | G/T | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099113 | CAATATCACTATAAG[G/T]AACTTAGGACAGGGT | 75725 |
rs239153503 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12018171 | CACTGTGTTCCACAA[C/G]GTCATTTCCATCCAA | 75725 |
rs239173680 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12098097 | GATGTTTCCAATGCT[C/G]CCCTCTTCCTCCAGG | 75725 |
rs239187560 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076095 | TGGTGTTTTGTTTTG[C/T]TTTGCTTTGCTTTGT | 75725 |
rs239188686 | snp | G/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12047997 | CTTTCATCTTGACAG[G/T]TTTTTTTTTAATATT | 75725 |
rs239189074 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12091247 | CACTCTCAAAGAAAT[C/T]GCTCTTCCCTATTCT | 75725 |
rs239189210 | snp | C/T | | | nc-transcript-variant, intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099520 | AATATGCTTCTTCTT[C/T]TTTTACATAAACATG | 75725 |
rs239217528 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11949222 | CACTGTGGTGTTTTC[A/G]TTTATGCAGAAATAC | 75725 |
rs239218005 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11991706 | TATCTAGAACTAGCA[C/G]TTGGTATTGTTAAAA | 75725 |
rs239239056 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11938968 | GAGTTCGAGGCCAGC[A/C]TGGTCTACAAAGTGA | 75725 |
rs239251533 | snp | A/G | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12081381 | ACTGTGTACTCTTGT[A/G]GACCTAAAGGTACCT | 75725 |
rs239257239 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11929434 | GTTTGTAGTTCTTTT[C/T]GGTAGTTCTTTTCCG | 75725 |
rs239269860 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949954 | GTTTGTATTTTGGAC[C/T]TCTGTCAGATAAAAA | 75725 |
rs239283702 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11942083 | ACACCAGTCAAGGAC[A/G]GATCTCACATGGAAG | 75725 |
rs239287273 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009410 | CCTTTATCATGCATG[C/T]ATAGTATTTTATCTC | 75725 |
rs239296395 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11916496 | TCAACCAACCAAACC[A/G]ATAGAACTGCATGTG | 75725 |
rs239298589 | snp | A/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010067 | ATAGGTGGAACAACA[A/T]TATGAACTAACCAGT | 75725 |
rs239335876 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024674 | TGCCCAAGAGTGGTA[A/T]AGCTGGGTTTTCAGG | 75725 |
rs239337655 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12032678 | ATCCACCCTCCCCCT[C/G]CTTCTAAGACTGTGT | 75725 |
rs239360147 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908678 | GGAATGTACTGATTG[A/G]GGAAAAAAAATCACC | 75725 |
rs239399006 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12026169 | TTGCTTTTAATACAG[C/T]TGTGTTCCTAAAACA | 75725 |
rs239408185 | snp | C/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12047259 | GAAACACCAAGTACA[C/T]GGCAGAACTTGACAA | 75725 |
rs239410270 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12098119 | TCCTCCAGGGAAGCA[A/C]CAGGCCCTGGCCTAC | 75725 |
rs239413588 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12075393 | CACACACAGACATAT[C/G]TATGCATGTAAATAT | 75725 |
rs239436974 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12027472 | CAGCTAAAGCAGCAC[A/G]TAGCCCTCCTTGCTG | 75725 |
rs239446198 | snp | G/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12048266 | TAGCACTAAAGAATA[G/T]GTACATAATATTAAG | 75725 |
rs239448412 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:11959516 | GTTGAAATATCCAGT[-/C]CTTTGAAAGCATTTC | 75725 |
rs239472470 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11948883 | TTGCTTCCATTGTGT[C/T]TCCAGATCCTGTGTA | 75725 |
rs239491909 | snp | A/G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12038401 | TTTGCAGCTCTTGCC[A/G/T]TTGCTTCTCGTGTGT | 75725 |
rs239505082 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12033874 | CTTTATCTTTCTGAA[A/C]ATTCTCCACACTGAT | 75725 |
rs239506122 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12068566 | TATACAAATATGAGT[A/G]GATTTTGCTAATAAT | 75725 |
rs239521628 | snp | G/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908342 | AAACGTTTCAAATAA[G/T]AAGGAGAGGGTTTCG | 75725 |
rs239524442 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12039099 | GTGAGGATTTCTCTC[G/T]CTTTGTTATTTGAAT | 75725 |
rs239563983 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031140 | ATTGATTCTTTGTAT[A/T]TTTTAATTGCTTTTA | 75725 |
rs239577977 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12024180 | CCCCATCCACCCTCC[A/G]TCTGCTCCATATCTC | 75725 |
rs239578079 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072458 | ACGTCCTGTCTGTGC[A/G]TCACCAGTAGCAGAG | 75725 |
rs239603242 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11958911 | TTATCGCACGAGTTT[A/T]ACTAGACAGTCCTCT | 75725 |
rs239612892 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054579 | CTGGGATTGAGGGAC[G/T]ATGTGGTCTGATTGT | 75725 |
rs239633788 | snp | G/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | GRCm38.p3 | 6:11908870 | GTATGCAAAACCCAC[G/T]GTATTTCTCGAGAGC | 75725 |
rs239637834 | in-del | -/GTTTGTTT | | | intron-variant | Phf14 | Mm_Celera | 6:12043971 | AACCAGTGTTTTGGG[-/GTTTGTTT]GTTTGTTTGTTTGTT | 75725 |
rs239651083 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055087 | CAAGTTTAATATTCA[C/T]CATGTCTCTTTTGCC | 75725 |
rs239666043 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11946055 | CTGAGGGTAATTTCT[A/G]TTTCTTAGATTAGTC | 75725 |
rs239672937 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095406 | GATTATCACCCAATC[C/T]AGAAGCCTTCTTCAT | 75725 |
rs239676743 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11988361 | TAGCAAAAAGACTGT[G/T]GGGAGTAAAGTCACA | 75725 |
rs239680648 | in-del | -/CTCCGACA | | | intron-variant | Phf14 | Mm_Celera | 6:11927792 | CGTCTTGCTCCTTTT[-/CTCCGACA]CTCTCACCTCTCTTT | 75725 |
rs239687615 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11949090 | TCTTCATATTGTATA[A/G]TTAATTAACTGGTCA | 75725 |
rs239734856 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11989332 | TTACTTGCAGATCTA[G/T]CATTTGTTTTGTCTG | 75725 |
rs239736688 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055690 | CCATGTGTGTTGCGA[C/T]AATAAAAATACTTTG | 75725 |
rs239748982 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11977602 | ATAGAATTGGAACTC[-/T]TTTTTTGTGATATTT | 75725 |
rs239834260 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11998524 | ACTGTGGCCTTGTAA[C/T]TCCCTCTTGGCATGA | 75725 |
rs239841653 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12053737 | TTTCTCTTTGTTTTT[C/T]TGCTTGTTGTTCATT | 75725 |
rs239848814 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024238 | CCACGTGGATGCCCC[C/T]ACCCTCCAACCCACC | 75725 |
rs239857102 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997826 | TTCCCCTTTGATGCT[A/T]TTCTGTGTTACCAAA | 75725 |
rs239857588 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11938902 | GGGCCGGGCAGTGGT[A/G]GTGCACGCCTTTAAT | 75725 |
rs239887606 | in-del | -/TTTA | | | intron-variant | Phf14 | Mm_Celera | 6:12068534 | ATGAGTCTTGACAAT[-/TTTA]TATATATATATATAT | 75725 |
rs239896552 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12056426 | GATGCACAAAAGTTG[C/T]CGGGTGTATAAATCT | 75725 |
rs239901127 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12002264 | AACATCTCTGCCTCA[A/G]ACACAAGGGTATCCA | 75725 |
rs239912215 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12050611 | TGTTTTTAACGTATA[C/T]TTTGGACTTCCTGCT | 75725 |
rs239913532 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024591 | GTCATGCTAGGTCTA[C/T]AGCCTCAGTAGTAGT | 75725 |
rs239921329 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11942737 | GTCTTCCAAAACATA[A/G]TCTAAGCAGTTTGAA | 75725 |
rs239926082 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12079997 | CTTTCTTCATTGTAC[-/T]GATTGTAGAAGAGGG | 75725 |
rs239980895 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11998541 | CCCTCTTGGCATGAC[A/C]GAGCATATTCTGCAC | 75725 |
rs239997156 | snp | G/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924859 | CACTAGCATCTTAAC[G/T]TCACCTTCAGATTCG | 75725 |
rs240010503 | in-del | -/AAGGA | | | intron-variant | Phf14 | GRCm38.p3 | 6:12050266 | GAAAAAGGAAGGAAG[-/AAGGA]AAGGAAAGGAAAGGA | 75725 |
rs240042827 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12058054 | GTTCACTTGGTGACC[C/G]CTCTGCTGTCTCATC | 75725 |
rs240043811 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11990166 | ACGGAATAATAGTAT[C/T]TACTTTTCAACTAGT | 75725 |
rs240055654 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11991182 | AAAATCTAGTTCTTT[G/T]GATTTGTTGAACATT | 75725 |
rs240059530 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12036004 | TTTATTACATTTATC[A/G]ATATTTATATTCTTC | 75725 |
rs240078234 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906124 | TAGAAACAAATAGAC[-/A]AAAGAAGAGTAGCCA | 75725 |
rs240082365 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052373 | GTCTGATATAAGAGA[G/T]GTTTTTATAAAGCAA | 75725 |
rs240103304 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11949591 | GGATTCTGACTTCAT[A/G]TTCTTTGGCTGTGTA | 75725 |
rs240122637 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12070823 | CTCCTACTAGAATGA[C/T]CCACTAACCTCTATT | 75725 |
rs240135329 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010354 | GACCTGTTAAATTGT[A/G]ATATCTCTCTGTGAA | 75725 |
rs240139033 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060625 | TGCCGTGATGCTGGG[C/T]GGCAAGTTCCTAGCA | 75725 |
rs240139651 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032059 | CATTCTGTTAGTCAG[C/T]GTCTTTTGGGAGCAT | 75725 |
rs240147415 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11919319 | TACACTAAAAATAAA[G/T]GCTAATTTTTTGAGG | 75725 |
rs240154283 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12050358 | TGTAGATTTGCTAAG[-/T]TCTACTTGTTTATTT | 75725 |
rs240162503 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12071744 | GAATCTTGCCAACTG[C/T]CCTACATTTGGGAAT | 75725 |
rs240163127 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11996590 | CCAAAACTCAGCAGA[A/T]CTTTTGTAGAGTTTT | 75725 |
rs240186639 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054952 | ACACACATACACATA[C/T]TCAGGATGGATAGGT | 75725 |
rs240206793 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11913511 | GATAAAATGACAATT[G/T]GAGTTATTTTTATGA | 75725 |
rs240207958 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11944313 | CTAGTGTAGGGTCTT[G/T]GAAGCTGCAGATAAA | 75725 |
rs240211153 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12019785 | GCCAAAAAAAACCTA[A/G]GCAACAACAAAGAGC | 75725 |
rs240243837 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11941721 | TAATATATATAAAGT[A/G/T]CTTGAAATTTGTTTT | 75725 |
rs240264199 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11923195 | TAACAATTTCCCTGC[A/T]TTTTGAGCCAAGCCA | 75725 |
rs240282338 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11936552 | CTACACTAAAGATAC[A/G]GAAACAGGCAAGGTG | 75725 |
rs240287475 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916179 | ACACACACATTCTCT[C/T]ACACAAACTTATATC | 75725 |
rs240289805 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12000087 | TGTGTACAGCAGTGG[A/C]TTGAAGGTTTACTGT | 75725 |
rs240313656 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12079320 | CAAGTATTTAATTGG[G/T]CTCATGGTTTCAGAA | 75725 |
rs240326136 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12020420 | GGACTGAAACCTCCC[A/G]CAATCAATCACTTGC | 75725 |
rs240326234 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010935 | AAAGTGAGAGCAAGA[C/T]TGAACTGTAAGCCTC | 75725 |
rs240365316 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12002957 | AGAGTTTTGTGCACA[A/G]GACAGAGACTCAATT | 75725 |
rs240381446 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12050926 | GACCAACAATAACAA[C/T]GGCTATTGTATATTG | 75725 |
rs240390238 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011784 | ATAAACTTCTCATAT[C/T]AAAATTGCTATTTTT | 75725 |
rs240393647 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12094857 | AGTATTTAAAGCACT[A/G]ATACTCTGGCTCTGT | 75725 |
rs240398184 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917781 | ACAGCAACCAAAAGC[C/T]ACAGAGATCACACAT | 75725 |
rs240413426 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918042 | TGAGTAGAGTTACTA[A/G]TAGTGAATTTTGTGT | 75725 |
rs240434163 | in-del | -/A | | | intron-variant | Phf14 | GRCm38.p3 | 6:12028914 | ACCCTTGCACACCAG[-/A]AAAAAAAAAAGTCGG | 75725 |
rs240440995 | in-del | -/TTAG | | | intron-variant | Phf14 | Mm_Celera | 6:11923291 | GTGCCAATCGGATTT[-/TTAG]TTTCAACATGCTCTT | 75725 |
rs240465205 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12049928 | CCTCTGGGATTTTAT[A/G]TGACATACAGGTTGG | 75725 |
rs240477321 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12082639 | ATGCATGAATCTAGT[C/T]GCAGTTTGTATAACC | 75725 |
rs240486252 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12087174 | CAAGTCAAGTGGATC[A/C]GGGACCTCAACATAC | 75725 |
rs240501187 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12050542 | TAGCCCCTTGCTAAA[A/G]GTCTAAACATTTAAT | 75725 |
rs240503490 | snp | A/G | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12040683 | CAAATGACATTACTT[A/G]ACTTATAGCAAAGAT | 75725 |
rs240509419 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11928369 | AATGACTTCTTCCTA[A/G]GGTTGACTAACAGGA | 75725 |
rs240509935 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924940 | TTCTGAGGCTTACTT[-/A]CTTACTGGAGTTACA | 75725 |
rs240523621 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12084431 | ATCCATACTTTTCAT[C/G]CTACTTCACCCGTGA | 75725 |
rs240534492 | in-del | -/TA | | | intron-variant | Phf14 | Mm_Celera | 6:12023831 | TGTTGTTGTTGTTTT[-/TA]TTTTTTTTATTTTTT | 75725 |
rs240546119 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11954510 | CTTCTATAGTAATGT[A/G]TCCTGTCTGTCCTGT | 75725 |
rs240549957 | snp | A/C | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008079 | TGTCAGTCACTAAGA[A/C]TATAACTTCTGTTTG | 75725 |
rs240600197 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921042 | ACATTAGGGTACTTG[G/T]ACTTAAGGTAATAAG | 75725 |
rs240603801 | in-del | -/CTT | | | intron-variant | Phf14 | Mm_Celera | 6:11948921 | AACCCAGTGCACTGA[-/CTT]CTTCTCCCACGTCAC | 75725 |
rs240608695 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11955197 | AATATTTTACTGGGC[A/G]TGATGGTGGACTCTT | 75725 |
rs240614089 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12029926 | TTTCAGCGGGTGATG[A/G]GTCTTTTCTCTAGTT | 75725 |
rs240639923 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12096656 | TACAAACCATCACAG[G/T]TGGTATGAACTTATT | 75725 |
rs240661037 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11990364 | TTCATAAGCTCCAAC[A/G]AACAAAGAATTCTCT | 75725 |
rs240676552 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12097279 | CACACTGGGTGGAGC[G/T]TGAGCACTAAGAGCC | 75725 |
rs240676684 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11929528 | ATCACAAATAAGTCA[A/T]TAGATTGCTATTATT | 75725 |
rs240698938 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11951268 | TAGATGTGTGTCTTG[C/G]TTTGCTGTGTTTCCA | 75725 |
rs240713168 | in-del | -/TTTT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12015550 | CTTTGGTTTGGGTTG[-/TTTT]TTTTTTTTTTATGAA | 75725 |
rs240715659 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11944124 | CTATAAAATAAGGGA[A/G]AGTTTGTCTCTATAA | 75725 |
rs240721423 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11993628 | TGAATTTGGGTATTG[C/T]GGGAAAAGCTCAGTT | 75725 |
rs240721465 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008959 | ATTAATATTTGCTAG[A/G]TTAAAATTGGATATG | 75725 |
rs240760960 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12087817 | ATTTTTTTTAACTGT[A/G]ACCACTAGAAAATTT | 75725 |
rs240763295 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12094178 | GCATATCAAGAAAGC[C/G]AAAGTCGTAATGAAT | 75725 |
rs240769872 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11991256 | ACATCTCCAATATAA[A/G]TACATGCTAAGTTTT | 75725 |
rs240780405 | in-del | -/AA | | | intron-variant | Phf14 | Mm_Celera | 6:12046092 | GTAAAAAATGCAGAG[-/AA]AAAAAATGTATTTTA | 75725 |
rs240792456 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043373 | AAGATAGGTTCATCA[C/T]TTTTATGATGTTTGT | 75725 |
rs240799488 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11981199 | TTCCCTGGCATTTCT[A/T]GGAGATGAAATCTTA | 75725 |
rs240820701 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11912638 | AGATGTCACAGTAAA[A/C]GATGCTTACCTTCGG | 75725 |
rs240827251 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11977767 | AATTGGACATTTATA[A/T]AGGACTCCTTACAGA | 75725 |
rs240834402 | in-del | -/TTG | | | intron-variant, cds-indel | Phf14 | Mm_Celera | 6:12008136 | GTAAAGTTAATAGGT[-/TTG]TTTTTTTGAGAAGAT | 75725 |
rs240840292 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11978728 | ATGGCTGGAGCCATG[A/G]GACCCTCCATGTGTA | 75725 |
rs240855739 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11986643 | TTTTTGATTAGACAT[C/G]AGTAGTATTTGTTTC | 75725 |
rs240882511 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032434 | ATAAATAGCAGTAAG[C/T]AGAAACATGTTTTAA | 75725 |
rs240888590 | snp | C/T | | | synonymous-codon, utr-variant-3-prime, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:12081026 | AGCTGAAAAGAAAAA[C/T]GCATCTCAGGAGCTC | 75725 |
rs240895813 | in-del | -/TTTTG | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011683 | ACTTTAAAAATATTC[-/TTTTG]TTTTTTTTTTAAGGA | 75725 |
rs240921137 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12064134 | AGAATTCTGAATAGC[A/T]TACAATCCTGTTTAA | 75725 |
rs240924198 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12033427 | AGTTTTTGCCGTGTT[-/C]CCCATCACAGTCCTT | 75725 |
rs240942306 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11913976 | TCCTTTATGGATTCC[C/T]AAGTTCATTCAGTCA | 75725 |
rs240947488 | in-del | -/GA | | | intron-variant | Phf14 | Mm_Celera | 6:12057152 | TAACCTGAATCCCAT[-/GA]AAAAAAAAGATTTCT | 75725 |
rs240955523 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12064898 | TGTTGCTTAGGGTTG[A/G]AGACAAAATTTTATG | 75725 |
rs240957750 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12058254 | AGGTGACAAAGTGTT[C/T]CCTGAACAGTTATTC | 75725 |
rs240964044 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11998030 | AGGCTTTGAAGTTTC[-/A]AAATACCTTGGCTTT | 75725 |
rs240974472 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12044999 | AAGTGTGTTATTGTA[G/T]TTGTACAATTAAAAT | 75725 |
rs240992891 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11936638 | CATACTTTTGCCACT[A/C]TAAAGTGGGTGGAGC | 75725 |
rs240993764 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11956003 | ATGTGATCTCCTGTC[A/C]TAGTTTCCCCTCCGA | 75725 |
rs241003197 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906195 | GTTCCTTTCTATATA[A/T]GCCAACCTCTAAATC | 75725 |
rs241006952 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927548 | ACATTAAGACCTTTT[C/T]GTATTTCGCTCCCAT | 75725 |
rs241019147 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906529 | CCTTAAAAGTTCTGT[A/G]AGCCAGGCAATGTGG | 75725 |
rs241024532 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072257 | ATGTTGGGATGAGAA[A/G]GAAATCATCATGAAG | 75725 |
rs241028995 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947206 | CATGGCAGCAGGCAA[A/G]CAAGCATGGACTTGG | 75725 |
rs241056224 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927969 | CAAACAAAAAATTCC[A/T]TGGATTGTGTTACTC | 75725 |
rs241088918 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11978109 | CTTTAGGTTTCCTAT[-/A]AAGCGCTTTTTTCTT | 75725 |
rs241089030 | in-del | -/TT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12035664 | GATAAATCTTGTTGG[-/TT]TTTTTTTGGTTTTTT | 75725 |
rs241097801 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906645 | GGACAGCCAGGGCTA[C/T]ACAGAGAAACCCTGT | 75725 |
rs241098861 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12072511 | ACATTTACGACATCT[C/T]CACATAATGCAGAGG | 75725 |
rs241111803 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12095538 | CTAGATAGTAAGTTC[A/G]CTGATCCCACCCTAC | 75725 |
rs241120655 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12095177 | GGCTAGAACACATAC[A/C]AAAAAAAAAAAAAAA | 75725 |
rs241145500 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12096515 | GCATCTTCATCAGAA[A/G]GCTTCTAGCAGAGTA | 75725 |
rs241150759 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12064384 | ATCTGTGTACTACAT[A/G]CGTGCAGTACCCATG | 75725 |
rs241151625 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11920613 | GATCCAGCACCCACA[C/T]TGGGCAGAATATAGC | 75725 |
rs241155157 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12086472 | TTGGGTATTGTCCTT[A/C]CCGCTAATAAATTTC | 75725 |
rs241158344 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11936730 | AATTAGTACAGTTTG[G/T]ATAGCAGCCCTGCAG | 75725 |
rs241158631 | in-del | -/AC | | | intron-variant | Phf14 | Mm_Celera | 6:12016065 | GTTCTTAACTTGGAA[-/AC]AGTTTCCAGGCATGT | 75725 |
rs241171745 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12065160 | TTGATTACTTACCGA[C/T]TCACTGAAATAGCTC | 75725 |
rs241173561 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12073091 | CGGAGGAGTTCCCAG[C/T]CATAAAACAGAAAGA | 75725 |
rs241184676 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11973995 | ATTTGTTTCATAACT[C/T]CTGTTAGTGCCCATG | 75725 |
rs241185130 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12016101 | CATTTATCCTAAACT[G/T]AAATATATTATCATT | 75725 |
rs241203316 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12065905 | TTTTTTTTTTTCTGT[C/T]ATGTATCTAGTACTT | 75725 |
rs241222082 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12036954 | TTTTGGCCGGGCAGT[A/G]GTGTCACAAGCCTTT | 75725 |
rs241238367 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11937707 | TATGTTTTAAAACTG[A/G]TACCATTTAAAGTAT | 75725 |
rs241249976 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11938703 | CTCATCACAGAAGTG[A/C]CAGATTACTGATTCA | 75725 |
rs241250369 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12077862 | CCTGGAAATTTTTTT[-/A]CTCCTCTCTGTGATC | 75725 |
rs241257622 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12003966 | TTACTGTTATAGTTT[C/T]GAGCTTGGTAGACTC | 75725 |
rs241269124 | in-del | -/GTG | | | intron-variant | Phf14 | Mm_Celera | 6:12013824 | CATTTAGGTAAAGTT[-/GTG]GTGCTATGCACACTT | 75725 |
rs241300615 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12077035 | AACTTCTATGCAATA[A/G]TAAGGATTTCCATCT | 75725 |
rs241308726 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11963341 | AGTTTTAATGATCCT[C/T]CTTTTATATTTTTTT | 75725 |
rs241312870 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12042606 | ATATCAAGACATGAA[A/G]ACAGAGTTTATCTGT | 75725 |
rs241325105 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11953918 | CCCATTTGATGCCCT[C/G]TCTTCTTGCTGGAGA | 75725 |
rs241343903 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12031110 | ATTTTCTCTAAAAAA[A/C]CATCTCTTTGTTTCA | 75725 |
rs241348378 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12022802 | CAGAGAGGTTAATTG[A/G]GAAGTTCTGAGGAAA | 75725 |
rs241357107 | in-del | -/GTTT | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12047996 | CTTTCATCTTGACAG[-/GTTT]GTTTTTTTTTAATAT | 75725 |
rs241369943 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12060880 | GCATTGTATCAACTC[-/TT]TGACACATGCATTCA | 75725 |
rs241387093 | in-del | -/AGAGGAGTGC | | | intron-variant | Phf14 | Mm_Celera | 6:11936390 | GGCTTCACAATACCT[-/AGAGGAGTGC]TTCTAAAACATATTG | 75725 |
rs241408123 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12075835 | TAGATCCTCATTTTT[-/C]CTCACTTATTCATAG | 75725 |
rs241416108 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12070214 | ATGTTTCACTTGTTA[A/T]TGTTATTTTTAGTGT | 75725 |
rs241423594 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11943290 | AGGTGGCTATGGCAG[C/T]CTTTCTTTTATCTCC | 75725 |
rs241428641 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036336 | AGACTGTAGCCTCCA[C/T]ACACATTTGCACACT | 75725 |
rs241437548 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023553 | ACTGGTCCAGCAAGA[A/T]ATGCCTACTGATGGT | 75725 |
rs241461663 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12022003 | CTAGCTTGTTGCCCC[C/T]AGATTGATCAGCCTG | 75725 |
rs241497410 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12015872 | TGTTTATTAAAAAGG[A/G]CTATAGTAGAAATTT | 75725 |
rs241501404 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11934106 | AAGTGGCATCCTTGA[A/C]TTTTTATTTGGATGT | 75725 |
rs241536715 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12014189 | TTCAGTAAGCTTAGA[A/C]AATGAGACTATTTTG | 75725 |
rs241552631 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:11952478 | TATTTTTTAAATGAA[-/TT]TTTTTTTTATACTCC | 75725 |
rs241566114 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905895 | AGCCAGCCAAGTAAA[A/C/T]GTCAGCAGCCCTGGG | 75725 |
rs241567724 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12052450 | CCTGTTTCTTTTGGA[A/G]TTTTATGTTAGATAG | 75725 |
rs241604216 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12091831 | AACGATACGGAAACC[A/G/T]TTCTGGAATGCATCA | 75725 |
rs241611591 | in-del | -/TT | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12047997 | TTTCATCTTGACAGG[-/TT]TTTTTTTTTAATATT | 75725 |
rs241611883 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11980109 | TGGCTCAGATTGTAA[A/G]GTGTTTGACATGGAA | 75725 |
rs241630796 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12059333 | TGGATACCATCACAG[C/T]CCTTACAACTTTGAC | 75725 |
rs241654556 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053150 | GAAGCAAGAATTGCA[A/G]AAGAGACCTCCCTAA | 75725 |
rs241664550 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031426 | GCTGTATATTCATTT[G/T]CTTTCAATTCTAGAA | 75725 |
rs241666438 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906719 | AAGAGCATAACTAGC[G/T]GACAGAAATGCCTAT | 75725 |
rs241670917 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11980931 | ACTAATATGTATATT[A/G]TTTCAGGGCTCAGTC | 75725 |
rs241672912 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11959368 | TGTTTTCTAATGACC[A/G]TGGGTGATTCCTGTA | 75725 |
rs241685245 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959840 | TAATTTAATTTCTGT[G/T]GTCACATAAGAGTTT | 75725 |
rs241689601 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12046909 | TTTAATTGACTTTTT[A/T]TGCTCTAAACCGTGA | 75725 |
rs241693514 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12037443 | TGCTTAGTATTAAGA[C/G]TTCTCTTGTACAGAA | 75725 |
rs241724101 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12031933 | ATGAGTATGTACTGT[A/C]TTACCCTCTCTTTTC | 75725 |
rs241726722 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11915712 | TCCACCTCACCAAAG[G/T]ATTGCTCCCAAGTGG | 75725 |
rs241738275 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11991004 | AAAATATTAGGCATC[A/G]TACCAGACGTTGGAG | 75725 |
rs241760449 | in-del | -/TG | | | intron-variant | Phf14 | Mm_Celera | 6:12019346 | ATACATGTATGATTT[-/TG]TGTGTCTATACTATT | 75725 |
rs241760468 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12020487 | AGAAAATAGAGTTAT[C/G]TCTAATATGACTATT | 75725 |
rs241802691 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12020796 | AAAATGAGTTAAATA[-/T]TTTTTTTTATGTTAA | 75725 |
rs241817624 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12021236 | CTCCATGACCCCTTA[G/T]GCCTTTAAAACCATT | 75725 |
rs241821616 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12065942 | ACCAACATTTCTGAT[A/G]TGTTACTAGAGCCTG | 75725 |
rs241849937 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908042 | TTAAAGCTGGCCATA[A/G]TTTCTACAATGTGAT | 75725 |
rs241878529 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12021546 | AAGGGCCACGCAAAA[-/T]TTTTTTTTGTTGTTT | 75725 |
rs241884401 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12014091 | TGGTCTCTTGATTAT[C/T]TGTGATCTGGAGGAT | 75725 |
rs241894957 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11917886 | CATATAGGCTCTCAG[-/A]AAAAAGAGTTTAAGC | 75725 |
rs241897674 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066968 | CCACTCCTAGGCATA[A/T]ACCCAAAAGATACTT | 75725 |
rs241902441 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12059794 | GAAGGAGGTTTCAGC[C/T]TTTCTGACTCTGTAG | 75725 |
rs241904332 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11931640 | TTGAGCTGAAAACAA[A/G]TCACTTTGCTTTGAA | 75725 |
rs241941606 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12026905 | TCTATTGGCTAGCAA[A/G]CATGACACACATTTG | 75725 |
rs241946584 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12074261 | CTTTCTATTTGACTT[C/G]TTGCTAAAATAAAGA | 75725 |
rs241957057 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11928781 | CATATAATCCCCATT[C/T]GTCTACTGCCCTGGC | 75725 |
rs241983649 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11929752 | AATGTTAAGGTATGG[A/G]GATGCGGAAATGTTA | 75725 |
rs241992472 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12035857 | GTGCCACCACTGCCT[A/G]GCAAATCATGTTTTC | 75725 |
rs241994279 | snp | C/T | | | nc-transcript-variant, intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099688 | AACTCTGAAATTATC[C/T]TTTTAACATTTTTTT | 75725 |
rs242023256 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12019586 | TCTTCATCACCTATT[G/T]CAGCATTTACAAAGA | 75725 |
rs242028416 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12050598 | ACTCCAGGTAGTTTG[G/T]TTTTAACGTATACTT | 75725 |
rs242046032 | in-del | -/GTG | | | intron-variant | Phf14 | Mm_Celera | 6:12068768 | ATTTATTGGGTTGTT[-/GTG]GTGTGTATGAGACAT | 75725 |
rs242064094 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11939757 | CCACAAAATATTTAA[A/C]CATATCATTTACAAT | 75725 |
rs242087119 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029857 | TAGCTCAACCATCAT[C/T]CATTGACTTAATAAC | 75725 |
rs242115131 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11981030 | AGACTATTTTTCCTG[C/G]TCTCGGCATTTCTTG | 75725 |
rs242142457 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12016871 | TTAACAAATCTGTAG[A/G]ACTTTTACAGCTTTA | 75725 |
rs242143521 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12030168 | TTGGCTAGCATTACC[A/G]CAAGATCTTTTCTAT | 75725 |
rs242144938 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12005643 | TCCCCTCCCATTGAC[A/G]ACAGATAAGGCCGTC | 75725 |
rs242190430 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11910299 | TTTAGTAAGACATGG[A/C]ATGTGAGAATTCCAT | 75725 |
rs242194518 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031660 | GTTTTGGAGAAAGTT[C/T]TAAGAGGTGCTAAGA | 75725 |
rs242200165 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079819 | CAGTAGTAGTTGTTG[A/G]AAAAGTAGTCAAAAT | 75725 |
rs242201217 | in-del | -/A | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083042 | GCAGTTCAGCTGCAC[-/A]GGGGGGTTGCCCTAA | 75725 |
rs242226434 | in-del | -/TTA | | | intron-variant | Phf14 | Mm_Celera | 6:12004609 | TTCTTACATATTAAT[-/TTA]TTAAGGCAAGGGGCA | 75725 |
rs242250529 | in-del | -/TGTT | | | intron-variant | Phf14 | Mm_Celera | 6:11910640 | TTTAAAAACTGTGAC[-/TGTT]TGAGATATGAATTGA | 75725 |
rs242250566 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12006544 | AGCGATTGGTGGTAA[A/G]ACCAGAAAAATTACT | 75725 |
rs242260789 | in-del | -/TTTTGC | | | intron-variant | Phf14 | Mm_Celera | 6:11961830 | TATTAATTTGTTGTG[-/TTTTGC]TTTTGTATTTTTGAG | 75725 |
rs242277656 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024539 | CAAATATCTGCATCT[G/T]ACTCTTTCAGCTGCT | 75725 |
rs242279415 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924835 | CCACCCCCATTAGAC[-/TT]TTTTTTTTCACTAGC | 75725 |
rs242280276 | in-del | -/AAA | | | intron-variant | Phf14 | Mm_Celera | 6:11939023 | GAGAAACCCTGTCTC[-/AAA]AAAAAAACAAAAACA | 75725 |
rs242318663 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11946672 | TATACTTGGGGGCAG[A/G]GGGGGATGGAGTGAA | 75725 |
rs242319515 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12098347 | TGGTAAACTTCTCCC[A/C]AGCAGGCTTGCATAG | 75725 |
rs242320508 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12058329 | TCTCAGAACCCAGTT[A/G]TTGAAAAAATTGGGT | 75725 |
rs242320577 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12052332 | CTTGTTTTGTAGCAG[A/C]GGTTGAGATTTAGAA | 75725 |
rs242335070 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11973478 | TGATTTCATCCCTGA[A/G]TTTGATTATTAACTC | 75725 |
rs242368941 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037167 | GGATTAAGGCACATA[G/T]TTGGGGTTTGGTGCT | 75725 |
rs242397388 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11980402 | ACTTCTTTTTTTTTT[A/T]AATAGAGATTATATT | 75725 |
rs242412959 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12065890 | ATTCCAAAGCATGTG[-/T]TTTTTTTTTTCTGTC | 75725 |
rs242414062 | snp | C/T | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100240 | ACGCACCGGCCATGG[C/T]AGTGCAAGCAGCAGC | 75725 |
rs242430933 | snp | C/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925622 | TGTGTTAAGTTGATA[C/G]ACAAAACTAGGAAGT | 75725 |
rs242440497 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:11918574 | GTACGTAATAAAATA[-/C]CACCTTATCACATTC | 75725 |
rs242443367 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916847 | GAACTGGGAACCATC[C/T]ACCCCACCTGATCTA | 75725 |
rs242457149 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909079 | TAAAACAAGGAGGGG[A/G]CCATGGATGATAAAC | 75725 |
rs242496860 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12093590 | AGACTTCCTTCCTGT[C/T]CTCTCTGGCCCTTCC | 75725 |
rs242504445 | in-del | -/AAAAAAAAAAAAAAAAAA | | | intron-variant | Phf14 | Mm_Celera | 6:12071125 | CTGAGAGCCCATATT[-/AAAAAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA | 75725 |
rs242506336 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12001867 | TTTCCTGCATCTACT[A/G]CAATGTTCATGTGAT | 75725 |
rs242515548 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985633 | TTTGTTATTGACAAG[G/T]TCTGGCCTTCCTCAT | 75725 |
rs242543590 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11926456 | GCGTGCGTGGCCGTA[C/T]GTTGTCTGAGTGAGG | 75725 |
rs242543667 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094108 | AAACAGCCTCTGCTC[C/T]GAGCTACACTCGGTG | 75725 |
rs242549197 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12054255 | CCTGCAGAGGCCAGA[A/G]GCAGACACTGAATTC | 75725 |
rs242571949 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11999269 | CTGTATTTCTAGTCA[C/G]TGAATGTTTGAGAAG | 75725 |
rs242573637 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12002821 | TAGGGTAAAATGGAT[C/T]TTTTTAATTAATGTT | 75725 |
rs242586429 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031422 | TATGCTGTATATTCA[-/T]TTTTCTTTCAATTCT | 75725 |
rs242586789 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11994372 | CTGGATCCTACTCTG[A/G]GCCTATTGCTGGACC | 75725 |
rs242612009 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12084621 | GGAATCAAACCCTTT[A/C]TCTTCTGCAAGAACA | 75725 |
rs242618850 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12075689 | TAAAATTTTTAAAGA[A/C]AATAGAAACCTTTCC | 75725 |
rs242626576 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11986584 | ATGGAAATTTAGGTC[C/T]AACATGTAAAATGTA | 75725 |
rs242631340 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924435 | GGAGACTATAAGACA[-/AG]ACAAGACAAGAGTCT | 75725 |
rs242633199 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11944902 | GAGGAAGGATGGTGT[C/G]TGGGTATAGATGTAA | 75725 |
rs242638804 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924084 | TTTAATGTTCAATAA[C/T]ATAAGTAGTGTCTTC | 75725 |
rs242639936 | in-del | -/AAAAAAAAAAG | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908772 | TGAGTGAAAAAGAAT[-/AAAAAAAAAAG]AGTAAATCAGAACTT | 75725 |
rs242641404 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11995338 | TACTTTGTATTTATG[C/T]TGTGGAATTTAGGAT | 75725 |
rs242646242 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12085511 | ACATGGGTGCTAGGA[A/G]CTAAACTTGGATCCT | 75725 |
rs242663542 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12027635 | CATAATTTTTCCCTT[A/T]TAAGGCCCAAGCTGA | 75725 |
rs242681796 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11961385 | TGCTATCATTCTCTA[A/G]CTATGCTGGGTTTTT | 75725 |
rs242688697 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906558 | GCGTACACCTTTGAT[-/C]CCAGCAACTGGGAAG | 75725 |
rs242693467 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11962530 | GCTTACTTGCAGTTA[C/T]TTGCATTTATGCTTT | 75725 |
rs242704344 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11932493 | GCTAATTAAAGGCTT[G/T]CATGAGCTACTCAAT | 75725 |
rs242708165 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918026 | GGAGATTACAAAACA[C/G]TGAGTAGAGTTACTA | 75725 |
rs242712221 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12035069 | TTTTGTTGTTGTTGT[A/T]GTTGCATCATGAGAA | 75725 |
rs242752888 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11952933 | TGGTTACTAAAATTT[A/G]ATACTAAAGAAATTA | 75725 |
rs242753440 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12002427 | GATATTATACCCCAG[C/T]CGGACCTAAGGCTAG | 75725 |
rs242770409 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11926660 | AAGTCATTTCTATTT[C/T]CCCCAGCATCACAGT | 75725 |
rs242782725 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12055258 | GCAAGCTGGGAGTGT[A/G]AGGCCAACCTGGTTT | 75725 |
rs242789080 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12058465 | GGAGGTGGAGTGGGG[A/G]TGAGAGCTACACTGA | 75725 |
rs242793372 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11909897 | TGTTTTGTTGATTTT[A/T]AAAATAATCTTATTA | 75725 |
rs242822750 | in-del | -/TGCA | | | intron-variant | Phf14 | Mm_Celera | 6:11930017 | GTTTTTAGGAACTAG[-/TGCA]TGCATGTCTTTTGAG | 75725 |
rs242824353 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12041257 | GGTGTTTGACAGTTA[A/T]TTGCTGTAGGATAAG | 75725 |
rs242830734 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925273 | AGTGTTTCTATTCGT[A/G]CACAAAACATCATGG | 75725 |
rs242840379 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11923742 | ATTTGTGGAATAAAT[A/G]AATGAGTTTAATTGG | 75725 |
rs242858758 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11910286 | TCAGGTGACTTTCTT[C/T]AGTAAGACATGGAAT | 75725 |
rs242875287 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12090450 | AAGAGATGTAAGAAG[A/G]TATTTGTTTTGATTC | 75725 |
rs242896521 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916957 | CGTCCTTAGGAACAG[C/T]CCTCTATGGTACACT | 75725 |
rs242911758 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12091317 | GTGGCATTTCATGCC[C/T]AATTTCTAGCTTTAT | 75725 |
rs242913946 | in-del | -/TTCTACCTAGCT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021954 | GTGTGTGTGTGCGTG[-/TTCTACCTAGCT]TGTGTGTGTGTGCAT | 75725 |
rs242927215 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11920376 | CTGAGTTCAACCAGC[C/T]AGCCAGAGTCAGCCA | 75725 |
rs242939191 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12093519 | TTTCTTTTCCTGTAA[A/G]ACAGGAACTTCCTCA | 75725 |
rs242951732 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11997345 | AGTTTTCTATGTTAT[A/G]TAGCGTATTATATTT | 75725 |
rs242965082 | snp | C/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:11988987 | CAGACCACTGGCAGC[C/T]GCTGCCTACTGAGAA | 75725 |
rs242980103 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083623 | CTCAGTTCAGTGGTT[C/G]ACTGTGAGCATCTGC | 75725 |
rs242985192 | snp | A/C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12084062 | TCCTAGCTGTTCTGG[A/C/G]ACTTATGTATACTAG | 75725 |
rs242998881 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083107 | CGTGGATCTATTTCA[A/G]AAAACCCATATTTAC | 75725 |
rs243000528 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11958673 | AAAATTTTGTAATAG[A/G]CTGTCTAAATACTTG | 75725 |
rs243003643 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11948954 | AGCCCTGTTGTCATA[A/G]AAGGAAGAGGAGGGT | 75725 |
rs243012182 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959411 | CATCTCAGAGGGGTC[A/T]TAACCTCCCAGCTGA | 75725 |
rs243035437 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12070125 | AGGAAATGAGGGGAA[C/T]GAAGCACAGTGAGAT | 75725 |
rs243035444 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061908 | ACATGTGACCCCATG[A/G]AAGAACAAGATCAAG | 75725 |
rs243049011 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11960533 | AAAAATGATAAAAAC[A/T]TTAGACTTTTTCTGA | 75725 |
rs243062238 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11914423 | GCAAGATATATGTCA[C/T]TCTTAAGATCAAGAA | 75725 |
rs243063399 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949580 | CAAATAACTCTGGAT[G/T]CTGACTTCATATTCT | 75725 |
rs243071855 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12062337 | GAAGCGCACCTGTCT[A/G]TACATGGATGGATGG | 75725 |
rs243079082 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12035637 | GTTTCTGGGATATTA[A/C]ATTGTAAGTAGGATA | 75725 |
rs243111023 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11932650 | AAGCAGTGTCCTGTT[G/T]ATCAGGGAGACTGAA | 75725 |
rs243122665 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11933626 | TGTCCCTACCACCAC[C/T]ACCACCACCACGGAG | 75725 |
rs243123447 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11950658 | TGTATCTTGTCTTTC[A/G]GCAGCATTTATTAAA | 75725 |
rs243129134 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12037665 | GCTACTGAATGTAAG[C/G]CATCTTAACTATCAA | 75725 |
rs243170455 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12084248 | TATAAATATGAGGTT[G/T]ATGATGCTGCTTGTC | 75725 |
rs243172258 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12051788 | TTTATATTCTTGCTT[G/T]AAATGCCAGTGGAAG | 75725 |
rs243204865 | snp | A/G | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099075 | CCTCTTCCTGTCTTA[A/G]GGTTTCTATGGAAGT | 75725 |
rs243207994 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11995697 | CCTTTCTCCTCCCCT[A/C]CAGCTCTCCTCCAAG | 75725 |
rs243218826 | snp | A/C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032349 | TAGTTGTGAGTCATG[A/C/T]TTTTTACTTATTCAT | 75725 |
rs243249891 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083886 | CCATACTTTGGTCTT[C/T]CTTCTTCTTGGGCTT | 75725 |
rs243255874 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12044584 | CTTTGTATTTGTATC[-/A]AATATTAATGTAGTA | 75725 |
rs243258928 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12077409 | GTTGCTTCAGGGATC[C/T]TTCATGAAACAAATG | 75725 |
rs243278758 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12032869 | CTCTTTGGTTGGTGA[A/G]TTAGCCCCTGTGAGC | 75725 |
rs243289036 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11979868 | AGTGGTCTTTATTGG[A/G]AAAAAAGGTATTGTG | 75725 |
rs243294931 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:11953892 | GTGACTGTGGGATTG[-/C]CCCCCCCTCCCCCAT | 75725 |
rs243297529 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12078618 | ATACAGTTTATTAAC[A/G]AAGTAATATTAGTCT | 75725 |
rs243304135 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918529 | TGGAATACACATCTA[C/G]CATGTCTCAGACCTT | 75725 |
rs243316203 | snp | A/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12040671 | ATAAGGAAGAAGCAA[A/T]TGACATTACTTGACT | 75725 |
rs243326568 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11943766 | ATTTTGAAGAGATTA[A/T]TCCAAGACCTTCAGA | 75725 |
rs243335781 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11952141 | GACGTTCAGAATCCA[G/T]TCCCATGGATGTTTG | 75725 |
rs243363757 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959115 | GGAGTTGTCCTCCTT[A/T]TATCACTGTTGTAGG | 75725 |
rs243382439 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11911772 | CACAAATATGCATAC[A/G]CACTCGGAAATATAA | 75725 |
rs243392986 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12034095 | GAAGATAGCATAAGT[C/T]GTACCCTAGAAAATA | 75725 |
rs243421559 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060504 | GTGATGAATCAGTTT[A/G]TAACACTTTAATGTT | 75725 |
rs243438585 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11944725 | AGACAGCCACAGGCA[C/T]AGTATATTGCTTGTT | 75725 |
rs243450342 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12078770 | TCTTACAGAGGAACC[C/T]AGTTCTACCAGCACC | 75725 |
rs243453978 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12054813 | ATTTTTGTTTGGTTG[A/G]TTGGTTTTGGTTTTG | 75725 |
rs243455356 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060810 | GCCAAAGAAAGACTA[A/T]AATCCACAAGTACCA | 75725 |
rs243490906 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11916971 | GCCCTCTATGGTACA[C/G]TTGTCCCCTTTCCAT | 75725 |
rs243506829 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11952579 | CCATGTGGATGTCCC[C/T]AACGCCCACCCCCAC | 75725 |
rs243528996 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030424 | AGTTGTCTTTTTGCA[C/T]TGGCAGTCCTTCAAA | 75725 |
rs243529134 | in-del | -/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12047649 | ATTGTATTGTTTCAA[-/T]TTTTTCATCTATAAT | 75725 |
rs243539317 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12050019 | TTCCTGTCCTGATGT[A/C]GTAGTATTGGCACTT | 75725 |
rs243593348 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917325 | AGTTGAAGAACAGTT[C/T]ACATTGCAGCCTAGA | 75725 |
rs243597718 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11909503 | GCAAGGAAAGATGCC[C/T]CTGGGGATATCATCT | 75725 |
rs243602974 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12061516 | AGCCTCTATTGAAAC[A/T]CTTTACTGTCTTCAG | 75725 |
rs243603556 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12069547 | ACCAACCCACTTCCT[G/T]CAGGCCTAATCATCC | 75725 |
rs243648508 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11909999 | CAATATAAATTTGCC[G/T]AAACTGTACCCAACT | 75725 |
rs243655787 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061838 | GACACATGACTTGGT[A/G]TCCTTTACAGGTTGT | 75725 |
rs243660194 | in-del | -/CTA | | | intron-variant | Phf14 | Mm_Celera | 6:12029682 | TCCCTATATTTCTTC[-/CTA]CCTTATCCTGCCTTA | 75725 |
rs243660332 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910386 | ATCATGACAAGATCA[A/G]GTTATGTTCCAAACA | 75725 |
rs243662553 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12094804 | TATTTTAATAATGTT[A/G]TTGAAAAACAAGCCC | 75725 |
rs243667512 | in-del | -/G | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12048079 | TTAAATTTCCTCCAT[-/G]TAAAGCATTTAGCTA | 75725 |
rs243669592 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910236 | ACCCTGAGGGAGAGA[-/G]GGTCATCTCACTGCC | 75725 |
rs243673093 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12075797 | AAAGTAAAAGCCACT[G/T]ACTTCACTCCTTCTT | 75725 |
rs243682218 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061961 | TTGTCACAGTCTGGT[C/G]AATTCCCTATTGAAA | 75725 |
rs243686802 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11988211 | CTAATATATAAAGCA[A/C]GGTCTTTCTAAAGTG | 75725 |
rs243688367 | snp | A/G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12056159 | CTCAGAGCTGGCATC[A/G/T]TTTATGCCCCAGTCA | 75725 |
rs243688505 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924546 | TTTATTTCAGCTTAT[C/T]CATCACAGCTAACTA | 75725 |
rs243696877 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12043840 | GTATAGGGAATACTG[A/C]CTGTTGTGCTTCATT | 75725 |
rs243700564 | in-del | -/TG | | | intron-variant | Phf14 | Mm_Celera | 6:12092623 | ATGGCGTAAACCCAC[-/TG]TGTGTGTGTGTGTGT | 75725 |
rs243710479 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12069143 | AATAGATATGCATAT[A/G]TGTATATATACTTTA | 75725 |
rs243718919 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908249 | CAAATTTACTTTTAC[C/T]CAAAAGTTCTTCCTT | 75725 |
rs243720293 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12056793 | GCTGTAGCCCACGAG[C/T]GTTTGAGTATTTACT | 75725 |
rs243743984 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12036730 | TTTCTCTCCAAGGGC[A/G]CTATCGTGTTTTCTC | 75725 |
rs243758515 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925379 | ATGACAGGAACTCAA[A/G]CAGGTCAGGAACTTG | 75725 |
rs243762183 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Phf14 | Mm_Celera | 6:11962765 | CCAAAAGGAAGGCCT[A/G]CTATCAGAGGCAGCA | 75725 |
rs243766101 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11913817 | CTTTTTATTTGAAAC[A/T]TGGCTACATAATATT | 75725 |
rs243799449 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12069834 | AGAAATAATTCTTCA[G/T]TTTTCTGTTTCATGC | 75725 |
rs243826009 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11942349 | AGCAGTGGATTGAGG[C/G]TCATAGTGGGAAGAC | 75725 |
rs243832751 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12070361 | GAAAACTACAAAGAT[A/G]GTTAAGATGTTTATC | 75725 |
rs243838511 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906008 | TCCAAATATTAAAGC[A/T]TTTACACTCACCTGA | 75725 |
rs243854583 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917975 | GATGTTAGTGAAAGG[C/T]AGCAAAGTGCCGGCC | 75725 |
rs243876741 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12035696 | GTTTTTGTTTTTTTT[-/G]TTGTTGTTGTTGTTT | 75725 |
rs243892436 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12068146 | GGGGAAATCAGTTTT[A/G]TATTCTGGGTCTGGC | 75725 |
rs243896886 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083776 | CAGGTGAGGCAGTCT[C/T]TGGACGGTCATTCCT | 75725 |
rs243916158 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918387 | AGGACATGGTGGTTC[A/G]TTCCTAACATGCTAG | 75725 |
rs243957858 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12019679 | TTAATCCCAATATTT[A/G]GAAAGCAGAGCCAGG | 75725 |
rs243966767 | in-del | -/TGT | | | intron-variant | Phf14 | Mm_Celera | 6:12016295 | GCAGATTTGGGCTGA[-/TGT]TGTCAGATGGCTCAA | 75725 |
rs243970735 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072498 | GTTCTTTAGAAGGAC[A/G]TTTACGACATCTTCA | 75725 |
rs243973946 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12000009 | ACCCATACTTCCAAG[A/C]TGTGCTTATTATGTA | 75725 |
rs243975307 | snp | C/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010886 | TTAGAGATAAGCAGT[C/G]CTTTCATCTCCATGA | 75725 |
rs243976405 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12026741 | AAGGGTTGGAGGAAC[A/G]GGTCAACCCTCAATC | 75725 |
rs243980179 | in-del | -/GG | | | intron-variant | Phf14 | Mm_Celera | 6:11980081 | ATTAAGATTATCTTA[-/GG]GTGCTAGGGAGATGG | 75725 |
rs243983992 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12000854 | AAAGTAACTATCATT[A/G]TGTCTGCTCTAAAGA | 75725 |
rs244001115 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060697 | CAGGGCGCTGTGCTT[C/T]TGAACTTCCTTGTGT | 75725 |
rs244023074 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12064943 | TGGTTAAATACAGAA[A/G]ATAGAACATTAGCGG | 75725 |
rs244042855 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12019984 | CCAGTTTAGCCAACT[C/T]AATGAGCTCCACAAG | 75725 |
rs244064962 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11911087 | AGCACTGAAAAGAAA[A/T]TTTAAAGACGATAAA | 75725 |
rs244066170 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11930754 | TGAAATGTTAAGTTT[C/G]GAAGGCAGCATGGGG | 75725 |
rs244075795 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11944692 | TGCCAGGCAATGTTG[-/A]TTACGGAGGGCTGTT | 75725 |
rs244076321 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076295 | CCTAGCTCCTTCTAT[C/T]CAGGTGACCGTGGTT | 75725 |
rs244108903 | in-del | -/TTTTT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12069253 | GTTATATATGATGTC[-/TTTTT]TTTTTTTTTTAAGAC | 75725 |
rs244126756 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12033695 | TATGTATGTACTTCC[G/T]TTTCATTGTCCAGTC | 75725 |
rs244128466 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12078416 | GTTACCTACAGAGAA[-/C]AAAAGACGACAACAG | 75725 |
rs244141159 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11923496 | AGAGTAACAAACAGT[A/C]ATTTACTTGATTATA | 75725 |
rs244217000 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12049198 | TTTAAAGTGGCTTCT[G/T]TTCCAGATCATGTAC | 75725 |
rs244223485 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12034349 | AAGAATCAGATGATC[A/G]GGTAGGAAGTGGGCT | 75725 |
rs244236073 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12027492 | CCTCCTTGCTGCAGG[A/G]AAAGTTAAGTTTAAT | 75725 |
rs244261418 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11941641 | CAAAGGAACTTTAAA[-/T]TGTTTCCCTTTTGTA | 75725 |
rs244262317 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11980402 | CTTCTTTTTTTTTTT[-/A]AATAGAGATTATATT | 75725 |
rs244290133 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12070652 | TAAATTTAGCCTCAA[A/G]CAAGTTTTTAGAACA | 75725 |
rs244299723 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008649 | CAAACGATTATATTT[C/T]AGTTATCTTTCAAAA | 75725 |
rs244312121 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095758 | AGTGAACTTTTAGCT[C/T]TCCAGTTATGCCATG | 75725 |
rs244321416 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11944196 | CCCCCAAATATAGCA[G/T]CTTATTTAAAACAAT | 75725 |
rs244339298 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11975162 | TCTTTTTGTATTTTG[C/T]ATTTTCTTTGATTGT | 75725 |
rs244342461 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985132 | TTTTCCACCAAGATC[C/T]ATATTTTTCACAGGT | 75725 |
rs244353482 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11944888 | TCATTATAACTATCG[A/G]GGAAGGATGGTGTGT | 75725 |
rs244354796 | snp | A/C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12052097 | CAGTTCCCCGTTCCC[A/C/T]TTCCCCCATTACTAC | 75725 |
rs244359493 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12022752 | GTGTGTACAAATGGA[A/T]GTGTAAATGTGGGTA | 75725 |
rs244375572 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11930521 | TGTGTGCTTTGAAGG[-/T]TTTTTTTGTTTTTGT | 75725 |
rs244375633 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12015073 | TCCCCCGTGTGTTTT[C/T]AGATCTCAGGCTTAC | 75725 |
rs244382011 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11928611 | GGATGAAATAGTCCA[A/G]AGATAAGTTTATAAG | 75725 |
rs244390935 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11998260 | AAGGCACTCTCAGTG[C/T]TCCTCTCTCCCTCCT | 75725 |
rs244391755 | in-del | -/TTTG | | | intron-variant | Phf14 | Mm_Celera | 6:11955716 | CCCATGCTTATATTT[-/TTTG]TTTGTTTGTTTGTTT | 75725 |
rs244392937 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12045504 | GGGGTATTATTCTGT[A/G]ATTTTCTTTCTCTCT | 75725 |
rs244398747 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12080788 | GAGAGCACTGTTCGG[G/T]AGCAGGTGTTCAGAA | 75725 |
rs244398828 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11976734 | TTTTATCTTAGCTAG[A/G]AAATAAGTAATCTAA | 75725 |
rs244408434 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11955828 | GTACAACAGTTCCTG[C/G]GATGTAGTTGGGTTT | 75725 |
rs244431876 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12081776 | ATTCACTTCAACTTA[C/T]ACTTCCAGGTCTCAG | 75725 |
rs244432392 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11989627 | TCATCTGCTTTTTTA[C/T]GGAGTTTAGTCCAAT | 75725 |
rs244444625 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11972204 | gttagagtcacacca[A/C]ggtattttatattgt | 75725 |
rs244445355 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11998882 | GAGACGTTTCTGGAA[C/T]GCGAACAAATGTCTG | 75725 |
rs244455626 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11990882 | CATATATGTTTTCAT[A/G]CATGTATATCTATCT | 75725 |
rs244458919 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11937689 | GTATAGCATTTTTTT[-/A]ATTATGTTTTAAAAC | 75725 |
rs244465754 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11975701 | AGCTCTCGCCTGAGT[C/T]TCAGTGGTCAGAGTA | 75725 |
rs244465920 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11935573 | TACATTTTAAGATCA[C/T]ATATATGTGTTAGTG | 75725 |
rs244466649 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11957523 | TCCATAAGTCTCAGT[A/G]TCTCTGGTTTTATGT | 75725 |
rs244513745 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11991393 | AGAGACATAGAAATG[C/T]AGATTATTTATTTAA | 75725 |
rs244545377 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032405 | CCTAAATGTGCTTTA[C/T]TAATTAAAAATATAT | 75725 |
rs244561361 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947746 | ATGCTAGACAGACAC[A/G]TTGTCAGTGAACTGT | 75725 |
rs244579071 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11962377 | ATGTGTGTGTGTGTG[G/T]ATATGTGGATATATG | 75725 |
rs244579128 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12042454 | TATGGAAATATTTCA[C/G]CAAGATCTGTTTAAA | 75725 |
rs244585003 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12087964 | TACTACATCATTTCA[A/T]ACAATTAAAGGATCT | 75725 |
rs244594137 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11919184 | AGTTGTATGATAATC[C/T]AAATCTTGTCTTTCC | 75725 |
rs244626214 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12038315 | AATGCTGAGACAAAG[A/G]ACTCATTCGCATTCC | 75725 |
rs244643863 | in-del | -/TGTGCTGTT | | | intron-variant | Phf14 | Mm_Celera | 6:12068005 | ACAAACTCTTTTGTA[-/TGTGCTGTT]TGTCATCCTAAGCGT | 75725 |
rs244645175 | in-del | -/GT | | | intron-variant | Phf14 | Mm_Celera | 6:12017247 | TTTGAAAAAATGAGA[-/GT]ATGTTATATGTGCAC | 75725 |
rs244646363 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010196 | CTCAGTACAGGGAAA[C/T]GCCAGGGCCAAGAAG | 75725 |
rs244656098 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12020795 | AAAATGAGTTAAATA[-/TT]TTTTTTTTTATGTTA | 75725 |
rs244659823 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11977560 | TAAAGCACGTTTATA[C/T]TGGTTTCTAGTTGTT | 75725 |
rs244663989 | in-del | -/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12048299 | CAAACACACTTAATG[-/T]TTTTTACAATTAGTG | 75725 |
rs244664997 | snp | A/G | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099227 | CTGATGCAGAGGCAT[A/G]GAGGGGTGCTAATTA | 75725 |
rs244678497 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:11990699 | AATTTCATTGTAGTG[-/TT]ATTTTACATAACAAT | 75725 |
rs244689537 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11920238 | TGGGGGAGAAGTGTA[G/T]TGAGAGAGAGAGGAG | 75725 |
rs244692837 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12027169 | AACTCATAGTCTTCA[A/G]GTCCTGTCCTCAGGG | 75725 |
rs244695917 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12085910 | TCAGAAAGGTTGTTA[A/G]TTGGCATATGGTCTA | 75725 |
rs244696636 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11992836 | TTACAGTTCAGGATA[C/T]TGGTCCTCAGGCTGA | 75725 |
rs244712023 | in-del | -/GG | | | intron-variant | Phf14 | Mm_Celera | 6:12028994 | AGCCTTTGGATTACA[-/GG]CGTGAAAGTACATTT | 75725 |
rs244750775 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11914224 | CGTTTCCTCTTGTTC[G/T]GGTGTTATAGGTGCA | 75725 |
rs244751809 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12082586 | TTGAATCCTCCCTGC[-/T]TCTGACTTCTGAGCT | 75725 |
rs244756585 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11980368 | TTTAGGTTAAGTGTA[A/T]ATAGGTTAAATGCAT | 75725 |
rs244774008 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12079154 | ATTCTATGCTGATTG[C/T]ACCCATTTAGACAGG | 75725 |
rs244779136 | snp | A/G | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099140 | GGGTTTGTTAGGCTT[A/G]TGGGCCCATAGTCCA | 75725 |
rs244797891 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12065990 | TTATAATCTCTTTAA[-/T]TTTTTCCCATCCTTT | 75725 |
rs244811254 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11932181 | TAAATTCCTAGTTAA[A/T]TTTACAGGTCAAAGA | 75725 |
rs244816503 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12049996 | ATAATTTTCATGTAA[A/G]ATACCACTTCCTGTC | 75725 |
rs244830542 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11948201 | TGGTCCATTATCATT[G/T]CAGGAAGCATGGCAG | 75725 |
rs244859225 | snp | C/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11945920 | TGTTGTACTGACTAG[C/G/T]GATGTTGGTGTTGTG | 75725 |
rs244860323 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11993511 | TGATGATGAGTATTA[A/G]CTACAGAAGTAGAAA | 75725 |
rs244860876 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11954576 | TTGATTACAGTGCCC[C/T]GCTCTACTGATGGCA | 75725 |
rs244890274 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12097477 | TTGTAGTCAAACACA[-/T]TTTGCTTTTTCTAAT | 75725 |
rs244903620 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11946476 | GGCTATTTTGCTGCC[A/C]GTTTGGCATTTGGAA | 75725 |
rs244919229 | in-del | -/TTTG | | | intron-variant | Phf14 | Mm_Celera | 6:11961700 | TAAAATTCAGGTTTT[-/TTTG]TTTGTTTGTTTGTTT | 75725 |
rs244935757 | in-del | -/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12088654 | TTTTTCATTTTTTTC[-/T]TTTTTTCTATTAGAT | 75725 |
rs244957712 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12020744 | CCAAGTCTTTTAAAA[A/C]TTCAGTGTCTCTCAA | 75725 |
rs244957807 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12029112 | GTGTTCCTTTTAAGG[A/G]TCCTGTAGAACGCAG | 75725 |
rs244971337 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12061185 | AGCTGCCTTAGGCTT[A/C]CAGCGAAGCCTGAGC | 75725 |
rs244974871 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12093145 | TGAATACATACCTCT[C/T]ATTGCAGCTGTAATT | 75725 |
rs245005177 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12042378 | TAAACACTCAGATTT[G/T]CAAACTTTAAACACA | 75725 |
rs245007815 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11929226 | GAGATGATTATTATT[A/T]TTTTTTATCTAAATT | 75725 |
rs245008998 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12021707 | AGCAACATGCTCAGG[A/T]CTGTCACAGTAATAC | 75725 |
rs245009742 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11939311 | GGGCATGGGTAATGC[C/T]GCACTGAGGACCTTT | 75725 |
rs245020450 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11985309 | GCTGTGTAGAAATTG[A/G]TTGCTTCACTCCTGT | 75725 |
rs245029120 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12055790 | TCTGGTAGAGGAGTC[A/G]CATGGTAGATGACAT | 75725 |
rs245036850 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12081851 | ATACTGACCTAGCTT[C/T]CTTACACAACCTGGC | 75725 |
rs245062115 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11930070 | GAGAAGCTCTAGTTT[A/G]AATTTCCCCAGAATC | 75725 |
rs245063603 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12001382 | TGTTTGTTTAGAGTT[A/G]CTCCAAGATATATTA | 75725 |
rs245068586 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12097307 | GCCTTCAAAGCCCAC[C/T]CCCTACAACAAGGCC | 75725 |
rs245069658 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12074073 | CACAATTGTCTGCCT[C/T]CCATAGATAACAGTA | 75725 |
rs245077189 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12098033 | CAAGTAGCATCTTCT[A/T]GTTAAGTTAATCTGT | 75725 |
rs245102052 | snp | A/G | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12047405 | TTAGAAAGTTCATTT[A/G]CAGTATACTTTAACC | 75725 |
rs245121735 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947775 | GTATACCTACACTTC[C/T]TCCTATTGTTTTGAA | 75725 |
rs245123150 | snp | A/C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12098629 | TTCTCTTTGTCCCTC[A/C/T]GTCTTTAAACTCCCT | 75725 |
rs245123394 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12088929 | TCTTCTAAGCAAGAA[C/T]TTTGAATGTACCTGC | 75725 |
rs245138789 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11999862 | ATAAGATATAGGGGT[-/A]AAAGCAAGTTTGGAA | 75725 |
rs245156817 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12074986 | TCATCTGTATTTTTC[C/T]AGTTATTAGGATAAA | 75725 |
rs245159764 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11993464 | GAACAAGTTTTCAGT[A/G]GGGTTGGGAATGACC | 75725 |
rs245164009 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11991283 | TTTTAAGCCCTTGGT[A/G]CTCATTTTCTTAGAA | 75725 |
rs245167367 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12071024 | TAGGAAGGGTTTATT[C/T]GGGGCTTATAGTTCC | 75725 |
rs245180376 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11977875 | TGTTATTTATCCCGT[G/T]TGTACACATGTACAT | 75725 |
rs245189324 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11948754 | TCTCCATTTTATTCC[A/G]TCTAGGACCCCATCT | 75725 |
rs245189418 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11939601 | CTTTCAGGATGGTCA[C/G]TGGGTGTTGTGACAT | 75725 |
rs245195358 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11978266 | AAACTTTTTATATAG[C/T]CTTGGAATATATTGC | 75725 |
rs245198573 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12090087 | GGACAATGAGCAAAG[A/G]AGCTGTTAAGTGAGA | 75725 |
rs245212635 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11916350 | TTGACAATGTTTCAT[A/G]TAGATGAGCATCTGA | 75725 |
rs245215238 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11979226 | CAATAGATAGGGAAC[A/G]GGTACATTTTCTTTT | 75725 |
rs245270711 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11917165 | TAAACTTTATTTGAC[A/C]TTGATTCAGAATGGA | 75725 |
rs245288490 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908495 | AGTAGGAGCCACATC[C/T]GAGGCAGGGACCACT | 75725 |
rs245290416 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11940452 | ATTGTCCATCCTTTC[C/G]TCTTTGTGGCTAGCT | 75725 |
rs245303441 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12057241 | TTTGTTTAGAATCTG[-/A]ATATTGCATATCAGT | 75725 |
rs245307725 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11914414 | ATAAGCCAGGCAAGA[A/T]ATATGTCACTCTTAA | 75725 |
rs245311611 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060141 | GAACCGAAGCAGGCA[A/G]GTTCCTGTGAGTCCC | 75725 |
rs245347267 | snp | A/C | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009562 | GTAAAGATACATTTT[A/C]AGGGCAGGGAGATAG | 75725 |
rs245362833 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12074892 | AGGAATTACGATGGG[A/G]TTGTGAAGCATTAAA | 75725 |
rs245366472 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12098900 | AAATTTGCTTACAAA[A/G]GTCAGGTATTCCAAA | 75725 |
rs245373564 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12027215 | GCAGGACCATCAGCT[A/G]CACTGCTCCCATTCT | 75725 |
rs245410355 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11914967 | TTAGACACATAGTGA[G/T]TACAATCACATAATG | 75725 |
rs245427588 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037619 | ACTTTATTTGTGGTC[C/T]GTGAGGAAATGAAGG | 75725 |
rs245439949 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12054447 | AAGAGATTTATTGAC[A/G]GAGGGGGAAACCAGA | 75725 |
rs245443069 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11999697 | GTGGCACAGGAGGAG[G/T]AGCTCGGTATGTGGA | 75725 |
rs245446662 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12059321 | ATTTGATAAGGTTGG[A/C]TACCATCACAGTCCT | 75725 |
rs245464495 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906876 | TCTATCGAGCTATAC[A/T]GGACGAAAGTGACAG | 75725 |
rs245469485 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12068307 | GTTTATCTTCTCTGA[C/T]TTTGGAGTTGTCATG | 75725 |
rs245474180 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11940401 | TCTGTGTTTAGTGAC[A/T]GATTATGGGATGGAT | 75725 |
rs245480376 | snp | A/C | | | upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907536 | TGCGGCTGTCCTCTA[A/C]GGTGCCTGAATAGGT | 75725 |
rs245506943 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12019899 | AACCCTCATAAAAAA[C/G]CTGTGCATAGTAGTC | 75725 |
rs245518814 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12073165 | TGTTGCCAGTGCTGC[C/T]GCTTGTGTCTTCTCT | 75725 |
rs245522839 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12053608 | AGTAAATATATTTGC[A/T]GATTATTTGTTCATT | 75725 |
rs245525379 | in-del | -/TTTTTTTT | | | intron-variant | Phf14 | Mm_Celera | 6:11935160 | TCAATGCTATCTTAA[-/TTTTTTTT]TTTTTTTTTTTTTTT | 75725 |
rs245525487 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11920986 | GACTTATGCTTCCCT[C/G]AAATCCATGAAGCCA | 75725 |
rs245553015 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054058 | TTCTATATCCTCTTA[C/T]GTGCACTTTTCAAAA | 75725 |
rs245566703 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921823 | TCCTGGGAATAAACA[C/T]GTCACCAAGTCTCTG | 75725 |
rs245578241 | in-del | -/CAAA | | | intron-variant | Phf14 | Mm_Celera | 6:11921845 | AAGTCTCTGTACCTT[-/CAAA]CAGCTTCCCAGATAC | 75725 |
rs245580890 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12057592 | TTTTCTTTTTAGAAC[-/A]AAAAAAGGGACAGAA | 75725 |
rs245581330 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11921540 | TCTAAGTCAATCCTA[C/G]TAAAACACATTCTGT | 75725 |
rs245585981 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916068 | CTCTAGTCCTCTTTG[C/T]CAACTAAGTTTTCTA | 75725 |
rs245610151 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12062276 | TATGGGTTAGCTCAG[G/T]GTTTCCAGCCATGCA | 75725 |
rs245620110 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11938837 | ATCATACAGATGTTG[A/G]CAGTCCATTAACACA | 75725 |
rs245638627 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:11926902 | TTTTTAACTTTTTAA[-/TT]TTTTTTTGAGACTTT | 75725 |
rs245656711 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12056912 | GTGTGTTAGAAATTA[A/C]TAACTATATATAACT | 75725 |
rs245661492 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12003158 | TTAAATCTAAATTCA[A/G]TTGACTTGAGTGTGT | 75725 |
rs245661838 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12089388 | AGTCAAGCACTTAAA[A/G]CAACAGTATGAAAGC | 75725 |
rs245668814 | in-del | -/CTA | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906859 | TAGGTACACAGCATC[-/CTA]CTCTATCGAGCTATA | 75725 |
rs245673991 | snp | C/T | | | synonymous-codon, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11933458 | GGAAGAAGAAGAAAA[C/T]GGAGAAAGACCTAGA | 75725 |
rs245675026 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12047758 | GTCGCTATGTAACAC[A/T]GTGTTCTTTTGTCTT | 75725 |
rs245680055 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12092131 | GGCCTGCTTTTGACC[C/T]CCTTTTCTTCTCTGG | 75725 |
rs245694471 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12080934 | TATTCTAGAATCAGG[A/T]TAGTACATTGTTTTG | 75725 |
rs245694725 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11915581 | ATAAGAAGCCACTAT[A/C]GTGTGTCTAAGATCA | 75725 |
rs245706960 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023275 | GTTAGTTTTTTCTAA[C/T]TTATTTTGCCTTGAG | 75725 |
rs245742558 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083501 | GTCCCCGGGAGTTCT[-/G]GGGGGGGTCTGACTT | 75725 |
rs245745707 | snp | G/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925588 | TTCCTCAAGGGAGGC[G/T]CCTTTGATTACTCCA | 75725 |
rs245746651 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11916441 | GTTTAGCATGTGTTT[A/G]ATCTCTCCCAGGCTC | 75725 |
rs245790197 | in-del | -/TAGCTGTGTC | | | intron-variant | Phf14 | Mm_Celera | 6:11947706 | CTTCTCCATCTGGTT[-/TAGCTGTGTC]TGTATCTACCAGAAG | 75725 |
rs245791994 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12005698 | CATGGGTCCCACCAT[A/G]TGTACTCCTTGGTTG | 75725 |
rs245800216 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997236 | AGTGACATCCCAATG[C/T]AAAAACTTTACGCAG | 75725 |
rs245807011 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11930989 | TCCTGTTGTTAGATT[-/A]AGATTATGACTAAGA | 75725 |
rs245811382 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12015413 | ATTACTGGCCTGGAG[C/T]TTGCCAAGTAGGTGT | 75725 |
rs245814453 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12023726 | TTTGCTGGATCCTGG[A/G]GATTTGAACACACAT | 75725 |
rs245825092 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12016202 | AATATCCAGCAAGCA[C/T]CTTTGTGAAAAGAGT | 75725 |
rs245825492 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11958142 | GAGAGAGAGAGTGGG[A/C]AGCCTTGTCTAGTCT | 75725 |
rs245830895 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094089 | GTTTCTTAATTTGTT[C/T]ATCAAACAGCCTCTG | 75725 |
rs245871300 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12033163 | TCTCCATGTCAGGCA[A/G]TCTCTGGATGGCCTT | 75725 |
rs245895647 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054781 | GGTTTGTTGTTGTTG[-/T]TTGTTGTTATTTGGG | 75725 |
rs245897815 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11920555 | ATCAAGCAATAAAAG[A/T]TTCTTTAGCATGGCT | 75725 |
rs245913778 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052841 | TTAAAGACATTGTTT[C/T]CTTCTAATTTATTAA | 75725 |
rs245914582 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12085749 | TTTTTTTTCAGTTAA[A/G]TATGATTATAATTTC | 75725 |
rs245923093 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12084570 | CCAGAGAGGCCAGAA[C/T]CTGCAGAGCTAGTAA | 75725 |
rs245925205 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997636 | CACCTGAAAAAAAAA[A/T]TTTTTATTTACATTT | 75725 |
rs245925348 | in-del | -/TT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12068533 | AATGAGTCTTGACAA[-/TT]TTATATATATATATA | 75725 |
rs245942901 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031008 | TTACTGTCTGTTGTT[C/T]GCCCCCTTTCTTTTA | 75725 |
rs245946825 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036137 | ATAAATTGAGTGTGG[A/T]AGGGCATGCTTGTAA | 75725 |
rs245948955 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11961346 | TAATGCTCACTGCAG[C/T]CATGCTTCCTGTGAT | 75725 |
rs245992788 | snp | C/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924040 | CTTAACCTTAGCCAT[C/T]AGGGATGGAACTTCT | 75725 |
rs245993982 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12044658 | GTTCACATTAAAAAT[C/T]GGCTTTGTTTGATCT | 75725 |
rs246008266 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11962875 | TCCTGTAGCAGTCAT[A/G]AAGCATGAGGGAAAG | 75725 |
rs246010146 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12089914 | GGTGCCCTTATAAGC[A/G]TGCATATGGTGGCTT | 75725 |
rs246029816 | in-del | -/TTGTTGTTGTTC | | | intron-variant | Phf14 | Mm_Celera | 6:12035058 | AAGTTAGGGATTTTG[-/TTGTTGTTGTTC]TTGTTGTTGTTGTTG | 75725 |
rs246054146 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024074 | CTGTCCTGGGACTCA[C/T]TTTGTAGACCAGGCT | 75725 |
rs246054424 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12031493 | GTTTTTCATTTTGTA[A/G]TGATTTTTTTCAGTT | 75725 |
rs246060532 | in-del | -/TTCCAGACGTATTTCT | | | intron-variant | Phf14 | Mm_Celera | 6:12078120 | TAGTGATGCCTTAGC[-/TTCCAGACGTATTTCT]GTTACATGTTATACA | 75725 |
rs246085181 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11943339 | AGAATGTTTAGATAA[C/G]ATGGCTAGCAAGAAT | 75725 |
rs246086263 | snp | C/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100034 | TGTCTGTTTTGGGGA[C/G]CTGCCATCCAAAAGA | 75725 |
rs246086348 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11932912 | TGATTAAGTTACAGT[C/G]AACTTCTCATTAAAA | 75725 |
rs246089464 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11979080 | GTATTGAACAGTATT[A/G]TAATATTTAGAAAAT | 75725 |
rs246109809 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024448 | TGGTCCTCCTACAGG[G/T]CCGCCCTTTTCAGCT | 75725 |
rs246131416 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12080011 | CTGATTGTAGAAGAG[A/G]GTTTTGTTGTTGTCT | 75725 |
rs246139493 | in-del | -/CTCCCC | | | intron-variant | Phf14 | GRCm38.p3 | 6:12018392 | ACATCTCAAATGCCA[-/CTCCCC]CCCCCCTTTCCTTTA | 75725 |
rs246140987 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11934387 | GAAGTAAGGCTTTTG[A/C]GTACATTAGAAGAAG | 75725 |
rs246142353 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12033410 | CTAAAGTCTGCTGCT[A/C]CAGTTTTTGCCGTGT | 75725 |
rs246148034 | in-del | -/AGC | | | intron-variant | Phf14 | Mm_Celera | 6:12077993 | CAAATCTTCAGAATA[-/AGC]AGCAGAAGAAAAACC | 75725 |
rs246151248 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11941587 | AAGGTAATTTTGCTG[-/T]TTTTTTTCCTGTTAG | 75725 |
rs246159614 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12018586 | ACGCACATGGAGACT[G/T]ACCTACATATGTCTG | 75725 |
rs246168999 | snp | G/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009934 | CCCATCTTTTATTAT[G/T]TTTTTTATTAGATAT | 75725 |
rs246170924 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12031885 | TAGATGTTAAAAATT[A/G]CAATGTTCTCTTGGT | 75725 |
rs246198181 | in-del | -/TTT | | | intron-variant | Phf14 | Mm_Celera | 6:11937430 | TTTTTTAAATGAAGA[-/TTT]TTTTTTTTAAGATTT | 75725 |
rs246222220 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11995682 | TCTAGTCTCCTGTTC[C/T]CTTTCTCCTCCCCTC | 75725 |
rs246232897 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11996110 | CCGCCTAATATTTGG[C/T]TGTGGGTCTCTGCAT | 75725 |
rs246233325 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11922643 | AATGATTTTATTAGA[A/G]CACCGATTCTCAGTT | 75725 |
rs246233567 | in-del | -/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12024424 | GGGTCCAAATTAATT[-/G]GAAACTGCTGGTCCT | 75725 |
rs246277309 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12034569 | GGGAACTATGATTCA[C/G]TGTTTGATCAGTGTT | 75725 |
rs246286879 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11986870 | CAGAAATGGATTGTA[C/T]ATCTTCAGGATCAGT | 75725 |
rs246289976 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12047823 | GACTCTGCTTGCCCT[A/G]CAGGTGTGATGAATG | 75725 |
rs246290246 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11955067 | GGCTGGAGGTATAAG[A/C]ATGTGTGAGCTGCCT | 75725 |
rs246290789 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12068939 | TTAAATACTTCATGC[C/T]AACAAGACAGGTCAA | 75725 |
rs246301428 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12014689 | AGACTTATCTGAAAA[A/C]ATCTAATAACTAGGA | 75725 |
rs246323487 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959762 | AGTACAGATAATTTT[A/T]AAATATATCTTAAAT | 75725 |
rs246325905 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12048971 | GTAGGGGAAGATACA[C/T]GGCATCTGCCTCTGG | 75725 |
rs246390867 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061454 | ATATTTCTAAAACAA[A/G]GTTTTCTTTTACCTT | 75725 |
rs246407120 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040119 | TTTTACTTGTTGAAC[C/T]TAAATGTGAAGCTAT | 75725 |
rs246424583 | snp | C/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12016492 | GTAAAAGGATGAGCG[C/G/T]GCACTGAGTGAGACG | 75725 |
rs246427599 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908610 | TGGAGTAGATAAAAG[A/G]GCTATTGTAGTTGTC | 75725 |
rs246497456 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909267 | CAAGATCCTCCTGCC[C/T]CAGCCTTCCAAGAGT | 75725 |
rs246515441 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12095888 | AGTCCATAAGGGAGG[A/G]ACAGAGACAAGAAAC | 75725 |
rs246524752 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12016943 | GGGAGTGCCCTGTGT[G/T]TGCTCTCATGTGGCC | 75725 |
rs246524935 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12006142 | GCTACTAGAATAAAA[C/T]CTAAGTGGCAGCTTG | 75725 |
rs246554594 | snp | A/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:11988925 | AAATAATTGCATTCC[A/T]TCAGAGCCTAATCCC | 75725 |
rs246575366 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12001701 | AAGCTTGTCTTGTTT[C/T]CAATTATAGTGGAAT | 75725 |
rs246580419 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12007383 | GTAATGCTTTATGTA[A/G]AGATTCTGCCGAAAT | 75725 |
rs246604421 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12067046 | TTAACCACTCCATGG[A/G]TTCTCAGACAAGCCA | 75725 |
rs246643751 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12018513 | CTGCAGAATAAAGTA[C/T]TTCCTCTCCCACTGA | 75725 |
rs246648618 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060208 | ACCACGCCTAGCCGT[A/G]CAACTTCAGAGAAGA | 75725 |
rs246649811 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11976681 | CTATTTTATTTGTTA[C/T]ATAAAATTTTATTTT | 75725 |
rs246651001 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905774 | CAACAACAAAAAAAA[-/C]CTCAAGTGCTATCCA | 75725 |
rs246653599 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12015121 | TAGTTTATTGGCACA[A/G]CCCTGTACATATAAG | 75725 |
rs246656409 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11998830 | GCAGGCTCAAGGCTC[A/G]GGGCTGACGATTCTA | 75725 |
rs246667961 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12057574 | GGGGAAACATGGTTA[A/T]TTTTTTTCTTTTTAG | 75725 |
rs246681933 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11929937 | TAGCATCTTTGTCTT[A/G]TACTTGATGCCTGTA | 75725 |
rs246688306 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909345 | TTTAGTATTGAGGGG[-/AA]AAAAAAAAATACGTA | 75725 |
rs246692673 | in-del | -/GGTTT | | | intron-variant | Phf14 | Mm_Celera | 6:12003671 | GTAGCTGTGTTCACA[-/GGTTT]TGTTTTGTTTTTTAC | 75725 |
rs246703684 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11926604 | CTTTTCCCACCAAGC[A/T]CAGTGTGGAGAAGTC | 75725 |
rs246716762 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12037276 | ACTATAGGAATTATC[A/C]AATTAGATTTTGGTC | 75725 |
rs246717773 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12004261 | GTAGCTTGAAAGCTT[C/T]CTGATTTTGTTTTTC | 75725 |
rs246722542 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11995746 | GGGTACCAATCTGGT[C/T]TGGTATATCAAGTTG | 75725 |
rs246734801 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024506 | AGGAGTCAGCTGCTC[C/T]TGTCCATTGGTTGAG | 75725 |
rs246736564 | snp | C/G | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11925892 | TTTCACTTCCTCCTT[C/G]TCGGAGCTGTATCCG | 75725 |
rs246744492 | in-del | -/ACATACATACATACATACATAC | | | intron-variant | Phf14 | GRCm38.p3 | 6:12019294 | CATACATACATGCAT[-/ACATACATACATACATACATAC]ATACATACATACGTA | 75725 |
rs246751438 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11976554 | TTTAAAGGATTTTAA[A/G]GAGTCTTAAGACCAA | 75725 |
rs246797557 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11935806 | AGGCTGATTTCTCTA[C/G]AACAGCCTGTGTAAA | 75725 |
rs246807004 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11978464 | ATGTTTTAAAGTTGC[-/T]TTTTTGTTTTCTTTT | 75725 |
rs246822774 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12098548 | TTTCAACAGGCAGCT[A/G]GGGCTCAGCTCCTCT | 75725 |
rs246849515 | snp | G/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | Phf14 | Mm_Celera | 6:11926761 | GAGGCAGGTGAAGCC[G/T]TTGGCCGCTTCTCTC | 75725 |
rs246868512 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094256 | AATAAGCTTAGGTTT[C/T]AGGACAAGAATCTCA | 75725 |
rs246891910 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12017887 | GGTTTCTGAAGGAAG[A/G]AAATGGCAGAGATGC | 75725 |
rs246902834 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095048 | TTGCAGGAAATCCAC[C/T]ACGTCAAGTGCGTGG | 75725 |
rs246910401 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12085097 | CCCTAGGATCCACAT[A/G]ATGGTGAGAACTAAC | 75725 |
rs246911599 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11999977 | TTTTCTTGCTTTCTG[-/A]GGATGATGATATTCT | 75725 |
rs246941514 | in-del | -/TT | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040034 | ATTAGTATCTAGGTA[-/TT]TTTTTCCAGAAATAT | 75725 |
rs246945708 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11915278 | GGCATGATGGGCCCA[A/G]ATTGAACAGGGAGCA | 75725 |
rs246950177 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12016914 | TGCAGATCACACCTG[C/T]TTCCTGTGGCACAGG | 75725 |
rs246958862 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12071347 | CCCTAGAATTTTCTC[C/T]TGATAGTTAAAGGGT | 75725 |
rs246959862 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12079521 | TTTCCCACACATTTC[C/T]ACCAACTGAGACCAA | 75725 |
rs246962980 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12006670 | GTAGTATATTAAATG[A/G]CATAATTTTAGCAAT | 75725 |
rs246997048 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11961925 | TTATATAAAGGGGTC[A/G]CCATGCTAGATTTGA | 75725 |
rs247009429 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11962971 | TAGAACACTGGAAAG[C/T]ATATCAAAAGCGTTC | 75725 |
rs247009780 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907212 | CAAGCAATCAGGTCA[G/T]CCCAACAACAGAATG | 75725 |
rs247021502 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11944886 | CATCATTATAACTAT[C/T]GAGGAAGGATGGTGT | 75725 |
rs247052405 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12072305 | TTGGAGAGAAGAAAG[G/T]GTCTGGTGCTGTAGC | 75725 |
rs247065206 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11953561 | CTTCCCATCTTCTTG[A/G]CATAGAGGAGTGACT | 75725 |
rs247074747 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11936154 | TTGAGAAACCTGTAG[G/T]TCTACTCTAGAGTAG | 75725 |
rs247097370 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11946892 | CTTGAGCCCACCAAG[A/G]AATACTACCATTGAA | 75725 |
rs247106933 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910096 | ATTTTAATTAGGGCT[A/G]GAGACAATAGTGCTA | 75725 |
rs247112094 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12041764 | ACTACCATCTTCTCC[G/T]TATCCTCCAGCTCCA | 75725 |
rs247142578 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12096550 | CTACCAGGCAGCTAA[A/G]ATGAGGGTCTTAAAG | 75725 |
rs247171124 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11936997 | CTCATTGAGGAAGAA[A/T]TTGTAGAAGAGTTTG | 75725 |
rs247177563 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12073794 | AAACATTTTAGCTTT[A/C]GTGAATTGGTGACCA | 75725 |
rs247191285 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12059154 | AAATAGTAAGCAGGG[-/T]TTTTTTTGCTGTGGG | 75725 |
rs247191894 | in-del | -/A | | | intron-variant | Phf14 | GRCm38.p3 | 6:12028597 | ATTTTTTTTGTAAAT[-/A]AAAAAAATACAGTTT | 75725 |
rs247192378 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12035017 | TAAAAAGTAGAACTT[A/T]GTGATTTAAAGTCGT | 75725 |
rs247240273 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12087303 | TCTGTAAGGCAAAGG[A/G]AAAGATCTTCAGTAA | 75725 |
rs247244570 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12095183 | AACACATACCAAAAA[A/C]AAAAAAAAAAATGGC | 75725 |
rs247261557 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11976297 | AGACTCATCTCTGAG[A/G]GATCTGGGACCCCAG | 75725 |
rs247263193 | in-del | -/GT | | | intron-variant | Phf14 | Mm_Celera | 6:11978577 | CCTGCTTCTATGAGA[-/GT]GTTTCCCAATCCACC | 75725 |
rs247267897 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12022200 | AAGATGCCATAAAAC[A/G]AGCCAGTACACTAAG | 75725 |
rs247271828 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037492 | CAGGTCTGCTGGCTT[C/T]CACTCTGGTTCCCAC | 75725 |
rs247289459 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12069902 | GTTCCTTCCTGGAAT[A/G]TAAATTATTTCCTTG | 75725 |
rs247294753 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12025778 | TGTAATTTCCCGTTT[A/T]TCTAAGTACTAATAT | 75725 |
rs247311023 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12018460 | TCTGCTGAGGGTGGG[C/T]AACTCCCATTATTCC | 75725 |
rs247312755 | in-del | -/TG | | | intron-variant | Phf14 | Mm_Celera | 6:11940628 | CGGCCTACTCCTCTC[-/TG]TGGCTGGAGCTATGT | 75725 |
rs247324229 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12070404 | AGAAACATTCAGAGA[A/G]CATAATTGTCAAGGG | 75725 |
rs247331678 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11955352 | CAGAATGCTTACTCT[C/T]TTAATAATAGCCACA | 75725 |
rs247335171 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907296 | AACCACAGCTAAGAG[A/G]CCACCCTGGCAAAGA | 75725 |
rs247345471 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947389 | AACATTAAAGCCTAT[A/G]GGAACCATTCTCCTT | 75725 |
rs247410625 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12062732 | CCAAAACCTAATTGC[A/G]TATATGGTTTCCACA | 75725 |
rs247415855 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11939195 | GCTTGTCACTTACCT[C/T]TGACGTTCAAAAGAG | 75725 |
rs247419251 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11934438 | GCTCTCTCAGACGTT[C/T]AGAGAGTTGTTTTAA | 75725 |
rs247441223 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12063403 | AGTAGTATACATGGC[C/T]ATTATTCAATATGCC | 75725 |
rs247452077 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12051763 | GAAAGTGGCAGCCTA[A/G]CTGGTGTCATTTATA | 75725 |
rs247468081 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060763 | CGGTATGTTTCCTTT[C/G]ACGATGAATTTATTA | 75725 |
rs247485631 | in-del | -/AAAA | | | intron-variant | Phf14 | Mm_Celera | 6:11918118 | ATAAAATAAAAAAGG[-/AAAA]AAAAAAAAAAAGGTA | 75725 |
rs247489980 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12052177 | CCAAACCTGCCCCCA[C/G]TTCTTTTCCCTCTTC | 75725 |
rs247496342 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11958573 | AAAAAAGACAAAAGA[A/G]ATCTCTTTAAGCATT | 75725 |
rs247540020 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12020160 | TTAGGAAACTGAGAA[C/T]ACAAGTGAATCCTGG | 75725 |
rs247566611 | in-del | -/TTTT | | | intron-variant | Phf14 | Mm_Celera | 6:12058703 | CAAATGCTCTTTGTC[-/TTTT]TTTTTTTTTTCCTAT | 75725 |
rs247575920 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055170 | GAATAAAACAGGTTT[A/T]CCAGGAGGGGAGAGT | 75725 |
rs247577632 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12043438 | GTATAGAAAACATTC[A/G]TGTAGGTGGTGGCTT | 75725 |
rs247591598 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12077737 | AAGGACAGCCCTTCA[A/G]AGGGTTATGCGATCA | 75725 |
rs247598997 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11911628 | TAGAAGCTCCCAAGA[C/T]ACAAGCTCACAAGGC | 75725 |
rs247626992 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11923647 | CCTCCTCATTGCATT[C/T]GGTGATTTGATGTCT | 75725 |
rs247644702 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12000568 | AGTGCTTTTTGTTGT[G/T]GTTGTTCTCAGATTG | 75725 |
rs247647271 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11937487 | CTGTAGCTGTCCTCA[G/T]ACACTCCAGAAGAGG | 75725 |
rs247652170 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12020604 | CTTCCTTGGTCTTCC[C/T]GAAGATCACACATTA | 75725 |
rs247655486 | in-del | -/GCCAG | | | intron-variant | Phf14 | Mm_Celera | 6:12019688 | TATTTGGAAAGCAGA[-/GCCAG]GCCAGGTGGACCTCT | 75725 |
rs247658400 | in-del | -/CTA | | | intron-variant | Phf14 | Mm_Celera | 6:12069315 | AAATCCTGTATGGAC[-/CTA]CTACCTCTGTAGACT | 75725 |
rs247667248 | in-del | -/GAGATGG | | | intron-variant | Phf14 | Mm_Celera | 6:11992905 | AAAGGACATGCAGTA[-/GAGATGG]GTTTTCCTACATCAA | 75725 |
rs247668046 | in-del | -/CAACTATGAATAG | | | intron-variant | Phf14 | Mm_Celera | 6:12021509 | CAAACCACATATTCT[-/CAACTATGAATAG]CAACATACCTGTCAG | 75725 |
rs247707623 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12012611 | CTGTAATTTTCATCC[A/C]TTAAGTTTTCACTCC | 75725 |
rs247707708 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12064479 | CTGGGAATTGAACAC[C/T]GGGCCCTCTGAAAGA | 75725 |
rs247709028 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12052615 | ATATTACCCTATGCT[A/G]TATTTTACATAAGGA | 75725 |
rs247743454 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12087803 | TTAATTAAATTTTAA[-/T]TTTTTTTAACTGTGA | 75725 |
rs247762767 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11920092 | GAAGTAAAGTTAGTT[A/T]GTAGGAGGAAGCACC | 75725 |
rs247780620 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997022 | TTCATAAAAATTTAT[G/T]CAGGCAATGCTCAGA | 75725 |
rs247781579 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12058484 | GAGCTACACTGAGTA[A/C]TATCTAGGCTCTGTC | 75725 |
rs247784800 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12065231 | TTATACCATTGTCCA[A/G]AATCACAGTGACAGC | 75725 |
rs247787829 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927778 | CTGAGAGTTTGGAAC[A/G]TCTTGCTCCTTTTCT | 75725 |
rs247816651 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12059165 | AGGGTTTTTTTTGCT[A/G]TGGGTAACACTATTA | 75725 |
rs247823354 | snp | C/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12041042 | CATGTTGTCACAGTT[C/T]CTACATGATATGTTC | 75725 |
rs247843866 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029247 | TTGCCTTAACTGTAG[G/T]ACATGTGTTGACTTT | 75725 |
rs247848295 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11928215 | AACTAATGAGTTCAC[A/G]CCAGCCGTCAACACT | 75725 |
rs247872800 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053865 | TAAAATTGGAGGAAT[A/G]TGTACAAGGTCAAGG | 75725 |
rs247878751 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12061787 | CCACTTGTCAGTGTA[C/T]ACTCATGTCTTTCTT | 75725 |
rs247888513 | snp | G/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008918 | AACTTTGAAAGGAAT[G/T]TATATGTACACAATT | 75725 |
rs247907817 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12096127 | TCCACCAGTTTTTAG[A/G]GACTATAGTTAAGGT | 75725 |
rs247955953 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12046233 | AAACATTCTGATCAA[C/T]GTAGAAGCAGTCTTG | 75725 |
rs247960080 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11920882 | CATACATTTACTTGA[C/T]TTAAGTTTCTCAGGC | 75725 |
rs247979180 | snp | A/C | | | synonymous-codon, nc-transcript-variant | Phf14 | Mm_Celera | 6:11990040 | ATAGAAGTTGAATGT[A/C]CCAGCAATCTTACGA | 75725 |
rs247985504 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921318 | TGTGGGGAAATAATT[C/T]CGTGTTATCTTCAGC | 75725 |
rs248005107 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12086795 | GTCTGAGCCAGTAGA[A/G]CACATCCACAGCAGC | 75725 |
rs248014523 | in-del | -/TA | | | intron-variant | Phf14 | Mm_Celera | 6:12055837 | TCTGGAAGGGAAATC[-/TA]TATAAAGAGAGCAGA | 75725 |
rs248031056 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12051472 | CAGTGGGGTACCCTA[A/G]ATGGAAATGCCTTTG | 75725 |
rs248034277 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12003197 | ATTTTGTCTGCATTT[C/T]TAAGGCAGTACCCAT | 75725 |
rs248041266 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12056877 | ACATGTTATTCATAT[A/G]CTGTGCTAAATCTTC | 75725 |
rs248048674 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12067339 | TATTATAATATAATC[-/T]TTTTTATTTATATTG | 75725 |
rs248073462 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12051038 | TAAATAATAATTTTA[G/T]CAAAATATTTTCTAT | 75725 |
rs248074641 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057364 | TGTGTAGAAGCCAGA[C/G]ACAGCCTCAGATGTC | 75725 |
rs248080415 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11915477 | TTCTAGGACAGCCAC[A/G]GCTACACAGAGAAAC | 75725 |
rs248083091 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12003467 | ATGTAGCAGGCTGAG[A/C]TACAGCCCACACCAA | 75725 |
rs248085651 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11995035 | GTGAATTCTTCCATT[G/T]TTATTTACTGGTGTT | 75725 |
rs248089313 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11931590 | TATTATGAATGATTT[-/A]AAAATTCAAATTTTC | 75725 |
rs248089405 | snp | A/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925534 | AGTGCTTGATCACTA[A/T]TTGAGAAAATACCTT | 75725 |
rs248098000 | in-del | -/GG | | | intron-variant | Phf14 | Mm_Celera | 6:12034596 | GTTGGAAGGCAGTAT[-/GG]ACAATGCTTTCTTTC | 75725 |
rs248100300 | in-del | -/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908870 | GTATGCAAAACCCAC[-/G]GTATTTCTCGAGAGC | 75725 |
rs248101226 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12004406 | TCTTTGAAGTCCTGT[A/T]ATTTTTATTTCCCAT | 75725 |
rs248107692 | in-del | -/GT | | | intron-variant | Phf14 | Mm_Celera | 6:11947508 | ATCAACACCCTAGCG[-/GT]GTGTGTGTGTGTATG | 75725 |
rs248120184 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11918333 | TTATTATGGTAATCA[C/T]TTCATAGTGTTTATA | 75725 |
rs248142574 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918238 | AGAAGTTCCAGGCCA[A/G]CATTAGCTATAGTGT | 75725 |
rs248147182 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12051857 | ACTCTAGTTTATTAA[A/G]TGTATAATTTAAGTA | 75725 |
rs248149987 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11918677 | GGTATCGGCCTGTCA[G/T]CCCAGCATGTGGGAG | 75725 |
rs248155325 | in-del | -/AAGT | | | intron-variant | Phf14 | Mm_Celera | 6:11909828 | AATATTGGTAATAAA[-/AAGT]AAGTAGATATATAGA | 75725 |
rs248168588 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11911285 | ATAGTGGAGACCTGA[A/G]TGTCTTGAAGAGAGT | 75725 |
rs248189292 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12000334 | ATTTTAGGCCTGTCG[A/C]TGTCCTCTTCTCTTT | 75725 |
rs248192094 | snp | A/C | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011526 | GGACTGATAGTGAAC[A/C]TAAATTTGACTGTCA | 75725 |
rs248199948 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12088051 | ATTTGTACAGAATTT[G/T]TAACCATCTTCTTCA | 75725 |
rs248208391 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12078455 | CCTGAAACTGGCGTT[C/G]CAGATGGTTGTGAGC | 75725 |
rs248218090 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12043634 | TCAGTGTTCACTGCA[C/G]TAACTTATCACAGTT | 75725 |
rs248225745 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030144 | GTTATGTGCCTTTGG[C/T]TACTCTGCTTGGCTA | 75725 |
rs248234157 | in-del | -/TAT | | | intron-variant | Phf14 | Mm_Celera | 6:12051173 | AGTCATACCTAGAAA[-/TAT]TATTGTTTCAGATAA | 75725 |
rs248244864 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12001238 | TCAGACAGTCTGTAC[A/T]TCAACCCCTCAAATC | 75725 |
rs248245578 | in-del | -/GTGTGTGTGT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12053236 | GACAGGAGCCTCGTG[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 75725 |
rs248251973 | in-del | -/GTAC | | | intron-variant | Phf14 | Mm_Celera | 6:12027987 | ACAAAAGAGAACAGT[-/GTAC]GTATGAAAGGTTCTG | 75725 |
rs248255129 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12044274 | GGGGGGGGGGCTGTA[A/G]GGGTCGCGACCCACA | 75725 |
rs248255182 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036487 | AAAATGGATTACCTT[G/T]AATTAAGTTGACTTG | 75725 |
rs248261933 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11951986 | AGAAAATATGATGAC[A/G]TGGTAGGTCAGATGT | 75725 |
rs248277621 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12020650 | TATAAAACATTTTAC[A/T]AACTTCAAAAGTTCC | 75725 |
rs248295035 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032740 | CTGTCCTGGCATTCC[C/T]CTACACTGGGGAATA | 75725 |
rs248327425 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11957450 | ACGAGGCATTGGTGT[A/T]CTGTTCAAGAATTTC | 75725 |
rs248332339 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11944476 | ATGCTACCCCACTGG[C/T]GATTTCAGAGCGGTT | 75725 |
rs248344615 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12036875 | CATCATATTTTATCC[A/G]TTATTTGTCTATCAG | 75725 |
rs248359640 | in-del | -/AT | | | intron-variant | Phf14 | Mm_Celera | 6:12028802 | CTTATCAAGTCTCTC[-/AT]GTGTTAATAGACACA | 75725 |
rs248362534 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905641 | GTCAGGCATGATGGT[A/G]CATGCCTTTAATTCC | 75725 |
rs248414251 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11979756 | ACATTAATCATGTTA[-/T]TTAGTATTTTTAATC | 75725 |
rs248415185 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11993855 | TTATCCCCCTCTTGG[C/G]CCACCCTCTGATTTT | 75725 |
rs248417714 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906258 | TAACGGTTGAACTTG[A/G]ATTGAAGCAGTGTTT | 75725 |
rs248420268 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12092320 | ATGTCTTCTTGCCAG[A/G]CCAATCACTATACCT | 75725 |
rs248428757 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947584 | GATTATTGTGACAGG[C/T]AGAATGTCATTTATC | 75725 |
rs248442582 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12034740 | CATTGAGGAATTTCC[C/T]GCAGTGTCTTGGCTG | 75725 |
rs248454004 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12034056 | TGTAAGAACTTATGT[A/G]AAAACAAAATGCTGA | 75725 |
rs248457353 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11980499 | TGTATGCAGTGCTAT[A/G]TCCTTTAATATCTGT | 75725 |
rs248485265 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12034553 | GGAGATGTGAGGGGA[A/G]GGGAACTATGATTCA | 75725 |
rs248509892 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12076268 | AGCTTACAGATAACG[A/G]GATAGATAATTCCTA | 75725 |
rs248519851 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11981283 | TGTGAGCCTAAGGTA[C/T]AGGAGTTGTGTTGCA | 75725 |
rs248530602 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11960351 | GTAGAGAAAGGCGGC[A/G]TTTAATACATCACTG | 75725 |
rs248544112 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950098 | TAGAGGGATTGGATT[C/T]AGTCTTAGTTATTTT | 75725 |
rs248564327 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12028740 | TTTTTTCAAAAAGTG[A/G]CTGTGTAAAACTCCA | 75725 |
rs248592681 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11960616 | AAACCAGAACCTTTT[A/C]AACTAGGATAAAGCA | 75725 |
rs248612726 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12037136 | AATGAGCTAGGGGTA[A/G]AGGGAATTAACAGTA | 75725 |
rs248618746 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12087904 | ATCTTAAAAAGATAT[A/T]GAAAAACCCTGAAGT | 75725 |
rs248641109 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12079440 | CATGACAGAGATAAG[G/T]CTAGTCTCTTAAACC | 75725 |
rs248643650 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12089207 | TTCACTCGAACTTGC[A/G]AAAGTTGATTAGAAA | 75725 |
rs248645340 | snp | A/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12081438 | AAAGAGATGTGGGCC[A/T]CCGTAACAGCCTCTC | 75725 |
rs248673961 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11957077 | ACCTGAATAATTTTT[A/G]ATCTTAGCCATTCTG | 75725 |
rs248676902 | in-del | -/CCACCA | | | cds-indel, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11933615 | CCTCCCCTTCTGTCC[-/CCACCA]CTACCACCACTACCA | 75725 |
rs248681194 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11942113 | GGTTTATTTGGGAGG[A/G]AATATACAGAGACTG | 75725 |
rs248687375 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11954416 | TTACACATGCGGTAG[A/G]TGTTTATTGAGAAAG | 75725 |
rs248702818 | in-del | -/GTATAT | | | intron-variant | Phf14 | Mm_Celera | 6:11922562 | CAATCGATATACTCA[-/GTATAT]ATGCTCACAGACTTG | 75725 |
rs248710693 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12081950 | CACAGGTACAGCCAC[A/G]TGCCTGTGTGGTTTA | 75725 |
rs248718954 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12031323 | TCTCTCTCCTCCCCC[A/G]TGTGTCTGTCTGTCT | 75725 |
rs248745892 | in-del | -/AACT | | | intron-variant | Phf14 | Mm_Celera | 6:12057068 | CCTCAGTCCCTGATG[-/AACT]AACTATATTTGTATC | 75725 |
rs248767630 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947411 | ATTCTCCTTCAAACC[A/G]TCATAGTCTCCTATG | 75725 |
rs248778108 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11957774 | GAGACTTGAAGTTCT[C/T]ATCATACAGATCTTT | 75725 |
rs248800180 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057079 | TGATGAACTATATTT[C/G]TATCTTCTAGTTGGA | 75725 |
rs248825629 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11946352 | GGATTAAAGGCATGC[A/G]CCACCACCACCACCG | 75725 |
rs248834670 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947951 | GACAAGTCTACCTTT[C/T]CAAGTAGCTTTTAAT | 75725 |
rs248845335 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11960380 | TGCATGAAGAGAAGA[A/G]GCTACACAGATTACA | 75725 |
rs248886636 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12068536 | TGAGTCTTGACAATT[A/T]TATATATATATATAT | 75725 |
rs248921430 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11960203 | TACATTGGTGTTCTC[A/G]TAAATAACTGAGCAA | 75725 |
rs248932039 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:11953521 | TTCCTTTTTCTTCCA[-/TT]TGTGACTTTTGAGTC | 75725 |
rs248933894 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010738 | GAGAATTGCTTTTTG[A/G]TACAATTAGAATGCA | 75725 |
rs248937798 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11940549 | CTCTTTGTTTTGTTT[C/T]TTGAGGTGGAGTCTT | 75725 |
rs248942615 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12070477 | CCTTGTCTGTGGTGC[A/G]ATTTTTTTCTCTTCA | 75725 |
rs248957615 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11911331 | AAATGATTGTAATTT[-/A]AAAAAAAAAATGACA | 75725 |
rs248958025 | in-del | -/TTT | | | intron-variant, cds-indel | Phf14 | Mm_Celera | 6:12009195 | AGTTGTAACGTTATC[-/TTT]TTTTTTTTTTTAAAT | 75725 |
rs248961142 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12031726 | CTGTGGATATCTGCC[A/C]ATTGGTTTATGATGT | 75725 |
rs248968993 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060983 | TTACCAATGGCCTTG[C/T]AGGTTCTGTGGTTTG | 75725 |
rs248969031 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12069036 | AAGCAAACAAAGCCA[A/T]ACAATACAAATGTGT | 75725 |
rs249000235 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061476 | TTTTACCTTCAGACC[A/G]AGTTTTAAAGTTTCA | 75725 |
rs249048872 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12065713 | TCCAGCCCTCAGAAA[A/G]AAGTAGGTGGATCTT | 75725 |
rs249061981 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11934722 | TCAGTTAAACATATC[C/T]GTGTCTCTGTCTGTG | 75725 |
rs249067363 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12059745 | CTCAGATGTAAGCTG[A/G]AAGGATTTTGACTTC | 75725 |
rs249080959 | snp | C/G | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099292 | TCTTACAGAGCCCAG[C/G]ACCACCAACTATGGG | 75725 |
rs249086292 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11932032 | GTCTTGAGATTGATA[A/G]TAATTTCTTTGAGTC | 75725 |
rs249125434 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030090 | TGAGTAGGTTAGCAG[G/T]GAGCATGGTTGAGTA | 75725 |
rs249133489 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12059677 | TATGGCAAGGTAGTG[C/G]AGAGGCTGCTTGGGA | 75725 |
rs249145154 | in-del | -/CTC | | | intron-variant | Phf14 | Mm_Celera | 6:12059196 | ACAGTAGTTTAATTT[-/CTC]CTCATGTTCTATCAA | 75725 |
rs249154248 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12020691 | AATCAAACACTTAAA[A/G]GTCCAGCCTCTTTAA | 75725 |
rs249160388 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12071963 | TGCAAAGTACTTAAA[-/T]TTTTTGACATAAATA | 75725 |
rs249163207 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12069125 | AATACATATTTATAT[A/G]TAAATAGATATGCAT | 75725 |
rs249169425 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060066 | CCTATCATCGTCACA[C/G]CCTAAGCACTATAAA | 75725 |
rs249171453 | snp | G/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924375 | CAGTCCCCAGAATGC[G/T]GTTTTCTTAGTGAGG | 75725 |
rs249189311 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12012831 | TACTATTAAAACTTA[C/T]GGACAATAATGCCTG | 75725 |
rs249195335 | snp | A/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12099872 | TGTCTGATTTTTGTC[A/G]TCTCCTGGCGTACTT | 75725 |
rs249195717 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11941401 | CTTTTTAATTAAAGC[A/G]TGATTTTTCTGATTT | 75725 |
rs249197769 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12091467 | TTGTATTCACACACC[A/G]TGTACTTGAGCTCTT | 75725 |
rs249199049 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11928568 | GTTTATTAAGGTGGA[A/G]TCATTCCCAGACATT | 75725 |
rs249224564 | in-del | -/GGTTT | | | intron-variant | Phf14 | Mm_Celera | 6:12083162 | TGGTGATAATGGTTG[-/GGTTT]TTTTGTTTTTGTTTG | 75725 |
rs249240078 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076701 | ACGCATGGTGATATT[C/T]ACTGGGTTTTTGGCA | 75725 |
rs249253265 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11932057 | TGAGTCATTCAAAAT[A/C]TGTTTTCATTTCTTA | 75725 |
rs249268040 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921163 | AGAGAGAAGCAGAGA[C/T]TGCATTTGTTGTTTG | 75725 |
rs249272088 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949881 | TTGTATTCATGTCAT[C/T]TTCCCGTGTTTTTTA | 75725 |
rs249284830 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921753 | GTTTAAATATTAAGC[C/T]GATACTTTTTTTAGT | 75725 |
rs249318230 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950401 | GCTCCTTCAACAAGG[C/T]TACATCTCCTAATCC | 75725 |
rs249321845 | in-del | -/CTCTCTCTCTCTCTCTCTCTTTCTCTCTCTCT | | | intron-variant, utr-variant-3-prime | Phf14 | GRCm38.p3 | 6:12039487 | TTTTCTGTTTTTCTG[lengthTooLong]CTCTCTCTCTCTCTC | 75725 |
rs249331648 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12081970 | TGTGTGGTTTATGCA[G/T]TTACTTAGTTAATGA | 75725 |
rs249333519 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11942977 | ACCCAACCCTTTCCA[C/T]CCAGGATGAGAGGAT | 75725 |
rs249351296 | snp | A/C | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908818 | GTGAGCAGCTGTGAA[A/C]ATATCCATGCCAATT | 75725 |
rs249360640 | snp | C/T | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12099902 | TTCTCATAGCAGTAG[C/T]CACAAAGGACATGTT | 75725 |
rs249365334 | in-del | -/GCAAA | | | intron-variant | Phf14 | Mm_Celera | 6:11929332 | TCTTTGCTATATAAC[-/GCAAA]GGGAGTTAACTAGAT | 75725 |
rs249384366 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12050853 | AGAATTATCTAGGTA[A/G]TCTACAAGAGTCTAA | 75725 |
rs249394433 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12092468 | TTTTCCATATTCTAT[G/T]ATTCAAGTATGTGGT | 75725 |
rs249407977 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12063868 | CCAGTATCAGAAAAA[C/T]ATTCAGCATTTTGAA | 75725 |
rs249410505 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12074388 | TGCTTAGGGATGGAA[A/C]CCACGGGATCCTGAT | 75725 |
rs249424734 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12041910 | AAAAAATTCATACAC[A/G]GTTACTTGTTTAAAA | 75725 |
rs249432845 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12023997 | cactgcccagctTGT[A/T]tttatttatttattt | 75725 |
rs249437141 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12003093 | CAAATAGTATATAAA[C/T]AAACAAAATAGTCTG | 75725 |
rs249442617 | in-del | -/ATTTT | | | intron-variant | Phf14 | Mm_Celera | 6:11994926 | TTAGGACACAATGAC[-/ATTTT]ATTATGTTCAAAAAA | 75725 |
rs249443766 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11948103 | CTTAGTTAGGACTTT[A/G]TTCCTGTGAACAGAC | 75725 |
rs249448513 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12058208 | GTGCCTTCCAAGTGT[C/T]GAGCTTACAGGTATG | 75725 |
rs249449808 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12075528 | CCTACCTTCCATCTG[A/G]CTGCAAACTTTTATA | 75725 |
rs249472989 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12005316 | GTAAATGAACTATTT[A/G]TATTTATTTTATCAA | 75725 |
rs249473017 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947675 | CCTCTCCTGAGATGT[-/G]GGATTACAGGCATGT | 75725 |
rs249496108 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11994827 | TCCTTTCACAATAGC[C/T]ACAAATAATATAAAA | 75725 |
rs249497404 | in-del | -/TCTC | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909131 | TGGCATGGTTTGTTT[-/TCTC]TCTCTCTCTCTCTCT | 75725 |
rs249500973 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12003571 | TTTCCAAATGCCTGG[C/T]TTGTGTTCAGTCAAT | 75725 |
rs249506611 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11910639 | TTTTAAAAACTGTGA[C/T]TGTTTGAGATATGAA | 75725 |
rs249554276 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11940115 | CTCTTCCCAGTGATG[A/G]CAGACTAGGCCATCT | 75725 |
rs249556088 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11948982 | GGTAAGAAAGTGTGT[A/G]ATGCTCATGGACTTA | 75725 |
rs249558405 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11996882 | GAGTAGAGGTATCTT[G/T]CTGTTTGTCATTACC | 75725 |
rs249595639 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927495 | AGAAACAGAATGATA[C/T]AGGCTGTTGTATCTG | 75725 |
rs249598050 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12098782 | GAATCTTTAAATGTA[G/T]TTTTCAGAGAATTTT | 75725 |
rs249612810 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11940791 | GCTTTTATCGTTTAT[A/G]TTGATAGTAGCTAGC | 75725 |
rs249626964 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12049139 | TTGCATACCCAAAGT[A/G]AAACAAACTTGTCTG | 75725 |
rs249644085 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11992630 | AATGACTCAAACTGT[A/G]GAGTTTGTTGTGTTA | 75725 |
rs249652350 | in-del | -/TCTCTCTCTC | | | intron-variant | Phf14 | Mm_Celera | 6:12097533 | ACTAAACTAACAACG[-/TCTCTCTCTC]TCTCTCTCTCTCTCT | 75725 |
rs249656768 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12061013 | GATTTCATGTATGTT[G/T]TGGAGTATAATCTGC | 75725 |
rs249658468 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055002 | GTACAGGTATTAAAC[A/T]TCATCGTATTTTGTT | 75725 |
rs249669252 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11919979 | CATCTCTCACATCTG[G/T]CATACAGCAGTTTTC | 75725 |
rs249678875 | snp | A/T | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099088 | TAGGGTTTCTATGGA[A/T]GTGACAAAACAATAT | 75725 |
rs249712487 | snp | G/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040243 | ACATTTGATCCTCAC[G/T]CTTTACTGATCCAGT | 75725 |
rs249719730 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909342 | GGGATTTAGTATTGA[A/G]GGGAAAAAAAAATAC | 75725 |
rs249720405 | in-del | -/TCTGTCTA | | | intron-variant | Phf14 | Mm_Celera | 6:12085382 | CTGTCTGTCTGTCTG[-/TCTGTCTA]TCTGTGTGTTCTATG | 75725 |
rs249750628 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11979301 | CATTAGCTAGAGGAA[C/T]GACAAAGTTTCCTCC | 75725 |
rs249763187 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12080104 | ATTCAACTATTATGT[A/G]ATTTATTTAAACTTG | 75725 |
rs249776396 | snp | C/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924001 | ATGATTACGTTTCTC[C/G]TCCTCTCATAGTGTG | 75725 |
rs249788458 | in-del | -/TC | | | intron-variant | Phf14 | Mm_Celera | 6:11940431 | CCCCGGGTGGGGTAT[-/TC]TCTGGATTGTCCATC | 75725 |
rs249795137 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11917051 | CAACTTGCCAGCCAG[A/G]GTGGCAGTTACCCAT | 75725 |
rs249809273 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12090912 | GCTCCTGAGGGAGAA[A/C]AGTAGTCTTGCCTGA | 75725 |
rs249825176 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11998349 | cagctatggagagct[A/G]caaacaggaagcaaa | 75725 |
rs249853751 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12075786 | GCACGGTTATGAAAG[G/T]AAAAGCCACTGACTT | 75725 |
rs249857391 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12073117 | AAAGAAGCCTTAGGC[A/G]GTTCTCTGAAGTAAA | 75725 |
rs249868280 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11946980 | AGAATTGAATCCAGG[A/T]CTTCACACCTCCTTA | 75725 |
rs249895597 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959071 | TTCTAAAGAGAGACT[G/T]AGTGACCATCCTGGA | 75725 |
rs249899453 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054337 | CCAGGAAAGTTTCCC[C/T]AGGAATTTGTTTTGG | 75725 |
rs249900984 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12024627 | GCCTTGGGGCCTCCC[C/G]TTGTGGTATGGTGGG | 75725 |
rs249901865 | in-del | -/GTGTGTGTGTGTGT | | | intron-variant | Phf14 | Mm_Celera | 6:11941868 | AATGTTGCTGTATTG[-/GTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 75725 |
rs249928381 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11915526 | AAACAAACAAACAAA[C/T]AGACAAAGACTTCTA | 75725 |
rs249944540 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083301 | ACCTCTGTGAGGGTG[C/T]TCTCCCACCCACCCA | 75725 |
rs249946388 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11938743 | TCAAGAATTCAGTTT[C/T]TTCCCATTCACAGGT | 75725 |
rs249954237 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11990686 | TAATATTTAAGAAAA[A/T]TTTCATTGTAGTGAT | 75725 |
rs249964645 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11959707 | CTTTACCTGGGACAC[A/C]CTTAACCATGGTTCT | 75725 |
rs249975799 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12017772 | CTCTATTTATTCTTT[A/T]TGTTCATTAAAAATT | 75725 |
rs249981465 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076063 | TTAACTATAGAAGTG[C/T]GGGTGTCTTCATATT | 75725 |
rs249981589 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Ndufa4, Phf14 | Mm_Celera | 6:11907699 | GTCTCGACTGGTGAG[A/G]CAGGCACTTTTCAGG | 75725 |
rs249991263 | snp | C/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12047251 | AAGTACTTGAAACAC[C/T]AAGTACATGGCAGAA | 75725 |
rs249994576 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054949 | CACACACACATACAC[A/T]TACTCAGGATGGATA | 75725 |
rs250042200 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11955480 | GAGAAGTGTAGTCTC[-/A]AGTAGATTGCTAGGA | 75725 |
rs250074950 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11915854 | TTGATTTGTCATAAA[A/G]TGAGTTTGCTGAGCA | 75725 |
rs250075896 | in-del | -/TA | | | intron-variant | Phf14 | Mm_Celera | 6:12061346 | CACGATTTGAAATTC[-/TA]TGACTTAAGTAGACT | 75725 |
rs250088069 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916649 | GAACCTATGTGGCTT[G/T]CTCTGTTCCTTTCTG | 75725 |
rs250088250 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908257 | CTTTTACCCAAAAGT[C/T]CTTCCTTGGGGCAGG | 75725 |
rs250118889 | in-del | -/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12081619 | TTTTTATTTTTATTC[-/T]TTTTTTACTATAGTC | 75725 |
rs250136608 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11996853 | TAATATAGCCATGGT[A/C]GTCATTCTTACAAGA | 75725 |
rs250140887 | in-del | -/TTT | | | intron-variant | Phf14 | Mm_Celera | 6:12035663 | GATAAATCTTGTTGG[-/TTT]TTTTTTTTTGGTTTT | 75725 |
rs250159990 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12038980 | AGATCTATTTTGACA[A/G]TCAGAGCTATTACCA | 75725 |
rs250174444 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12067397 | TACTCTTTTTTCCTA[C/T]CATTTAAGCAGGCCT | 75725 |
rs250184829 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12018615 | TGTTACATATGTACC[A/G]GGAGCCTGGTTACAG | 75725 |
rs250185160 | in-del | -/TGT | | | intron-variant | Phf14 | Mm_Celera | 6:11952151 | ATCCAGTCCCATGGA[-/TGT]TTGTAGGTGTTTTAA | 75725 |
rs250188149 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12054514 | GAATAGGGAGAACAC[A/G/T]GGGTTTACATAGGGT | 75725 |
rs250189413 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11997551 | CTGTGTGCTGTGTGC[A/T]CGTGAACAGCATTTC | 75725 |
rs250191912 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032550 | TGTGTGAGTGTGTAG[G/T]TGTATTACTAGAATT | 75725 |
rs250205013 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12033071 | CTCTCAGGAGACAGC[A/T]ATGTCAGGCTCCTGT | 75725 |
rs250213327 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12057306 | TGTGTATGTAAAAGG[-/T]TTTTTTTTTTGGTGA | 75725 |
rs250250512 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12023585 | GCCAGAATTGTGGCA[A/G]TAACCAACCACTTTG | 75725 |
rs250260792 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11939432 | GTAATGAAAGCTGCA[A/G]ATGAACCCAGGATGT | 75725 |
rs250265363 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:11953892 | AGTGACTGTGGGATT[-/G]CCCCCCCTCCCCCAT | 75725 |
rs250289587 | in-del | -/TTT | | | intron-variant | Phf14 | Mm_Celera | 6:11932337 | ATCCTTATCTCCCTC[-/TTT]TTTTTTTTTCCACTT | 75725 |
rs250293778 | snp | C/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:11989175 | ATTTTTCCTTCCCAT[C/T]CCCTTCTTTTGTGAA | 75725 |
rs250302707 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11945377 | CCCTGCCTCCCACCC[C/T]GGAATGATGGCATCT | 75725 |
rs250344502 | in-del | -/TA | | | intron-variant | Phf14 | Mm_Celera | 6:12092328 | TGCCAGACCAATCAC[-/TA]TATACCTTCCAGGGT | 75725 |
rs250355261 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11989834 | ATGTATTTCTGAGAA[C/G]TAACGAGACTATGCA | 75725 |
rs250389781 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11962488 | TTTAATTTAGATTGA[-/T]TAGAACTATTTTTAT | 75725 |
rs250391282 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031241 | TTGTTCTAGAGCTTT[G/T]GGGTGTGCTATTAAG | 75725 |
rs250398945 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060676 | GTGTGGGCCACAGAT[A/G]ATCTCCAGGGCGCTG | 75725 |
rs250423386 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12091406 | AGTTCATGATGTGAC[A/G]TCTCTGTGTACAGCA | 75725 |
rs250450966 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12031794 | ATGACCTTCATGCTA[A/G]TGTTTGAAGGTCAAT | 75725 |
rs250458062 | snp | C/G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083184 | TTTTGTTTGTTTTTT[C/G/T]TTTTTTTTTTTAATT | 75725 |
rs250463152 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024580 | TTCGGAGGGCAGTCA[C/T]GCTAGGTCTACAGCC | 75725 |
rs250475097 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053364 | TGAAAGATAACCTGA[A/G]TTCATTTTGTCATAG | 75725 |
rs250501094 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11954071 | TTGATTTTTTTGTTG[A/T]CCCTCAGGGCTTCAG | 75725 |
rs250507908 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12084479 | TTAGTGTTTTTATTA[C/T]TTTTAGATTTGTTTT | 75725 |
rs250532979 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12034420 | ATGGCTACAACACAT[C/T]TCAGAATATGTTGAA | 75725 |
rs250559576 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11997737 | TGAGGGTGCTCCCCT[A/G]TGTATCTACCTGTCT | 75725 |
rs250561427 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959540 | GCATTTCTTGATTTG[C/T]GAATGAGAAGAACGA | 75725 |
rs250566077 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11954735 | TCACTGGAATCACTC[C/T]CATGGTCACCAACAG | 75725 |
rs250577569 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12034038 | ACAAAGCAAAACAAC[A/G]GATGTAAGAACTTAT | 75725 |
rs250583703 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12045306 | AGGCCTAGTTAACAC[A/G]GATTTTTCAAATTCT | 75725 |
rs250595200 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12078141 | ACGTATTTCTGTTAC[A/G]TGTTATACACTAAAC | 75725 |
rs250597289 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12085420 | CGGGGACTTGTGTTC[A/C]TGTATGCAATAACTG | 75725 |
rs250610633 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12065889 | ATTCCAAAGCATGTG[-/TT]TTTTTTTTTTTCTGT | 75725 |
rs250613688 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11951683 | AATCATCTATATCTT[C/T]ATAAAATTCAAGACA | 75725 |
rs250629394 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12078800 | CTACATGGGGATTGA[A/G]AACCATCTATAGTTG | 75725 |
rs250631591 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949600 | CTTCATATTCTTTGG[C/T]TGTGTAGGTAGGAGG | 75725 |
rs250643182 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12085700 | CCATAACAAAATAAC[C/G]AGAGGTTGCATTGGT | 75725 |
rs250666916 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959349 | AAGCTGGAGTGTAAA[-/T]TTCTGTTTTCTAATG | 75725 |
rs250668903 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008525 | TTCTGGATCATTTAC[A/G]TTAGGATATATAGAT | 75725 |
rs250699233 | in-del | -/TTTCTATGTCTGGA | | | intron-variant | Phf14 | Mm_Celera | 6:11977068 | TAAGTTCAGCTCAGT[-/TTTCTATGTCTGGA]TAACTGAACTTCATT | 75725 |
rs250709144 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11914835 | CATAGTTGTGTGGTT[A/C]CATATTTATTATTTT | 75725 |
rs250713413 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12062062 | ATTTAAACAATGAAT[C/T]ATTTTCATACTAATC | 75725 |
rs250720636 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11952643 | GTCTCTTATGTTTAT[C/T]TGTGATTGAACACAG | 75725 |
rs250722997 | in-del | -/AAAACAA | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905728 | GTGTGAGGATGCCTC[-/AAAACAA]CAGCCATAACATAAA | 75725 |
rs250728666 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11944291 | ACTTGAGAATCTTTG[A/G]ATGGTTCTAGTGTAG | 75725 |
rs250738667 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908544 | TCAGGACTTTCAGAA[A/G]TTCACCAATAAGATT | 75725 |
rs250741103 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11998530 | GCCTTGTAACTCCCT[C/T]TTGGCATGACCGAGC | 75725 |
rs250747738 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009315 | TTTGTCGGTTTGTCT[A/G]GCATCTCATTTATTT | 75725 |
rs250748175 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032891 | CCTGTGAGCTCTGGG[G/T]AGTCTTGGTCGATAT | 75725 |
rs250758247 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11978154 | ATCAAGTTGGATGTC[A/G]TACTTTTATAGAGCT | 75725 |
rs250794075 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11945206 | TTGTTTGTTTGCCTA[C/T]AGTTGGAGGGGATAC | 75725 |
rs250822692 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11957574 | GACTTGACCTTTGTA[C/G]AGTTCACATTTTTCT | 75725 |
rs250856841 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052065 | CCTGGAGTCTGAGAC[A/T]ATGTGTTGGCTACCC | 75725 |
rs250858606 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11999384 | GTTAAGAGAATGTTT[C/G]AATGTTAACTTTGAA | 75725 |
rs250868257 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11995909 | TTGAAGACCAAGCTA[C/T]GCATGTGCTATATAT | 75725 |
rs250894839 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11998099 | TCTTTTTGCCCATTT[A/T]CTGTTTTTTATTGTA | 75725 |
rs250908091 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11918585 | AATACCACCTTATCA[C/T]ATTCTGTACCTGCAC | 75725 |
rs250908461 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12068396 | ATTAAATTCAGCAAA[A/G]TACTTAATAAAATCC | 75725 |
rs250922934 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12096438 | TCAGTCCATTATCAT[C/G]AAGGCAAGAGCATGG | 75725 |
rs250939067 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11989944 | TCTAAGTGCTGGCTT[A/C]CTTAGATTTAGTGGC | 75725 |
rs250950090 | snp | A/C | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009114 | GTGGCTGGGAATTGA[A/C]CCTCTCTGAGAGCAG | 75725 |
rs250957133 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12096998 | CCTTGAGCTACAGAC[A/G]CTCTGCAACAATCCA | 75725 |
rs250993035 | snp | A/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011206 | AGTTTATATAGATAC[A/T]GATCCATTTTGGATA | 75725 |
rs250997000 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060961 | TGAAATGATAGGAAC[G/T]TGGCCCTTACCAATG | 75725 |
rs250997722 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11990979 | TTCCCAACTGTGGTT[A/G]ATTCTTTGGAAAATA | 75725 |
rs250998325 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12027059 | GAGCTGTAAGGAGGA[A/T]GTTGAACTGGAAAAA | 75725 |
rs251000027 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12019867 | GCCCAACTATGTAAA[C/G]CTAAATTTGATCTCT | 75725 |
rs251001194 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12048868 | TGTAATCCTAGCACT[-/G]GGAGGGGCAGACACT | 75725 |
rs251015304 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918816 | CTTTTATTTATTTGG[A/G]GGACAGGGTCAAACT | 75725 |
rs251025319 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11912466 | AAAAGCAATGACAAA[A/T]TTTTTTATATTGTCC | 75725 |
rs251057135 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12019703 | AGCCAGGTGGACCTC[C/T]GATTTCTAGGCAAGC | 75725 |
rs251070338 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997767 | GTTTCTCCCAAGTGC[-/T]AAGATTACAGGCGTA | 75725 |
rs251070416 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12020376 | ATACAACCAAGAACT[A/C]CCAGCTCATTGGTGG | 75725 |
rs251073312 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11931023 | TACATTCTGTGACTA[A/G]AACGTTGGGCTAGTA | 75725 |
rs251083077 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11923818 | TTGTATTATGTTCTT[C/T]TTTCCTCTTAGTAAT | 75725 |
rs251099858 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11977010 | CAGAAGGGCAGTGCA[A/G]TAGGTCTAATAGGGC | 75725 |
rs251102551 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12001023 | GGGTTTCCCATAGCC[C/T]AGGCTGCGCTCAAAC | 75725 |
rs251196584 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066126 | TCTCTCTCTTTCTTT[G/T]TCTCATTTTATTTTT | 75725 |
rs251207463 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12017825 | CCTTGTAGTAATGGT[A/G]CTTAAACAGTGGTGA | 75725 |
rs251212831 | in-del | -/TTTG | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011430 | TTTTTAATTAACTTT[-/TTTG]TTTGTTTGTTTGTTT | 75725 |
rs251220271 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12049504 | TTACATACCAGCTGA[A/T]GCAATGGGTGTTTCT | 75725 |
rs251243587 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12018456 | TCCCTCTGCTGAGGG[C/T]GGGCAACTCCCATTA | 75725 |
rs251244142 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12078876 | GAAATGGATGTGGTA[C/T]GCATATGTAATTGCA | 75725 |
rs251256013 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12073478 | ATGTGCATTTTTCGC[A/G]TATGTTCTTATGAGT | 75725 |
rs251260299 | in-del | -/GTGTGT | | | intron-variant | Phf14 | Mm_Celera | 6:11916131 | CACAATATTAAACAA[-/GTGTGT]GTGTGTGTGCGCGCA | 75725 |
rs251264268 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905864 | TTGGGGAGGCGAGAT[A/C/T]GAGATGAGCTCACGA | 75725 |
rs251270997 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11946760 | CTGTGATAGGTTCTT[A/T]AGTAGTGTAGCCTAA | 75725 |
rs251282346 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11938780 | GTAGAATTCTCATAT[A/T]TTTCTCTCTTAAGCC | 75725 |
rs251296992 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11928885 | AAAGAGCTAGTGGAA[A/T]ATGATTTTATTTTAA | 75725 |
rs251308069 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072207 | CTAAAGATTTAGCCC[A/G]TCATGTGGTGTTAGT | 75725 |
rs251319920 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12030709 | TGTTTTGGATTTCAG[A/G]ATAACTCTGTCCTCA | 75725 |
rs251321077 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009007 | TTTTGTTTTAATATT[C/T]ATTTTTTTTATATGA | 75725 |
rs251323270 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11919166 | CATGCAGGTTTTTTT[-/A]AAAGTTGTATGATAA | 75725 |
rs251327116 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11938602 | TTGAGATAATTGGCA[G/T]AGATAGCTTAGTCAT | 75725 |
rs251327395 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947195 | CATGGTGTGAGCATG[A/G]CAGCAGGCAAGCAAG | 75725 |
rs251327399 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11921881 | TACAAACCAGAGACG[-/A]AGCCAGAGAACCAAG | 75725 |
rs251339169 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11939063 | CAGACTCTGTTTCAC[G/T]AGGTCGTTTCCTAGC | 75725 |
rs251356350 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917590 | CTACAAGTTCCCAGA[G/T]TTTTACCCACTGAGC | 75725 |
rs251365479 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083077 | TTTCAAAATCACTGA[A/G]ACATTTTTTTCCTAC | 75725 |
rs251379957 | snp | A/C/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | GRCm38.p3 | 6:11906482 | CTGGTAGGCTGGGAG[A/C/G]GGAATCTCTTCGGGA | 75725 |
rs251381454 | in-del | -/CTATTGATGGTAT | | | intron-variant | Phf14 | Mm_Celera | 6:12025092 | GATTACCAATTTGTC[-/CTATTGATGGTAT]CTTTTGACTTACAGT | 75725 |
rs251385569 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11994101 | ATTGTTGGTCCAATG[A/C]CTGAGAGATCTCAGG | 75725 |
rs251402236 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12034219 | TTGGTGCAACAAAAG[A/C]GACAAGTGAAGATGA | 75725 |
rs251406137 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12016805 | TCTTAATTTTATTGT[C/G]CAAGTTATCTTTTCT | 75725 |
rs251412853 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11913652 | TAAACCTTCTATTAG[-/A]AAAAATGAAGTATTT | 75725 |
rs251418212 | in-del | -/TTAGTTGTAAC | | | intron-variant | Phf14 | Mm_Celera | 6:12046894 | TCCTTCCTTGGTGTT[-/TTAGTTGTAAC]TTAATTGACTTTTTA | 75725 |
rs251421336 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11912467 | AAAGCAATGACAAAA[-/T]TTTTTATATTGTCCT | 75725 |
rs251425241 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11999504 | AATTCCCAAGACCTA[C/T]ATGGTTGCTTCAAAC | 75725 |
rs251435642 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12097385 | CGAACACATGAGTCT[A/T]TGGGGACCAAACCCT | 75725 |
rs251450101 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12064680 | CTACTTATTAGTGTT[C/T]TCCTTGCCCATATTC | 75725 |
rs251453949 | in-del | -/TACAAGC | | | intron-variant | Phf14 | Mm_Celera | 6:11911628 | TAGAAGCTCCCAAGA[-/TACAAGC]TCACAAGGCTGGAGG | 75725 |
rs251468957 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12088552 | CAGATGAAATGGGAG[C/T]GGGATCAGAAGTTCT | 75725 |
rs251484209 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12065697 | TGATGCATGCTTCTG[C/G]TCCAGCCCTCAGAAA | 75725 |
rs251486129 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12000042 | ACATTAAGTGATTAA[A/G]TAAATTGCTGGTGGT | 75725 |
rs251489595 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12025937 | TACCTGAAAAAGAAC[-/A]AAATAAAAATAGAGA | 75725 |
rs251515922 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11937320 | CTTGGGATGTCTGAC[C/T]TACTAGTTAGTTATC | 75725 |
rs251530173 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927904 | GTGGGGAGGAACTCT[G/T]CGAGTTGGAAGGCAG | 75725 |
rs251537054 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12038635 | AAATGAACATTTTAT[A/G]ATGTGACTATTAATC | 75725 |
rs251546142 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094294 | ACCCTTGAGCCTGGC[A/T]TTGAAGGCACGTGTT | 75725 |
rs251554033 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927639 | TCTTATCTTGAAGCA[C/G]TGGGAGCATACGCAG | 75725 |
rs251567619 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095476 | GATTCACACTACTAA[C/T]GCGTGTTTAAGAAAA | 75725 |
rs251585122 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11928405 | CTTTGCTGAAAGGTA[C/G]TACTGGTGCATAGGT | 75725 |
rs251589325 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Phf14 | Mm_Celera | 6:11992088 | TCCTCCTCTTACAAG[A/G]ATGCCGAGAAAGACG | 75725 |
rs251590532 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11987427 | CCTTTGTAAATTCTA[C/G]TGTTTATTCTTAAAT | 75725 |
rs251608992 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12043747 | GAAGAGCCAGCAGTC[A/G]GTTCTCCAGATGCTC | 75725 |
rs251610916 | in-del | -/TGTGTA | | | intron-variant | Phf14 | Mm_Celera | 6:12022706 | GGATTCGTGTGTGTG[-/TGTGTA]TATGTGTGTACATAT | 75725 |
rs251623910 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12026601 | CCATGATCTACTGAA[-/T]TTTCAGGACTTTTGT | 75725 |
rs251630125 | in-del | -/GACTTTGTAGTACT | | | intron-variant | Phf14 | Mm_Celera | 6:11950862 | TCCCCAGGGTTGTGA[-/GACTTTGTAGTACT]GACTTCCTTCTTTGT | 75725 |
rs251654851 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076958 | GTTAGTAAGGGGAAA[G/T]AGAAGGAGTCTTTGT | 75725 |
rs251659437 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12073130 | GCGGTTCTCTGAAGT[A/G]AACGTTTGTGTTCAC | 75725 |
rs251676511 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12014876 | GAGAAAAGGAGCTAT[A/C]GTGGCAGGAGCTTGC | 75725 |
rs251684775 | snp | A/G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12053072 | TGCCCCTACAGTCAG[A/G/T]TGTGAGGTAGAAAAA | 75725 |
rs251710734 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11919482 | GCTGCCCTTAGGCCC[C/T]AGGTAACTCAGTATG | 75725 |
rs251737684 | in-del | -/CGGGCGGG | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11926096 | CGGGGGAAGGGGCGC[-/CGGGCGGG]CGGGCGGGCGGGCGC | 75725 |
rs251742284 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12029413 | ATTAATTGGCAATTT[A/C]ATTTTTTTAAATTTA | 75725 |
rs251759423 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12037200 | ATTGTGGTATCTAGA[A/C]AATTATGTGTTATAA | 75725 |
rs251775439 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11950510 | ACTCTTACCTAGAAA[A/C]ATCATGGTCTCGCTA | 75725 |
rs251779568 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072414 | CTTGCAGAATAAGAA[C/G]CTTGTTTAGTCGATG | 75725 |
rs251786958 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11920479 | CTACAGAGGCTAGAA[A/G]CTTCCAGAACTAGGC | 75725 |
rs251790318 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906760 | AGTTTTAGGAATGAA[C/T]TCTGAAAACAGACTG | 75725 |
rs251797652 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11914767 | ATAGCAAACCAGAAC[C/T]GAAGGTCAGTACATC | 75725 |
rs251851743 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12079427 | GCGGCAAAAAGAGCA[C/T]GACAGAGATAAGGCT | 75725 |
rs251857508 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11943194 | AATAGGCTGGGGGTG[A/G]GTGACTTCTCCAGTA | 75725 |
rs251863814 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043218 | TGAATTGATTCCACA[C/T]TTTACGTGGGATTGG | 75725 |
rs251863973 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052343 | GCAGCGGTTGAGATT[C/T]AGAATTGATGACCTG | 75725 |
rs251869221 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11915104 | ATACGAGAAAGGAAT[A/T]TGGCAGTATGAAGAG | 75725 |
rs251889135 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043758 | AGTCGGTTCTCCAGA[A/T]GCTCATGTTTCTAGG | 75725 |
rs251921276 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11912334 | CTGAGTTAGGAATAC[C/T]GACAGATGGAGTTTT | 75725 |
rs251926288 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11913431 | ACAATTATATTAATA[C/T]AAATTGAAGACAGAT | 75725 |
rs251942842 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11911501 | ATAAAAAGAAGGCTG[A/G]GGAGATGTCACCATA | 75725 |
rs251968391 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11993261 | GAACTCAGGACCTTC[A/G]GAAGAACAGGCATTG | 75725 |
rs251973320 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12079879 | CTGATATCTCATTCA[C/T]CTATAAAGCTTCAGA | 75725 |
rs251975246 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060229 | TCAGAGAAGACTGTT[C/T]CCTTAAGAAATGTAG | 75725 |
rs251997247 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11985749 | CCTATTTACAACACT[A/G]TTACAATTTACTATT | 75725 |
rs252009777 | snp | A/G | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099452 | ATAACTCTAGCTTGT[A/G]TCAAGTTAACAAAAA | 75725 |
rs252013046 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054676 | TGCTGGGAATGGATG[A/T]TATAGCCTTTAGAAT | 75725 |
rs252022426 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12025866 | TTAAAATCTTCATAA[-/G]GTAGTTTTTGTTTTG | 75725 |
rs252026981 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11993951 | CCAACCCCTACTCCA[C/G]CAGACCTCCCCACTC | 75725 |
rs252031292 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11999941 | TAGACAGTGGCTTCC[A/C]GATTCCCGGACATTC | 75725 |
rs252060556 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11922450 | GAACAGGATAGATAT[G/T]AGTCCAATTTCGACA | 75725 |
rs252122744 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11960755 | AACATTTTCTTTGTC[G/T]GCAAGCAAACAGATA | 75725 |
rs252125876 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12043188 | TGCAAGCTGGCTGTT[-/G]GCAGATATAAATAAT | 75725 |
rs252126223 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11916489 | ACTAAAATCAACCAA[A/C]CAAACCAATAGAACT | 75725 |
rs252126514 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11994499 | GAGGTACTTGAAGCA[A/G]TCCCACTAAAATTGG | 75725 |
rs252127912 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11980867 | ACTGCGTGTGTTTGT[A/G]TATTATTAAATATAT | 75725 |
rs252133091 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11991578 | AATGAATTTTAAGTA[A/G]TAATTGAAAGCTATA | 75725 |
rs252166420 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12028612 | AAAAAAAATACAGTT[A/T]TAAGGAGAGAGAATG | 75725 |
rs252182270 | snp | A/C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11981580 | TGAAATCAACCAAGT[A/C/G]GAAACAAGAAGAACT | 75725 |
rs252208443 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030047 | TTCTTTCGAGGGACA[C/T]CTAAGTTGTTTCCAG | 75725 |
rs252220182 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12022794 | TTAAAGTCCAGAGAG[A/G]TTAATTGAGAAGTTC | 75725 |
rs252220558 | in-del | -/TCTT | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008675 | AAAAAATAGGTTTCA[-/TCTT]TCTTCTAGAATTGTT | 75725 |
rs252222147 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12030522 | TAGTGGAATTGCTTT[A/G/T]AATTTTTCTCTATTT | 75725 |
rs252223429 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12082411 | GCACTCATGCACGCA[C/T]ATAATCTTTTTAAAA | 75725 |
rs252237044 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11974421 | TGTGTAGCCAATCTG[C/T]TAGTCTATGTCTTTT | 75725 |
rs252282850 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023421 | ACCCAACTTCATTTG[C/T]TATTTTAAGTCCACT | 75725 |
rs252286135 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12023134 | TCATCAAAGGCAAGG[A/G]TGTTTTAAAAAGTAA | 75725 |
rs252292570 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12033435 | CCGTGTTCCCCATCA[C/T]AGTCCTTGTGTCCTT | 75725 |
rs252309537 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12071080 | GGCTGGGAAGCATGG[A/G]AACAGGCAGGCATGG | 75725 |
rs252317615 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11920751 | AATGTAAGCTAATAA[A/T]GAGAACACATGAAAA | 75725 |
rs252324080 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11916341 | TTGGGTTTATTGACA[A/G]TGTTTCATGTAGATG | 75725 |
rs252329255 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021969 | TTCTACCTAGCTTGT[G/T]TGTGTGTGCATGTTC | 75725 |
rs252337350 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12003990 | TAGACTCAAATGTTG[A/C]GACTTGGTTCCAGTC | 75725 |
rs252383561 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12063635 | CTTATAACTGAGATA[A/G]CATCACTATTTCCTT | 75725 |
rs252389861 | in-del | -/CACACACACACA | | | intron-variant | Phf14 | GRCm38.p3 | 6:12041576 | ATGCACACACACACG[-/CACACACACACA]CACACACACACACAC | 75725 |
rs252393581 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12015370 | CCTTTTCTTAAAATC[A/G]GTCTACCTTATTTTT | 75725 |
rs252394753 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12005209 | ATGAAAGTTAAGGTA[A/C]GATGAGTACCAAAAA | 75725 |
rs252395621 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12060259 | GAGGGGATCTTGGGG[-/A]AAAAACTGTTAAGCA | 75725 |
rs252400010 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12058191 | GAATTGCTAATTCTC[C/T]TGTGCCTTCCAAGTG | 75725 |
rs252428417 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12087366 | AAATTCCACACAGTG[A/G]AAACACAAGATATGT | 75725 |
rs252433191 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12052417 | CACAATTTCCTGCAA[A/G]CATAACAAATAGAGT | 75725 |
rs252433221 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12058607 | GCACTGAGAATGGTG[A/G]TCCCTGTGCGTGGAC | 75725 |
rs252465074 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947256 | CATCTTATCTACCGT[-/G]GGAAGTAGACAGACA | 75725 |
rs252517642 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11936036 | GGCTAATAGTTTTGT[A/C]AGTCTTTCTAGTTAC | 75725 |
rs252518421 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12032191 | ATTTTTGTGGTAGTG[A/G]TGGTGGTGGTGGTGG | 75725 |
rs252519478 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12046183 | TGACATATTATATAG[C/T]CCCTGTACTTAGATC | 75725 |
rs252522578 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12080373 | CAAAAATAGGATGAA[A/G]TATTTTTCCAGGTGC | 75725 |
rs252535655 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927309 | GTGCTTTAAAACAGC[A/G]GGTACCGTGGCCCAG | 75725 |
rs252558665 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12046781 | ATTTTTTAAGTTACT[C/T]TTCTTTGGACATATG | 75725 |
rs252560845 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12036684 | GTCAAGTCTCTTGTG[A/G]TATGTAAGTGCTCTA | 75725 |
rs252573518 | in-del | -/TTTT | | | intron-variant | Phf14 | Mm_Celera | 6:12057683 | GTCCAAATGCTTTAA[-/TTTT]TTTTTTTTTTACTGA | 75725 |
rs252585857 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037033 | CCAGCCTGATCTACA[G/T]AGTGAGTTCCAGGAC | 75725 |
rs252593777 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12024858 | GATTGGGTGTAAGGT[A/G]GAATTTCAGGGTTGT | 75725 |
rs252594037 | in-del | -/TTTG | | | intron-variant | Phf14 | Mm_Celera | 6:12060014 | GATTGGCATGGTTAT[-/TTTG]TTTGTTTTGTTTGTT | 75725 |
rs252598324 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905916 | CAGCCCTGGGCTGAC[A/T]GCAAAGCTACAAACT | 75725 |
rs252616357 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031145 | TTCTTTGTATTTTTT[A/T]ATTGCTTTTATGTTA | 75725 |
rs252630580 | snp | A/C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032241 | tgtgtgtctgtgtgt[A/C/G]tgtgtgtgtctgtgt | 75725 |
rs252631464 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11955660 | ATGGCCTACAACTGT[A/G]GGTTTAGTAACATTA | 75725 |
rs252649895 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947150 | CATTTAATAGGGGTT[C/T]ATAGTTTCAGAGAGT | 75725 |
rs252659611 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Ndufa4, Phf14 | Mm_Celera | 6:11907926 | CCGCAGGACAGGTCG[A/G]GTCTCCAGCCGCCGG | 75725 |
rs252675412 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12092902 | ATCTCACATAAATGA[A/G]TAATGCAGACTTAGT | 75725 |
rs252684811 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970211 | TCTTCCCTGTGATGG[C/T]CATCTTCTGCTACAT | 75725 |
rs252687911 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985174 | GACATGAGTTTCCTC[A/T]TGCTGAATAGACCTT | 75725 |
rs252699920 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12093940 | AACTTTCTTAAGATC[C/T]GCCAGTTGTCCTTCA | 75725 |
rs252703648 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083946 | TTCTGAAATTTGGGG[C/T]TTATCATACCATGTG | 75725 |
rs252715669 | in-del | -/AGA | | | intron-variant | Phf14 | GRCm38.p3 | 6:12077996 | ATCTTCAGAATAAGC[-/AGA]AGAAGAAAAACCAAG | 75725 |
rs252732517 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11960450 | TGAACTCCACAGGAC[A/G]CATAGGGGAGGTTAG | 75725 |
rs252745150 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12073748 | TCAGTAAAAAATGTG[A/C]TATCACACTTTTGTT | 75725 |
rs252765578 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12084442 | TCATCCTACTTCACC[C/T]GTGATTCTCTGCATT | 75725 |
rs252773279 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12021352 | AGGAAACCACTTCCC[A/G]GAAGATTTCAACTCA | 75725 |
rs252777615 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950306 | GCTGGGTGGAGGATG[G/T]GTGGAGAGGGAGAGA | 75725 |
rs252810178 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12079013 | GTAAATCAAGATTGC[A/T]GGAAACATGTCTGCT | 75725 |
rs252822868 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11939163 | CACTGGGATGGTGAA[C/T]TATAGTGCTCATTTG | 75725 |
rs252847172 | in-del | -/TTTG | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011684 | CTTTAAAAATATTCT[-/TTTG]TTTTTTTTTAAGGAA | 75725 |
rs252862460 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Phf14 | Mm_Celera | 6:11953436 | GATTTTCAAGGAGAC[A/G]GATGCTGGAAGGTTG | 75725 |
rs252886352 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12030818 | CTTTCTTTCTTGGGA[C/G]ACTGTTAGTGGCTGC | 75725 |
rs252891986 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030878 | TAAAGTTTTTACCTG[C/T]TCTTGATTTACTTTG | 75725 |
rs252892578 | in-del | -/TTACATG | | | intron-variant | Phf14 | Mm_Celera | 6:12077132 | AGTACTAGACCATTA[-/TTACATG]TCCCTTGTGTGCCTA | 75725 |
rs252913491 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12014938 | GAAGCAGAGGGAGAC[C/G]AATGCTTGTTCTCAG | 75725 |
rs252920495 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11963448 | TGCTATACCAAAAGT[C/T]CCCCTTACCCACCCA | 75725 |
rs252931371 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11942210 | GGCAACAGTGGGAAT[A/G]TATTTGGCAGTTAGT | 75725 |
rs252932110 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12003112 | AAAATAGTCTGATTT[-/C]TCCCCCAAATTGTCT | 75725 |
rs252949791 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917100 | GTCTTGTCTTGTCTC[A/T]TTCTCTCTGCCCAGC | 75725 |
rs252958919 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11932754 | GCTACAAGTTGACTA[C/T]CATAGATCTTTGCTT | 75725 |
rs252978581 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12068703 | TTTTTTGGAAACAAG[C/T]GTATTGTCGGCGTTC | 75725 |
rs253001776 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12069241 | GACATTAATTCGGTT[A/G]TATATGATGTCTTTT | 75725 |
rs253013540 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023570 | TGCCTACTGATGGTG[G/T]CCAGAATTGTGGCAA | 75725 |
rs253036685 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12013605 | ATAAGAATTATAACA[C/G]TAATTATGGAGAGGG | 75725 |
rs253064757 | in-del | -/AA | | | intron-variant | Phf14 | Mm_Celera | 6:12082369 | TCAGTAGACACCTAT[-/AA]ACACACATGCACTCA | 75725 |
rs253073978 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12024096 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCCGC | 75725 |
rs253077047 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12015875 | TTATTAAAAAGGACT[A/G]TAGTAGAAATTTGCT | 75725 |
rs253077922 | in-del | -/TG | | | intron-variant | Phf14 | Mm_Celera | 6:12015548 | GACTTTGGTTTGGGT[-/TG]TTTTTTTTTTTTTTA | 75725 |
rs253080119 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060415 | TAAATAATAGATTCA[-/T]TTTTTTCTATCATCT | 75725 |
rs253080205 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083178 | TTTGTTTTTGTTTGT[-/G]TTTTTCTTTTTTTTT | 75725 |
rs253087572 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043844 | AGGGAATACTGCCTG[C/T]TGTGCTTCATTACGG | 75725 |
rs253088134 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12062235 | ATTGTAGAACAGGGG[A/G]ATACTTGGCAAGTTT | 75725 |
rs253091003 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12059049 | TGCATGAAAATTGAT[A/G]AAGAATTAACTTATG | 75725 |
rs253091772 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12016852 | TGTGATTATAAATGA[C/T]ATTTTAACAAATCTG | 75725 |
rs253100663 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11932169 | ATTTTTGAACCTTAA[A/C]TTCCTAGTTAAATTT | 75725 |
rs253111323 | in-del | -/TG | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021637 | GCTTATATAGCAGAC[-/TG]AGCTCTCAACACTCA | 75725 |
rs253153775 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11932958 | TAAGTAATTATCTTT[A/C]GGTCACTATACTGCT | 75725 |
rs253153843 | snp | A/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924917 | GGCTTGGCTCCTGTC[A/T]GCCTTGTTTCTGAGG | 75725 |
rs253160672 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11928174 | ATTGATAGAATCTCA[A/C]ATCAAAATGGCCTGG | 75725 |
rs253182744 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053520 | ACTGTGCCCTTGGTG[A/G]AATCAGAATAGGAAA | 75725 |
rs253196957 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12013723 | GAGTATAATTACATT[A/G]TACTTATATATATAA | 75725 |
rs253201554 | in-del | -/GAATAAG | | | intron-variant | Phf14 | GRCm38.p3 | 6:12064278 | ATCAAAGAAACTCTT[-/GAATAAG]CTGAAACAGTTTTCT | 75725 |
rs253213017 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009566 | AGATACATTTTAAGG[A/G]CAGGGAGATAGCTAA | 75725 |
rs253231326 | snp | C/T | | | intron-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100307 | ATTAACCATAACAGC[C/T]TCCAAACTCCAAGGA | 75725 |
rs253246987 | in-del | -/GT | | | intron-variant | Phf14 | Mm_Celera | 6:12021947 | TGTGTGTGTGTGTGT[-/GT]GCGTGTTCTACCTAG | 75725 |
rs253247982 | in-del | -/AGCA | | | intron-variant | Phf14 | Mm_Celera | 6:11940286 | TTATAGATGACAGTG[-/AGCA]AGCATTCACTTCTGT | 75725 |
rs253251062 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12073837 | GAAAGTAAAAGAGGT[-/A]CCCCATACATAATCA | 75725 |
rs253253862 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12056815 | GTATTTACTTTGTCT[C/T]TGTGGACATGCTCGC | 75725 |
rs253255569 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12002858 | ATAAAGAAAATAACA[A/G]TAATCAGAATTCTCT | 75725 |
rs253275910 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010437 | CCGTTTCCTTTTTTC[C/T]ACCTATTATCCTCAG | 75725 |
rs253276044 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12070559 | TAGATCTGCATAAGA[A/G]TGATAATAACCTTGT | 75725 |
rs253294459 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11943151 | CCACTAGCAAGCTAG[A/C]TCAGGTTAAGAGGCA | 75725 |
rs253329209 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925422 | GATGCAGAAGCCATG[A/G]AGGAGTTCTGTTTAC | 75725 |
rs253350022 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11933491 | GAAAAAGGAGAAAGA[A/G]AAGGAGAAAGAAAAG | 75725 |
rs253351428 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11944067 | AAATTTTGTGATAAG[C/T]TTTTGTAAGGAGATG | 75725 |
rs253364732 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11934993 | TTAATTAAGCTTATT[A/G]TAGATTTTGTGGGCT | 75725 |
rs253370967 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12048542 | GCCCTGTAATATAAA[A/G]TGGTACTAAGAGGAT | 75725 |
rs253388665 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11937583 | TTCGGAAGAGCAGTC[A/G]GGTGCTTTTACCCAC | 75725 |
rs253419951 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12093651 | TACTCACTGCTTTGT[C/T]TAACTATGTGCTTTA | 75725 |
rs253449655 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12039114 | TCTTTGTTATTTGAA[G/T]CTACTGTGGTATTAT | 75725 |
rs253458492 | in-del | -/GACAGGA | | | intron-variant | Phf14 | Mm_Celera | 6:12053222 | TTCCACACTGACTTT[-/GACAGGA]GCCTCGTGGTGTGTG | 75725 |
rs253464980 | in-del | -/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12049590 | ATTTATTTTGTATGA[-/T]TTTTTTTTGCAATGA | 75725 |
rs253468185 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12084372 | ACCTTACCCCTAAAT[A/C]TCTCAGTCTTTACAT | 75725 |
rs253479837 | snp | G/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040575 | TGAAATAATGTATAA[G/T]GATACTAGTAATTTA | 75725 |
rs253482401 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12094092 | TCTTAATTTGTTCAT[A/C]AAACAGCCTCTGCTC | 75725 |
rs253493594 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11961042 | CCAAAACTGTTTGAA[A/G]ATATACCCTTAGGGA | 75725 |
rs253498028 | snp | A/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11925938 | TATTGTCTCTGACAG[A/T]AGGCCCTCCGCTGTG | 75725 |
rs253500825 | in-del | -/ACTT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12042322 | CGTTCACATTTGTTA[-/ACTT]ACTTACTTTCCTGTT | 75725 |
rs253501611 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11986517 | ACCTAAATTTATTAG[A/G]TTTTTTTGTTGTTGT | 75725 |
rs253508690 | in-del | -/TTGGTT | | | intron-variant | Phf14 | Mm_Celera | 6:12054813 | TTTTTGTTTGGTTGA[-/TTGGTT]TTGGTTTTGGTTTTG | 75725 |
rs253509311 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11919008 | CATTGGCTGACAGCC[C/G]TGAGAGATGCTTTGT | 75725 |
rs253517440 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12094469 | GCATTCATTGCCTGG[C/G]AAGATATGAGACCTT | 75725 |
rs253519300 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908927 | ACAATAGATGGAGTG[A/G]TTTTGTTTCTTAGGA | 75725 |
rs253530097 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11909644 | CGAGAGAGTAACAAT[C/T]TTGGTAATCCTTTAT | 75725 |
rs253534683 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11931003 | TTAGATTATGACTAA[G/T]ATGTTACATTCTGTG | 75725 |
rs253540193 | in-del | -/CTGTGTG | | | intron-variant | Phf14 | Mm_Celera | 6:11997536 | CTTTGTGTTGCAAAC[-/CTGTGTG]CTGTGTGCTCGTGAA | 75725 |
rs253574037 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12098098 | ATGTTTCCAATGCTG[C/T]CCTCTTCCTCCAGGG | 75725 |
rs253578871 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061433 | AATTTATATATTTTG[A/G]GAAAGATATTTCTAA | 75725 |
rs253597082 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11991809 | GAAGGTTAAGGCAAG[A/G]TGATAATAAGGTCAA | 75725 |
rs253609736 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11987913 | TCCTGTCTTTAGTGT[G/T]AGTTATGGCTGTTGC | 75725 |
rs253613470 | snp | A/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12048007 | GACAGGTTTTTTTTT[A/T]ATATTACAACATTCT | 75725 |
rs253615159 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12055899 | TTCATTAGGATTAGG[A/C]AGGATCAGAATGCCA | 75725 |
rs253639670 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083080 | AAAATCACTGAGACA[-/T]TTTTTTTCCTACGTG | 75725 |
rs253646626 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12024272 | CCTCTAAAGTCCCAG[A/G]GGCCTCCAGTCTCTT | 75725 |
rs253666949 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924127 | TTGCTATCAGGTTGT[A/G]GAGATCAAGTAACAA | 75725 |
rs253689814 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12050406 | TTTTCGTGTATGCAC[A/G]TCTGTATGAGGGTGT | 75725 |
rs253694608 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12056658 | AGAATATCTGGTTTG[C/T]CTAAAAGTGTTTAGT | 75725 |
rs253701137 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916534 | GTCCACAGAATGGCA[C/T]GTGCAGACAAAGAAG | 75725 |
rs253708421 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917063 | CAGGGTGGCAGTTAC[C/T]CATATACTTCTCTGT | 75725 |
rs253713067 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11946407 | TCTAGTTGTTCATCA[A/G]ACTTACAGACTTTCT | 75725 |
rs253722367 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11917284 | CATGCTACAAGAATT[A/C]ACAGAAATATTGAGT | 75725 |
rs253723791 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925177 | ATGGACATCTATAAT[A/G]TTTCTAAATTTTGGT | 75725 |
rs253724363 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11937950 | TATACTGAGTTCTCA[A/G]TTGCTTCCCTGTACT | 75725 |
rs253765491 | snp | A/C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11917575 | GAATCACTCCAACGT[A/C/G]TACAAGTTCCCAGAG | 75725 |
rs253775356 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910216 | ATTTACAAATTCCTC[A/G]TGCTAACCCTGAGGG | 75725 |
rs253804227 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12023610 | ACTTTGTACTTAAGT[C/T]TAAAGTCTGCACTGA | 75725 |
rs253805704 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12041976 | GTGTGGGTTTAATGC[C/T]TTTAAGGGGCTCTTC | 75725 |
rs253811403 | in-del | -/ATA | | | intron-variant | Phf14 | Mm_Celera | 6:12092549 | CAATGTGACTAGCCT[-/ATA]ATGTTTGTGGTTATT | 75725 |
rs253814683 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917753 | GGAAGAGGTACCTAC[C/T]TCACATGTGTGGACA | 75725 |
rs253814752 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083602 | TCCTCCATCTGGGAC[C/G]CCATGCTCAGTTCAG | 75725 |
rs253815204 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12076181 | TTTATTTAGAAAACC[A/G]GTGAAATATTATAAT | 75725 |
rs253832877 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910996 | AAACCACCTAGAAAT[C/G]ACAGTATTGGACTGG | 75725 |
rs253853330 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12053976 | ATTCACAATGTTATA[A/T]AGAAGGAAATCAATT | 75725 |
rs253888689 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12084002 | GCAGGAGGATCACCC[C/T]GAGCTACACCTTTGT | 75725 |
rs253890557 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12076305 | TCTATCCAGGTGACC[A/G]TGGTTTCCATCTTGT | 75725 |
rs253893260 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12076881 | TTAAAAGAAAAGAAG[A/G]TAGATAGGTTTTATT | 75725 |
rs253907561 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12096783 | ACAGCTGTTCCTGCT[C/G]TCATGAGTGACTTTA | 75725 |
rs253926226 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12070021 | TATGTGGCCTTTCAA[G/T]TGTAGCCTAATACTG | 75725 |
rs253929637 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12045432 | ATGAAAATAACTTGT[-/A]AAAATCCTTTGAATA | 75725 |
rs253933613 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12046460 | TGGATCAGTGGAATA[A/G]TATATGGCATTTGTC | 75725 |
rs253980432 | snp | C/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12040859 | GATGGGTTTCTGTTT[C/T]AGTTTTGAGAAATCA | 75725 |
rs253993610 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11995725 | AAGAAGAGGAATCCC[C/T]ACCTTGGGTACCAAT | 75725 |
rs254007708 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12032873 | TTGGTTGGTGAGTTA[A/G]CCCCTGTGAGCTCTG | 75725 |
rs254014451 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057471 | CTTGAATCAAGCTGC[A/G]TTCCCTGTCTCCATT | 75725 |
rs254023924 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12068771 | TATTGGGTTGTTGTG[-/C]TGTATGAGACATATA | 75725 |
rs254042499 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12073135 | TCTCTGAAGTAAACG[C/T]TTGTGTTCACTAGAT | 75725 |
rs254046227 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11909925 | TTAGCCTAGTTCCTA[C/G]ACATAATAATTTGAC | 75725 |
rs254048288 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12058082 | ATCTTGGTTTTATTT[A/G]GTATCACTTAGTTTA | 75725 |
rs254065441 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12033400 | CTCTCCTCGGCTAAA[C/G]TCTGCTGCTCCAGTT | 75725 |
rs254068036 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11926553 | CCTAACGTCAGGGGC[A/T]GCCAGGCTCTCTGCA | 75725 |
rs254088295 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12075409 | TATGCATGTAAATAT[A/G]ACTTGCTGAATCTGT | 75725 |
rs254089162 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11918556 | CCTTAGATTTAAACC[C/T]CTGTACGTAATAAAA | 75725 |
rs254090111 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11980285 | AAAAAGGCAGAGGTG[C/G]CTTCTGCAAACCAAT | 75725 |
rs254108955 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11994673 | ATAGCATACATAAGC[A/G]ACCCCAAAATGTCTA | 75725 |
rs254125587 | in-del | -/AT | | | intron-variant | Phf14 | Mm_Celera | 6:12020089 | GATTGAGGAAGGCAC[-/AT]ATATGTATATTCATC | 75725 |
rs254132939 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927369 | TGATGTGAAGAGGTG[A/G]TGAACTTGTATGTTC | 75725 |
rs254146245 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11919320 | ACACTAAAAATAAAG[A/G]CTAATTTTTTGAGGT | 75725 |
rs254146309 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094645 | GAATGTCACTAATAT[C/T]GCGGAAATGGATACA | 75725 |
rs254191151 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12027949 | CCAATTTTGCCACTC[-/TT]TATTAATTAGCACAG | 75725 |
rs254212848 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11920410 | ACAAGAAAGGGTGAG[C/T]TTATTCAGCAGTAAG | 75725 |
rs254229832 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11988572 | TCCCTTCTCTTGAGG[A/G]TGTTCACCATACTAG | 75725 |
rs254232885 | in-del | -/AAAAAA | | | intron-variant | Phf14 | Mm_Celera | 6:11988276 | TCTAATTATTGTTCC[-/AAAAAA]AAAAAAAAAACCTAC | 75725 |
rs254233180 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906920 | AAATCAATTTTGCCA[A/G]TGTCAAGTTTTCCAA | 75725 |
rs254234333 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12078771 | CTTACAGAGGAACCC[A/G]GTTCTACCAGCACCT | 75725 |
rs254239709 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095267 | GTTTCTGCTGTCTCA[C/T]ACTGCGGTTGTGGAG | 75725 |
rs254244787 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12085548 | AGCAATTTAAGTTAA[A/G]TGCTGAGCCTTCTTC | 75725 |
rs254265780 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12030432 | TTTTGCACTGGCAGT[A/C]CTTCAAATACAGTAC | 75725 |
rs254269116 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11914151 | AGTCTCTCACTAGCC[A/T]AGAGCATGTGGATTT | 75725 |
rs254275242 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11962551 | TTTATGCTTTGTGTT[A/T]AAATGCTTGAGCATT | 75725 |
rs254277597 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11998049 | ACCTTGGCTTTTATG[-/T]TTTTTTTTTCTCTTC | 75725 |
rs254301337 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12086035 | GTTAAGTACCACAGC[A/G]CTGAGGCAGCCTGAG | 75725 |
rs254317476 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11954558 | CTACTGTCCTCTATG[A/G]CTTTGATTACAGTGC | 75725 |
rs254327115 | in-del | -/CTCTGCTGCAC | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100172 | GCAAAGCAACTGCAG[-/CTCTGCTGCAC]TTGCCGTTGTAGCAG | 75725 |
rs254329372 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11955218 | GTGGACTCTTTTAAT[A/C]CTAGTACAGAGGCAG | 75725 |
rs254344498 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970997 | ACCAGAAGAGGTATT[A/G/T]CTGGATTTTCTGGTA | 75725 |
rs254383145 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12073413 | GATCCACTTGCTTCA[C/G]TCTCCCAAGTGCTGG | 75725 |
rs254401721 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11946983 | ATTGAATCCAGGACT[C/T]CACACCTCCTTAGTA | 75725 |
rs254407970 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947190 | ACCATCATGGTGTGA[A/G]CATGGCAGCAGGCAA | 75725 |
rs254438248 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083692 | ACAGCCATATCAGGC[A/G]CCTGTCAGCAAGCAC | 75725 |
rs254456929 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12025326 | CAGTACAATTCTAAA[A/T]TTTAAATATATATAA | 75725 |
rs254478322 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12018076 | ATTAAAATAGAAGGG[G/T]TGTGTGTAAGGATCT | 75725 |
rs254478430 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076460 | CATTAAATGATCATG[C/T]TACCCTAGCCTTCTC | 75725 |
rs254487122 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031095 | TGTCAGTCTTACTGA[-/T]TTTTCTCTAAAAAAC | 75725 |
rs254488687 | snp | A/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008972 | AGGTTAAAATTGGAT[A/T]TGAGGTAATATCACA | 75725 |
rs254493207 | in-del | -/ATAAATAAATAAATAAATAA | | | intron-variant | Phf14 | Mm_Celera | 6:12013285 | TCTTCCCCCTCCCCC[-/ATAAATAAATAAATAAATAA]ATAAATAAATAAATA | 75725 |
rs254511248 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950334 | AGAGTGCATGCACTA[A/T]CTGGGAATGGCTTGG | 75725 |
rs254538496 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029138 | CGCAGATTGTCACAC[A/T]ATTATTGCACAAAAT | 75725 |
rs254543555 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12041416 | ATGTAAAAAACAGAC[A/G]AAAGGATCTCTGTGA | 75725 |
rs254549142 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12021737 | CGTCATAAACTTGGT[A/G]CCAGTTTATCTTATG | 75725 |
rs254558331 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12035467 | CCAGGAAAGCTAAAC[C/T]TTTAAGTAAATTTGT | 75725 |
rs254575620 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11938904 | GCCGGGCAGTGGTAG[C/T]GCACGCCTTTAATCC | 75725 |
rs254579406 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11998871 | TGGAAGGAACAGAGA[C/G]GTTTCTGGAATGCGA | 75725 |
rs254585586 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009686 | TAATCCCTTTGCTGT[A/G]GAGGAAGAGACAAGA | 75725 |
rs254621247 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11942763 | TTGAATCCTATACTA[C/T]ACCTTGCACACTCCG | 75725 |
rs254648447 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12036061 | GCTCGAGAGAGGCCT[A/G]TCTGTGAAATGCTTC | 75725 |
rs254659279 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12064249 | TATTTTATGCCTAGG[C/T]CAATTTTTAAACCAT | 75725 |
rs254731348 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12058266 | GTTTCCTGAACAGTT[A/C]TTCTTTCTGATAGGC | 75725 |
rs254732567 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927549 | CATTAAGACCTTTTT[A/G]TATTTCGCTCCCATT | 75725 |
rs254744189 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12027459 | AAGCAACACTCCTCA[A/G]CTAAAGCAGCACGTA | 75725 |
rs254745915 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12075273 | ATTGCGGCACTATCT[A/T]ATTTCTACCCTCCAG | 75725 |
rs254765587 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12058668 | ATTTACTTAAATACG[G/T]TGACTTAACTGCCAT | 75725 |
rs254781375 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12095049 | TGCAGGAAATCCACC[A/G]CGTCAAGTGCGTGGA | 75725 |
rs254785422 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12090496 | TGTAAAGCATAAATA[G/T]CTAGACTCCAGGTCC | 75725 |
rs254786383 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11928015 | GACAGTTTGCATTGT[A/G]ATTTGCTACAGAATC | 75725 |
rs254788211 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11920159 | AAATGACAAGTCACA[A/G]AAATGCTTGACAGAA | 75725 |
rs254790395 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12063170 | GGTTTGCTGGCTGTT[-/A]AGTTTCTGTGTAGGG | 75725 |
rs254792596 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924275 | CTCCCCCAGTATATG[A/G]GGGAGTAAATATATT | 75725 |
rs254805469 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040387 | CTTAAAATTCCATTG[C/T]TTATCATTGTGGGTT | 75725 |
rs254808667 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12063253 | ACTTTAACTTAATTA[C/T]TAATAAAGCTTAGGA | 75725 |
rs254818354 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11948862 | TTTCATGCACAGGAG[C/G]TTAGCTTGCTTCCAT | 75725 |
rs254850976 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11935581 | AAGATCATATATATG[G/T]GTTAGTGTCTTTTTC | 75725 |
rs254882780 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12032801 | CCATTGATGTCCCAC[-/A]AGGCATTCCTCTGCT | 75725 |
rs254893983 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11920619 | GCACCCACATTGGGC[A/G]GAATATAGCTGCCTG | 75725 |
rs254898291 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12086475 | GGTATTGTCCTTACC[G/T]CTAATAAATTTCACT | 75725 |
rs254911799 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11958928 | CTAGACAGTCCTCTA[G/T]TGTTGTGAATTACTA | 75725 |
rs254931191 | in-del | -/TTC | | | intron-variant | Phf14 | Mm_Celera | 6:11981090 | GAGGTCCCATGAGGT[-/TTC]TCCCTTCCACCTAGG | 75725 |
rs254976757 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11959629 | GAGCAAAGACAGGAC[A/G]CTAAACCTGCTTTAA | 75725 |
rs254981047 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12001766 | TCTATAGGCTTGCTG[C/T]AAGTTGCCATTATTA | 75725 |
rs254985542 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079588 | TCTCATTTAATCCAC[C/G]ATAGCCTCTTTACCA | 75725 |
rs254987409 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12087178 | TCAAGTGGATCAGGG[A/G]CCTCAACATACAGTT | 75725 |
rs254995591 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11974068 | AGAGTGGGGTGTTGA[A/T]GTCCCCCACTATTAT | 75725 |
rs255015920 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12020422 | ACTGAAACCTCCCGC[A/C]ATCAATCACTTGCAG | 75725 |
rs255016049 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036520 | TTTTGTCGTCTATCA[-/T]TTTTTTAAATTTAGA | 75725 |
rs255017690 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12073881 | GTTCCCCTAAAACTC[G/T]CTTTCAGTCTGAGGT | 75725 |
rs255023142 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12041655 | CTCCCCTGACACATA[A/C]TATTGGGAAATAAAT | 75725 |
rs255028254 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12050121 | AAGATATGTAAGAAT[A/G]AGAGGAAAAGAAAGG | 75725 |
rs255040990 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083630 | CAGTGGTTGACTGTG[A/G]GCATCTGCCTCTGTA | 75725 |
rs255043742 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11993725 | TTGATCATGATGCAT[A/G]CTTGTAATCTCAGTA | 75725 |
rs255077014 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947522 | GGTGTGTGTGTGTGT[A/G]TGTGTATGTGTGCAC | 75725 |
rs255084294 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11917376 | ACTTTGAGCCCTTCC[A/C]CAAACTAGAAACATT | 75725 |
rs255091655 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12013143 | CTATGTTTTAGTTCC[A/C]TGCTGCTTAAAACTT | 75725 |
rs255117103 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11998718 | TTTTTGAAGCAGAGG[-/A]AAAAAAAAAAAGAAA | 75725 |
rs255121465 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11939259 | GTCCGTGTTTCTGTT[A/G]TGAGCCATGTACAGG | 75725 |
rs255145042 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12021066 | TGCTACAGTTGGACT[C/G]CACTTTCACCGGTAG | 75725 |
rs255146142 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11960268 | GCAGTTGAGATCTTC[A/G]CTGCACATGTTAGGA | 75725 |
rs255147172 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12069471 | TATTTTCTTTATTTA[C/T]ATTTCAAATTTCCTA | 75725 |
rs255181462 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11950251 | GTAGGTATGGCTCTG[A/G]AGCAGTAGCTGAGAG | 75725 |
rs255215848 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12097410 | AACCCTATTCAAACC[A/G]CTAAGGTCCGCTGCC | 75725 |
rs255225847 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11941925 | GTGTCTGAGTGTTTC[C/G]ATAAGGATCCTGTGT | 75725 |
rs255238039 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11932432 | AATAAAAATTGTGCT[A/G]GGTTGCTGTGGACTC | 75725 |
rs255256475 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12013233 | TAGGAGAATAATTGT[C/T]AGAGACCAGTCTGAG | 75725 |
rs255268797 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11919863 | GACTATGTAGAGGGA[-/T]TTTTTTAATCTATCA | 75725 |
rs255273941 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11991459 | CAAAGTTGTTGGTAA[A/T]GAATTTCTTTAGACC | 75725 |
rs255278719 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12002960 | GTTTTGTGCACAGGA[C/G]AGAGACTCAATTAAA | 75725 |
rs255310293 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11955994 | ACATTTCAAATGTGA[A/T]CTCCTGTCCTAGTTT | 75725 |
rs255312001 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12067867 | TTCCCATTGCCTTCT[A/G]TGATGTCATACCAAC | 75725 |
rs255319409 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12098584 | TTTAAATCAGCTTCC[G/T]TTCCTAGTCTTTCAG | 75725 |
rs255374989 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11929692 | AGAGGAGGAGTGTGA[A/G]CTAAGAATATTTAGA | 75725 |
rs255375655 | snp | C/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100182 | TGCAGCTCTGCTGCA[C/G]TTGCCGTTGTAGCAG | 75725 |
rs255387337 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11939667 | GGAGGACTAGAAGTT[C/T]TAGGCCAACCTTGGG | 75725 |
rs255394723 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11992499 | AATCTTACTTTCCTG[C/T]CTTATGTTGAAGTTG | 75725 |
rs255415071 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12093200 | CTCATGTCTCCTCCT[A/G]TTTCCCACTATTTAG | 75725 |
rs255416245 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11958415 | CTTTGTGAAGTAAGG[C/T]CATTTTGAAAAACAA | 75725 |
rs255435824 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12098327 | TATGCGTGCAGAGCA[C/G]CTGTTGGTAAACTTC | 75725 |
rs255450790 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12026745 | gttggaggaacgggt[C/T]aaccctcaatcagtc | 75725 |
rs255468824 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12067720 | TTTTTGTTTTTGTTT[C/T]TTGTTTTTACCATAC | 75725 |
rs255471827 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11911174 | ATAATAAGAGAAGAA[A/G]CATCTACAGCATCAT | 75725 |
rs255492974 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12053489 | CTAGCAAGAGCTGAT[A/C]TTACAGGACTGTGCC | 75725 |
rs255514462 | snp | G/T | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099037 | ATTACTAAGAAAAAT[G/T]TCTAACTTAAGATCT | 75725 |
rs255517721 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060595 | TCTCTTCCTTGAGTG[A/G]CAGTTATGCAACAGT | 75725 |
rs255521480 | in-del | -/GGAATGAT | | | intron-variant | Phf14 | Mm_Celera | 6:11945377 | CCTGCCTCCCACCCC[-/GGAATGAT]GGAATGATGGCATCT | 75725 |
rs255531342 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11978855 | GTCCTTTCTCTAGCT[C/T]TTCCATTGGGGACCC | 75725 |
rs255532938 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12018849 | CCTCTCTGAGGACAA[C/G]CATGCTAGGCTCCTG | 75725 |
rs255534005 | in-del | -/TTG | | | intron-variant | Phf14 | Mm_Celera | 6:12006074 | GATATAAATGTTTTC[-/TTG]TTGTTGTTGTTGTTG | 75725 |
rs255545066 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12080148 | AGAAGTACAGAATGA[-/T]TTTTTTGGAGATAAC | 75725 |
rs255551318 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12090625 | TAGCTTTGTAATTAC[A/G]CTAAGAAGGGATAAC | 75725 |
rs255554443 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11920667 | TGAAATGCCTTCTTT[A/T]TCAAAACTTCCAGGA | 75725 |
rs255582704 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12053803 | AAAGAAAATTTCATA[A/C]AGCCATTCACAGTGT | 75725 |
rs255583043 | snp | A/G | | | intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:12045645 | ACACCCCAATTGTCT[A/G]CCAGCATGAGAAAGA | 75725 |
rs255594544 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11979575 | AGCTCTGATAAGATC[A/C]CTTTCTCCTTCCACT | 75725 |
rs255596187 | snp | C/T | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099061 | AAGATCTATTTTTGC[C/T]TCTTCCTGTCTTAGG | 75725 |
rs255618109 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11914939 | AAGAAGACATGAAGC[A/C]GACAAAATCACCTTA | 75725 |
rs255625950 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12046391 | AACTACATAATCTTA[C/T]TTTTAAATCCCAGAG | 75725 |
rs255653443 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11930484 | GTTGAAATGAATGTT[A/G]CTTTGAGAGATCCTG | 75725 |
rs255687581 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11993031 | CATCGGAGAGGTCTA[G/T]AATGAATTTTATCCT | 75725 |
rs255694267 | snp | A/G | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12040620 | CTAGAAAAAATACTC[A/G]TAATTCTTAGGAAAA | 75725 |
rs255727384 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11909747 | TGGTAGTGAGTACAG[C/T]GAGGCTGCTAGTAAC | 75725 |
rs255727756 | in-del | -/TGAT | | | intron-variant | Phf14 | Mm_Celera | 6:12072666 | AGTTGAAAATAAAAC[-/TGAT]TGTATTTACAAATCA | 75725 |
rs255730419 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12080295 | AAATCAGAAATAACA[A/G]AAAAGCAAGACTACT | 75725 |
rs255738575 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11915427 | AGGCAGGACGATTTC[G/T]GAGTTCAATGCCAGA | 75725 |
rs255739312 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11931895 | CACACATACCTGGCT[A/C]CAGAGGTCTGAAACC | 75725 |
rs255774286 | snp | A/G | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12012423 | TTTAAGTTTAGTAGC[A/G]TCTTCGAATGGAAGC | 75725 |
rs255779801 | in-del | -/TTT | | | intron-variant | Phf14 | Mm_Celera | 6:12051901 | CAACCTGTCTGTGAC[-/TTT]TTTTCTTTCACAACT | 75725 |
rs255801910 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12001407 | ATATTATTTGAGTCT[A/G]TTGTGAAAGGTGTTA | 75725 |
rs255806287 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907375 | GAGCATGTTTGCGGC[A/C]CAGGCCTACCTACAC | 75725 |
rs255834127 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12065468 | GTTTGGTGACTTCCG[A/G]TTTTCTGATTTTGTC | 75725 |
rs255852928 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12002377 | CTCATCAATAGATAG[A/G]TCATCCAGACAAAAA | 75725 |
rs255853742 | in-del | -/AC | | | intron-variant | Phf14 | Mm_Celera | 6:12092661 | TGTGTGTGTGTGTGT[-/AC]ACAAACATTTATTTG | 75725 |
rs255857828 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11993517 | TGAGTATTAACTACA[A/G]AAGTAGAAATAAAAT | 75725 |
rs255862670 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12097049 | ACGCCTCTTTCTAAA[-/T]AAAACAATTGGTCAG | 75725 |
rs255865174 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11994135 | CCAGGTTAATTGAGA[C/G]TACTGGTCCTCCTAC | 75725 |
rs255897854 | snp | C/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12007860 | CTAGTCTTTCAGGGT[C/G]CACTGACACACAGTG | 75725 |
rs255911336 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11938172 | TTTCTAATTTTGAGA[A/T]GTTTTCTTTTGCCAT | 75725 |
rs255914760 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11915732 | CTCCCAAGTGGCACT[A/G]TAACTGTGTCTTCAA | 75725 |
rs255948335 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11991037 | TTATGACTGTAATTA[C/T]TTTTTTGCTTCAGAA | 75725 |
rs255960268 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11977339 | AACATAATCACTATG[C/T]AGTCACTATGTTTAA | 75725 |
rs255990227 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11928339 | GAAGGAAAACAAGGA[A/G]AGGGAAAGGAGGTAA | 75725 |
rs255991149 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12075230 | GACTACAAACTTTTT[-/A]AAAAAATTTTTTCTT | 75725 |
rs256001160 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12034798 | CGTGCCTCATCAGAC[A/T]TGCAGTGCCTGAGTG | 75725 |
rs256013869 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12029002 | GGATTACACGTGAAA[A/G]TACATTTGATAGTAG | 75725 |
rs256025741 | snp | C/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908075 | CTAGATTCTTAGGTC[C/G]TGGCACTATTGAAGA | 75725 |
rs256039088 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12035621 | CATAGTTAATTATAT[A/T]GTTTCTGGGATATTA | 75725 |
rs256053665 | in-del | -/AC | | | intron-variant | Phf14 | Mm_Celera | 6:12075091 | ATGCCCCCATATCAA[-/AC]ATATAATAATAATAA | 75725 |
rs256054042 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12030780 | GAAATAATTTGAGGA[C/G]TATTGGCACTATTTC | 75725 |
rs256078433 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12096921 | ACATAGAAGTGTAGA[C/T]TTAACTTTGAGAGAT | 75725 |
rs256092974 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12088474 | TGGAATGTGTGTGGC[C/T]TGCCTTGAGTCTGAT | 75725 |
rs256104510 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12074289 | AGAATATACTTTTGT[A/G]TGGTTAAGTAAAAAG | 75725 |
rs256112055 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12026946 | TGGACTTTCCAGAGG[G/T]TTAGGTAACTATTAG | 75725 |
rs256127863 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12081789 | TACACTTCCAGGTCT[C/T]AGGAAGCCATGGAGA | 75725 |
rs256129127 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916429 | TCTAGCTCAATGGTT[G/T]AGCATGTGTTTGATC | 75725 |
rs256131645 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12089758 | TGCTAAATAGCTCAC[A/G]CTAGAGAATAAGCCC | 75725 |
rs256134240 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12023719 | TCTGACTTTTGCTGG[A/G]TCCTGGAGATTTGAA | 75725 |
rs256152747 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12046625 | TGATGAGTAAGTCAT[A/G]GTAGATAACTATCTC | 75725 |
rs256159467 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11946936 | TTTTTCTCTATCCTA[-/T]TTTTTTCTCTTGTTA | 75725 |
rs256182686 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11916867 | CACCTGATCTAGAGA[A/C]TATTACAGAGCTTTG | 75725 |
rs256195550 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12067986 | AGCTATAGACACAAA[C/T]ATAAACAAACTCTTT | 75725 |
rs256199913 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12037764 | CAACCAAGCACAGCA[A/G]ATACTTAGTAGTAAT | 75725 |
rs256200985 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11939780 | TTTACAATTTTTATT[A/G]AAATGATGGTTCCAA | 75725 |
rs256202413 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11976896 | AATGCTGGAAGAACA[C/T]TGAACATTTTCACAG | 75725 |
rs256206994 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12082274 | TTAAGAATGCTTACC[A/G]CTTATAGAAGACTGG | 75725 |
rs256213923 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11957535 | AGTGTCTCTGGTTTT[A/T]TGTCGAGTTCCTTGA | 75725 |
rs256216108 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11979950 | GCTATATAGAACCTT[-/A]AAGGAAATTTTATGT | 75725 |
rs256217185 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11922019 | AAGGTAGGAAATCAA[A/G]CAGGGCAGTAAACTG | 75725 |
rs256262264 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024213 | ACCTCCTCCCTACCC[C/T]ACCCCATCTCCACGT | 75725 |
rs256267577 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11930736 | TCTTTCCTTTTTTCC[A/T]CATGAAATGTTAAGT | 75725 |
rs256271368 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11958385 | TTTCGAATATTGAAA[C/G]TTTGAAAACTCCATC | 75725 |
rs256290729 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11948536 | AATGATTACTAGTTG[C/T]ATTAGTCTCTTTATG | 75725 |
rs256298885 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | Ndufa4, Phf14 | Mm_Celera | 6:11907743 | AGACCAGGGTCATCC[C/G]GCGGTCCGCTGGCAG | 75725 |
rs256321562 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11951348 | ATTTTTGTTTGTTAA[-/T]TTTTTTAAATGTGTT | 75725 |
rs256341816 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12077106 | ATAACTCTTCACTCT[C/T]TTCCACCCAGAGTAC | 75725 |
rs256343684 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11934143 | AATGAACACCCTGAA[-/T]TTTAACATTTATTCA | 75725 |
rs256354720 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949141 | CAATAATTTAAAATG[C/T]CATGGAATCTTGTTT | 75725 |
rs256392000 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:11915448 | CAATGCCAGAGTGTG[-/TT]CTACAGAGGGAGTTC | 75725 |
rs256396255 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11950240 | CATGGTAGCAAGTAG[C/G]TATGGCTCTGGAGCA | 75725 |
rs256400636 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950584 | TCTGGGTCTTGCATT[C/T]AGGCCTTTGTTTTGA | 75725 |
rs256400914 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072886 | GAGGAAGAGTGAAGG[A/G]GTCGAGAAGGAGTGG | 75725 |
rs256409782 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11946677 | TTGGGGGCAGGGGGG[A/G]ATGGAGTGAAGATGC | 75725 |
rs256410482 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11942211 | GCAACAGTGGGAATG[C/T]ATTTGGCAGTTAGTT | 75725 |
rs256426891 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095090 | TCAAGTTTTCAGCTC[C/T]GTGTGAAAAGCCACA | 75725 |
rs256432594 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11971908 | caggcatggtgattc[C/T]accagaggttctttt | 75725 |
rs256435553 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024566 | TGCTTGTTGGGTCTT[G/T]CGGAGGGCAGTCATG | 75725 |
rs256450135 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12044323 | TAGCACCTTGACTAC[C/T]TTGTGTAGGCATAAG | 75725 |
rs256459660 | in-del | -/ATGGAAGGA | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908461 | AGCACACAGTCTACC[-/ATGGAAGGA]ATTTAAAAGGGAAGG | 75725 |
rs256471634 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11938459 | TGTGGCCCACTGTTA[C/T]GGAACACTGTGGGGC | 75725 |
rs256475887 | in-del | -/TTC | | | intron-variant | Phf14 | Mm_Celera | 6:12002244 | AAGATGACATTTCAG[-/TTC]TTAACATCTCTGCCT | 75725 |
rs256479698 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11943299 | TGGCAGTCTTTCTTT[A/T]ATCTCCACCTCAGGA | 75725 |
rs256493573 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031991 | TGTTACATATTAAAA[A/T]TTTTAGGTGTGTTTT | 75725 |
rs256497863 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12017487 | AGATTACATTTGCTG[A/G]TGAATGTTAACAGTT | 75725 |
rs256507941 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12021889 | AAGCATGAGCAGATG[C/T]ACAGACGGTGTGTGT | 75725 |
rs256540965 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036903 | CAGGAGTTTAACTTT[A/T]TATTGGCTTTGTTTT | 75725 |
rs256549124 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906356 | CAACTTCCTTACATG[G/T]ATTAAATTATATGAA | 75725 |
rs256575734 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11963257 | TAAAATATGCATTTC[C/T]AAGTTCTCATCTTTG | 75725 |
rs256590200 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12003381 | GGAGCTAATGCAGAG[A/C]TAATGCAGAGCGAGG | 75725 |
rs256590752 | in-del | -/GGCA | | | intron-variant | Phf14 | Mm_Celera | 6:11953966 | CTCTCCCTACTGTTG[-/GGCA]GGCAGTCCTGAGAGT | 75725 |
rs256615040 | in-del | -/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12040437 | GGGCATTTGGAATAG[-/T]TTAAACTTTAGCATT | 75725 |
rs256621539 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12059850 | TTAAGCATTTTAACT[C/G]ATAAATTATATATCT | 75725 |
rs256663519 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054284 | TCCTTGAGCTGGTGG[G/T]GGTAAGCCACTCAGT | 75725 |
rs256664640 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12016934 | TGTGGCACAGGGAGT[A/G]CCCTGTGTGTGCTCT | 75725 |
rs256676262 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12097114 | TCCAGGACCAAGAAA[A/G]CAGTTCATTGGGGCT | 75725 |
rs256699981 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072716 | GCTTGTCATAATACA[A/G]TTAAATCATGTTCTA | 75725 |
rs256700216 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12047092 | ATTCATTTTTAAAAC[A/T]CTGAAATAATACAGA | 75725 |
rs256701101 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11928803 | TGCCCTGGCTCCTGG[C/T]GAGTATATGTGAGCT | 75725 |
rs256707779 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060186 | CACAGACTGAGGCCA[A/G]CACGAAACCACGCCT | 75725 |
rs256707843 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053996 | GGAAATCAATTTACT[A/G]CAATTATAGAAGCTG | 75725 |
rs256713906 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11921434 | GCTTGAATATGTGAA[A/G]GTGGCTTTGGAATTG | 75725 |
rs256717284 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12004091 | AGAGCCGTAATGGTG[A/C]CATTCTCTCTGCACT | 75725 |
rs256719600 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11995346 | ATTTATGTTGTGGAA[C/T]TTAGGATTTAAAAAC | 75725 |
rs256740443 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12033107 | AGCACTTCTTGGCAT[C/T]CATAATAGTGTGTGG | 75725 |
rs256742200 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054534 | TTACATAGGGTTTCT[G/T]GGGGATGGGGAGGAG | 75725 |
rs256756306 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11978541 | CTGCCCCCTGAAGTT[C/T]CTTATTCCATCCCTC | 75725 |
rs256768049 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921973 | CATTTGGCTTCTGCT[C/T]CCAGACCATAGTATA | 75725 |
rs256772098 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11958083 | CCTCTTTTGTTGTCT[A/G]ATTGCTCTGGCTAGG | 75725 |
rs256820753 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12016069 | TTAACTTGGAAACAG[A/T]TTCCAGGCATGTAAC | 75725 |
rs256829922 | in-del | -/TA | | | intron-variant | Phf14 | Mm_Celera | 6:12061143 | AATACCGTTAAGTCT[-/TA]ATAAGAATAGCTTTT | 75725 |
rs256834152 | in-del | -/TTTTTT | | | intron-variant | Phf14 | Mm_Celera | 6:12019818 | TTTAGGGGCTGAGGC[-/TTTTTT]TTTTTTTTTTTTTCA | 75725 |
rs256839306 | snp | A/C | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009113 | GGTGGCTGGGAATTG[A/C]CCCTCTCTGAGAGCA | 75725 |
rs256851695 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11999218 | ATGTAGTAGTTATGA[A/G]TAAGATGTTCCTCAT | 75725 |
rs256855527 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11962919 | ACTGATTTATACTTT[G/T]GAATAGTAAATGCCT | 75725 |
rs256866193 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12054125 | TTAAGATAATTGTAT[A/C]CACAATATACAAGTT | 75725 |
rs256870199 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11973500 | TATTAACTCCCTTCT[A/T]CTCCTCTTGGGTGAA | 75725 |
rs256908853 | snp | G/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925365 | CACCAAAGGAAGTCA[G/T]GACAGGAACTCAAGC | 75725 |
rs256923743 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12005656 | ACAACAGATAAGGCC[A/G]TCCTCTGCTACATAT | 75725 |
rs256924851 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12068648 | GCACCCTGTTTACTG[C/T]ACCTTGAACTTAAAT | 75725 |
rs256927774 | in-del | -/AAG | | | intron-variant | Phf14 | Mm_Celera | 6:12048751 | ACAGGTACAGGGACT[-/AAG]AAGATGGCTTGGTAG | 75725 |
rs256966135 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023829 | GTTGTTGTTGTTGTT[G/T]TTATTTTTTTTATTT | 75725 |
rs256966169 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11993168 | tgtaagtacactgta[A/G]ctgtcttcagacact | 75725 |
rs256966862 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12061120 | AGTATCCAGGAAAAA[A/C]TTATGTTAATACCGT | 75725 |
rs256968312 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11921560 | ACACATTCTGTACAT[A/C]TAAAGGTAGTCATAA | 75725 |
rs256982460 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12006597 | GTATGAAATGCTGAA[G/T]AAAGTCTTGGAATAT | 75725 |
rs256991786 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997750 | CTATGTATCTACCTG[C/T]CTGTTTCTCCCAAGT | 75725 |
rs257020421 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11931459 | GTGCACAAGGGCTTG[C/T]CTTTGAAGTATTTAG | 75725 |
rs257036481 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011619 | GGCCCTATAAACATG[A/G]TCATTATTTTCATGT | 75725 |
rs257069205 | in-del | -/AAGTTTA | | | intron-variant | Phf14 | GRCm38.p3 | 6:12023606 | AACCACTTTGTACTT[-/AAGTTTA]AAGTCTGCACTGAAT | 75725 |
rs257080102 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924041 | TTAACCTTAGCCATT[A/G]GGGATGGAACTTCTA | 75725 |
rs257095643 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12001353 | CTTGAAGTTTTTGTC[A/C]CAAGTCTTTTACTTG | 75725 |
rs257103686 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11992569 | GCTTCCTCCTCCTGA[A/G]TGTTGGATTGTAGGC | 75725 |
rs257104511 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985386 | GGAGGAGTCTTTCAG[G/T]TCACAACCAGCTTGA | 75725 |
rs257133788 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037184 | TGGGGTTTGGTGCTG[A/T]ATTGTGGTATCTAGA | 75725 |
rs257150265 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031436 | CATTTTCTTTCAATT[C/T]TAGAACATCTTTAAT | 75725 |
rs257162172 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12081866 | TCTTACACAACCTGG[C/G]CACAGCTCCCTAGGA | 75725 |
rs257165219 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037449 | GTATTAAGAGTTCTC[C/T]TGTACAGAACAGTTT | 75725 |
rs257172337 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11957634 | ATTTGTTGAAAATGC[G/T]GTCTTTTTTCCATGA | 75725 |
rs257175211 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12017540 | ATAGAAGGACTTAGG[C/T]TGTTCTTAGAGATCC | 75725 |
rs257175579 | in-del | -/CTTTCTCTG | | | intron-variant | Phf14 | Mm_Celera | 6:12062686 | ATGTACTAAATTTTC[-/CTTTCTCTG]CTTTCTCTGTATTAT | 75725 |
rs257191259 | in-del | -/AAAAAC | | | intron-variant | Phf14 | Mm_Celera | 6:11936514 | AATCTTAGATATTCT[-/AAAAAC]AAAAACAAACACAAA | 75725 |
rs257202480 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11916924 | CCAGGTTTCAGTTAC[A/G]TATTTAGGAATAAGG | 75725 |
rs257204950 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12026449 | GACATGAGCCTGGAA[G/T]TCCAGTCCTTTGTCT | 75725 |
rs257206674 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12017838 | GTACTTAAACAGTGG[A/T]GAAAAGATTGCCCAG | 75725 |
rs257208843 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12033001 | GGGACCCTGTGCTCA[A/G]TCCAATGGTTGGCTG | 75725 |
rs257231814 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12018231 | TTTGTTCCTTTGTCT[C/T]CCTAGACCAGTGGCT | 75725 |
rs257241963 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060100 | AGTGTAGTAACTCAT[G/T]CCTATAGTTTCAAGA | 75725 |
rs257254964 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008925 | AAAGGAATTTATATG[C/T]ACACAATTGAATGTT | 75725 |
rs257258908 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:11914286 | GAGATTGACTCAGGT[-/C]CCCCTGTTCTACAGC | 75725 |
rs257265714 | in-del | -/TTT | | | intron-variant | Phf14 | Mm_Celera | 6:12044125 | TCTCTTATACATTTC[-/TTT]TCATTGTGGTAAGCA | 75725 |
rs257270419 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12070898 | CAAACATCTTTCATG[C/T]TCCTTGGAAAACCAT | 75725 |
rs257274463 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11929448 | TTGGTAGTTCTTTTC[A/C]GTTAACCTGATCAAA | 75725 |
rs257290672 | snp | A/C | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009473 | ATACTTATTCATTTA[A/C]TTAATTAATTTGCAA | 75725 |
rs257291844 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11943368 | ATAAAATTATCATGA[A/G]GTTTGAGTTGCATTG | 75725 |
rs257300402 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985461 | CAATAGAGAATTAAC[-/T]TCTGCTTCCAGGAGA | 75725 |
rs257309401 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12018543 | AGACCAGACAAGGCA[A/G]CTCTGTCAGAGAACA | 75725 |
rs257361813 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11934388 | AAGTAAGGCTTTTGC[A/G]TACATTAGAAGAAGG | 75725 |
rs257361862 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11944320 | AGGGTCTTTGAAGCT[A/G]CAGATAAATCTGTTG | 75725 |
rs257375754 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11935787 | ACATAGACTGACCTA[C/T]GGAAGGCTGATTTCT | 75725 |
rs257382506 | in-del | -/CA | | | intron-variant | Phf14 | Mm_Celera | 6:11940978 | GAGTCTAGAGTCTCT[-/CA]GACATCAAATGCATA | 75725 |
rs257384073 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12098221 | ATGTTTACTTTGTTT[A/C]CCCAAATATTCTTTT | 75725 |
rs257386061 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921789 | TGGAGGTGCAAAATC[C/T]AGCAGCAGCTGAGAG | 75725 |
rs257392593 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12054631 | TGGGGTATTTTTTTT[G/T]TAACTTGCAGGTCAG | 75725 |
rs257427773 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037258 | AGTATCTTTGAACTG[G/T]CAACTATAGGAATTA | 75725 |
rs257427934 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12047788 | TTGAAATGAGTAGTT[G/T]CAACATTCAGATCCA | 75725 |
rs257428308 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12055132 | AGTTCATTTTGTTGC[A/G]CTCTAAGACAGGTAA | 75725 |
rs257494986 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12006179 | ATCTAGTCTGTAGAG[C/G]AGTGGCCTGCAGATG | 75725 |
rs257509811 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12048889 | GGCAGACACTGGCAG[A/G]TCTCTGGAGTGGCTG | 75725 |
rs257514380 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12094252 | TCTAAATAAGCTTAG[A/G]TTTCAGGACAAGAAT | 75725 |
rs257519014 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11936585 | ATCATGAGATACTTT[A/T]CTTTACTGTGCACTT | 75725 |
rs257538121 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12031593 | GTGTTTGGTCAAGTT[A/C]TTTTCTTTTTTACAT | 75725 |
rs257575210 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11954641 | ACATTCTTTCTGTCA[A/G]TGCAGACTCAATATT | 75725 |
rs257577640 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927864 | ATCAGCCAGGTACTC[C/G]TGGCACATGCCTTTA | 75725 |
rs257607927 | in-del | -/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12050139 | GGAAAAGAAAGGGAA[-/G]GGAAGGGAAGGGGAG | 75725 |
rs257608672 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12094961 | GTGCAGTCACAGTAC[A/G]GGAGCACTGCTGAAG | 75725 |
rs257657428 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11943988 | TAACACACATCAATC[-/A]TATTGATCTTAGAGA | 75725 |
rs257657671 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11946658 | TTTCTCATTTACTCT[A/G]TACTTGGGGGCAGGG | 75725 |
rs257665648 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12096234 | ATCACTCATTTACAT[C/G]GTACTGTGGTTTGAA | 75725 |
rs257681344 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12046135 | GATGAACCAAATAAT[A/G]GTATTCTTTATAACA | 75725 |
rs257694836 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11997881 | GAATAGTGTTTGTTA[A/G]ACATTACTGTGATGG | 75725 |
rs257698001 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12086912 | AAGACATTTTAGTTA[A/G]TCTCTTCTGGAAATG | 75725 |
rs257743778 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11975562 | GGTGAGTGGTCTTGG[A/T]TTTTGTTAGTAAGAT | 75725 |
rs257751629 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12050718 | CATTTTCCCCACGGG[A/G]AGGGAGTTGGGAATG | 75725 |
rs257752329 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11989644 | GAGTTTAGTCCAATA[C/T]GATAATTTCTCTAAT | 75725 |
rs257752917 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11998564 | TTCTGCACCATTATA[C/T]GTTGGAAACTTACAG | 75725 |
rs257763087 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12037399 | AAATTTAATTAATCC[A/C]AGTATATGTTAAAAG | 75725 |
rs257763694 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11990192 | CTAGTATGTACTAGT[A/T]AGAAGTTATTTTACA | 75725 |
rs257767017 | in-del | -/ACACACACAC | | | intron-variant | Phf14 | GRCm38.p3 | 6:12026646 | ATTTGACAACTGGAT[-/ACACACACAC]ACACACACACACACA | 75725 |
rs257776890 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060038 | TTTGTTTGTTCTTGT[C/T]ATCTTGCCATTTCCT | 75725 |
rs257804831 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11955060 | TCTCTGGGGCTGGAG[G/T]TATAAGCATGTGTGA | 75725 |
rs257809889 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030319 | ATCACCTGTAGGAGG[G/T]TTGTGGTTGAATTTT | 75725 |
rs257815521 | in-del | -/TTAT | | | intron-variant | Phf14 | Mm_Celera | 6:11998559 | GCATATTCTGCACCA[-/TTAT]ACGTTGGAAACTTAC | 75725 |
rs257818672 | snp | A/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907053 | CCTCTCTTGGATTCT[A/T]ATCACTCAACGTACC | 75725 |
rs257826730 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947947 | TAAAGACAAGTCTAC[C/T]TTTTCAAGTAGCTTT | 75725 |
rs257827293 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11961796 | AGGAGCTCTTAGCAT[A/G]AGGTCATTTATTAGT | 75725 |
rs257846372 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12041719 | GTAGTAATATATCAG[A/C]GTCACAGGGAGAATT | 75725 |
rs257879145 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910428 | ACCAGCTTGAATGCT[A/G]TTTGGAAAGAGCCGT | 75725 |
rs257907451 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11952324 | TCTTGGTAATTGTCT[A/T]CTTTGAATACAGATT | 75725 |
rs257930633 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024678 | CAAGAGTGGTATAGC[A/T]GGGTTTTCAGGTAGA | 75725 |
rs257983157 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11990509 | AGTAACCATTTATCG[-/T]ATACTTTAGTGTGTA | 75725 |
rs257993611 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030220 | GTGTTGCTTTCTCTC[G/T]CAGTCTATGTGCAAT | 75725 |
rs258000251 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12064439 | TGGGATTGCAGGGCT[A/G]CAGGTTGTGAACTGC | 75725 |
rs258001683 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11911245 | GTTTTAGGTTCTCCC[A/T]GTGCTGAAGGCACTT | 75725 |
rs258002053 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11962171 | CTTTATTTTGAGCAT[A/G]TGTCAGTCCATTACC | 75725 |
rs258016474 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12070678 | GAACAAAATGAGAAA[G/T]CAGCCACCTTTTGAC | 75725 |
rs258016658 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12084849 | AAAGACAAGTGGTTG[A/C]TTCCATTTCTGTATG | 75725 |
rs258041803 | in-del | -/A | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008837 | TACTCTAGAATTGAT[-/A]ATACAGAAAGCTAGC | 75725 |
rs258051643 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12078639 | ATATTAGTCTGCACA[C/G]TTAGACTGTACAGAT | 75725 |
rs258057110 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11912662 | CCTTCGGAAGCAATC[A/G]GAAACCTACCCCTGT | 75725 |
rs258074788 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11905747 | CCATAACATAAACAA[A/G]CAAACAAACAACAAC | 75725 |
rs258096006 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12070374 | ATAGTTAAGATGTTT[A/G]TCGAAGTTTTCATAA | 75725 |
rs258107415 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12058405 | AATGAAGACAGCAAG[A/T]GATGTCTACTTAGTC | 75725 |
rs258110452 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12005821 | CAACTCCTCCGTTGT[A/G]GTCAGAAAAAATGTT | 75725 |
rs258135275 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12078987 | TTTCCTTCTTTATCA[A/G]TGTTGTTATTGTAAA | 75725 |
rs258149464 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11952195 | TGTTTGCTGAGTGGC[A/G]CATACAGTTTTTAGA | 75725 |
rs258166958 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12072267 | GAGAAAGAAATCATC[A/T]TGAAGATTCAAGAAA | 75725 |
rs258177742 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11979125 | ATAAAATTATTTGTA[A/G]ATCTATTGATTTTAA | 75725 |
rs258190029 | in-del | -/C | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009534 | ATCTCTTAAATATGA[-/C]CTTTTTTTTCTTGTA | 75725 |
rs258201598 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11979970 | AAATTTTATGTATAT[C/T]CTACTTGATATTTTT | 75725 |
rs258209451 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11953121 | TCATAGCTGTAAGGT[A/G]AAAAAGAGTTTTTGA | 75725 |
rs258215250 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927696 | CCACACTTGCAGTCC[A/G]TCTGACATAGTTTAA | 75725 |
rs258216262 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12064523 | GTAACCACTGAGCCA[C/T]CTCTATAGTCCTGAA | 75725 |
rs258225961 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11945530 | CATCACTGTGGGTTC[A/G]CCTTGATCAGTGGAA | 75725 |
rs258234592 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11920316 | TTAGTCAGAGGCCAA[A/G]AGAGAAGCCTGATCA | 75725 |
rs258247585 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11937194 | ACCCTTTCTCTTGAA[A/C]AACCATCTGTGTTTC | 75725 |
rs258285523 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11946294 | TGTAGACCAGGCTGG[C/T]CTTGAACTCAGAAAT | 75725 |
rs258286101 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12027380 | CATGTTTTTCTTCCA[C/T]TTGGCTAGCCCTTCT | 75725 |
rs258302321 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12027815 | TTTAATGAACAAAAC[C/T]TTCCAAAAACGATTT | 75725 |
rs258321823 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11998480 | TTGCTCTTCTGGGTA[C/T]CAGTCTTTCTTGGGG | 75725 |
rs258357663 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11921048 | GGGTACTTGTACTTA[A/T]GGTAATAAGGCCACA | 75725 |
rs258360521 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12054455 | TATTGACGGAGGGGG[-/A]AACCAGAAGGGTGGC | 75725 |
rs258367652 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12020577 | TGTCTCACTGTTAAG[C/T]CACAAACTTTCCTTC | 75725 |
rs258416286 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12057281 | TTTCATTGTCTGTGC[C/T]TGTAGGTGCTTGTGT | 75725 |
rs258424977 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11915223 | CTGGATAAATCACAG[A/G]AACTCATAGCACAAT | 75725 |
rs258432233 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12029502 | CTATACCCTCACCCC[A/G]CCCTGCTTCCCAACC | 75725 |
rs258449133 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12087820 | TTTTTTAACTGTGAC[C/T]ACTAGAAAATTTGTA | 75725 |
rs258484462 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12021195 | AACCACCTATCCGTG[A/C]CTCTCAGTGCCAGAT | 75725 |
rs258485262 | snp | C/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925782 | GGAACTAGAGAATCT[C/G]TGAATATTCTTAAAG | 75725 |
rs258487019 | snp | C/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12081243 | ACAATTCAACTTTGA[C/T]TTAAAGGCCAAACCA | 75725 |
rs258505882 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12003400 | TGCAGAGCGAGGCCG[C/T]GGGGAAGGTCTGCTT | 75725 |
rs258563645 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918477 | ACACCTTGTCTCCAG[A/G]AAATAAAACCAGAGC | 75725 |
rs258567393 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11957034 | GGACTGTTCCTCTTT[C/T]ACCACATCTTCCACA | 75725 |
rs258579719 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947351 | CTTTTAAGCAGTTCT[A/G]CCAACTGAGGGCCAA | 75725 |
rs258598365 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12051534 | CTGAAATAGCATTTT[A/G]TAGTTTTACTTATTT | 75725 |
rs258600330 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12057542 | TAGTTATTTAATATA[C/T]TTTGTTATGTGGGGG | 75725 |
rs258604309 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12025770 | CTGCTATATGTAATT[A/T]CCCGTTTATCTAAGT | 75725 |
rs258619367 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12042621 | AACAGAGTTTATCTG[A/T]CTTTGTAAATTTAGA | 75725 |
rs258651315 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918414 | CTAGTAATTGCAGAG[C/G]TTTAGGCAAGAAATC | 75725 |
rs258662363 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094204 | TGAATGTTCTAAATG[G/T]TGATAGAAGAGGCTA | 75725 |
rs258670305 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12085991 | TGTTATCTCTTTAGT[C/T]CTGTTACTTAGCTCA | 75725 |
rs258684016 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12052137 | TTCAATTTCCTGACC[A/G]TCCGTGCATCTCCCC | 75725 |
rs258696923 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12036964 | GCAGTAGTGTCACAA[A/G]CCTTTAATCCCAACA | 75725 |
rs258702121 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12084942 | GAAAGCCACTATATG[C/T]GCATATTCAGTACTT | 75725 |
rs258715808 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12043300 | GAGGAATTTTAGACT[A/C]TCCTACCACCCACTC | 75725 |
rs258716098 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12035838 | GTGCTGGGATTAAAG[A/G]CATGTGCCACCACTG | 75725 |
rs258727841 | in-del | -/AAA | | | intron-variant | Phf14 | Mm_Celera | 6:12032579 | TTAGAGACACTTTTT[-/AAA]TTAAAATTTATTAGA | 75725 |
rs258728753 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036434 | AGAGAAATATTTAAG[C/T]ATGCAGGATGGAATC | 75725 |
rs258755461 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079284 | GTGATAAAACACCAC[A/G]ATCAAGGGCACTGAC | 75725 |
rs258797171 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023872 | CAAAACAGGGTTTCT[C/T]TGTATAGCCCTGGAT | 75725 |
rs258799891 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12037146 | GGGTAAAGGGAATTA[A/G]CAGTAGGATTAAGGC | 75725 |
rs258799919 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031113 | TTCTCTAAAAAACCA[G/T]CTCTTTGTTTCATTG | 75725 |
rs258803864 | in-del | -/TTGTT | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12081282 | CTTTTGGTTTCTTTA[-/TTGTT]TTGTTTTGTTTTGTT | 75725 |
rs258804643 | in-del | -/AAG | | | intron-variant | Phf14 | Mm_Celera | 6:12034497 | GCATCTTTCTTCTGT[-/AAG]AAGAGCTCTGATCAA | 75725 |
rs258818489 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906225 | CTGCTATTTGGCTAA[C/T]TTGTCCTACAATGGG | 75725 |
rs258819413 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12072356 | TCTTTAAAAAGCAGA[C/T]TTTCCCTACATGAGG | 75725 |
rs258820871 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072311 | AGAAGAAAGTGTCTG[A/G]TGCTGTAGCCCAGCT | 75725 |
rs258881020 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906681 | AAAACCAAAAGTTCT[A/G]TGAACATAATCTCTG | 75725 |
rs258896283 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11946020 | TGACTCCATTTACTT[C/G]TCGCTATTTCATTGT | 75725 |
rs258904798 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072529 | CATAATGCAGAGGTT[C/G]TTACTGTGCTTAAGT | 75725 |
rs258923603 | in-del | -/ATAAATAAATAAATAAATAAATAA | | | intron-variant | Phf14 | Mm_Celera | 6:12013284 | TCTTCCCCCTCCCCC[-/ATAAATAAATAAATAAATAAATAA]ATAAATAAATAAATA | 75725 |
rs258934896 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12073093 | GAGGAGTTCCCAGCC[A/C]TAAAACAGAAAGAAG | 75725 |
rs258936375 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12065204 | TTAACTTCCTCTCAT[C/T]ACACTCAGTATTTAT | 75725 |
rs258950197 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11937154 | TTTTGGCAAAATTTA[C/T]CAAATTTTAAGTAGG | 75725 |
rs258967735 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11991086 | TTTTAATTTTGTGGG[-/A]TTTTTTGTTGTGGTT | 75725 |
rs258969814 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12030729 | CTCTGTCCTCATAAA[A/G]TGAATTGGGTAGTGT | 75725 |
rs259003137 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12063458 | CTTGTGTCTGCTCAG[C/T]TTATATAGAATAAAT | 75725 |
rs259003483 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12059359 | TTGACAGTGCCCAGT[C/G]TATATGGCAAGTCTA | 75725 |
rs259016192 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12065915 | TCTGTCATGTATCTA[A/G]TACTTGTACTTACCA | 75725 |
rs259022689 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11938709 | ACAGAAGTGACAGAT[C/T]ACTGATTCAGTTTCT | 75725 |
rs259023773 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11928192 | CAAAATGGCCTGGCA[A/G]TTGTGGCAACTAATG | 75725 |
rs259038687 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12053720 | AGACACATTTTTCTG[C/T]TTTTCTCTTTGTTTT | 75725 |
rs259041717 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008111 | GTTACTTCATAAAAG[A/G]CATTGAGTTGTAAAG | 75725 |
rs259077681 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11951113 | CTTGTTTCTTTGATC[C/T]TTGCTGTTGTTCTTT | 75725 |
rs259083621 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11928727 | AAATGTTTGATCCCT[A/G]AAAGAACTAAAAACT | 75725 |
rs259084950 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11981008 | ACTTGGTGCTCTTGA[A/C]CACAGAAGACTATTT | 75725 |
rs259086455 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11959370 | TTTTCTAATGACCGT[A/G]GGTGATTCCTGTAAA | 75725 |
rs259096762 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959847 | ATTTCTGTGGTCACA[A/T]AAGAGTTTTTCAAGA | 75725 |
rs259100303 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12056922 | AATTAATAACTATAT[A/G]TAACTCTTGATGCTA | 75725 |
rs259100920 | in-del | -/AA | | | intron-variant | Phf14 | Mm_Celera | 6:11939104 | AACAAAACAAAAGAC[-/AA]AAGTGATTTAGAAGT | 75725 |
rs259117902 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12003160 | AAATCTAAATTCAAT[C/T]GACTTGAGTGTGTTC | 75725 |
rs259132475 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12014329 | CTGCAGAGTCACATG[C/G]CATAGCTGATCCTGA | 75725 |
rs259133003 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12053576 | AAGTAACAGTAGAAA[G/T]AAGATAACTATGTAG | 75725 |
rs259133940 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12022862 | TAAAGAAATAAATTC[C/T]CATATTCTCATATTC | 75725 |
rs259149078 | snp | A/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925597 | GGAGGCTCCTTTGAT[A/T]ACTCCAGCTTGTGTT | 75725 |
rs259175437 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11943456 | GCTTCAGGCCTCCCA[A/G]TGCACACATGCGCAT | 75725 |
rs259181330 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12046051 | AGAGATGTAGCTCCA[A/G]CTGTCATTTAGCCTG | 75725 |
rs259181968 | in-del | -/GCCATTCAG | | | intron-variant | Phf14 | Mm_Celera | 6:12075990 | CAATAATATCACTTA[-/GCCATTCAG]GCCCTTAGTGAAGGA | 75725 |
rs259207406 | in-del | -/TTG | | | intron-variant | Phf14 | Mm_Celera | 6:12037768 | AAGCACAGCAGATAC[-/TTG]TTAGTAGTAATGATT | 75725 |
rs259220384 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11915046 | CACAAATGACTCTAT[A/C]GCTCTTCTTACAAAA | 75725 |
rs259239530 | in-del | -/ATAAA | | | intron-variant | Phf14 | Mm_Celera | 6:12077686 | CTATGTAAAGTTCTT[-/ATAAA]ATTTGCCTACAATGT | 75725 |
rs259246262 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057977 | AAATTCTTAATTCCC[A/G]TATTCTATGAGAGTA | 75725 |
rs259273389 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12057643 | GGTACTTACGTGGTT[A/T]AAAAAATTAGAAGAA | 75725 |
rs259309053 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055328 | CCCTGTCTTAGAAAG[-/T]AAAAAGAGGGACATG | 75725 |
rs259313756 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052270 | GGGCTCAAATTTCAC[G/T]ACAGTGCTGTGATCT | 75725 |
rs259319577 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12004954 | TCAAATTTTTCTGAT[A/G]TGTGGCTTATCATAT | 75725 |
rs259333494 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11996536 | AATTATATTTTATTA[A/C]GGATTTACTTGGCCT | 75725 |
rs259334598 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11996244 | CCCATGGGTTTGGGT[A/G]TCAGGTTAGGCCAGT | 75725 |
rs259345018 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11931135 | ACTGTGCTGAGACAT[G/T]GTTATAAAACAAAAA | 75725 |
rs259347897 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11972551 | GTCCCTGATTTTAGT[C/G]AGATTGCTTCGAGTT | 75725 |
rs259361473 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052178 | CAAACCTGCCCCCAC[G/T]TCTTTTCCCTCTTCC | 75725 |
rs259372516 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927358 | ATTCCAGTTAGTGAT[A/G]TGAAGAGGTGGTGAA | 75725 |
rs259378015 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12084591 | GAGCTAGTAACAGTT[A/G]TGAAGTGGGTGTGAG | 75725 |
rs259378960 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11919098 | TATTCATTTAGAACT[C/G]AAGCAATGTGAGCTC | 75725 |
rs259396414 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12036140 | AATTGAGTGTGGAAG[A/G]GCATGCTTGTAATCC | 75725 |
rs259400437 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043557 | CATATTATTTAAAAA[A/T]TTTTAATGGGCCTCA | 75725 |
rs259409656 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12002663 | CAATGTCAGGGATGA[C/T]GAAATATTTTCAAGG | 75725 |
rs259412457 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11961374 | GATTAATTATCTGCT[A/C]TCATTCTCTAGCTAT | 75725 |
rs259434899 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11919283 | CATAGTACATAGACA[C/G]AGATGTAGGCAAAAC | 75725 |
rs259460325 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11912976 | TGTTTTGTTTTAAAA[A/T]TTTAAATGATTTAAA | 75725 |
rs259469830 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Phf14 | Mm_Celera | 6:11987126 | AAGTAGTGCTTCGGC[C/T]ATTCGTAAGCTTATG | 75725 |
rs259473351 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12003214 | AAGGCAGTACCCATG[C/T]TTCTTCTCTCAGCTT | 75725 |
rs259484233 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11912849 | TGTCAGTGGTGGTCT[C/T]TGTGTGGTGACGCTT | 75725 |
rs259485921 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12044253 | CATAGGCAAGTCCTG[G/T]GGGGGGGGGGGGGGG | 75725 |
rs259489312 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060486 | TGACAGCTAATTTCC[A/G]CTGTGATGAATCAGT | 75725 |
rs259495516 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12068280 | ACGAGACATCTGTAG[A/G]AAGCAGTTGTAGTTT | 75725 |
rs259520164 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12045001 | GTGTGTTATTGTATT[G/T]GTACAATTAAAATGT | 75725 |
rs259532082 | in-del | -/TA | | | intron-variant | Phf14 | Mm_Celera | 6:11947070 | TTTTAAGACAGATTC[-/TA]TGTCTTGGTTACTTT | 75725 |
rs259569612 | snp | A/G | | | nc-transcript-variant, missense | Gm6578, Phf14 | Mm_Celera | 6:12099830 | GGAAGAGCTTCGAAA[A/G]GACCTCCTTCTTGAG | 75725 |
rs259575911 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11932621 | ACTTAGAAGGCTAAC[A/G]TGACACATGACACAA | 75725 |
rs259576769 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12091610 | GGTCATGAGGCATAA[A/G]TTAGTTCCTTACTGT | 75725 |
rs259580262 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060766 | TATGTTTCCTTTGAC[A/G]ATGAATTTATTAATC | 75725 |
rs259594519 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12041205 | TCTAAGTAATTTATA[C/T]CTTATAAATACACAT | 75725 |
rs259603883 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057189 | ATTCTTTTAAATTTA[-/G]AAAGGAACAATCCAC | 75725 |
rs259611121 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11994157 | TCCTCCTACAGGGCC[A/G]CCCTCCTCCTCAGCT | 75725 |
rs259619932 | in-del | -/TAAAA | | | intron-variant | Phf14 | GRCm38.p3 | 6:12082704 | AGTCAAATTTGCTTT[-/TAAAA]AAAAAAAGGGCTAGA | 75725 |
rs259622583 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12061210 | CTGAGCTGGCCACAT[A/C]CTTGCCATGGAAGGC | 75725 |
rs259625121 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079026 | GCTGGAAACATGTCT[A/G]CTGAATAAGAAATGA | 75725 |
rs259643297 | in-del | -/AAAA | | | intron-variant | Phf14 | Mm_Celera | 6:12063552 | ATAATTCATTGCTTG[-/AAAA]AAAAAAAAAACCTTA | 75725 |
rs259646896 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083459 | AGCCATGGGTCCCTC[C/T]ATGTGTACTCTTTGG | 75725 |
rs259648238 | snp | A/T | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100222 | CCTCTGGAGTGGTCC[A/T]GGACGCACCGGCCAT | 75725 |
rs259651065 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11931605 | AAAAATTCAAATTTT[C/T]ATAATGATTTGTAGA | 75725 |
rs259651070 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11923664 | GTGATTTGATGTCTA[C/T]AAATTTCACAATTTT | 75725 |
rs259673389 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12034672 | TCCTAGAACCTCTGG[G/T]TCTGTCTTTTGCCCA | 75725 |
rs259676806 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12098643 | CAGTCTTTAAACTCC[C/T]TGTATTTCTGTTCTG | 75725 |
rs259697574 | in-del | -/AATG | | | intron-variant | Phf14 | Mm_Celera | 6:11952473 | ATTATGTATTTTTTA[-/AATG]AATTTTTTTTATACT | 75725 |
rs259712835 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12030867 | TATAGATCTATTAAA[A/G]TTTTTACCTGCTCTT | 75725 |
rs259714520 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12090100 | AGGAGCTGTTAAGTG[A/G]GACCTAATGTATCAG | 75725 |
rs259715671 | snp | A/G | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099121 | CTATAAGTAACTTAG[A/G]ACAGGGTTTGTTAGG | 75725 |
rs259720595 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11994960 | AACAAGAACCTAACA[G/T]TTCACAATTTTTCAT | 75725 |
rs259723896 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11981245 | TTTTTACAGTGTTTC[C/T]ACTCCCTCTTAAATT | 75725 |
rs259730778 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11959770 | TAATTTTAAAATATA[C/T]CTTAAATATGAGGAA | 75725 |
rs259745669 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950043 | CCTTTGTACCAGGAA[C/T]ATTTACTTTGATGTA | 75725 |
rs259756249 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11994229 | TTCTGTCCATTGGTT[G/T]GATACAGATACCTGC | 75725 |
rs259769890 | snp | A/C | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924088 | ATGTTCAATAATATA[A/C]GTAGTGTCTTCAGCA | 75725 |
rs259789009 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985500 | GACAATGGAAGTAGA[C/T]TGTGTTTTGGGAGTC | 75725 |
rs259807878 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12091248 | ACTCTCAAAGAAATC[A/G]CTCTTCCCTATTCTA | 75725 |
rs259846304 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12091858 | ATCAAAGCCCCAAAT[A/G]TATTAGTCAGGCCCA | 75725 |
rs259880434 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12084113 | GATCCTCCTGTGTCT[A/G]GAGTGTTGACATTAA | 75725 |
rs259880623 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11910506 | CTGTTTAAAATCATA[A/G]TAATTGTGATTAGCA | 75725 |
rs259880853 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11980170 | CCCATGAGAGAAGCA[C/T]GTGGCTCTAATGCTA | 75725 |
rs259888762 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12029918 | TATTCTGTTTTCAGC[A/G]GGTGATGGGTCTTTT | 75725 |
rs259899788 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950554 | CAGTATATTTTCCTC[-/T]TATTAGTCTTTAGTT | 75725 |
rs259907798 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12022219 | CAGTACACTAAGTAA[A/G]TTTAATAACAACAAC | 75725 |
rs259941075 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11917860 | TTTGACCCTAAGGAA[A/G]TAAATAAAGGCATAT | 75725 |
rs259951833 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12001703 | GCTTGTCTTGTTTCC[A/G]ATTATAGTGGAATTG | 75725 |
rs259952456 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12046454 | TATTTTTGGATCAGT[A/G]GAATAATATATGGCA | 75725 |
rs259967814 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11936273 | AGAAATGATATACAT[C/T]GTCTATAGGGAAATG | 75725 |
rs259973852 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029811 | TTAGTCCTTACTCAA[C/T]ACCTAACCTCTGTGG | 75725 |
rs260035111 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909202 | TTGCTAAGTACCTAC[C/T]CTGTACCATATCTTG | 75725 |
rs260045359 | snp | A/C | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12047277 | CAGAACTTGACAAAA[A/C]CTAGTGAGAGTAATA | 75725 |
rs260045365 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12037631 | GTCTGTGAGGAAATG[A/G]AGGAGTGTAATCAAA | 75725 |
rs260047975 | in-del | -/AC | | | intron-variant | Phf14 | Mm_Celera | 6:12078408 | GTGCAAGTGTTACCT[-/AC]AGAGAACAAAAGACG | 75725 |
rs260053483 | snp | A/T | | | upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11907581 | CGATTGCCCTAAATG[A/T]CCCGACCACTTCTTC | 75725 |
rs260064457 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950876 | AGACTTTGTAGTACT[G/T]ACTTCCTTCTTTGTT | 75725 |
rs260081583 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12038415 | CATTGCTTCTCGTGT[A/G]TTTACAAGCACAGCC | 75725 |
rs260092903 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11909852 | GATATATAGAAATGC[C/T]ATGATTCAAAAGAAA | 75725 |
rs260109163 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12075707 | TAGAAACCTTTCCAG[G/T]CACCACTTATCTGCA | 75725 |
rs260112115 | snp | G/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908360 | GGAGAGGGTTTCGCC[G/T]AAACTGCTAAACTGA | 75725 |
rs260134337 | in-del | -/TGTGTGTGTA | | | intron-variant | Phf14 | Mm_Celera | 6:11947513 | CACCCTAGCGGTGTG[-/TGTGTGTGTA]TGTGTATGTGTGCAC | 75725 |
rs260139876 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997422 | CACCAGCCTAATCAA[C/T]GCTCCACTAAAACAC | 75725 |
rs260146342 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12068992 | TACAGAGATTCAAAT[A/G]CAGATTTTTCTATTT | 75725 |
rs260147912 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11943464 | CCTCCCAATGCACAC[A/G]TGCGCATGCACTCAC | 75725 |
rs260159503 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12044753 | AATATACTTCTTCAG[C/T]CATCAAGTTTAGTTT | 75725 |
rs260200898 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11941083 | TTTACTGAAGTTTAA[A/G]AACCACATCTTAGAC | 75725 |
rs260216297 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11914427 | GATATATGTCACTCT[A/T]AAGATCAAGAAAACT | 75725 |
rs260231524 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12069549 | CAACCCACTTCCTGC[A/G]GGCCTAATCATCCTT | 75725 |
rs260262485 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11931900 | ATACCTGGCTCCAGA[A/G]GTCTGAAACCTAAGG | 75725 |
rs260265772 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12067364 | ATATTGTCTGACAGT[A/T]TTCCCATTGTTGCTC | 75725 |
rs260281217 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906516 | ACTGAAAAGTGGCCC[C/T]TAAAAGTTCTGTGAG | 75725 |
rs260292371 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12075733 | CTGCAGCCCAGTTTG[C/T]TTAACTACAGTAGCA | 75725 |
rs260314522 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12027983 | AAATAACAAAAGAGA[A/G]CAGTGTATGAAAGGT | 75725 |
rs260323220 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031496 | TTCATTTTGTAGTGA[-/T]TTTTTTTCAGTTTCC | 75725 |
rs260343846 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949238 | TTTATGCAGAAATAC[A/T]TATTGATTATGCTCA | 75725 |
rs260382537 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11974180 | ATTCAGAATTGAGAA[G/T]TGATCTTGGTAGATT | 75725 |
rs260386377 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985949 | GTGCTGGAGTCAAAT[C/T]CAGGTCTTTCTCGTG | 75725 |
rs260391273 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11955037 | GAGTCCAGAGGAGGG[-/T]TTCAGATTCTCTGGG | 75725 |
rs260392214 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11941141 | TACTTGAGGATTGAG[C/T]GTTCCTTTTTTCCCT | 75725 |
rs260413152 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029454 | ATTAGATATTTTCTC[C/T]ATTCACATTTCAAAT | 75725 |
rs260416414 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11911852 | CATATAGACTTATTG[A/G]GGGAAAAGGAGCCTT | 75725 |
rs260423143 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076970 | AAAGAGAAGGAGTCT[C/T]TGTCCCAAAATAGTG | 75725 |
rs260424111 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12084160 | GCTTGACTGTCACTT[G/T]GAACGGTAATGATAG | 75725 |
rs260451952 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12084671 | AAGCCATCTCTCCTG[A/G]GCAGCTTTTATTCAC | 75725 |
rs260471981 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950528 | CATGGTCTCGCTATA[C/T]TGAAGTATTTTCAGT | 75725 |
rs260474881 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11960670 | ATTCATAGAGATTTG[A/G]CATCTCATTTTTATC | 75725 |
rs260485653 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11986138 | GCCATCACTAAGAGA[-/T]TTGTGAAAAGAAAAC | 75725 |
rs260514886 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12056735 | GCTGTAGCCCACAAG[C/T]GTTTGTAGAGGAAGC | 75725 |
rs260520451 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11961388 | TATCATTCTCTAGCT[A/G]TGCTGGGTTTTTTAG | 75725 |
rs260544685 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12071455 | TTAAGCCTCATGTGG[C/T]GGGGATTATATAGGA | 75725 |
rs260545953 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11952091 | ACTGGCAGAGTACCC[A/G]TGTTCTAGATTACAG | 75725 |
rs260569051 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11944991 | AAATAGGTAGCAGAA[A/G]TGATAGTGAGCACAG | 75725 |
rs260578541 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12050738 | AGTTGGGAATGTATA[A/C]GTCTTTTCACCTTGT | 75725 |
rs260590494 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12023324 | GGTTGTTGATAGTTC[C/G]TGTATGTGTATGTGT | 75725 |
rs260594593 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11953007 | AAAACCATTTCTTTG[A/G]CATTCTCTTATATGA | 75725 |
rs260600292 | in-del | -/TTC | | | intron-variant | Phf14 | Mm_Celera | 6:12097516 | AGAAGTCATTTTTTT[-/TTC]ACTAAACTAACAACG | 75725 |
rs260603942 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12075658 | TTCCTTCTCTGATTA[C/G]TCAAAGACACTATAT | 75725 |
rs260610428 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12027583 | ATGGCAGGTTCTGTT[C/T]TCTCTATGTCTAAAT | 75725 |
rs260659870 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12069932 | GTCTACTGTGTCCAT[A/G]CGGTGTAGATCACCC | 75725 |
rs260668451 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949091 | CTTCATATTGTATAA[C/T]TAATTAACTGGTCAT | 75725 |
rs260676083 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11940838 | TTGCCCTCGATATTT[C/T]TTGACATAAAAGTAA | 75725 |
rs260688152 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12021865 | AGAATTCAAACGGCA[G/T]AAATCTGGAAGCATG | 75725 |
rs260693420 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12062266 | TCCCATGGGGTATGG[A/G]TTAGCTCAGGGTTTC | 75725 |
rs260711839 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12034741 | ATTGAGGAATTTCCT[C/G]CAGTGTCTTGGCTGC | 75725 |
rs260712289 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:11943692 | CTGCTGAATAGCCAT[-/G]GGGTTTGTTTCTTAA | 75725 |
rs260718055 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11933028 | GTATATTCTAACATA[C/T]ATTTCATTTCTCATC | 75725 |
rs260743128 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12015353 | GAAGTCAACTTTGGT[C/T]ACCTTTTCTTAAAAT | 75725 |
rs260788506 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947199 | GTGTGAGCATGGCAG[C/G]AGGCAAGCAAGCATG | 75725 |
rs260790695 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12069616 | GAGATTATAACACAA[A/G]GTCATTTTACTCAGA | 75725 |
rs260807553 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12002302 | AAAAGAAACATTACT[A/G]CAGCTTAAATCACAT | 75725 |
rs260820559 | in-del | -/TG | | | intron-variant | Phf14 | Mm_Celera | 6:11923110 | TTGTTGCCCGTAGAC[-/TG]TGATCAATAATCACA | 75725 |
rs260821086 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12061941 | AGCACACATAAGTGA[A/T]CTAATTGTCACAGTC | 75725 |
rs260841766 | snp | C/G | | | nc-transcript-variant, intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099584 | CTCATTTAAAAGTAA[C/G]AACTAACAAAATCCA | 75725 |
rs260867923 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11917607 | TTTACCCACTGAGCC[A/G]AGTACCAGATCAGCC | 75725 |
rs260884736 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11932652 | GCAGTGTCCTGTTTA[C/T]CAGGGAGACTGAAAT | 75725 |
rs260889353 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12062382 | ACATGTACCATTCTC[A/G]TCCTTGCTGTGTTCA | 75725 |
rs260890173 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094031 | ACTGCTCACCCAATT[A/T]TACCATTCACAGTTA | 75725 |
rs260902604 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12043061 | TCTAATCCATTTCTC[A/G]TGCTGGGAAGAGATA | 75725 |
rs260923949 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032461 | TAAGGTTTTTCAAAC[-/T]TATCTAAAATTCAAT | 75725 |
rs260945303 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925633 | GATACACAAAACTAG[A/G]AAGTACAAGTGTTAT | 75725 |
rs260945858 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12060626 | GCCGTGATGCTGGGC[A/G]GCAAGTTCCTAGCAG | 75725 |
rs260962622 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12020651 | ATAAAACATTTTACA[A/G]ACTTCAAAAGTTCCA | 75725 |
rs261015372 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12054956 | ACATACACATACTCA[G/T]GATGGATAGGTATCA | 75725 |
rs261038065 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11923272 | TATTACCTAAACATA[C/T]TAGTGTGCCAATCGG | 75725 |
rs261045890 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12000108 | GGTTTACTGTGTGCC[C/T]AGAAGTCATCTTTAT | 75725 |
rs261049975 | snp | A/G | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099367 | TCACTAATTAGGAAG[A/G]TGCCCTACAGGCTTG | 75725 |
rs261079040 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12091549 | GGAACTGCAAAAGAT[A/G]CTTCTCAAATAGGGA | 75725 |
rs261080911 | snp | C/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011006 | TCCTCCTGTGTGAGA[C/G]ACACACCAGGAAAGA | 75725 |
rs261096640 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11992396 | CTCAAATGCTTTTTG[C/T]TTTTTGAAGGCAAAT | 75725 |
rs261110691 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12006968 | TGTTTTGTTTACTTA[-/TT]TTTTTTTGTATGGCA | 75725 |
rs261115178 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11980616 | CAAGTCTTCCTGCCT[C/G]TTAGTATCATTTCTA | 75725 |
rs261125921 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11916771 | GGTGAATGCAGCTGA[C/G]AAGATTTCACTTTAG | 75725 |
rs261132703 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12041118 | ATCCTAAATGAAGTA[C/T]AACATTAACTTTTGC | 75725 |
rs261178514 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11910138 | AAGCCAGTGTAAAGG[G/T]GGGGATTGCAAACTT | 75725 |
rs261182577 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12033971 | GGAAAACTGGCTCTC[C/T]ATGTGTAGAATGCAG | 75725 |
rs261194968 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12082730 | AGGGCTAGAACTTTG[A/G]GGGAACTTATAAGAG | 75725 |
rs261240665 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11931011 | TGACTAAGATGTTAC[A/G]TTCTGTGACTAAAAC | 75725 |
rs261247862 | snp | A/G | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12040735 | AGAGAAATGACAATG[A/G]ATGCTTACCATTTTT | 75725 |
rs261248661 | in-del | -/TTTGCTGAAAG | | | intron-variant | Phf14 | GRCm38.p3 | 6:12030288 | TCTGTATCTAGCTAC[-/TTTGCTGAAAG]TGTTTATCACCTGTA | 75725 |
rs261275659 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12041283 | ATAAGAAATGGAAGG[A/C]ATATTAAAATGTCAG | 75725 |
rs261276297 | in-del | -/GACAAATG | | | intron-variant | Phf14 | Mm_Celera | 6:11937807 | TCTTATAGAATATAT[-/GACAAATG]GACATAAAATATGTT | 75725 |
rs261276995 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12034300 | TAATACTCATAATAT[A/T]AAAAGTAATAATAAT | 75725 |
rs261284601 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11912738 | CCTCCAGTTTCCTAT[-/A]AAAGACTTATATCCC | 75725 |
rs261306519 | snp | A/C | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099150 | GGCTTGTGGGCCCAT[A/C]GTCCATTACTGAAGG | 75725 |
rs261312513 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12096671 | TTGGTATGAACTTAT[C/T]AAGAGCTGTGTCACT | 75725 |
rs261319177 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12050004 | CATGTAAAATACCAC[G/T]TCCTGTCCTGATGTA | 75725 |
rs261334736 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12091356 | TTGATCTACCTGAGG[C/T]GTGCACAGGTCTTGT | 75725 |
rs261346465 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11978511 | TATTTATATTTCAAA[A/T]GTTATCACCTTTCCC | 75725 |
rs261347458 | in-del | -/TGTA | | | intron-variant | Phf14 | Mm_Celera | 6:12051916 | TTTTCTTTCACAACT[-/TGTA]TGTTGAACCTTAAGG | 75725 |
rs261368698 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11980294 | GAGGTGCCTTCTGCA[A/C]ACCAATATAGAACAC | 75725 |
rs261372206 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12025956 | TAAAAATAGAGAGGC[A/T]AGGTGCTTAAATTCC | 75725 |
rs261378659 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12097287 | GTGGAGCGTGAGCAC[C/T]AAGAGCCTTCAAAGC | 75725 |
rs261382018 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12087379 | TGGAAACACAAGATA[C/T]GTAATTTTTGCCTCA | 75725 |
rs261397410 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11979174 | TATTGAGAATTTTGT[-/A]CATTGTATTTTAATC | 75725 |
rs261398790 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908714 | TATCAGAGAAAATTT[C/T]GTGGTATCAACAGAA | 75725 |
rs261412136 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12088298 | AAGTGATGTCGCTTA[C/T]TTGAAAATGATTAAT | 75725 |
rs261423484 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12026738 | GAGAAGGGTTGGAGG[A/G]ACGGGTCAACCCTCA | 75725 |
rs261430948 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11909936 | CCTAGACATAATAAT[A/T]TGACAACCAGGTGAA | 75725 |
rs261432230 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11976633 | CAGTAAACTTTTACT[A/G]TGCATTCATGATGCT | 75725 |
rs261451316 | in-del | -/AAAC | | | intron-variant | Phf14 | Mm_Celera | 6:11913171 | AAGAGCATGTCTTCA[-/AAAC]AAACAAACAAACAAA | 75725 |
rs261482798 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11977814 | TGAGTTGTTAGGATG[G/T]TAGTGAGATTTGCTT | 75725 |
rs261489143 | in-del | -/TAA | | | intron-variant | Phf14 | GRCm38.p3 | 6:12067440 | TGCATTTTTGTTGCT[-/TAA]TAAACAAATAGGAAG | 75725 |
rs261491749 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031065 | CTTTACCTCTAGTTA[-/T]TTTGGTATAAGAGTT | 75725 |
rs261492418 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11957465 | TCTGTTCAAGAATTT[C/T]CCCCTTGTACCCATA | 75725 |
rs261505733 | in-del | -/TGGAATGTTAC | | | intron-variant | Phf14 | Mm_Celera | 6:11948772 | TAGGACCCCATCTTG[-/TGGAATGTTAC]TTACCACTTTTAGTG | 75725 |
rs261513207 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12068580 | TAGATTTTGCTAATA[A/G]TTATAATACCTTATT | 75725 |
rs261523563 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11991313 | AGTAAATTGACTTAC[C/G]TCACAAGAAGTGTTA | 75725 |
rs261533911 | in-del | -/AGGG | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008395 | ACAAAACTCAATGAA[-/AGGG]AGGAAATTCTCTTGA | 75725 |
rs261540283 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11940698 | AGTTTACATCCACAA[A/G]TGCAAAAGGTTTAAA | 75725 |
rs261540865 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11958160 | CCTTGTCTAGTCTCT[A/G]ATTTTAGTGGGATTG | 75725 |
rs261542759 | snp | C/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12047443 | AATACAAAAATGAAG[C/T]ATAAATTGTATGGCA | 75725 |
rs261547004 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11980830 | TCTCTCAAATCCATG[A/G]CTGTTCTTTCTTTCA | 75725 |
rs261564038 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12020269 | GACAAGAATTCAATC[A/G]GGGCAGGAATCTGGA | 75725 |
rs261564836 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12018604 | CTACATATGTCTGTT[A/G]CATATGTACCGGGAG | 75725 |
rs261572182 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11918268 | TTTTTACTCTGTCTC[A/T]AAATAAACAAACAAA | 75725 |
rs261573307 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11977983 | TTTTGTTCACCTCTC[C/T]GAGTGCTAAGATTAC | 75725 |
rs261577884 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072477 | CCAGTAGCAGAGAGG[A/G]CGATGGTTCTTTAGA | 75725 |
rs261586977 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12024191 | CTCCATCTGCTCCAT[A/G]TCTCATACCTCCTCC | 75725 |
rs261620700 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11908514 | GCAGGGACCACTTAT[A/G]CAAGGACTTTATGTT | 75725 |
rs261629085 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11946064 | ATTTCTATTTCTTAG[A/G]TTAGTCTTTGGGTCA | 75725 |
rs261635089 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11937571 | GAACTCTGGACCTTC[A/G]GAAGAGCAGTCAGGT | 75725 |
rs261655783 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12074936 | TTTAGTCTGAAGGAT[G/T]CAGTGTGCTCATTTT | 75725 |
rs261663324 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11929226 | AGATGATTATTATTA[-/T]TTTTTTATCTAAATT | 75725 |
rs261680906 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11978873 | CCATTGGGGACCCTT[C/G]GATCAGTCCAATGGA | 75725 |
rs261716283 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11940402 | CTGTGTTTAGTGACT[G/T]ATTATGGGATGGATC | 75725 |
rs261721554 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12053755 | CTTGTTGTTCATTTT[G/T]ACTCCACTTTTCAGA | 75725 |
rs261730456 | snp | A/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12011163 | ACACTATTAATTGCA[A/T]GCTGGAATCTCATCT | 75725 |
rs261732053 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12096519 | CTTCATCAGAAAGCT[G/T]CTAGCAGAGTACTGA | 75725 |
rs261738455 | in-del | -/AA | | | intron-variant | Phf14 | Mm_Celera | 6:11927959 | TCTTAGAAAACAAAC[-/AA]AAAATTCCTTGGATT | 75725 |
rs261764501 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12004265 | TTGAAAGCTTCCTGA[-/T]TTTTGTTTTTCATTT | 75725 |
rs261766702 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12046234 | AACATTCTGATCAAC[A/G]TAGAAGCAGTCTTGA | 75725 |
rs261771070 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11915317 | CTCCGATTTAGTAAA[A/G]TCAGCTTGCACTCTG | 75725 |
rs261788441 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11990153 | TAATGAAATTATAAC[A/G]GAATAATAGTATCTA | 75725 |
rs261800249 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12073118 | AAGAAGCCTTAGGCG[A/G]TTCTCTGAAGTAAAC | 75725 |
rs261822878 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024649 | TATGGTGGGGCATCT[G/T]TTAGGTATATGCCCA | 75725 |
rs261827115 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11974582 | CTTACTTGATTTTTC[C/T]AGGGTGTCATTTCCG | 75725 |
rs261831134 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12017787 | ATGTTCATTAAAAAT[G/T]TAATTATTATTAACT | 75725 |
rs261867356 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11958802 | AAAAAGCAATAAAAC[A/G]TGGACAGTTCCTTTT | 75725 |
rs261867878 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11938757 | TCTTCCCATTCACAG[C/G]TTTAATCGTAGAATT | 75725 |
rs261872792 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12068148 | GGAAATCAGTTTTGT[A/C]TTCTGGGTCTGGCTT | 75725 |
rs261879591 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12033854 | GCAACTCATATGATA[A/G]ATTACTTTATCTTTC | 75725 |
rs261879617 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917664 | CTCCTGGGCCCCAAC[A/T]GTTGTGTATCCATAT | 75725 |
rs261933921 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12097308 | CCTTCAAAGCCCACC[C/T]CCTACAACAAGGCCA | 75725 |
rs261953547 | in-del | -/AG | | | intron-variant | Phf14 | Mm_Celera | 6:12061953 | TGAACTAATTGTCAC[-/AG]TCTGGTCAATTCCCT | 75725 |
rs261962392 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12041544 | GACCAACACACACAC[A/T]CACAAGCACATGCGC | 75725 |
rs261970329 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11945418 | TGGGTCTTCCCTACC[G/T]TAGTTATTTAACTTA | 75725 |
rs261999452 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12061613 | CTACTTTCACAGAAG[C/T]GGACTGGCTGGAGTA | 75725 |
rs262000160 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11936650 | ACTCTAAAGTGGGTG[G/T]AGCACTTGATGAGTT | 75725 |
rs262026358 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12012991 | TTTGCTACCTAGCAA[A/G]GCAGGCAATGTTATT | 75725 |
rs262039993 | snp | A/C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12017530 | AAATATCTTAATAGA[A/C/G]GGACTTAGGTTGTTC | 75725 |
rs262042081 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12065788 | AAAAACAAAGGCTGG[A/G]GAATAGGATGAGAGA | 75725 |
rs262059349 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12059738 | TGTCTTTCTCAGATG[C/T]AAGCTGAAAGGATTT | 75725 |
rs262064309 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11945365 | CATTCCCCCCCACCC[C/T]GCCTCCCACCCCGGA | 75725 |
rs262072529 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053390 | CATAGTATCTAATGG[A/G]TTTTGTTTGCTTGCC | 75725 |
rs262082681 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12095677 | ATATAGCAGCTAAGC[A/G]TGGCTTCCTCCACTT | 75725 |
rs262090374 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12045331 | AATTCTGCTAGATTT[C/T]ACCTCTGCCATTTAG | 75725 |
rs262093401 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11989547 | GTACTAAGCAGTGAC[G/T]TTGATAGATGTTCAC | 75725 |
rs262102480 | snp | A/C | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008841 | CTAGAATTGATAATA[A/C]AGAAAGCTAGCTTCT | 75725 |
rs262153740 | snp | C/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906740 | AAATGCCTATTAAAA[C/G]CACTAGTTTTAGGAA | 75725 |
rs262156030 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12097141 | GGCTGGTTTTACAGT[A/T]TCAGAGGTTTAGTCC | 75725 |
rs262183403 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12038364 | ACTTAGGGCCTAAGG[A/G]GCTGGAAACTGTAGC | 75725 |
rs262223500 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12067059 | GGGTTCTCAGACAAG[C/T]CAAAGTATCACAGTG | 75725 |
rs262228090 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11977561 | AAAGCACGTTTATAC[G/T]GGTTTCTAGTTGTTA | 75725 |
rs262245244 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060212 | CGCCTAGCCGTGCAA[C/T]TTCAGAGAAGACTGT | 75725 |
rs262279857 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12009884 | TTGCCTTTAATATAA[C/T]CTTGAGGAATTTTTA | 75725 |
rs262282684 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12070150 | GAGATGTCTTACGAG[-/A]AAAAAAGGGGCCATA | 75725 |
rs262285274 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11999916 | CTTGCTTAGCACAGG[A/G]GGGGTCCCCTAGACA | 75725 |
rs262287832 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095372 | ATGTTTCCTACTAAC[C/T]TCATCATTACCCACG | 75725 |
rs262297186 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11929942 | TCTTTGTCTTATACT[C/T]GATGCCTGTAGTGTT | 75725 |
rs262321591 | in-del | -/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12028583 | TAAACATAGTAGCAA[-/T]TTTTTTTGTAAATAA | 75725 |
rs262329277 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11922088 | ATTGACTTGCTGCAT[A/C]TAACTTGCTCAGCCT | 75725 |
rs262335241 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12086231 | TCACAAACAGGAATA[C/G]CATTTTTTTTTCTTA | 75725 |
rs262347967 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12037115 | CAAAACAAAACCCCT[C/G]ATTTTAATGAGCTAG | 75725 |
rs262355225 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12090014 | CTGATCCAAAGGAGA[C/T]GTGAGATTTCCATTG | 75725 |
rs262367515 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906614 | GAGGCCAGCCTGGTC[C/T]ACAGAATGAGTTCCA | 75725 |
rs262368844 | snp | G/T | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12039877 | AACCCTAGACTCATA[G/T]TTAATGCTATTTCTA | 75725 |
rs262378563 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11972543 | CTTGTCTAGTCCCTG[A/C]TTTTAGTCAGATTGC | 75725 |
rs262384109 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11954355 | TCTTAAAAGTAGGTG[A/G]CTGACACAGTTTTCA | 75725 |
rs262390957 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Phf14 | Mm_Celera | 6:12007024 | CAGAGGCAGTCTGTG[C/T]TACAGAAGAAGCCCA | 75725 |
rs262467216 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12096553 | CCAGGCAGCTAAGAT[A/G]AGGGTCTTAAAGCCC | 75725 |
rs262484392 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985991 | TTGTGTGGATGTGCT[A/T]TACATCCAACTACAG | 75725 |
rs262492418 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11961297 | AGTGGAAAGCAATTA[C/T]GGTTCTAAATCTACA | 75725 |
rs262503801 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036133 | ATATATAAATTGAGT[G/T]TGGAAGGGCATGCTT | 75725 |
rs262508135 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12087315 | AGGGAAAGATCTTCA[C/G]TAACCCTACCTTCTT | 75725 |
rs262521481 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12037495 | GTCTGCTGGCTTCCA[C/T]TCTGGTTCCCACTCA | 75725 |
rs262521503 | in-del | -/TT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12061660 | AAACATTGAACTGAG[-/TT]TTTTTTTTTTTAAGT | 75725 |
rs262523573 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11976310 | AGAGATCTGGGACCC[A/C]AGATGCCCTCCTTTT | 75725 |
rs262562616 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032118 | GAATAGTTTTGTTGA[G/T]TTCTGTTCATTTTCT | 75725 |
rs262579704 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11955427 | GTAAAATTAAGAAAA[C/G]CACACTTCTCATTTT | 75725 |
rs262592676 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055292 | GAGTAAGTTCCAGTC[-/T]AGCAAGGACTACATA | 75725 |
rs262607492 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12063787 | TGACCTAATGCCAAT[A/C]TAGATTTTAAGTTTG | 75725 |
rs262613077 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12094822 | GAAAAACAAGCCCCC[A/G]AGAAACAAACCATAT | 75725 |
rs262629161 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12085658 | TATTATCATGCAATA[C/G]ATTGTATTACATACT | 75725 |
rs262633868 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12095178 | CTAGAACACATACCA[-/C]AAAAAAAAAAAAAAA | 75725 |
rs262648488 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12015806 | ATACATTTTACAGAC[C/T]ATCTTGACAAAAGTC | 75725 |
rs262670212 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906128 | AAACAAATAGACAAA[A/G]AAGAGTAGCCATCAT | 75725 |
rs262673169 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927470 | ATTAAGTTTCAGTTA[A/G]GGCAACCCGAGAAAC | 75725 |
rs262682852 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12005272 | TTGAGTGTTTGTATT[A/G]CACAGTGTAGTGCAA | 75725 |
rs262720324 | in-del | -/GAG | | | intron-variant | Phf14 | Mm_Celera | 6:12014241 | AGCTTGTCCTTGCCT[-/GAG]AAGTCTCATGCTGTT | 75725 |
rs262755642 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12065016 | TTTCATTGTGGTTCA[A/G]AGGTGTCAGCTGTAG | 75725 |
rs262766335 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12016924 | ACCTGTTTCCTGTGG[C/T]ACAGGGAGTGCCCTG | 75725 |
rs262778540 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031903 | ATGTTCTCTTGGTTA[A/T]TTTTTTTTTCTTTCA | 75725 |
rs262780456 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11915676 | TGCTAACTTAGAATG[G/T]CTATTATCTAGAAAA | 75725 |
rs262787578 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12080056 | CATAGGAGGCAATTA[C/T]ACAGACATGATTTGC | 75725 |
rs262791971 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12069759 | ACCTCCCCTTGTTCT[C/T]AGTATTACTTTCTTT | 75725 |
rs262792920 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11930573 | TAGGAATAGGAGTTT[A/G]ATTTTAAAGTTATTT | 75725 |
rs262809298 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11960505 | TTCAGAACTGTGGGG[G/T]TTTTTGTACAACAAA | 75725 |
rs262814974 | in-del | -/GTG | | | intron-variant | Phf14 | Mm_Celera | 6:11996027 | TGTAGATCTTCTTAT[-/GTG]GTGGTCCTCGATTCT | 75725 |
rs262821345 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11955070 | TGGAGGTATAAGCAT[C/G]TGTGAGCTGCCTGGT | 75725 |
rs262826287 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12021488 | TAAGCATTCTGCCCC[A/T]GCTAACCAAACCACA | 75725 |
rs262861356 | in-del | -/ACACACACACACACACACACACAC | | | intron-variant | Phf14 | GRCm38.p3 | 6:12026645 | ATTTGACAACTGGAT[-/ACACACACACACACACACACACAC]ACACACACACACACA | 75725 |
rs262881160 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12074158 | GCAATGCTACTAAGT[A/G]GACTGATGGTCTCTC | 75725 |
rs262893596 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12015089 | AGATCTCAGGCTTAC[A/C]GGTGAGATGAGGGTT | 75725 |
rs262895589 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12063327 | TTAGGTTTCTTGCCA[A/T]CTTTCGCCATCTTGG | 75725 |
rs262898020 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11947920 | ACCTCTGTTTTAGAT[A/G]AATAGCCTCATTAAA | 75725 |
rs262907036 | snp | C/T | | | intron-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100355 | TTTTCAGTCATGTTC[C/T]GCCAACTTCAACATT | 75725 |
rs262911943 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12026869 | GTTCAAACTTATTGG[C/G]TAAACATATTGACCT | 75725 |
rs262912618 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11937681 | ATGTTTGGTATAGCA[-/T]TTTTTTTAATTATGT | 75725 |
rs262913556 | in-del | -/AA | | | intron-variant | Phf14 | Mm_Celera | 6:11985014 | TGTAATAAAAAATAT[-/AA]AAAAAAAAAAGATGT | 75725 |
rs262915302 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12078851 | CCCTCTTCTGTATTA[A/C]ATAGACACAGAAATG | 75725 |
rs262919025 | in-del | -/GTTAGGAAG | | | intron-variant | Phf14 | Mm_Celera | 6:11960277 | ATCTTCGCTGCACAT[-/GTTAGGAAG]GTCGGTACAAAGCAA | 75725 |
rs262928237 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030598 | TCTGCATATGCTGCT[C/T]GTATCTCTAATCTTC | 75725 |
rs262944299 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11926574 | GCTCTCTGCATCCAG[A/C]GCCCCCAAACCCAAC | 75725 |
rs262944947 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11952816 | TTTTCGTTATTGCTC[C/T]TTTATAGGTAACAGT | 75725 |
rs262981670 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11945369 | CCCCCCCACCCTGCC[C/T]CCCACCCCGGAATGA | 75725 |
rs263012181 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12086351 | TGGAAGTTGCTAGAT[A/G]CAAGTTCTTAAATCC | 75725 |
rs263031864 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079486 | GTAACACACTTCTTA[C/G]GGTATCACACTCGCC | 75725 |
rs263050432 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11954430 | GGTGTTTATTGAGAA[A/G]GAAGTAAAAACTAAT | 75725 |
rs263054035 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12058629 | TGCGTGGACCCTTTT[C/T]CTTGTCCTTCGAAGG | 75725 |
rs263063184 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12031345 | TGTCTGTCTCTCAAT[C/T]TCTCTCTTTTGTTTA | 75725 |
rs263065473 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12006336 | CCAAATGTAGGATAT[A/T]AACTTTTTTACTAAA | 75725 |
rs263068933 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12024253 | CACCCTCCAACCCAC[A/C]TGACCTCTAAAGTCC | 75725 |
rs263087687 | in-del | -/TATG | | | intron-variant | Phf14 | GRCm38.p3 | 6:12068554 | ATATATATATATATA[-/TATG]CAAATATGAGTAGAT | 75725 |
rs263103588 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053166 | AAGAGACCTCCCTAA[C/G]GAAGCAAATGAGAGA | 75725 |
rs263104519 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11946356 | TAAAGGCATGCGCCA[C/T]CACCACCACCGGCTT | 75725 |
rs263121887 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11920558 | AAGCAATAAAAGATT[C/G]TTTAGCATGGCTCAG | 75725 |
rs263129000 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11997708 | TGACCACATGTCTCT[G/T]CCCCCTGCTTCTATG | 75725 |
rs263165998 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12063134 | AGCAATGTCAAGGGT[A/C]AACTGAACAGTTAAG | 75725 |
rs263207764 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11951954 | TTTCAGTTTACACTA[A/G]ATACTAAGATTATGG | 75725 |
rs263216847 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057460 | AAACTAGGCTACTTG[A/G]ATCAAGCTGCGTTCC | 75725 |
rs263230401 | snp | C/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:11926213 | CTCCGACCGGTCTCC[C/T]TGGTCCTCTGCGCGT | 75725 |
rs263238391 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12003741 | ACTCTTACTGAAATG[A/G]TGCAAAATCTATTTG | 75725 |
rs263273414 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11995793 | AAACTCTCCTGCTGA[G/T]ACCTGACAAGGCAGC | 75725 |
rs263295913 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12005354 | TTTCTGAAACATTGG[A/C]TGGAATAAACAGTGT | 75725 |
rs263311013 | in-del | -/CTC | | | intron-variant | Phf14 | Mm_Celera | 6:12093192 | TACATTAGCTCATGT[-/CTC]CTCCTGTTTCCCACT | 75725 |
rs263313577 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052491 | GTGTAACGTTCCTTG[C/T]AGAAAAACATCCATT | 75725 |
rs263321020 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11996904 | GTCATTACCACACTA[A/C]CTGTGTGTATTTGAG | 75725 |
rs263342623 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12085456 | GCCAGAAGCATCAAA[A/T]TCTCTAAGCCTGAAG | 75725 |
rs263343377 | in-del | -/ATA | | | intron-variant | Phf14 | Mm_Celera | 6:12075093 | GCCCCCATATCAAAT[-/ATA]ATAATAATAATAATA | 75725 |
rs263343401 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11919986 | CACATCTGTCATACA[A/G]CAGTTTTCTTTTCAC | 75725 |
rs263364675 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036592 | GAAATTCATATCTGA[C/T]CATTCATTTAGGACT | 75725 |
rs263371784 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12002152 | CAATATCTAACCAAA[G/T]AGACTTCAAAGTAAA | 75725 |
rs263399400 | snp | A/T | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924309 | TTTCATTTCCTTGCA[A/T]ATTGTATTTGCTTTA | 75725 |
rs263408408 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12071026 | GGAAGGGTTTATTTG[A/G]GGCTTATAGTTCCAG | 75725 |
rs263418712 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11924814 | TTAGTTGTCTTCTCT[A/G]TATTTCCCACCCCCA | 75725 |
rs263441010 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12092158 | CTGGGGGGTGGGGGG[A/G]GAGGCCCAATTCAGA | 75725 |
rs263459359 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083637 | TGACTGTGAGCATCT[A/G]CCTCTGTATTTGTCA | 75725 |
rs263466478 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918279 | TCTCAAAATAAACAA[A/G]CAAACAGTAAAAGGG | 75725 |
rs263472458 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12092609 | TTTGTTGCTCTGTAA[C/T]GGCGTAAACCCACTG | 75725 |
rs263489849 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083843 | GCAGTGAGTATTTTA[G/T]TCCACCTTCTAAGAA | 75725 |
rs263503022 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11960305 | GTACAAAGCAAGCAG[C/G]CAGCTGTTGGTTTAT | 75725 |
rs263517832 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11960393 | GAGGCTACACAGATT[A/C]CATTGAGAAAGTTGC | 75725 |
rs263550916 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11950486 | CCATTCTTACTCAAA[A/G]CATCACAGACTCTTA | 75725 |
rs263559998 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12029368 | CCAGTCTTAGTACTG[A/G]AATCTTTATTATGTG | 75725 |
rs263565179 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12030113 | GTTGAGTAAGTGTCT[A/G/T]TGTGGTAAGGTGAAG | 75725 |
rs263572842 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12078337 | ATGCATGGTTGTTTT[A/G]GGGTTTTTTATTTAT | 75725 |
rs263577243 | in-del | -/G | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12008138 | AAAGTTAATAGGTTT[-/G]TTTTTTTGAGAAGAT | 75725 |
rs263597940 | in-del | -/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:11988864 | TTGCTCTCTTTGAGA[-/T]TTTTTCATAGTACAT | 75725 |
rs263614120 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11958488 | TTGGTTTCCTATTAA[C/T]TTTAAAGTTCTATTG | 75725 |
rs263624531 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12033422 | GCTCCAGTTTTTGCC[A/G]TGTTCCCCATCACAG | 75725 |
rs263657104 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12052390 | TTTTTATAAAGCAAT[A/G]TCAATGTAAAACACA | 75725 |
rs263667974 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12043827 | CTTATTCATCATTGT[A/G]TAGGGAATACTGCCT | 75725 |
rs263668532 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11996744 | TTCCAAAGTAAAGAT[A/C]CCTTCTTAGTCAGTG | 75725 |
rs263678033 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11913633 | GCATAAACTACCACT[A/G]ATTATAAACCTTCTA | 75725 |
rs263699090 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11948757 | CCATTTTATTCCGTC[C/T]AGGACCCCATCTTGT | 75725 |
rs263745119 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079327 | TTAATTGGTCTCATG[A/G]TTTCAGAACTGTAGA | 75725 |
rs263771723 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11918092 | TCGATCTTAAATGTT[G/T]TCATTACAAAAATAA | 75725 |
rs263790098 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11994694 | AAAATGTCTACCAGA[G/T]AATTTCTACAGCTGA | 75725 |
rs263791553 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061460 | CTAAAACAAAGTTTT[C/G]TTTTACCTTCAGACC | 75725 |
rs263799736 | in-del | -/CGCGCA | | | intron-variant | Phf14 | Mm_Celera | 6:12053251 | GTGTGTGTGTGTGTG[-/CGCGCA]TGTGTGTGTGTGTGT | 75725 |
rs263837838 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11911035 | CTCAGTTCTCTATCA[C/T]TTGCTTAGTGTGTGT | 75725 |
rs263877026 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11995966 | TGTGCTGTTAGGTTG[A/G]TGGTTCAGTCTCTGG | 75725 |
rs263902681 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12029968 | CTTACAACTTCATGC[G/T]GTCATTATTTTTAAT | 75725 |
rs263903766 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036273 | TCTCAAGAAAATAAA[G/T]AACAATTATAATGAG | 75725 |
rs263905295 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11918824 | TATTTGGGGGACAGG[A/G]TCAAACTGGCCTGGA | 75725 |
rs263909154 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11912615 | ATAATATAAAAAGAA[A/G]GCTGGGGAGATGTCA | 75725 |
rs263925114 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11986586 | GGAAATTTAGGTCCA[A/G]CATGTAAAATGTAGT | 75725 |
rs263947705 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12070601 | TATTAGGCTGGTCGC[A/G]AAAGCTTTCTGCCAA | 75725 |
rs263950422 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11944167 | AGTAGCTATCAGTTT[C/T]TATATAACAATTACC | 75725 |
rs263972790 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12078902 | TTGCAAACAAACACT[C/T]ATAAACCTAAAAGTA | 75725 |
rs264009644 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023673 | GATAGTCCTTTCGTC[C/T]TCTAACTCCGGCTAA | 75725 |
rs264012203 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12083263 | CCCCTTCAGAAACCC[C/T]CTATTCCATCACCCC | 75725 |
rs264041371 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11910294 | CTTTCTTTAGTAAGA[A/C]ATGGAATGTGAGAAT | 75725 |
rs264056865 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12075737 | AGCCCAGTTTGCTTA[A/G]CTACAGTAGCAACAA | 75725 |
rs264057128 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12088651 | TCTTTTTCATTTTTT[-/C]TCTTTTTTTCTATTA | 75725 |
rs264059711 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949408 | TTCATTTTTCATCCC[G/T]TTTAAAGACTTCTGT | 75725 |
rs264064434 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949672 | AGGACCCTCCATATC[A/T]ACAGTGTAGAGTTGT | 75725 |
rs264076559 | snp | A/C | | | intron-variant, utr-variant-3-prime | Phf14 | Mm_Celera | 6:12010079 | ACATTATGAACTAAC[A/C]AGTACCCCCGGAGCT | 75725 |
rs264101063 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11941816 | AGCTTTTTACATGAG[C/T]GCAAGCACTGGACCA | 75725 |
rs264115332 | in-del | -/TGATA | | | intron-variant | Phf14 | Mm_Celera | 6:12098005 | CCTCTCCCTCTCTCT[-/TGATA]CCTGGTTTTCTACAA | 75725 |
rs264116294 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11930948 | AAATGACTAGTTATG[-/A]AAAAAGTTATATTCC | 75725 |
rs264116983 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12021036 | GTACTGGGATCTCCA[A/G]AGTATTGCCTGGCTT | 75725 |
rs264137978 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12070185 | ACTAACTTCCATTGT[A/T]GTATGTTGTCACAAT | 75725 |
rs264144302 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12021982 | GTGTGTGTGTGCATG[C/T]TCTACCTAGCTTGTT | 75725 |
rs264155002 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12062695 | AATTTTCCTTTCTCT[A/G]TATTATATTGACTGC | 75725 |
rs264180813 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11943203 | GGGGTGGGTGACTTC[C/T]CCAGTAAAGCACACA | 75725 |
rs264185446 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12056784 | GTAGAGGAAGCTGTA[G/T]CCCACGAGTGTTTGA | 75725 |
rs264202589 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12056865 | GATAAAAATTTTACA[C/T]GTTATTCATATGCTG | 75725 |
rs264206706 | snp | C/T | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100123 | GAGGACGGATGGACT[C/T]TGGACTGCTAATGCT | 75725 |
rs264243715 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12060162 | TGTGAGTCCCACTTC[A/C]GTGGGTGCCACAGAC | 75725 |
rs264250644 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11939321 | AATGCCGCACTGAGG[A/G]CCTTTAGTGCTTTAT | 75725 |
rs264265936 | in-del | -/CG | | | intron-variant | Phf14 | Mm_Celera | 6:11959628 | TGAGCAAAGACAGGA[-/CG]CTAAACCTGCTTTAA | 75725 |
rs264301691 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055228 | ACCTCTAATCTCAGC[A/T]CTCAGGAGAATGAAG | 75725 |
rs264308927 | in-del | -/AG | | | intron-variant | Phf14 | Mm_Celera | 6:12084557 | GGAGCCTTTGGAGCC[-/AG]AGAGGCCAGAACCTG | 75725 |
rs264319153 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12095177 | GCTAGAACACATACC[-/A]AAAAAAAAAAAAAAA | 75725 |
rs264331402 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030884 | TTTACCTGCTCTTGA[-/T]TTTACTTTGGTAAAT | 75725 |
rs264331606 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12055513 | CTTGTCACACTCCAG[G/T]TCGGAAAATCCAGGA | 75725 |
rs264337991 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12000738 | GAGTTTCTCTAGATT[A/G]TAATCCTAATTAACT | 75725 |
rs264349809 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12049017 | ACATAGTTAAGTGCA[A/C]CCACGTAAAAGTATG | 75725 |
rs264367378 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12001105 | AAGTTCTGGGATTAC[C/T]GATGTGTACCACTGC | 75725 |
rs264373570 | in-del | -/GATTGACGAAGATGCCTGAAATGA | | | intron-variant | Phf14 | Mm_Celera | 6:11943417 | TGTAAGGTGGAGAGT[-/GATTGACGAAGATGCCTGAAATGA]GCTTCAGGCCTCCCA | 75725 |
rs264375209 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11992949 | AGATCAGATAATCCT[C/G]CACAGGACTAGCCTT | 75725 |
rs264377879 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916943 | TTAGGAATAAGGGAC[G/T]TCCTTAGGAACAGCC | 75725 |
rs264381996 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12049241 | CTGCAGATTGAAGTG[C/T]GCTGGCTACTCTTGT | 75725 |
rs264391681 | snp | A/G | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11923930 | CACCAGCATATCTTG[A/G]AGGCAGGTTGCTTTG | 75725 |
rs264418517 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083093 | ACATTTTTTTCCTAC[A/G]TGGATCTATTTCAGA | 75725 |
rs264426928 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11916990 | TCCCCTTTCCATTGG[C/T]TGGGTCATTCCACTC | 75725 |
rs264443721 | in-del | -/TGATAAGCAC | | | intron-variant | Phf14 | Mm_Celera | 6:11935086 | AAGCTTATATTTATA[-/TGATAAGCAC]TGATTAATTCCTAGA | 75725 |
rs264446883 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11998711 | TTGCTGCTTTTTTGA[A/T]GCAGAGGAAAAAAAA | 75725 |
rs264452097 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12053886 | AAGGTCAAGGCCAAC[C/T]TGGGGTTGTACCACT | 75725 |
rs264477184 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11921344 | TCAGCCATCCACTTT[C/G]AAGTAATTTTATAGT | 75725 |
rs264479367 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11940910 | TTTCTGTTGTAGCTG[A/T]TGTGTTCAGGCTGTT | 75725 |
rs264480380 | in-del | -/A | | | utr-variant-3-prime, intron-variant, nc-transcript-variant | Phf14 | Mm_Celera | 6:12081074 | CCAAAGAAGTAAAGG[-/A]ATTGTCCAGTGTGTT | 75725 |
rs264505042 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11915492 | AGCTACACAGAGAAA[C/T]CCTGTCTAAAACAAA | 75725 |
rs264517305 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11931765 | TTTAAAATCAACTTA[A/T]TTTGTGTCATATCTC | 75725 |
rs264550783 | snp | C/T | | | nc-transcript-variant, intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099712 | TTTTTTTAGTTCAGT[C/T]CTGGGTGAACCAAGA | 75725 |
rs264574736 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032752 | TCCTCTACACTGGGG[A/T]ATAGAACCTGTATAA | 75725 |
rs264575111 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12073899 | TTCAGTCTGAGGTAG[G/T]TTTTGCAGTGAGTAA | 75725 |
rs264587750 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11947639 | GTATCTTAAATACCC[C/T]GACACTCTAATCCTC | 75725 |
rs264591035 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12050603 | AGGTAGTTTGTTTTT[A/T]ACGTATACTTTGGAC | 75725 |
rs264603803 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12091874 | TATTAGTCAGGCCCA[C/T]GGTTTAAATGCACAA | 75725 |
rs264612003 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12041453 | GGTCAGTCACCCTAT[G/T]GATTTGGCAAATACC | 75725 |
rs264639168 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11927964 | GAAAACAAACAAAAA[A/G]TTCCTTGGATTGTGT | 75725 |
rs264642856 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11910321 | GAATTCCATCTGTCA[C/T]ACAGAACTGTTGGCT | 75725 |
rs264670464 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12098411 | CTTTTGTGGTTTGGA[A/G]ACTTTTTCCCAGGGA | 75725 |
rs264674785 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12048687 | AGGACATTTATTTTT[A/T]AAATGCAGTTTCCTA | 75725 |
rs264674982 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11992489 | TTTAAGAGAGAATCT[C/T]ACTTTCCTGTCTTAT | 75725 |
rs264681243 | in-del | -/TA | | | intron-variant | Phf14 | Mm_Celera | 6:12061672 | GAGTTTTTTTTTTTT[-/TA]AGTTAAAGATTTAGT | 75725 |
rs264699276 | snp | A/C | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | Mm_Celera | 6:11909081 | AAACAAGGAGGGGGC[A/C]ATGGATGATAAACTG | 75725 |
rs264705070 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11978950 | TCTCAGGAAACAGCC[A/G]TATCAGGCTCCTTTC | 75725 |
rs264735699 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12075693 | ATTTTTAAAGAAAAT[A/T]GAAACCTTTCCAGTC | 75725 |
rs264740714 | in-del | -/AAAAAA | | | intron-variant | Phf14 | GRCm38.p3 | 6:12082705 | GTCAAATTTGCTTTT[-/AAAAAA]AAAAAGGGCTAGAAC | 75725 |
rs264765024 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12072635 | TTAATGAGAATGTCT[A/G]CTAGCCAAAGAGACA | 75725 |
rs264766310 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11981318 | CATTACTTGGGGCTC[A/G]GCATCACATGGTTAC | 75725 |
rs264768552 | in-del | -/AACC | | | intron-variant | Phf14 | Mm_Celera | 6:12019780 | GCCTGCCAAAAAAAA[-/AACC]CCTAAGCAACAACAA | 75725 |
rs264779970 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11946453 | TGAGTGCTGGAATTA[C/T]AGGCATGGGCTATTT | 75725 |
rs264818359 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066969 | CACTCCTAGGCATAA[A/T]CCCAAAAGATACTTC | 75725 |
rs264820530 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12018478 | CTCCCATTATTCCCC[A/C]ACCCTAGCACATCAA | 75725 |
rs264828741 | in-del | -/A | | | intron-variant | Gm6578, Phf14 | Mm_Celera | 6:12099462 | TTGTGTCAAGTTAAC[-/A]AAAAAACTAGCCAGG | 75725 |
rs264839141 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11939199 | GTCACTTACCTCTGA[C/G]GTTCAAAAGAGCTCA | 75725 |
rs264842584 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11929839 | TAGATGTGGGATTCT[C/G]AGAATGCCTTGGTAC | 75725 |
rs264858977 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:11938676 | CCCCTTGGCAGAGGG[-/G]AAAAGCCAGGGCTCA | 75725 |
rs264874159 | in-del | -/TATATATA | | | intron-variant | Phf14 | Mm_Celera | 6:12032503 | TGTATATACATACAC[-/TATATATA]TATATATATGCATAT | 75725 |
rs264874760 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11935927 | TTTTACTTAAGAAAT[C/T]AATGTTTAGATTATT | 75725 |
rs264903594 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12052618 | TTACCCTATGCTGTA[C/T]TTTACATAAGGAATA | 75725 |
rs264916713 | in-del | -/TTA | | | intron-variant | Phf14 | Mm_Celera | 6:12044032 | ATGCCAGAAATAAAC[-/TTA]TTATTATTTGAAACT | 75725 |
rs264917124 | in-del | -/AGACTCTAGAGTC | | | intron-variant | Phf14 | Mm_Celera | 6:12055858 | GAGAGCAGAAGGTGA[-/AGACTCTAGAGTC]AGACTTACTCTTTTG | 75725 |
rs264917149 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Phf14 | Mm_Celera | 6:11997134 | ACAGATTAAGGAGCC[A/G]GTGAAGTTTGTGCCA | 75725 |
rs264920620 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11988630 | ATTATCTGACCTGAA[A/T]GTTACAATAAATGGA | 75725 |
rs264925668 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12044304 | AGGTTGAGAACCACT[A/G]TTCTAGCACCTTGAC | 75725 |
rs264937253 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:11934868 | AAATTTGCTTCACCA[-/TT]TTTTTTTTTTTACAT | 75725 |
rs264939165 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11952599 | CCCACCCCCACCCTA[A/C]CTGACCTCTAAACTC | 75725 |
rs264940892 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11914152 | GTCTCTCACTAGCCT[A/G]GAGCATGTGGATTTG | 75725 |
rs264972578 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12066134 | TTTCTTTTTCTCATT[C/T]TATTTTTTATTTATT | 75725 |
rs264983164 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11957440 | ATCTTATATCACGAG[C/G]CATTGGTGTTCTGTT | 75725 |
rs264988117 | in-del | -/TCG | | | intron-variant | Phf14 | Mm_Celera | 6:12021008 | TGTTCCTGTTTTTGT[-/TCG]TCATCTCAGGGTACT | 75725 |
rs265025973 | in-del | -/AA | | | intron-variant | Phf14 | Mm_Celera | 6:11918119 | ATAAAATAAAAAAGG[-/AA]AAAAAAAAAGGTAGC | 75725 |
rs265030187 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12060732 | TAGACTTGCTGAGTG[C/T]TGCAGTTTTTCACTA | 75725 |
rs265044364 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12000527 | TGAAAACCTAAAGCT[C/T]TCACACAATCAGCTC | 75725 |
rs265050556 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11930775 | CAGCATGGGGTAGTT[G/T]TTGACATCATGGAAA | 75725 |
rs265053644 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11923632 | ATCTTTGAAGAGTTT[C/G]CTCCTCATTGCATTC | 75725 |
rs265056068 | in-del | -/A | | | intron-variant | Phf14 | GRCm38.p3 | 6:12030681 | TCTAATGTGATAGTT[-/A]TCTGTTTTTATGTGT | 75725 |
rs265087132 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11927666 | GCAGGGCCTTTCACA[G/T]GCTCTGCTGCTAGAC | 75725 |
rs265111583 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12095779 | TTATGCCATGGCTGC[C/T]TCTCCACCCCTCAAT | 75725 |
rs265124573 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11921260 | TCTAGAGAGAGAATA[C/G]CTTTGTTTACTACTT | 75725 |
rs265125736 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12037231 | CTTAGGCACAAAGGA[A/G]TATTACTTCCAAGTA | 75725 |
rs265132706 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11974182 | TCAGAATTGAGAAGT[A/G]ATCTTGGTAGATTTT | 75725 |
rs265153106 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | Mm_Celera | 6:11906823 | GCTTAAGGCAAAGAT[G/T]AAGGCCCATCAGTGG | 75725 |
rs265161011 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12086653 | AGCTGGTTGGAAAAA[-/A]CAAGCCAGTAGCTGC | 75725 |
rs265161191 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11949039 | CTACTATTTGACATG[-/A]TAAAAAAGTGTATAG | 75725 |
rs265168137 | in-del | -/CTT | | | intron-variant | Phf14 | Mm_Celera | 6:12037767 | CAAGCACAGCAGATA[-/CTT]CTTAGTAGTAATGAT | 75725 |
rs265174062 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032688 | CCCCTCCTTCTAAGA[C/T]TGTGTTCCTTCCACC | 75725 |
rs265185934 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11986781 | TAGGGATGGGAGCAT[A/G]TGTTTCTTCGTAGAG | 75725 |
rs265201666 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036390 | ACACATATACATACA[C/T]AAACACACAAACAAA | 75725 |
rs265202246 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11961697 | AACTAAAATTCAGGT[G/T]TTTTTGTTTGTTTGT | 75725 |
rs265262368 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12064385 | TCTGTGTACTACATA[C/T]GTGCAGTACCCATGG | 75725 |
rs265271408 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11936742 | TTGGATAGCAGCCCT[G/T]CAGTATGGCTGTATT | 75725 |
rs265275526 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12016107 | TCCTAAACTTAAATA[A/T]ATTATCATTATCAAT | 75725 |
rs265287187 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11994051 | TCTGCTGTATATGTG[-/T]TGGGGGCCTCATATC | 75725 |
rs265292213 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12005742 | TGGGAGCTCTGGGGG[A/G]CTGCTTGGTATTGTT | 75725 |
rs265318793 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12070338 | AAAAGGAAGACCACT[A/G]TTCTTGGGAAAACTA | 75725 |
rs265329068 | in-del | -/GCA | | | intron-variant | Phf14 | Mm_Celera | 6:11911582 | CAAGTTCAGCCCCAT[-/GCA]TCTCCAATCCTAGAG | 75725 |
rs265329070 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12062427 | TGTTCTATGTCTCCT[A/T]TAGACATTCACAACT | 75725 |
rs265331215 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12022004 | TAGCTTGTTGCCCCC[A/G]GATTGATCAGCCTGC | 75725 |
rs265331241 | in-del | -/TCTCTCTCTCTC | | | intron-variant | Phf14 | Mm_Celera | 6:12022876 | CTCATATTCTCATAT[-/TCTCTCTCTCTC]TCTCTCTCTCTCTCT | 75725 |
rs265332905 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11918761 | AGTGTACCATGGATA[C/T]ATGAGAAACTGTCTC | 75725 |
rs265335274 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12014204 | CAATGAGACTATTTT[A/G]TACTCATGTTAATAA | 75725 |
rs265357990 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11934222 | GGATCTGTAGTCTCC[A/T]TTTCCAAGGAAAATA | 75725 |
rs265375850 | snp | A/C | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925761 | CTAGTTCTTAGGCAG[A/C]TGGATGGAACTAGAG | 75725 |
rs265377022 | in-del | -/AAAAA | | | intron-variant | Phf14 | GRCm38.p3 | 6:12022464 | AAGAGACTAAAGATC[-/AAAAA]AAAAAAAAAAAAAAA | 75725 |
rs265392894 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12094184 | CAAGAAAGCGAAAGT[C/T]GTAATGAATGTTCTA | 75725 |
rs265397140 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12043395 | GATGTTTGTGAAATA[A/T]GACTTAGAACAAGTT | 75725 |
rs265401870 | in-del | -/GCACA | | | intron-variant | Phf14 | Mm_Celera | 6:12053275 | TGTGTGTGTGTGTGT[-/GCACA]GTGCGTGTATGCGTG | 75725 |
rs265416705 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12079016 | AATCAAGATTGCTGG[A/G]AACATGTCTGCTGAA | 75725 |
rs265419639 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11953486 | TCCATATGCCTGCTT[C/T]ATGACTTGCCTGCTT | 75725 |
rs265425634 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030821 | TCTTTCTTGGGAGAC[A/T]GTTAGTGGCTGCTTC | 75725 |
rs265434822 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11945716 | TATTTTTACTCTCCA[A/G]CCACCAGCCTGAATC | 75725 |
rs265462736 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12024594 | ATGCTAGGTCTACAG[C/T]CTCAGTAGTAGTGTC | 75725 |
rs265482409 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12059093 | TGTCTTGTTAAAGTC[A/G]GATGGCTTTAAAAAC | 75725 |
rs265492285 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12053527 | CCTTGGTGAAATCAG[A/G]ATAGGAAATCCTGTT | 75725 |
rs265492607 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12007302 | CTTATGTTCTAAATT[G/T]AGATATAAATAACAG | 75725 |
rs265510027 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11997970 | AGAACTATTTGGGAA[A/C]GATTAAGAGGTGTGG | 75725 |
rs265536169 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12063391 | TTCTGTTCTTACAGT[A/G]GTATACATGGCCATT | 75725 |
rs265539449 | in-del | -/TAAC | | | intron-variant | Phf14 | Mm_Celera | 6:12049901 | GACTTTTTTATACTT[-/TAAC]TATTCATTTGACCTC | 75725 |
rs265545908 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12057601 | TTAGAACAAAAAAGG[A/G]ACAGAAACTACTTAA | 75725 |
rs265554663 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11926624 | GTGGAGAAGTCAATT[C/G]GAGATTCCGTGCAGT | 75725 |
rs265561579 | in-del | -/TC | | | intron-variant | Phf14 | Mm_Celera | 6:12057966 | AAAAACAGAAAAAAT[-/TC]TTAATTCCCGTATTC | 75725 |
rs265561836 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12004287 | TTTTCATTTCTTTAT[A/T]CTGTATGCATCTGGT | 75725 |
rs265566494 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11996159 | GGATGAAGCCTCTCA[G/T]ATGATAGTTACGCTA | 75725 |
rs265584076 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11919069 | CCTGTTGTTATGCCA[C/T]GGACTGTTTTGATTA | 75725 |
rs265605649 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12085776 | TTTCTAGATCAAAAC[A/T]CAGTAGGATTTACTT | 75725 |
rs265611118 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12036844 | TATTTTATTTATTTC[C/T]TGTATTCTAAATGAA | 75725 |
rs265619220 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12002459 | TACAGAATATTTTAC[C/T]CAAACCTAAAAGAAT | 75725 |
rs265620634 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12056726 | GTAGTGGAAGCTGTA[G/T]CCCACAAGTGTTTGT | 75725 |
rs265621909 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11944496 | TCAGAGCGGTTTGTT[-/A]AAAAACAAAAGAGCT | 75725 |
rs265641326 | snp | A/C | | | intron-variant, upstream-variant-2KB | Phf14 | Mm_Celera | 6:11925281 | TATTCGTACACAAAA[A/C]ATCATGGCCAAGAAG | 75725 |
rs265645171 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11917797 | ACAGAGATCACACAT[A/G]AACAAAAATTGATGG | 75725 |
rs265655853 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12093522 | CTTTTCCTGTAAGAC[A/G]GGAACTTCCTCAAGC | 75725 |
rs265681244 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12084068 | CTGTTCTGGGACTTA[A/T]GTATACTAGGCTGGC | 75725 |
rs265683396 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11960534 | AAAATGATAAAAACT[A/T]TAGACTTTTTCTGAA | 75725 |
rs265686805 | in-del | -/GTTGTT | | | intron-variant | Phf14 | Mm_Celera | 6:12006094 | GTTGTTGTTGTTGTA[-/GTTGTT]GTTGTTGTTGTTTTG | 75725 |
rs265699787 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11950796 | TGGGGTGCTGGAGGC[C/T]GCCTTTAGGTCTTCA | 75725 |
rs265706583 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12029737 | TTCCCACTCATGATC[A/C]AGTCATAACTAACTG | 75725 |
rs265733568 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12091089 | CTTTATATTATTTTT[C/T]AGTTGAGAGTTTCAT | 75725 |
rs265737453 | snp | A/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12040678 | AGAAGCAAATGACAT[A/T]ACTTGACTTATAGCA | 75725 |
rs265740290 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083061 | GGGTTGCCCTAAGCA[A/G]TTTCAAAATCACTGA | 75725 |
rs265758998 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12034108 | GTTGTACCCTAGAAA[A/G]TATAGATATGTAGGA | 75725 |
rs265767825 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11959205 | TTAATAAGCATTATG[A/G]CACACTGGAGTAGTG | 75725 |
rs265784247 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949224 | CTGTGGTGTTTTCAT[G/T]TATGCAGAAATACTT | 75725 |
rs265784579 | in-del | -/ACAA | | | intron-variant | Phf14 | Mm_Celera | 6:12051688 | ATGCTTACTGTGCTC[-/ACAA]ATCATGTGGAATAGA | 75725 |
rs265805915 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12061841 | ACATGACTTGGTGTC[C/G]TTTACAGGTTGTAAG | 75725 |
rs265815000 | in-del | -/TT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12088348 | GGTCCCATATTCTAA[-/TT]TTTTTTTTAATTCAA | 75725 |
rs265824675 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:12013403 | TGTTCTTTTTGGTTT[G/T]TTTTTTTTTTTTTTT | 75725 |
rs265825362 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11995107 | TTTTGGTGTTGATTT[A/G]TTAATCTATAAAATA | 75725 |
rs265831019 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12051489 | TGGAAATGCCTTTGA[A/G]AAGTTGCCAGCATCC | 75725 |
rs265832707 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12050051 | CCACTGTGATAGTAG[-/T]TTATTGAAATGCTCT | 75725 |
rs265844496 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11985677 | AGAAAAAAAATATGT[G/T]TATGCATTGCTAGTG | 75725 |
rs265846431 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11918356 | TGTTTATATATGTCA[A/C]ATTAGCATATTCAGT | 75725 |
rs265861549 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11911316 | CATTTTGGAGAGTCC[A/G]AAATGATTGTAATTT | 75725 |
rs265889922 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12078508 | TGACCCTAGTCGTCT[A/G]AAAGGACAGTGTTCT | 75725 |
rs265898895 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12030148 | TGTGCCTTTGGCTAC[C/T]CTGCTTGGCTAGCAT | 75725 |
rs265900426 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12071027 | GAAGGGTTTATTTGG[A/G]GCTTATAGTTCCAGA | 75725 |
rs265908352 | snp | G/T | | | intron-variant | Phf14 | Mm_Celera | 6:11944539 | ATGAGTGATCAAAGA[G/T]AAAGACAGAAGAGAT | 75725 |
rs265914701 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11949326 | CCGCCAGCCAACTTC[-/T]TTTAAGTTTCTACAT | 75725 |
rs265915602 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:12023073 | AATGGAGTAAGGCAT[A/T]TCAGAAGAAGAGAAG | 75725 |
rs265943365 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12083540 | TGTTGCTCCTCACCA[A/C]CCATGGGGCTAAAAA | 75725 |
rs265953383 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12076288 | GATAATTCCTAGCTC[C/T]TTCTATCCAGGTGAC | 75725 |
rs265960180 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12090823 | AAAGTCAGGAATGGT[-/C]TTATGGAACTCTCCT | 75725 |
rs265961628 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11950128 | TTCTGGTGCTGTATA[A/G]AGGCACCAGGACCAA | 75725 |
rs265968830 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12028760 | GTAAAACTCCATGTA[C/T]CTAAAAATTTAATAG | 75725 |
rs265969085 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:11998364 | CAAACAGGAAGCAAA[-/C]CCAGCCCAAGAGAGA | 75725 |
rs265972457 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:12021320 | TGGCTAACTCTGGAA[C/G]ACAGTTCTGTGCTCT | 75725 |
rs265991713 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11942162 | AGGAAAAAGGGAGCA[A/G]AGAGAGGAGGGATTG | 75725 |
rs266020483 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12057083 | GAACTATATTTGTAT[A/C]TTCTAGTTGGATGCA | 75725 |
rs266025819 | snp | C/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | Mm_Celera | 6:12100249 | CCATGGTAGTGCAAG[C/G]AGCAGCAACGAAGGA | 75725 |
rs266044891 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:11948300 | GAAGAGCTCTTTCAC[A/G]CTGGGCAGAGCCTTA | 75725 |
rs266061992 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11940292 | GATGACAGTGAGCAT[C/T]CACTTCTGTATTTGC | 75725 |
rs266091361 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11994114 | TGACTGAGAGATCTC[A/C]GGAGTCCAGGTTAAT | 75725 |
rs266094254 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12001388 | TTTAGAGTTACTCCA[A/G]GATATATTATTTGAG | 75725 |
rs266106792 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:12049937 | TTTTATATGACATAC[A/C]GGTTGGATTATAGGT | 75725 |
rs266111171 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11993493 | CCACTCAACAGAATG[C/T]TGTGATGATGAGTAT | 75725 |
rs266129304 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11917166 | AAACTTTATTTGACA[C/T]TGATTCAGAATGGAA | 75725 |
rs266132471 | snp | A/T | | | intron-variant | Phf14 | Mm_Celera | 6:11909898 | GTTTTGTTGATTTTT[A/T]AAATAATCTTATTAG | 75725 |
rs266161989 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12054455 | TATTGACGGAGGGGG[A/G]AACCAGAAGGGTGGC | 75725 |
rs266166456 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:11999727 | ATATCAAGAATGTTG[C/T]CTTTTTTTGAAAGGA | 75725 |
rs266182462 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11937431 | TTTTTTAAATGAAGA[-/T]TTTTTTTAAGATTTA | 75725 |
rs266185073 | snp | C/G | | | intron-variant | Phf14 | Mm_Celera | 6:11921924 | CTGGGTGTGATGAAA[C/G]CCTTAACCAAAGCAA | 75725 |
rs266190034 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12080769 | ATCTGGTTCCCCTAC[A/G]ACAGAGAGCACTGTT | 75725 |
rs266192395 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12032345 | GAAGTAGTTGTGAGT[C/T]ATGATTTTTACTTAT | 75725 |
rs266197657 | snp | A/C | | | intron-variant | Phf14 | Mm_Celera | 6:11991272 | TACATGCTAAGTTTT[A/C]AGCCCTTGGTGCTCA | 75725 |
rs266225065 | snp | A/G | | | intron-variant | Phf14 | Mm_Celera | 6:12082121 | AGGAAATGCTGATGC[A/G]TTCGCTCTTCACATG | 75725 |
rs266245473 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12027177 | GTCTTCAGGTCCTGT[C/T]CTCAGGGTCTCATAT | 75725 |
rs266249780 | snp | C/T | | | intron-variant | Phf14 | Mm_Celera | 6:12074621 | TCACTTCAATGTCTA[C/T]GATGGCCCACTAAAG | 75725 |
rs386859400 | in-del | -/AATATCTGTG | | | intron-variant | Phf14 | Mm_Celera | 6:12044216 | ATGTGAATATCTGTG[-/AATATCTGTG]TTTTCTGATGGTCAT | 75725 |
rs386859981 | in-del | -/TA | | | intron-variant | Phf14 | Mm_Celera | 6:12093888 | ACACACACACACACA[-/TA]CACACACACACACAC | 75725 |
rs386873054 | in-del | -/C | | | intron-variant | Phf14 | Mm_Celera | 6:12018403 | GCCACTCCCCCCCCC[-/C]TTTCCTTTACTCCCT | 75725 |
rs386876751 | in-del | -/ACTA | | | intron-variant | Phf14 | Mm_Celera | 6:12049903 | CTTTTTTATACTTTA[-/ACTA]TTCATTTGACCTCTG | 75725 |
rs386895369 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12038622 | GTTAAATTTAAAAAA[-/A]TGAACATTTTATAAT | 75725 |
rs386930484 | in-del | -/GCCCAGTCTATATGGCAAGTCTATATGACAGACAGT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12059580 | AGTCTATATGACTGG[lengthTooLong]GCCCAGTCTATATGG | 75725 |
rs386945411 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12022817 | AGAAGTTCTGAGGAA[-/A]GACAGGTGGCAAAAG | 75725 |
rs386957341 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12024425 | GGTCCAAATTAATTG[-/G]AAACTGCTGGTCCTC | 75725 |
rs386984654 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12001462 | AATTTTTTTTTTTTT[-/TT]GAGTTAACCTTGTAT | 75725 |
rs387006380 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:11997627 | CTCTTTGGTCACCTG[-/A]AAAAAAAAATTTTTA | 75725 |
rs387035664 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12028730 | GAATAATTTTTTTTT[-/T]CAAAAAGTGACTGTG | 75725 |
rs387046774 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12062946 | TGATACAGTTTTTTT[-/T]ATTTCATTAATTTCT | 75725 |
rs387053661 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12065900 | ATGTGTTTTTTTTTT[-/T]CTGTCATGTATCTAG | 75725 |
rs387062578 | in-del | -/TT | | | intron-variant | Phf14 | Mm_Celera | 6:12054632 | GGGTATTTTTTTTTT[-/TT]AACTTGCAGGTCAGG | 75725 |
rs387090791 | in-del | -/A | | | intron-variant | Phf14 | GRCm38.p3 | 6:12082705 | GTCAAATTTGCTTTT[-/A]AAAAAAAAAAGGGCT | 75725 |
rs387094884 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12050288 | GGAAAGGAAAGGAAA[A/G]GCTTTTTGTACTGTT | 75725 |
rs387117053 | in-del | -/TTTT | | | intron-variant | Phf14 | Mm_Celera | 6:12015560 | GGTTGTTTTTTTTTT[-/TTTT]ATGAAAAAGTAGATT | 75725 |
rs387133053 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12078319 | TATTTTTATTTTTTT[-/T]ATATGCATGGTTGTT | 75725 |
rs387163460 | in-del | -/GAGT | | | intron-variant | Phf14 | Mm_Celera | 6:12034907 | AAGAATGCAAGGAGT[-/GAGT]AATATTGCCCTCTTT | 75725 |
rs387191517 | in-del | -/G | | | intron-variant | Phf14 | Mm_Celera | 6:12083048 | CAGCTGCACGGGGGG[-/G]TTGCCCTAAGCAGTT | 75725 |
rs387193048 | in-del | -/TTGCTGAAAGT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12030289 | CTGTATCTAGCTACT[-/TTGCTGAAAGT]GTTTATCACCTGTAG | 75725 |
rs387196719 | in-del | -/TGTTCTACCTAGCTTGTGTGTGTGTGCA | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021952 | GTGTGTGTGTGTGCG[-/TGTTCTACCTAGCTTGTGTGTGTGTGCA]TGTTCTACCTAGCTT | 75725 |
rs387197570 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12051958 | TGGCTATCAGATCAT[-/T]TTTTAGTTTTTGTGT | 75725 |
rs387207253 | in-del | -/CA | | | intron-variant | Phf14 | Mm_Celera | 6:11916145 | AAGTGTGTGTGCGCG[-/CA]CACACACACACACAC | 75725 |
rs387217744 | in-del | -/T | | | intron-variant, downstream-variant-500B | Phf14 | Mm_Celera | 6:12048304 | ACACTTAATGTTTTT[-/T]ACAATTAGTGAGTAA | 75725 |
rs387227792 | in-del | -/ACACAC | | | intron-variant | Phf14 | GRCm38.p3 | 6:12026646 | ATTTGACAACTGGAT[-/ACACAC]ACACACACACACACA | 75725 |
rs387231023 | in-del | -/TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT | | | intron-variant, utr-variant-3-prime | Phf14 | GRCm38.p3 | 6:12039507 | TCTCTCTCTCTCTCT[lengthTooLong]CTCTGTCTCTCTCTC | 75725 |
rs387255816 | in-del | -/TCTCTCTCTC | | | intron-variant | Phf14 | Mm_Celera | 6:12097573 | CTCTCTCTCTCTCTC[-/TCTCTCTCTC]CTCCCTCTCCCTCTA | 75725 |
rs387314516 | in-del | -/AAGGGAAGG | | | intron-variant | Phf14 | GRCm38.p3 | 6:12050142 | AAAAGAAAGGGAAGG[-/AAGGGAAGG]GGAGGGGAGGGGAGG | 75725 |
rs387345925 | in-del | -/TTAAAGT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12023610 | ACTTTGTACTTAAGT[-/TTAAAGT]CTGCACTGAATCTGG | 75725 |
rs387348530 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12088356 | TATTCTAATTTTTTT[-/T]AATTCAAGTATGGCT | 75725 |
rs387365856 | in-del | -/CT | | | intron-variant | Phf14 | Mm_Celera | 6:12032282 | TGTGTGTGTGTGTGT[-/CT]GTGTGTGTGTGTGTG | 75725 |
rs387376381 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12063565 | GAAAAAAAAAAAAAA[-/A]CCTTATACTGATCCT | 75725 |
rs387381227 | in-del | -/TCTACCTAGCTT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021955 | TGTGTGTGTGCGTGT[-/TCTACCTAGCTT]GTGTGTGTGTGCATG | 75725 |
rs387392098 | in-del | -/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12069253 | GTTATATATGATGTC[-/T]TTTTTTTTTTTTTTA | 75725 |
rs387430212 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12028924 | ACCAGAAAAAAAAAA[-/A]GTCGGTTCGTTTTTT | 75725 |
rs387449905 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12028590 | AGTAGCAATTTTTTT[-/T]GTAAATAAAAAAAAT | 75725 |
rs387454053 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12079626 | TTCTATACTGACACT[-/T]AGTCTCATTAGTAGA | 75725 |
rs387572604 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12069439 | TCATCCTTTTTTTTT[-/T]CTTTTTTTTTATTCG | 75725 |
rs387587875 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12049598 | GTATGATTTTTTTTT[-/T]GCAATGAGAAATTAA | 75725 |
rs387588380 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12086242 | ATAGCATTTTTTTTT[-/T]CTTAACTGTGTTTAG | 75725 |
rs387592203 | in-del | -/ACTT | | | intron-variant | Phf14 | Mm_Celera | 6:12042330 | TTTGTTAACTTACTT[-/ACTT]TCCTGTTTATGCAAC | 75725 |
rs387594865 | in-del | -/AA | | | intron-variant | Phf14 | Mm_Celera | 6:12022479 | AAAAAAAAAAAAAAA[-/AA]GTTTCACATAGCAGA | 75725 |
rs387621486 | in-del | -/ATGT | | | intron-variant | Phf14 | Mm_Celera | 6:11962365 | TGTATGTATGTATGT[-/ATGT]GTGTGTGTGTGGATA | 75725 |
rs387650621 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12057693 | TTTAATTTTTTTTTT[-/T]ACTGATAAGGAAAAT | 75725 |
rs387653598 | in-del | -/AT | | | intron-variant | Phf14 | Mm_Celera | 6:12023835 | TTGTTGTTTTTATTT[-/AT]TTTTTATTTTTTGTT | 75725 |
rs387654890 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12017687 | GTGCTGAGCAAGTAT[-/T]GTCGGAAGGCCATCA | 75725 |
rs387668835 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12088660 | ATTTTTTTCTTTTTT[-/T]CTATTAGATATTTTC | 75725 |
rs387690536 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12035672 | TGTTGGTTTTTTTTT[-/T]GGTTTTTTGTTTTTG | 75725 |
rs387744030 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12028942 | CGGTTCGTTTTTTTT[-/T]CATCAAAGTAAACAT | 75725 |
rs387764808 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:11934870 | AATTTGCTTCACCAT[-/T]TTTTTTTTTACATAT | 75725 |
rs387768426 | in-del | -/ATATAT | | | intron-variant | Phf14 | Mm_Celera | 6:12032519 | TATATATATATATAT[-/ATATAT]GCATATACATATTTG | 75725 |
rs387774453 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12082715 | CTTTTAAAAAAAAAA[-/A]GGGCTAGAACTTTGA | 75725 |
rs387776570 | in-del | -/A | | | intron-variant | Phf14 | Mm_Celera | 6:12028604 | TTGTAAATAAAAAAA[-/A]TACAGTTTTAAGGAG | 75725 |
rs387803404 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12051962 | TATCAGATCATTTTT[-/T]AGTTTTTGTGTTTTG | 75725 |
rs387809284 | in-del | -/TT | | | intron-variant | Phf14 | GRCm38.p3 | 6:12001451 | TAGGGCTACTGAATT[-/TT]TTTTTTTTTTTGAGT | 75725 |
rs387864931 | in-del | -/T | | | intron-variant | Phf14 | Mm_Celera | 6:12064838 | TATGTTTTTTTTTTT[-/T]CTTCAAACTGAAACA | 75725 |
rs387867760 | in-del | -/GAA | | | intron-variant | Phf14 | Mm_Celera | 6:12078003 | GAATAAGCAGAAGAA[-/GAA]AAACCAAGGCCAAGA | 75725 |
rs578337654 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12085363 | TGTGTGTGTGTGTGT[C/G]TGTCTGTCTGTCTGT | 75725 |
rs578343864 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062352 | GTACATGGATGGATG[A/G]TATATAAACACATGA | 75725 |
rs578349451 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12075744 | TTTGCTTAACTACAG[C/T]AGCAACAAGTGTCCT | 75725 |
rs578357901 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12033315 | AGTAATATATCCCTA[G/T]GGCCTTTTCAAGCAT | 75725 |
rs578367096 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12050261 | GAAAGGAAAAAGGAA[A/G]GAAGAAGGAAAGGAA | 75725 |
rs578370613 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021954 | GTGTGTGTGTGCGTG[C/T]TCTACCTAGCTTGTG | 75725 |
rs578370945 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12096135 | TTTTTAGGGACTATA[G/T]TTAAGGTTGTTATAA | 75725 |
rs578382707 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11974118 | ACTTTGAGCTTCATT[A/G]AAGTTTCTTTAATGA | 75725 |
rs578387439 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970795 | TTTGTCCAAGAATTT[C/T]ATAAATTCATTGTTT | 75725 |
rs578400711 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11944696 | AGGCAATGTTGATTA[C/T]GGAGGGCTGTTAAAG | 75725 |
rs578404786 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | GRCm38.p3 | 6:11905961 | TCTGTGACTTCTCCC[A/G]TGACTGGGGCCCCCA | 75725 |
rs578482813 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973145 | TCTATTTCTTTAGGT[A/G]ATATAGGACTGTTTA | 75725 |
rs578487002 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11939109 | AAACAAAAGACAAGT[A/G]ATTTAGAAGTGATGG | 75725 |
rs578505568 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971225 | TGATGATTAAGGATG[G/T]TGAACATTTTTTCAG | 75725 |
rs578515163 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11912546 | TTTGGCTAGTGTCAA[A/G]CTCAGACAGGTAACT | 75725 |
rs578516744 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11962167 | CACTCTTTATTTTGA[A/G]CATGTGTCAGTCCAT | 75725 |
rs578581235 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12066092 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 75725 |
rs578598062 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12091757 | TTCGAGGGTCTCGAG[A/G]GGACCTCCTCCTAAT | 75725 |
rs578612155 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12041562 | CAAGCACATGCGCGC[A/G]TGCACACACACACGC | 75725 |
rs578618175 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | GRCm38.p3 | 6:12010505 | TCCATAGAAGCATTG[A/G]CTCTTTTTTATTTAA | 75725 |
rs578637876 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11983088 | TGAAATAACAAAAAA[C/T]CTAGGATAGCAAAAA | 75725 |
rs578698716 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032953 | TCAGCTCCTTCAGTC[A/C]TTTCTCTAACTCCTT | 75725 |
rs578710982 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11998041 | GTTTCAAATACCTTG[A/G]CTTTTATGTTTTTTT | 75725 |
rs578720774 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972281 | CTGTTTATCCTTTGT[A/G]TAGAGAAAGGCCATT | 75725 |
rs578721142 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11979934 | TCCAAAATGGTTATA[A/G]TGCTATATAGAACCT | 75725 |
rs578722921 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062331 | GTCACAGAAGCGCAC[C/T]TGTCTGTACATGGAT | 75725 |
rs578723730 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984544 | ATACCTGGGGATCCA[C/T]CCCATAATCAGCTTC | 75725 |
rs578726613 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957652 | CTTTTTTCCATGAAT[A/G]GTTTTAGCTCCTTTG | 75725 |
rs578732756 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11928414 | AAGGTAGTACTGGTG[C/T]ATAGGTGAGGTTTAA | 75725 |
rs578733049 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970704 | GGCTAATATTCACTT[C/G]TCAATGAGTGCATAT | 75725 |
rs578733978 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021591 | CAGGAGTCTTTAGTC[A/G]GCACTGTTCTCAAAA | 75725 |
rs578745804 | snp | A/C | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | GRCm38.p3 | 6:11905722 | ATGTATAGTGTGAGG[A/C]TGCCTCCAGCCATAA | 75725 |
rs578756495 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11974114 | GTTTACTTTGAGCTT[C/T]ATTGAAGTTTCTTTA | 75725 |
rs578769382 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11943972 | TTGGACTTACAGGAA[C/T]TTAACACACATCAAT | 75725 |
rs578775664 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:12005394 | ACTTATACTCCCCAT[A/C]TGCAGATAATTCCCA | 75725 |
rs578815014 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12085237 | TTACAGTAAAACTCC[C/T]TAAATTTCCCTTCAG | 75725 |
rs578838286 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11938913 | TGGTAGTGCACGCCT[G/T]TAATCCCAGCACTTG | 75725 |
rs578923454 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12066080 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 75725 |
rs578932835 | snp | A/C | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | GRCm38.p3 | 6:12099974 | TTCTTAATTTTAATA[A/C]GCTTTTGAGGGTTTC | 75725 |
rs578937599 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975755 | TTGCAGGGAAGGTGC[A/C]CAGATATCTGGCGTT | 75725 |
rs578954208 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11952476 | ATGTATTTTTTAAAT[G/T]AATTTTTTTTATACT | 75725 |
rs578956411 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | GRCm38.p3 | 6:12039513 | TCTCTCTCTTTCTCT[C/T]TCTCTCTCTCTCTCT | 75725 |
rs578960033 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973123 | TTGGAGACTATTAAT[A/G]ACTGCTTCTATTTCT | 75725 |
rs578964169 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11982364 | AGATCCAACACCCAC[A/T]CATGATAAAAGTCTT | 75725 |
rs578974254 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11960419 | GTTGCTGCTGGTGGA[A/G]ATGCTATCTTTATAC | 75725 |
rs578983633 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12059511 | AAGTCTATATGACAG[G/T]GCCCAGTCTATATGG | 75725 |
rs578992735 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11992794 | TCCTGACAAAAAACG[A/G]CATAAGGTTGAAGAG | 75725 |
rs578994328 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971513 | TCTTACAGCATAAGC[C/T]ATTGCTGTTCTGTTT | 75725 |
rs579003851 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12050222 | AAAGGAAAGGAAAGG[A/G]AAGGAAAGGAAAGGA | 75725 |
rs579004618 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11916190 | CTCTCACACAAACTT[A/C]TATCTGGATATTTTT | 75725 |
rs579059522 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972090 | CTATATTAATCCTGC[A/C]AACCCATGAGCATGA | 75725 |
rs579065655 | snp | G/T | | | intron-variant, upstream-variant-2KB | Phf14 | GRCm38.p3 | 6:11924922 | GGCTCCTGTCTGCCT[G/T]GTTTCTGAGGCTTAC | 75725 |
rs579086927 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970835 | GAGTAGTATTCCATT[A/G]TGTAAATGTACCACA | 75725 |
rs579088404 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11979606 | GACTCTTTGTCTTTA[A/G]TGTAAGTTAACGAAA | 75725 |
rs579108759 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957215 | GAGAATTCATTGTTT[A/G]GCTCTGTGCCCATTT | 75725 |
rs579122718 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973687 | CATTAAATTCTAAAA[A/C]GTCTTTAATTTCTTT | 75725 |
rs579179228 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11997763 | TGTCTGTTTCTCCCA[A/G]GTGCAAGATTACAGG | 75725 |
rs579183273 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062302 | ATGCACTGACGCGTT[A/G]CTGTGAGAAGGAGGT | 75725 |
rs579183752 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12097233 | GAGTTTGCATCTTGA[C/T]CTGAAAGCACCCAGG | 75725 |
rs579207033 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12076031 | TGTATATAGAGCCAG[A/T]TTAAGAAACCGTTTC | 75725 |
rs579214612 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984839 | GGCCTAGTCGGCCAT[C/T]ACTGGAAAGAGAGGC | 75725 |
rs579218923 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021970 | TCTACCTAGCTTGTG[C/T]GTGTGTGCATGTTCT | 75725 |
rs579225883 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032670 | CCTATTCCATCCACC[C/T]TCCCCCTCCTTCTAA | 75725 |
rs579226332 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11974143 | TAATGAATGTGGCTG[A/C]CCTTGTTTTTGGAGC | 75725 |
rs579265911 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11983497 | TTGAAGATATGGTCA[C/G]AGAGGAAAATTTCCT | 75725 |
rs579298713 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11914980 | GAGTACAATCACATA[A/G]TGAGTATTTGTTTCT | 75725 |
rs579301748 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:12057844 | CAGTGATTAATAGGG[A/C]GTCTGTGATAAGTTA | 75725 |
rs579302555 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12014253 | CCTGAGAAGTCTCAT[A/G]CTGTTAACCCAGTCT | 75725 |
rs579310136 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12029507 | CCCTCACCCCACCCT[G/T]CTTCCCAACCTACCC | 75725 |
rs579310319 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12079634 | TGACACTTAGTCTCA[C/T]TAGTAGAAGGCAGTG | 75725 |
rs579320017 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11962376 | TATGTGTGTGTGTGT[A/G]GATATGTGGATATAT | 75725 |
rs579322015 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11988139 | ACTTTTAAAAATTAT[A/G]TGCTAATTTTTTAAA | 75725 |
rs579324878 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973163 | ATAGGACTGTTTAGA[C/T]CATTAACCTGATCCT | 75725 |
rs579331579 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971420 | GGAATATGTTGGTGG[C/T]CTTTTTGTCTTATTG | 75725 |
rs579331758 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975714 | GTTTCAGTGGTCAGA[A/G]TACCCTCTGCAGGCA | 75725 |
rs579337474 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11949338 | TTCTTTTAAGTTTCT[A/G]CATATATTAAGAGAA | 75725 |
rs579385147 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12043959 | CTGCACTTAATAAAC[C/T]AGTGTTTTGGGGTTT | 75725 |
rs579393226 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12091963 | AGGAGGGATGGGGCA[G/T]CTGAAAGAGAGGAAG | 75725 |
rs579429062 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12066100 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 75725 |
rs579432707 | snp | A/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | GRCm38.p3 | 6:12099930 | GTTTCTGCTTCAGGT[A/G]ACCACATTCAGGGCA | 75725 |
rs579476671 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12024544 | ATCTGCATCTTACTC[C/T]TTCAGCTGCTTGTTG | 75725 |
rs579492695 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11981516 | CTAGAAAAAAGGAAG[A/C]AAATTCACCCAAAAG | 75725 |
rs579511934 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984923 | AAAAAAAAAATGGGA[A/G]TGGGTGGGTAGGGAA | 75725 |
rs579514995 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957814 | AGTTAGAGTCACACC[A/G]AGATATTTTATATTA | 75725 |
rs579520648 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975337 | TATTGTTTCTACTTC[C/T]CTTTTTAGTTCTTGG | 75725 |
rs579537814 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970885 | TGTTGAGGGACATCT[A/C]GGTTCTTTCCAGTTT | 75725 |
rs579537899 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12000549 | AATCAGCTCTTCTGC[A/T]TACAGTGCTTTTTGT | 75725 |
rs579547507 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11946323 | ATCCACCTGCCTCTG[C/T]CTCCCAAGTGCTGGG | 75725 |
rs579549497 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | GRCm38.p3 | 6:11908761 | TTATGGGTGAATGAG[C/T]GAAAAAGAATAAAAA | 75725 |
rs579558209 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972369 | AGGAGTTCTCTGTTG[C/G]AATTTTTGGGGTCAC | 75725 |
rs579585548 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12077740 | GACAGCCCTTCAGAG[C/G]GTTATGCGATCAAGC | 75725 |
rs579624301 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12097977 | CTCCCCCTCCCCCTC[C/T]CCCTCCCCCTCCCCC | 75725 |
rs579692707 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12018489 | CCCCAACCCTAGCAC[A/G]TCAAGTCTCTGCAGA | 75725 |
rs579710622 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12059547 | CTATATGACAGACAG[G/T]GCCCAGTCTATATGA | 75725 |
rs579710843 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973581 | GTGTGCTCTCTCTAG[C/T]TTCTTTTTGGAGCTA | 75725 |
rs579721417 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12092103 | CTGACTTTCTCAGAG[C/T]GGTGCATCCGGTGGC | 75725 |
rs579722930 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11940215 | GGTTGCAGACCCCTT[C/T]AGATCCTTGGGTGCT | 75725 |
rs579728289 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083081 | AAAATCACTGAGACA[A/T]TTTTTTCCTACGTGG | 75725 |
rs579731206 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12046087 | CCTAATGTAAAAAAT[A/G]CAGAGAAAAAATGTA | 75725 |
rs579735924 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11917001 | TTGGTTGGGTCATTC[A/C]ACTCTGGCAGGCAAC | 75725 |
rs579737717 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984398 | ACAATTTGCTAAACA[C/T]ATGAAACTCAAGAAG | 75725 |
rs579747914 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970417 | GGCATAGCCTCATAC[A/G]AGACAGCTATAACAG | 75725 |
rs579749643 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12069099 | TTAAATATTTCACAA[A/G]TTCCTATATGAATAC | 75725 |
rs579752178 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12030986 | ACATTATGATTTGTG[C/G]ATTTCCTTACTGTCT | 75725 |
rs579819990 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970877 | CATTCTTCTGTTGAG[A/G]GACATCTAGGTTCTT | 75725 |
rs579833058 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | Ndufa4, Phf14 | GRCm38.p3 | 6:11907648 | TGCATCTTTTTGATA[C/G]GTTTATTTTTTTATT | 75725 |
rs579843496 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11993114 | ATTTATTCATTCATT[C/T]ATTCATTCATTCATT | 75725 |
rs579856256 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11974850 | CCTGCCTTTATATGT[C/T]ACTTGACCTTTTTCC | 75725 |
rs579857948 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975815 | CCTGAAACAGGGCCT[A/G]TCCCAGAAGATGTGC | 75725 |
rs579863822 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11955933 | GGAGACAGCCTAGTT[A/G]GTAACTTTTTTTTTT | 75725 |
rs579864270 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971563 | CCATATCTTCGAGGC[A/G]TTTCCCCACTTCCTC | 75725 |
rs579881207 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957963 | AGCTGTTTATCAGGT[A/T]TAGGAGTTCTCTGGT | 75725 |
rs579980239 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12023893 | AGCCCTGGATGTCCT[A/G]GAACTCACTCTATAG | 75725 |
rs579992548 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12063199 | GGAATTTTGTGTGGT[A/G]CTACATCATTACTGC | 75725 |
rs579998564 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12033940 | AAAAAGAAAAGAACC[A/G/T]GAACAAATGGTACTG | 75725 |
rs579998684 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12097796 | AGGGCAGCAGGGGCA[A/T]ATCTCCACCAAATTG | 75725 |
rs580015963 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12005815 | CTTCCCCAACTCCTC[C/T]GTTGTGGTCAGAAAA | 75725 |
rs580020894 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032323 | TCTGTGTGTGTATGT[A/G]TGTGAAGAAGTAGTT | 75725 |
rs580024141 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12076118 | TGCTTTGTATTTTTT[C/G]CTTGTAAAATCTTTC | 75725 |
rs580025810 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972805 | TCCCTGCATCCCTGG[A/G]ATGAAAGCTACTTGG | 75725 |
rs580027099 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975882 | GTCTCCAAGGGACAC[A/G]GGACACAAGATGGCT | 75725 |
rs580028191 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11981644 | TTTGAGAAAATCAAC[A/T]AGATAGATAAACCCT | 75725 |
rs580052446 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11956935 | TTGCTGGATCTTCTG[A/G]TAGTACTATGTCCAA | 75725 |
rs580070596 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12092079 | ATCTTGAGGTCAGGA[C/T]ATCCGGAGCTGACTT | 75725 |
rs580074212 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11994090 | TATGCTGCATGATTG[G/T]TGGTCCAATGACTGA | 75725 |
rs580083421 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971807 | CATTTCTGGGTCTTC[A/C]ATTCTATTCCATTGA | 75725 |
rs580107350 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12044580 | CTGTCCTTTGTATTT[A/G]TATCAATATTAATGT | 75725 |
rs580124302 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12066112 | TCTCTCTCTCTCTCT[C/T]TCTCTCTTTCTTTTT | 75725 |
rs580126290 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984071 | TGGGCATATATCCAA[A/C]AGATGTCCCAACCGG | 75725 |
rs580132413 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12015724 | AATTCTAAATAATTT[A/G]TAGAAAAGTATGTTA | 75725 |
rs580134523 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973327 | TCCTTTTTTGTTTTT[G/T]ATTTTGTTAATTAGG | 75725 |
rs580150665 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970048 | TTTATTAGATATTTT[C/T]TTTATATACATTTCA | 75725 |
rs580161964 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083754 | ATGACTATATGGGAT[A/G]GATCCCCAGGTGAGG | 75725 |
rs580195645 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12061133 | AACTTATGTTAATAC[C/T]GTTAAGTCTTAATAA | 75725 |
rs580213893 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12020446 | CTTGCAGGCAGCCCA[A/G]TCTTATGGAGGCATT | 75725 |
rs580259137 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062366 | GGTATATAAACACAT[A/G]ACATGTACCATTCTC | 75725 |
rs580273296 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12005130 | TGGAACTTTAATGGG[A/G]AATTTGAGTATTTTC | 75725 |
rs580292653 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972456 | GTATCCCCTTGATGT[A/C]CTTTTCTTGTCGAAT | 75725 |
rs580313097 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:12085514 | TGGGTGCTAGGAGCT[A/C]AACTTGGATCCTCTG | 75725 |
rs580326295 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12033617 | ACAACTTTTTCTAGG[A/T]CCTTTTTTTATCTGC | 75725 |
rs580326650 | snp | A/C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11981560 | GAAATAATCAAACTC[A/C/T]TGGGTGAAATCAACC | 75725 |
rs580368870 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083374 | CATTGACATCGAACC[C/G]CCTCAGGCCCAAGGG | 75725 |
rs580380567 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12077747 | CTTCAGAGGGTTATG[C/G]GATCAAGCTGCAATG | 75725 |
rs580383213 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957818 | AGAGTCACACCGAGA[C/T]ATTTTATATTATTTG | 75725 |
rs580383955 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971699 | TGATAACTGCCAGTT[C/G]TGCCAGCCCCATTTG | 75725 |
rs580390868 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12097989 | CTCCCCCTCCCCCTC[C/T]CCCTCTCCCTCTCTC | 75725 |
rs580395192 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:12028406 | AATACCTAAGTTTAA[A/C]AATATTAAAATATAA | 75725 |
rs580397527 | snp | A/C | | | synonymous-codon, intron-variant, nc-transcript-variant | Phf14 | GRCm38.p3 | 6:11933789 | GTAAAGAGAAAGGGG[A/C]GATCAGCGTCTCAGA | 75725 |
rs580401994 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11917877 | AAATAAAGGCATATA[A/G]GCTCTCAGAAAAAAG | 75725 |
rs580406520 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12056617 | AGAAATTCAGTTTAA[C/T]TTTAAAATCTTTAGT | 75725 |
rs580406557 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11985449 | ACTGTATCTTCAGCA[A/G]TAGAGAATTAACTCT | 75725 |
rs580442027 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11956819 | ACATCTGGGTTCTTT[A/C]CAGCTTCTGGCTATT | 75725 |
rs580468294 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12093184 | GGCATACATACATTA[A/G]CTCATGTCTCCTCCT | 75725 |
rs580500523 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11940053 | ACTTCTTGGCCCTGG[C/T]ATTCCCCTGTACTGG | 75725 |
rs580533681 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975848 | CCTCTGCAGTCTGCA[C/T]GCTCACCTGCACAGA | 75725 |
rs580591241 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11981841 | TCTAGACAGATACCA[A/G]GTACCAAAGTTAAAT | 75725 |
rs580638859 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083418 | TGATGTCCAAAAAGG[C/T]CATCCTCTGCCACAT | 75725 |
rs580642939 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12060253 | AATGTAGGAGGGGAT[C/T]TTGGGGAAAAACTGT | 75725 |
rs580652664 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12006226 | AGCAGCGTGCTATGT[A/G]AGCTAGAGAGTTTAA | 75725 |
rs580659309 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032219 | TGGTAGTGTGTGTGT[C/G]TGTGTGTGTGTGTCT | 75725 |
rs580659697 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972890 | TTGAGTATTTTTGCA[C/T]CGATATTCATAAGAG | 75725 |
rs580668841 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11938439 | AGGTTTTCCCATTGA[A/G]CCATTGTGGCCCACT | 75725 |
rs580700184 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11948788 | GGAATGTTACTTACC[A/G]CTTTTAGTGTACCTT | 75725 |
rs580702298 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971248 | TTTTTCAGGTGCTTC[G/T]CAGCCATTCCGTATT | 75725 |
rs580707613 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12078927 | AAAGTAAAAAATATC[A/T]AAGTATGTGGCCATT | 75725 |
rs580799846 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062282 | TTAGCTCAGGGTTTC[C/T]AGCCATGCACTGACG | 75725 |
rs580802043 | snp | C/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021896 | AGCAGATGCACAGAC[C/G/T]GTGTGTGTGTGTGTG | 75725 |
rs580812910 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12088072 | ATCTTCTTCATAATG[A/G]CCACATTCTAGAGCC | 75725 |
rs580820255 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11974116 | TTACTTTGAGCTTCA[C/T]TGAAGTTTCTTTAAT | 75725 |
rs580823584 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11943985 | AACTTAACACACATC[A/G]ATCTATTGATCTTAG | 75725 |
rs580826090 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11986321 | CTTCCTTCCTTCCTT[C/T]CTTTTTCTTTTTTTT | 75725 |
rs580828187 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12035755 | TGTGTAGCTCTGGCT[C/G]TCCTGGAACTCACTC | 75725 |
rs580832619 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12029414 | TTAATTGGCAATTTC[A/T]TTTTTTTAAATTTAA | 75725 |
rs580837392 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975510 | TGTGTTGGGGTGCCC[A/T]GGACTGGCTGAGGTG | 75725 |
rs580841614 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12064316 | TTTAAATTTATATTA[C/T]TTTGCATATACGTGT | 75725 |
rs580842471 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11974539 | TCTGTTCTTGCGGCT[A/G]TCTTCTTTTAGGCTT | 75725 |
rs580881944 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083777 | AGGTGAGGCAGTCTC[A/T]GGACGGTCATTCCTT | 75725 |
rs580881959 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984632 | GCTGTCTCTTGTGAG[A/G]CTATGCTGGGGCCTA | 75725 |
rs580888087 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970729 | GCATATCTCATGACT[A/T]ATTTGTGATTGAGTT | 75725 |
rs580906172 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | GRCm38.p3 | 6:11905786 | AAACCTCAAGTGCTA[G/T]CCAACCTTCAAAATG | 75725 |
rs580922098 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032544 | TATTTGTGTGTGAGT[A/G]TGTAGTTGTATTACT | 75725 |
rs580934658 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11995582 | CCAAGTTCTAGTCTC[A/C]CATTCCCTTTCTCCT | 75725 |
rs580946775 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975920 | CTGCTCTGGTGGTCA[G/T]AGCCCTCCCAGGCAC | 75725 |
rs580952771 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11956987 | TGATTTCCAGAGTGG[C/T]TGTACAAGCTTGTAA | 75725 |
rs580956932 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971872 | TGTTTATCACAATTG[C/T]TCTGTAGTACAGCTT | 75725 |
rs580959251 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11923286 | ATTAGTGTGCCAATC[A/G]GATTTTTTCAACATG | 75725 |
rs581045423 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12057193 | TTTTAAATTTAGAAA[G/T]GAACAATCCACCAAT | 75725 |
rs581069756 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11986257 | CTTCCTTCCTTCCTT[C/T]CTTCTTTCCTTCCTT | 75725 |
rs581071611 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971109 | GGAGTGTTCCTCTTT[C/T]TCCACATCCTCGCCA | 75725 |
rs581085407 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11911573 | CCCTAGAACTCAAGT[C/T]CAGCCCCATTCTCCA | 75725 |
rs581101134 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12075100 | ATATCAAATATAATA[A/G]TAATAATAGTAATAA | 75725 |
rs581102921 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12078424 | CAGAGAACAAAAGAC[A/G]ACAACAGATGGAGCC | 75725 |
rs581112625 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12096132 | CAGTTTTTAGGGACT[A/G]TAGTTAAGGTTGTTA | 75725 |
rs581126172 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12028997 | CCTTTGGATTACACG[G/T]GAAAGTACATTTGAT | 75725 |
rs581136218 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975507 | GGGTGTGTTGGGGTG[C/T]CCTGGACTGGCTGAG | 75725 |
rs581158076 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11948257 | AAGGAGCTGAGAGTT[G/T]TAATCTTGATCAGAA | 75725 |
rs581181938 | snp | G/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | GRCm38.p3 | 6:11905714 | ACGGCCAGATGTATA[G/T]TGTGAGGATGCCTCC | 75725 |
rs581184577 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12091723 | TCCAGATATTTGACC[C/T]GTCCAGCAGGTCCAG | 75725 |
rs581192758 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12066082 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 75725 |
rs581213293 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11982396 | GAAAGATCAGGAATT[C/G]AAGGCTCATACCTAA | 75725 |
rs581217079 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | GRCm38.p3 | 6:12039515 | TCTCTCTTTCTCTCT[C/T]TCTCTCTCTCTCTCT | 75725 |
rs581217271 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | GRCm38.p3 | 6:12010154 | CATTGGAAAGAGAGG[C/T]CCATTGGTCTTGTAA | 75725 |
rs581221143 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973140 | CTGCTTCTATTTCTT[C/T]AGGTGATATAGGACT | 75725 |
rs581346377 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973919 | GGTACCATGTGGCGC[G/T]GAGAGGAAGGTATAT | 75725 |
rs581354664 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970540 | ATAGTCCATCCTTTC[C/G]TCTTAGCTCCAAACT | 75725 |
rs581355945 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062325 | AAGGAGGTCACAGAA[A/G]CGCACCTGTCTGTAC | 75725 |
rs581376286 | snp | A/C | | | intron-variant, utr-variant-3-prime | Phf14 | GRCm38.p3 | 6:12010104 | GGAGCTCATGTCTAG[A/C]TGCATATGTAGCAGA | 75725 |
rs581378116 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12065890 | ATTCCAAAGCATGTG[G/T]TTTTTTTTTTCTGTC | 75725 |
rs581416833 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11947540 | TGTATGTGTGCACAT[A/G]TATATGTTTGCTTGT | 75725 |
rs581460106 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12071957 | GATTTTTGCAAAGTA[C/T]TTAAATTTTTTGACA | 75725 |
rs581468307 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12035785 | CTGTAGACCAGGCTG[A/G]CCTCGAACTCAGAAA | 75725 |
rs581471531 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12094649 | GTCACTAATATTGCG[A/G]AAATGGATACATTAA | 75725 |
rs581474854 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11982155 | TATCGATGCAAAAAT[A/C]CTCAATAAAATTCTC | 75725 |
rs581485897 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12050003 | TCATGTAAAATACCA[C/T]TTCCTGTCCTGATGT | 75725 |
rs581491545 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12020272 | AAGAATTCAATCGGG[C/G]CAGGAATCTGGAAGC | 75725 |
rs581492253 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970951 | GGAGCATGTGTTCTT[A/C]TTACCAGTTGGAACA | 75725 |
rs581506627 | snp | C/T | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | GRCm38.p3 | 6:11909164 | CTCTCTCTCTCTCTC[C/T]CTCTCTCTCTCTCAG | 75725 |
rs581586728 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12088828 | TTTCACAGGACCAAG[A/G]GCCTCTCCTCCCATT | 75725 |
rs581597105 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972904 | ACCGATATTCATAAG[A/G]GAAATTGGTCTGAAG | 75725 |
rs581601519 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11938886 | TTAATTATCAGACTC[G/T]GGGCCGGGCAGTGGT | 75725 |
rs581609864 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975502 | TTTTCGGGTGTGTTG[G/T]GGTGCCCTGGACTGG | 75725 |
rs581618265 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972037 | GATGGGGATTGCATT[A/G]AATCTGTAGATTGCT | 75725 |
rs581624648 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12049907 | TTTTATACTTTATTC[A/G]TTTGACCTCTGGGAT | 75725 |
rs581633301 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984515 | ATGAGAGGATGGATC[A/T]TCTATAGACTGCCAT | 75725 |
rs581639099 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11923461 | CTCTCTGAATGTGTG[C/T]ATTCTTTCTCTGGTT | 75725 |
rs581708453 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11940643 | TGTGGCTGGAGCTAT[A/G]TGTGTGCCACTGTGC | 75725 |
rs581725439 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12019322 | CATACATACATACAT[A/T]CATACGTACATACAT | 75725 |
rs581736006 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957120 | TGGAATCTCAGGGTT[C/G]TTTTGATTTGCATTT | 75725 |
rs581765903 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083786 | AGTCTCTGGACGGTC[A/T]TTCCTTCAGTCTCAG | 75725 |
rs581767288 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032660 | CCAAAAAACCCCTAT[C/T]CCATCCACCCTCCCC | 75725 |
rs581770153 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062296 | CCAGCCATGCACTGA[C/T]GCGTTGCTGTGAGAA | 75725 |
rs581786992 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083238 | CAAATGTTTTCCTCT[C/T]TCCAGGTCTCCCCTT | 75725 |
rs581825139 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12041612 | CACACACACACACAC[A/G]AAATTACCCCCGCTA | 75725 |
rs581825546 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11983114 | AAAAACTCTTCTCAA[G/T]GATAAAAGAACCTCT | 75725 |
rs581835680 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11962265 | GAAAGTCCCCTATAC[C/T]CTCCCCTTTAACTTT | 75725 |
rs581841912 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973745 | ATTGAGTAGAGTGTT[A/G]TTCAGTTTCCACATG | 75725 |
rs581848109 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970515 | GATCCCCGGGTGGGG[C/T]AGTCTCTGGATAGTC | 75725 |
rs581925059 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12085367 | TGTGTGTGTGTCTGT[C/G]TGTCTGTCTGTCTGT | 75725 |
rs581932408 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12013299 | CATAAATAAATAAAT[A/G]AATAAATAAATAAAT | 75725 |
rs581956294 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973147 | TATTTCTTTAGGTGA[A/T]ATAGGACTGTTTAGA | 75725 |
rs581966124 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11939938 | TTTGCTTTTGACTGG[C/T]TAGCTTTTTTTTTAT | 75725 |
rs582012863 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12031077 | TTATTTTGGTATAAG[A/G]GTTTGTCAGTCTTAC | 75725 |
rs582015088 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12066095 | CTCTCTCTCTCTCTC[C/T]CTCTCTCTCTCTCTC | 75725 |
rs582026948 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11993118 | ATTCATTCATTCATT[C/T]ATTCATTCATTTATT | 75725 |
rs582030645 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12091800 | GGGTAGAGAGAGACG[A/G]GGGCCTTGTGCGAAT | 75725 |
rs582042982 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975823 | AGGGCCTGTCCCAGA[A/G]GATGTGCTGCCTCTG | 75725 |
rs582045761 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12023982 | AAAGACGTGTGCTAC[C/G]ACTGCCCAGCTTGTT | 75725 |
rs582048333 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971624 | GTGGAGGTCTTTGAT[C/T]CACTTAGACTTGAGC | 75725 |
rs582139235 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12097937 | ACTGCCGCCACACCC[G/T]CTCCCTCTCCCTCTC | 75725 |
rs582142451 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972334 | TTCCTGCTACTGCAC[G/T]GAAGCTGTTTATCAG | 75725 |
rs582145441 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11979942 | GGTTATAGTGCTATA[C/T]AGAACCTTAAGGAAA | 75725 |
rs582145795 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957682 | GTCAAAGATCAAGTG[A/C]CCATAGGTGTGTGGG | 75725 |
rs582152377 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12059526 | GGCCCAGTCTATATG[A/G]CAAGTCTATATGACA | 75725 |
rs582155033 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11932697 | CACTGTTTTATGTGC[C/T]ATTGTATTGTCTAGC | 75725 |
rs582161576 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11993084 | AGATACTCAGATTTT[C/T]TTAAGGATTTATTTA | 75725 |
rs582163217 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12085355 | ATTGTGTGTGTGTGT[C/G]TGTGTGTCTGTCTGT | 75725 |
rs582167868 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971533 | CTGTTCTGTTTAGGA[A/T]TTTTTCCCCTGTGCC | 75725 |
rs582176248 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12053234 | TTTGACAGGAGCCTC[G/T]TGGTGTGTGTGTGTG | 75725 |
rs582191340 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11938927 | TTTAATCCCAGCACT[C/T]GGGAGGCAGAGGCAG | 75725 |
rs582260514 | snp | C/T | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | GRCm38.p3 | 6:12099976 | CTTAATTTTAATAAG[C/T]TTTTGAGGGTTTCCT | 75725 |
rs582269758 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032962 | TCAGTCCTTTCTCTA[A/G]CTCCTTCATTGGGGA | 75725 |
rs582277286 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062340 | GCGCACCTGTCTGTA[C/T]ATGGATGGATGGTAT | 75725 |
rs582284794 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12030683 | CTAATGTGATAGTTT[C/G]TGTTTTTATGTGTTT | 75725 |
rs582288774 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975768 | GCACAGATATCTGGC[A/G]TTCAGACCTGCCTCC | 75725 |
rs582396795 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032824 | CCTCTGCTACATATG[C/T]GGCTGGAGCCATGAG | 75725 |
rs582397048 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11953955 | TTATAAGTTCTCTCT[C/T]CCTACTGTTGGGCAG | 75725 |
rs582397199 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11916200 | AACTTATATCTGGAT[A/G]TTTTTCCTTCTACAT | 75725 |
rs582399855 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11979623 | GTAAGTTAACGAAAG[A/G]AAAAAGTCAGGTTGT | 75725 |
rs582403615 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970855 | AATGTACCACAGTTT[C/T]TGTATCCATTCTTCT | 75725 |
rs582406349 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11960425 | GCTGGTGGAGATGCT[A/G]TCTTTATACTGAACT | 75725 |
rs582407501 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12082071 | AAAACAGGAAATGCT[C/T]AGGCATGCAAACACT | 75725 |
rs582409627 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | GRCm38.p3 | 6:11906846 | ATCAGTGGGAGTTTT[A/G]GGTACACAGCATCCT | 75725 |
rs582422021 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12057380 | ACAGCCTCAGATGTC[C/T]ATTCCTGGGGATTCC | 75725 |
rs582476920 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:12092086 | GGTCAGGACATCCGG[A/C]GCTGACTTTCTCAGA | 75725 |
rs582501323 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11927972 | ACAAAAAATTCCTTG[G/T]ATTGTGTTACTCTTA | 75725 |
rs582507478 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975730 | TACCCTCTGCAGGCA[A/T]GCTCTCCTCTTGCAG | 75725 |
rs582511437 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11950846 | TACTGTATGCACTGT[C/T]TCCCCAGGGTTGTGA | 75725 |
rs582539339 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11997779 | GTGCAAGATTACAGG[C/T]GTATGCCACCGCCAC | 75725 |
rs582553205 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11945040 | ATGTGATTCTGTCTC[C/T]AGAAGTTTGTGTGTA | 75725 |
rs582561243 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972216 | CCAAGGTATTTTATA[C/T]TGTTTGTGACTATTG | 75725 |
rs582564243 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:12097532 | TCACTAAACTAACAA[A/C]GTCTCTCTCTCTCTC | 75725 |
rs582587205 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12022692 | TCTCTTTTATATGTG[A/G]ATTCGTGTGTGTGTG | 75725 |
rs582593099 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12076032 | GTATATAGAGCCAGT[G/T]TAAGAAACCGTTTCT | 75725 |
rs582597666 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984840 | GCCTAGTCGGCCATC[A/T]CTGGAAAGAGAGGCC | 75725 |
rs582602566 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12066104 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 75725 |
rs582623738 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12015166 | TCCTGCAATTAGTCA[A/G]CCAATTAATTTGAGG | 75725 |
rs582637425 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957289 | TCTTTATATATATTG[C/G]ATATTAGTTCCCTAT | 75725 |
rs582650552 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971438 | TTTTGTCTTATTGAC[G/T]GTGTCTTTTGCCTTA | 75725 |
rs582668975 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11916152 | TGTGCGCGCACACAC[A/G]CACACACACACACAC | 75725 |
rs582707320 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11962474 | TTGCTAATATATCAG[C/T]TTAATTTAGATTGAT | 75725 |
rs582712996 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12096623 | TTCTGGATAGTACCA[C/T]TCCCTGGGCCAAGCA | 75725 |
rs582713991 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11988263 | TATTTAAATTAGTAT[C/G]TAATTATTGTTCCAA | 75725 |
rs582716674 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12001438 | TTTCTTTATATAGTA[A/G]GGCTACTGAATTTTT | 75725 |
rs582719334 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11940054 | CTTCTTGGCCCTGGC[A/G]TTCCCCTGTACTGGG | 75725 |
rs582732957 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11932707 | TGTGCCATTGTATTG[C/T]CTAGCTTTGCTTTTG | 75725 |
rs582754591 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12044153 | AAGCACCAACCATAA[A/G]ATTATTTGTCACTTT | 75725 |
rs582756946 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12091965 | GAGGGATGGGGCAGC[G/T]GAAAGAGAGGAAGTA | 75725 |
rs582820127 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | GRCm38.p3 | 6:12008626 | ATTATTTTTTTCTAG[A/G]GTATTTTCAAACGAT | 75725 |
rs582823848 | snp | C/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | GRCm38.p3 | 6:12099961 | AATGTCTATATTGTT[C/G]TTAATTTTAATAAGC | 75725 |
rs582824431 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12064344 | TGTGTGTGTGTGTAT[C/G]TGTGTGTGTATTGCC | 75725 |
rs582835934 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12059391 | ATGACAGTGCCCAGT[C/G]TATATGGCAAGTCTA | 75725 |
rs582842516 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12054930 | CTTATCAAATACACA[C/G]ACACACACACACATA | 75725 |
rs582847434 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973170 | TGTTTAGACCATTAA[C/T]CTGATCCTGATTTAA | 75725 |
rs582849158 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12080160 | ATGATTTTTTGGAGA[A/T]AACTGGCATTAATTT | 75725 |
rs582853581 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11983718 | AGTGGACTCCAGAAA[A/G]TCAAATAACCCCATT | 75725 |
rs582861620 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11981529 | AGAAAATTCACCCAA[A/G]AGGAGTAGATGGCAG | 75725 |
rs582869624 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:12075770 | GTCCTCTCTGAGCAT[A/C]GCACGGTTATGAAAG | 75725 |
rs582876148 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021962 | GTGCGTGTTCTACCT[A/G]GCTTGTGTGTGTGTG | 75725 |
rs582887575 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957817 | TAGAGTCACACCGAG[A/G]TATTTTATATTATTT | 75725 |
rs582916233 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12048758 | ACAGGGACTAAGATG[G/T]CTTGGTAGGTAAAGT | 75725 |
rs582938482 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984454 | CCTTAGAATTGGGAA[C/T]AAAACACCCATGGAA | 75725 |
rs582944509 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970443 | AACAGGGTCCCTTCA[G/T]CAAAATCTTGCTGGC | 75725 |
rs582947547 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12033467 | TATCTTCTAATCGAA[A/G]GTTCCACTATCCCCC | 75725 |
rs582948804 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984797 | ACCCCGGAGCTCTTG[A/T]CTCTAGCTGCATATG | 75725 |
rs582955316 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11974121 | TTGAGCTTCATTGAA[A/G]TTTCTTTAATGAATG | 75725 |
rs582970216 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12077741 | ACAGCCCTTCAGAGG[A/G]TTATGCGATCAAGCT | 75725 |
rs582974066 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970816 | TTCATTGTTTTTAAT[A/T]GCTGAGTAGTATTCC | 75725 |
rs582976793 | snp | A/T | | | nc-transcript-variant, intron-variant | Gm6578, Phf14 | GRCm38.p3 | 6:12099557 | TTATTCATGATACAG[A/T]CTTCAAATTACCTCA | 75725 |
rs582978050 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11944800 | TGATGTAAAGAATTA[A/G]AGGACATTGCATACA | 75725 |
rs582990016 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11982131 | CTTCAGACCAATTTC[C/T]CTTATGAATATCGAT | 75725 |
rs583032623 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12088335 | ACAGCTTTTTTAATG[A/G]TCCCATATTCTAATT | 75725 |
rs583059278 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11946237 | TTTTTTTTTTTGAGA[C/G]AGGGTTTCTCTGTGT | 75725 |
rs583069708 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984968 | ATGGGGGACTTTTGG[A/G]ATAGCATTGGAAATG | 75725 |
rs583077654 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12025253 | GATCCACTTGGACTT[A/G]AGCTTTTTGCAAGGT | 75725 |
rs583094050 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12019298 | CATACATGCATACAT[A/G]CATACATACATACAT | 75725 |
rs583114673 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973659 | AAGTTTGGGTATGTT[A/G]TGGCTTCATTTTCAT | 75725 |
rs583126808 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11940317 | ATTTGCCAGGCACTG[C/G]CATAGCCTCACAAGA | 75725 |
rs583182044 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975077 | GAAAATCTTTATTCT[C/T]ATCTACTCTTATTAT | 75725 |
rs583196710 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11956762 | GTAGTACTCCGTTGT[A/G]TAAATGTACCATATT | 75725 |
rs583204801 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11917869 | AAGGAAGTAAATAAA[G/T]GCATATAGGCTCTCA | 75725 |
rs583290219 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062285 | GCTCAGGGTTTCCAG[C/T]CATGCACTGACGCGT | 75725 |
rs583292207 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11940147 | CTGCTACATATGCAG[C/G]TAGAGACATGAGCTC | 75725 |
rs583296122 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12092111 | CTCAGAGTGGTGCAT[C/T]CGGTGGCCTGCTTTT | 75725 |
rs583301831 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083781 | GAGGCAGTCTCTGGA[C/T]GGTCATTCCTTCAGT | 75725 |
rs583312746 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime | Ndufa4, Phf14 | GRCm38.p3 | 6:11907657 | TTGATAGGTTTATTT[A/T]TTTATTTTTTGCATA | 75725 |
rs583367365 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984881 | GCAAACTTTGTATGC[C/T]CCAGTACAGGGGAAC | 75725 |
rs583367582 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970879 | TTCTTCTGTTGAGGG[A/G]CATCTAGGTTCTTTC | 75725 |
rs583375512 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12061655 | CCTTCAAACATTGAA[C/G]TGAGTTTTTTTTTTT | 75725 |
rs583389318 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11994129 | AGGAGTCCAGGTTAA[C/T]TGAGACTACTGGTCC | 75725 |
rs583412396 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12034488 | TTTGAGATTGCATCT[C/T]TCTTCTGTAAGAAGA | 75725 |
rs583416412 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12086582 | TTCTCCACAGAGCTA[A/G]AGATGGGGAGATTTT | 75725 |
rs583424702 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12063214 | GCTACATCATTACTG[C/T]TTTTTCTCCAATATA | 75725 |
rs583426787 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11981675 | TAGCTAGACTCACTA[A/G]AGGGCACAGGGACAA | 75725 |
rs583430871 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12006069 | ATTTTGATATAAATG[C/T]TTTCTTGTTGTTGTT | 75725 |
rs583434916 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972815 | CCTGGAATGAAAGCT[A/G]CTTGGTCAGGATGTA | 75725 |
rs583455815 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11959468 | CATTAGACTCCTTAA[A/C]CGTCACCACTTGCCT | 75725 |
rs583485297 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12033634 | CTTTTTTTATCTGCA[A/G]TTTTCATAATTTCAT | 75725 |
rs583491479 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12085556 | AAGTTAAGTGCTGAG[C/T]CTTCTTCCCAGTGTC | 75725 |
rs583505684 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11981561 | AAATAATCAAACTCC[G/T]GGGTGAAATCAACCA | 75725 |
rs583512925 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11909794 | AGGACCTTTGCTGAA[A/C]ATTTTATTTGGAATG | 75725 |
rs583533819 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984077 | TATATCCAACAGATG[C/T]CCCAACCGGTAAGAA | 75725 |
rs583539053 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11956941 | GATCTTCTGGTAGTA[C/T]TATGTCCAATTTTCT | 75725 |
rs583543022 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971848 | TGTCACTGTACCAGT[A/T]CCGTGCAGTGTTTAT | 75725 |
rs583545205 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973335 | TGTTTTTTATTTTGT[A/T]AATTAGGACACTGTC | 75725 |
rs583550573 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11920707 | CAATGTGACATACAG[C/G]CATACAGAAAGACAT | 75725 |
rs583576727 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083769 | GGATCCCCAGGTGAG[A/G]CAGTCTCTGGACGGT | 75725 |
rs583590563 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975886 | CCAAGGGACACAGGA[C/T]ACAAGATGGCTCTCT | 75725 |
rs583666631 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12044659 | TTCACATTAAAAATT[A/G]GCTTTGTTTGATCTC | 75725 |
rs583671876 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062481 | GGCTAGGATTGCTGG[C/T]TATTTGAGTGCAATC | 75725 |
rs583678475 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12068454 | GTAATTTTATCCACT[A/G]TTGATTTTCCTTATA | 75725 |
rs583687074 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12005151 | GAGTATTTTCCCTTT[A/G]ATATTCTTTACCATT | 75725 |
rs583691359 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975503 | TTTCGGGTGTGTTGG[A/G]GTGCCCTGGACTGGC | 75725 |
rs583697970 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12070212 | CAATGTTTCACTTGT[C/T]ATTGTTATTTTTAGT | 75725 |
rs583703009 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11947544 | TGTGTGCACATGTAT[A/T]TGTTTGCTTGTTGAT | 75725 |
rs583733679 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975876 | AGACTGGTCTCCAAG[G/T]GACACAGGACACAAG | 75725 |
rs583741533 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:12028705 | ACACTGTTTTGTAGA[A/C]AGTGCAGACTGAATA | 75725 |
rs583749696 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12056761 | GAAGCTGTAGCCCAC[A/G]AGTGTTTGTAGAGGA | 75725 |
rs583753459 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11985456 | CTTCAGCAATAGAGA[A/C]TTAACTCTGCTTCCA | 75725 |
rs583755958 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11956864 | TATGAACATAGTGGA[A/G]CATGTGTCCTTCTTA | 75725 |
rs583806748 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957910 | GAGAAAGGCCATTGA[C/T]TTGTTTGAGTTAATT | 75725 |
rs583811371 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972484 | AATTGCTCTGGCTAG[A/G]ACTTCAAGTACTATA | 75725 |
rs583813675 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11935702 | CACATAGACTGACCT[A/G]TAGAAAAGTGCCCAC | 75725 |
rs583868464 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12078322 | TTTTATTTTTTTTAT[A/G]TGCATGGTTGTTTTG | 75725 |
rs583886106 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12098000 | CCTCCCCCTCTCCCT[C/T]TCTCTCCTGGTTTTC | 75725 |
rs583886726 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12093924 | CACACACACACACCA[C/T]AACTTTCTTAAGATC | 75725 |
rs583905072 | snp | C/T | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | GRCm38.p3 | 6:12099916 | GTCACAAAGGACATG[C/T]TTCTGCTTCAGGTAA | 75725 |
rs583915511 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12049909 | TTATACTTTATTCAT[C/T]TGACCTCTGGGATTT | 75725 |
rs583932710 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11994072 | GCCTCATATCAGCTG[A/G]TATATGCTGCATGAT | 75725 |
rs583972567 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972892 | GAGTATTTTTGCACC[A/G]ATATTCATAAGAGAA | 75725 |
rs583976310 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083464 | TGGGTCCCTCCATGT[A/G]TACTCTTTGGTTGGT | 75725 |
rs583991769 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12019326 | CATACATACATACAT[A/T]CGTACATACATGTAT | 75725 |
rs583993961 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973807 | TGAAGATCAGCCTTA[A/G]TCCATGGTGATCTGA | 75725 |
rs584000269 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984520 | AGGATGGATCTTCTA[G/T]AGACTGCCATACCTG | 75725 |
rs584015736 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970517 | TCCCCGGGTGGGGTA[A/G/T]TCTCTGGATAGTCCA | 75725 |
rs584018112 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11940963 | GACCTTGTATACTTT[A/G]GAGTCTAGAGTCTCT | 75725 |
rs584043209 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970730 | CATATCTCATGACTA[A/C]TTTGTGATTGAGTTA | 75725 |
rs584066263 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11923455 | TTCCTCCTCTCTGAA[A/T]GTGTGTATTCTTTCT | 75725 |
rs584117769 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975381 | ATTCCATCACCTGTT[C/T]GGTTGTGTTTTCCTG | 75725 |
rs584143105 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | GRCm38.p3 | 6:11908859 | TGGATGAGTGTGTAT[A/G]CAAAACCCACGGTAT | 75725 |
rs584150078 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12050252 | AAAGGAAAGGAAAGG[A/G]AAAAGGAAGGAAGAA | 75725 |
rs584153003 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12096134 | GTTTTTAGGGACTAT[A/T]GTTAAGGTTGTTATA | 75725 |
rs584169142 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984875 | GGACAGGCAAACTTT[A/G]TATGCTCCAGTACAG | 75725 |
rs584173711 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984773 | GTGCAACATTATGAA[C/G]TAACCAGTACCCCGG | 75725 |
rs584231726 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:12029444 | AGGCATTTTTATTAG[A/C]TATTTTCTCTATTCA | 75725 |
rs584237792 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12079036 | TGTCTGCTGAATAAG[A/G]AATGACAATATGCCC | 75725 |
rs584260811 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11948796 | ACTTACCACTTTTAG[C/T]GTACCTTTACAAAGG | 75725 |
rs584262969 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971275 | TATTCCTCAGTTGAG[A/G]ATTCTTTGTTTAGCT | 75725 |
rs584265164 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:12078497 | TGCTGGAGAATTGAC[A/C]CTAGTCGTCTGAAAG | 75725 |
rs584268862 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11914293 | GACTCAGGTCCCCTG[C/T]TCTACAGCAAGCACT | 75725 |
rs584271602 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12028999 | TTTGGATTACACGTG[A/G]AAGTACATTTGATAG | 75725 |
rs584279041 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975508 | GGTGTGTTGGGGTGC[C/G]CTGGACTGGCTGAGG | 75725 |
rs584281034 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11961330 | TTGGCTTCTTGAAAA[A/G]TAATGCTCACTGCAG | 75725 |
rs584354345 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11996041 | TGTGGTGGTCCTCGA[C/T]TCTTCCAGCTCCAGT | 75725 |
rs584355049 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12075127 | ATAATACTAATAATA[C/T]TAATACAACTGAAAT | 75725 |
rs584360036 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11944487 | CTGGCGATTTCAGAG[C/G]GGTTTGTTAAAAAAC | 75725 |
rs584361894 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971932 | TTCTTTTATTGTTGA[A/G]AATAGTTTTAATATC | 75725 |
rs584368386 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11976230 | TCCCAGAAGCTGTGT[C/T]GCTTCTGCAGTCCGC | 75725 |
rs584368694 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957000 | GGCTGTACAAGCTTG[C/T]AATCCCACCAGTAGT | 75725 |
rs584370782 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | GRCm38.p3 | 6:11905787 | AACCTCAAGTGCTAT[C/T]CAACCTTCAAAATGT | 75725 |
rs584377325 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021946 | GTGTGTGTGTGTGTG[C/T]GTGCGTGTTCTACCT | 75725 |
rs584470331 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12057194 | TTTAAATTTAGAAAG[G/T]AACAATCCACCAATG | 75725 |
rs584474153 | snp | C/T | | | nc-transcript-variant, intron-variant | Gm6578, Phf14 | GRCm38.p3 | 6:12099741 | GATGGCCTCTTTATG[C/T]TTCTTTCAACAGTCC | 75725 |
rs584488126 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032554 | TGAGTGTGTAGTTGT[A/T]TTACTAGAATTTAGA | 75725 |
rs584495734 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062327 | GGAGGTCACAGAAGC[C/G]CACCTGTCTGTACAT | 75725 |
rs584495836 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11998026 | AGGACAGGCTTTGAA[A/G]TTTCAAATACCTTGG | 75725 |
rs584496822 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11938963 | TTTCTGAGTTCGAGG[C/G]CAGCATGGTCTACAA | 75725 |
rs584498744 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11986262 | TTCCTTCCTTCCTTC[C/T]TTCCTTCCTTCCTTC | 75725 |
rs584511093 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971121 | TTTTTCCACATCCTC[A/G]CCAGCATCTGCTGTC | 75725 |
rs584525482 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11974071 | GTGGGGTGTTGATGT[C/T]CCCCACTATTATTGT | 75725 |
rs584531039 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11941908 | TGTGTGTGTGTGTGT[C/G]TGTGTCTGAGTGTTT | 75725 |
rs584568688 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11982626 | GAAGTCAAAATATCA[A/C]TTTTTGCAGATGATA | 75725 |
rs584570402 | snp | C/T | | | intron-variant, utr-variant-3-prime | Phf14 | GRCm38.p3 | 6:12039566 | CTCTTTCTCTCTCTA[C/T]CTGTTACAATATTCA | 75725 |
rs584574230 | snp | C/G | | | intron-variant, utr-variant-3-prime | Phf14 | GRCm38.p3 | 6:12010279 | GATAGCATTGGAAAT[C/G]TAAATGAAGACAATA | 75725 |
rs584576582 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973144 | TTCTATTTCTTTAGG[G/T]GATATAGGACTGTTT | 75725 |
rs584618917 | snp | A/G | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | GRCm38.p3 | 6:11905721 | GATGTATAGTGTGAG[A/G]ATGCCTCCAGCCATA | 75725 |
rs584626250 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11948316 | CTGGGCAGAGCCTTA[A/G]CGTAGGAGGCCTCAG | 75725 |
rs584627982 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11912455 | GTAATTAAAAAAAAA[A/G]CAATGACAAAATTTT | 75725 |
rs584692906 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12084812 | TGTCTGTGACATCCC[A/T]GAAGAGCTTTGTCCA | 75725 |
rs584698054 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12091754 | TTATTCGAGGGTCTC[G/T]AGGGGACCTCCTCCT | 75725 |
rs584702077 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12066086 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 75725 |
rs584706225 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12089856 | AAGCACAGATTAGCA[A/G]AAGAGACAGCTTCTA | 75725 |
rs584724460 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032851 | TGAGTCCCTCCATGT[A/G]TACTCTTTGGTTGGT | 75725 |
rs584725077 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11989392 | CTATAGTTTAAAATA[G/T]TCTGTGATAAAAGAC | 75725 |
rs584729523 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971503 | CAATTCTTGATCTTA[C/T]AGCATAAGCCATTGC | 75725 |
rs584735058 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12037085 | CTCTGTCTCAACAAA[A/G]CCAACAAAACAAAAC | 75725 |
rs584756780 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970697 | GTTTCTGGGCTAATA[C/T]TCACTTGTCAATGAG | 75725 |
rs584807406 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12072456 | GTACGTCCTGTCTGT[C/G]CGTCACCAGTAGCAG | 75725 |
rs584815141 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12094652 | ACTAATATTGCGGAA[A/T]TGGATACATTAAGTG | 75725 |
rs584819302 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021383 | GTGATGATGGTGATC[A/T]AAATCAGCTAATTTC | 75725 |
rs584822742 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032668 | CCCCTATTCCATCCA[C/T]CCTCCCCCTCCTTCT | 75725 |
rs584825135 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11979770 | TATTAGTATTTTTAA[A/T]CATTAGTAGTTGCAT | 75725 |
rs584826325 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11978824 | TATGGGGTTGCAAAC[C/T]CCTTCAGCTCCTTCA | 75725 |
rs584828850 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12050212 | AAAGGAAAGGAAAGG[A/G]AAGGAAAGGAAAGGA | 75725 |
rs584828998 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957347 | CCCAATTTGTTGGTT[A/G]CCTTTTTGTCCTATT | 75725 |
rs584830932 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984535 | TAGACTGCCATACCT[A/G]GGGATCCATCCCATA | 75725 |
rs584833028 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972238 | TGACTATTGTGAAGG[G/T]TGGTGTTTTCCTAAT | 75725 |
rs584842335 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11928413 | AAAGGTAGTACTGGT[A/G]CATAGGTGAGGTTTA | 75725 |
rs584848714 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957186 | GCTTCTCGGCCATTC[G/T]GTATTCATCAGTTGA | 75725 |
rs584927658 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973099 | ATTTGGTCCTGAGCT[G/T]TTTTTGGTTTGGAGA | 75725 |
rs584933789 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11982156 | ATCGATGCAAAAATC[C/T]TCAATAAAATTCTCG | 75725 |
rs584935599 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11960415 | GAAAGTTGCTGCTGG[C/T]GGAGATGCTATCTTT | 75725 |
rs584943545 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11938900 | CTGGGCCGGGCAGTG[C/G]TAGTGCACGCCTTTA | 75725 |
rs584944731 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12076030 | TTGTATATAGAGCCA[G/T]TTTAAGAAACCGTTT | 75725 |
rs584974591 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975734 | CTCTGCAGGCAAGCT[C/T]TCCTCTTGCAGGGAA | 75725 |
rs584983003 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12066077 | CTCTCTCTCTCTCTC[C/T]CTCTCTCTCTCTCTC | 75725 |
rs584984846 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | GRCm38.p3 | 6:12010133 | GAAGATGGCCTAGTC[A/G]GCCATCATTGGAAAG | 75725 |
rs585017425 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12066096 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTCT | 75725 |
rs585048023 | snp | C/T | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | GRCm38.p3 | 6:12099967 | TATATTGTTCTTAAT[C/T]TTAATAAGCTTTTGA | 75725 |
rs585053657 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973150 | TTCTTTAGGTGATAT[A/G]GGACTGTTTAGACCA | 75725 |
rs585063108 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11940005 | TGAAAGTCCCCTATA[C/T]CCCACCCCCCACTCC | 75725 |
rs585075924 | snp | A/G | | | intron-variant, downstream-variant-500B | Phf14 | GRCm38.p3 | 6:12081631 | ATTCTTTTTTACTAT[A/G]GTCACTTGTTATCTT | 75725 |
rs585085210 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12059447 | AAGTCTATATGACAG[G/T]GCCCAGTCTATATGG | 75725 |
rs585102191 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972055 | TCTGTAGATTGCTTT[C/T]GGCAGTATAGCCATT | 75725 |
rs585108362 | snp | G/T | | | intron-variant, upstream-variant-2KB | Phf14 | GRCm38.p3 | 6:11924833 | TTCCCACCCCCATTA[G/T]ACTTTTTTTTCACTA | 75725 |
rs585153952 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11932698 | ACTGTTTTATGTGCC[A/G]TTGTATTGTCTAGCT | 75725 |
rs585194816 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062299 | GCCATGCACTGACGC[A/G]TTGCTGTGAGAAGGA | 75725 |
rs585196400 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971707 | GCCAGTTGTGCCAGC[A/C]CCATTTGTTGAAAAT | 75725 |
rs585207574 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12097205 | AGGCAGACATGATAC[C/T]AGAGAAGGAACTGAG | 75725 |
rs585219517 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11959634 | AAGACAGGACGCTAA[A/G]CCTGCTTTAAGTATT | 75725 |
rs585220134 | snp | A/C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12097954 | TCCCTCTCCCTCTCC[A/C/T]TCTCCCCCTCCCCCT | 75725 |
rs585252093 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12053239 | CAGGAGCCTCGTGGT[G/T]TGTGTGTGTGTGTGT | 75725 |
rs585261148 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984883 | AAACTTTGTATGCTC[C/T]AGTACAGGGGAACAC | 75725 |
rs585313945 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12041882 | ATTGAGCTGGTCAAG[G/T]ACATTACTTTGAAAA | 75725 |
rs585320125 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11983195 | AAAAACTGCATGGTA[C/T]TGGTATAGTGACAGA | 75725 |
rs585326439 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11917870 | AGGAAGTAAATAAAG[A/G]CATATAGGCTCTCAG | 75725 |
rs585326623 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11962272 | CCCTATACCCTCCCC[C/T]TTAACTTTTTTTAAT | 75725 |
rs585357092 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975799 | TGGCTGAAGATGAAG[G/T]CCTGAAACAGGGCCT | 75725 |
rs585359409 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970301 | ATAGGGTTGCAGACC[C/T]CTTCAGCTCCTTGGG | 75725 |
rs585366119 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032208 | GGTGGTGGTGGTGGT[A/G]GTGTGTGTGTCTGTG | 75725 |
rs585373277 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12060244 | CCCTTAAGAAATGTA[G/T]GAGGGGATCTTGGGG | 75725 |
rs585376547 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11993122 | ATTCATTCATTCATT[C/T]ATTCATTTATTTATT | 75725 |
rs585383751 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971638 | TTCACTTAGACTTGA[A/G]CTTTGTGCAAGGAGA | 75725 |
rs585385813 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975830 | GTCCCAGAAGATGTG[C/T]TGCCTCTGCAGTCTG | 75725 |
rs585388551 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11956818 | GACATCTGGGTTCTT[A/T]CCAGCTTCTGGCTAT | 75725 |
rs585462926 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083043 | GCAGTTCAGCTGCAC[A/G]GGGGGTTGCCCTAAG | 75725 |
rs585485547 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12030877 | TTAAAGTTTTTACCT[A/G]CTCTTGATTTACTTT | 75725 |
rs585521936 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12076829 | GAACATATTCAGATT[C/T]TAAAATAATTTGCCA | 75725 |
rs585547659 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12024068 | CCCTGGCTGTCCTGG[A/G]ACTCATTTTGTAGAC | 75725 |
rs585557409 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975249 | GTATTCTGTTGCTGA[A/C]TCTTGCATCTATAGT | 75725 |
rs585588610 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957690 | TCAAGTGACCATAGG[A/T]GTGTGGGTTTATTTC | 75725 |
rs585590220 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12085359 | TGTGTGTGTGTGTGT[C/G]TGTCTGTCTGTCTGT | 75725 |
rs585591793 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11974774 | GGATCTGCATAACAT[C/G]TGTCCAGGATTTTCT | 75725 |
rs585598556 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062347 | TGTCTGTACATGGAT[A/G]GATGGTATATAAACA | 75725 |
rs585603467 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11945899 | TGTAGCAGTACTGAC[A/T]AGGTTTGTTGTACTG | 75725 |
rs585623092 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970883 | TCTGTTGAGGGACAT[C/T]TAGGTTCTTTCCAGT | 75725 |
rs585625138 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972352 | AGCTGTTTATCAGGT[A/G/T]TAGGAGTTCTCTGTT | 75725 |
rs585626574 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11946316 | CTCAGAAATCCACCT[A/G]CCTCTGCCTCCCAAG | 75725 |
rs585628618 | snp | A/G | | | upstream-variant-2KB, intron-variant | Ndufa4, Phf14 | GRCm38.p3 | 6:11908459 | TGAAGCACACAGTCT[A/G]CCATTTAAAAGGGAA | 75725 |
rs585630191 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11981459 | TCCAAAAAGAAACTG[C/G]AGAGAGCACACACTA | 75725 |
rs585680932 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12063168 | ATAGGTTTGCTGGCT[A/G]TTAGTTTCTGTGTAG | 75725 |
rs585709216 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11916154 | TGCGCGCACACACAC[A/G]CACACACACACACAC | 75725 |
rs585735852 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971561 | GCCCATATCTTCGAG[C/G]CGTTTCCCCACTTCC | 75725 |
rs585740265 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11955086 | TGTGAGCTGCCTGGT[A/G]TGGGTGTGGGTCTTT | 75725 |
rs585744064 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11916611 | CTTGCTCGCCCCGAT[A/T]ACTCAAGCTTTAAGA | 75725 |
rs585777868 | snp | A/G | | | nc-transcript-variant, downstream-variant-500B | Gm6578, Phf14 | GRCm38.p3 | 6:12100157 | GCCCACGGAGGACTG[A/G]CAAAGCAACTGCAGC | 75725 |
rs585794407 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12092007 | GAGGGATGGGGCAGC[A/G]GAAATTTTCTTTTGG | 75725 |
rs585804947 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11993086 | ATACTCAGATTTTCT[A/T]AAGGATTTATTTATT | 75725 |
rs585807254 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12059542 | CAAGTCTATATGACA[G/T]ACAGGGCCCAGTCTA | 75725 |
rs585812169 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973526 | GTGAATTTGCTTCCT[C/T]TAGTTCTAGAGCTTC | 75725 |
rs585813978 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12050217 | AAAGGAAAGGAAAGG[A/G]AAGGAAAGGAAAGGA | 75725 |
rs585885671 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12092087 | GTCAGGACATCCGGA[A/G]CTGACTTTCTCAGAG | 75725 |
rs585908086 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12018485 | TATTCCCCAACCCTA[C/G]CACATCAAGTCTCTG | 75725 |
rs585911747 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984857 | TGGAAAGAGAGGCCC[A/T]TTGGACAGGCAAACT | 75725 |
rs585914134 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12069056 | TACAAATGTGTTGTC[A/T]GTCTCTGATATATAA | 75725 |
rs585919762 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970861 | CCACAGTTTCTGTAT[C/T]CATTCTTCTGTTGAG | 75725 |
rs585920235 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984084 | AACAGATGTCCCAAC[C/T]GGTAAGAAGGACACA | 75725 |
rs585934169 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | GRCm38.p3 | 6:11906866 | CACAGCATCCTCTAT[C/T]GAGCTATACTGGACG | 75725 |
rs586011414 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12053028 | CCTTCAAGTCTAAAC[C/T]CAGACACTGTGTGAA | 75725 |
rs586021680 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12022869 | ATAAATTCTCATATT[C/T]TCATATTCTCTCTCT | 75725 |
rs586021821 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12076033 | TATATAGAGCCAGTT[G/T]AAGAAACCGTTTCTT | 75725 |
rs586025380 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12033918 | CACACACAGAAAAGA[A/G]CAAATGAAAAAGAAA | 75725 |
rs586029462 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12085602 | AATGCCACAAAATAA[C/T]TATGTGACTGTATCA | 75725 |
rs586034505 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12033607 | TTATTTCTGCACAAC[A/T]TTTTCTAGGTCCTTT | 75725 |
rs586040561 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11981539 | CCCAAAAGGAGTAGA[C/T]GGCAGGAAATAATCA | 75725 |
rs586123184 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957022 | ACCAGTAGTGGAGGA[C/G]TGTTCCTCTTTCACC | 75725 |
rs586143383 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12066108 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTTTCT | 75725 |
rs586146853 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12097751 | ACCGCAGGCCACGCC[C/G]CCTCGCCAGTCACGA | 75725 |
rs586164895 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083515 | TGGGGGGGGTCTGAC[C/T]TGTTGACACTGTTGC | 75725 |
rs586249406 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12069459 | TTTTTTATTCGATAT[G/T]TTCTTTATTTACATT | 75725 |
rs586251316 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12019318 | CATACATACATACAT[A/T]CATACATACGTACAT | 75725 |
rs586255897 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12044268 | TGGGGGGGGGGGGGG[A/G]CTGTAGGGGTCGCGA | 75725 |
rs586266892 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972442 | TTCCTTTCCAATTGG[A/T]ATCCCCTTGATGTCC | 75725 |
rs586274804 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12015427 | GTTTGCCAAGTAGGT[A/G]TGGCTGGCCAGTGAC | 75725 |
rs586274933 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | Phf14 | GRCm38.p3 | 6:11933788 | AGTAAAGAGAAAGGG[A/G]CGATCAGCGTCTCAG | 75725 |
rs586282546 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973320 | TTATGTCTCCTTTTT[C/T]GTTTTTTATTTTGTT | 75725 |
rs586284878 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984070 | CTGGGCATATATCCA[A/G]CAGATGTCCCAACCG | 75725 |
rs586295195 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970035 | TTTTTATGTGTTTTT[A/T]ATTAGATATTTTCTT | 75725 |
rs586299332 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11940068 | CATTCCCCTGTACTG[A/G]GGCATATAAAGTTTG | 75725 |
rs586332103 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11986286 | TTCCTTCCTTCCTTC[C/T]TTCCTTCCTTCCTTC | 75725 |
rs586357859 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972889 | ATTGAGTATTTTTGC[A/T]CCGATATTCATAAGA | 75725 |
rs586368969 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11937689 | GTATAGCATTTTTTT[A/T]ATTATGTTTTAAAAC | 75725 |
rs586378131 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062362 | GGATGGTATATAAAC[A/T]CATGACATGTACCAT | 75725 |
rs586379269 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984833 | AAAGATGGCCTAGTC[A/G]GCCATCACTGGAAAG | 75725 |
rs586385534 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12021966 | GTGTTCTACCTAGCT[C/T]GTGTGTGTGTGCATG | 75725 |
rs586389431 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11974123 | GAGCTTCATTGAAGT[G/T]TCTTTAATGAATGTG | 75725 |
rs586391252 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12002629 | AGAAAATGACTGAAT[A/G]ATGAAGTTCTAGAAA | 75725 |
rs586401847 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11945025 | GGACTTGAAATTTGG[A/G]TGTGATTCTGTCTCC | 75725 |
rs586406174 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970828 | AATTGCTGAGTAGTA[C/T]TCCATTATGTAAATG | 75725 |
rs586413242 | snp | C/T | | | intron-variant, upstream-variant-2KB | Ndufa4, Phf14 | GRCm38.p3 | 6:11905974 | CCGTGACTGGGGCCC[C/T]CAGCCAGATGATTAG | 75725 |
rs586418892 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12085513 | ATGGGTGCTAGGAGC[G/T]AAACTTGGATCCTCT | 75725 |
rs586470563 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12057202 | TAGAAAGGAACAATC[C/T]ACCAATGAACCAGTT | 75725 |
rs586475487 | snp | C/T | | | nc-transcript-variant, intron-variant | Gm6578, Phf14 | GRCm38.p3 | 6:12099787 | TTTCTTATGGTTTCT[C/T]TCCTGTGTACAGTAC | 75725 |
rs586484338 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12057657 | TTAAAAAATTAGAAG[A/G]ATATTAATATAGTCC | 75725 |
rs586489120 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984513 | TGATGAGAGGATGGA[C/T]CTTCTATAGACTGCC | 75725 |
rs586495469 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970472 | GCATATGCAATAGTG[C/T]CTGGGTTTGGTGGCT | 75725 |
rs586497176 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11923456 | TCCTCCTCTCTGAAT[G/T]TGTGTATTCTTTCTC | 75725 |
rs586526834 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11940421 | ATGGGATGGATCCCC[A/G]GGTGGGGTATTCTGG | 75725 |
rs586579858 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083772 | TCCCCAGGTGAGGCA[C/G]TCTCTGGACGGTCAT | 75725 |
rs586601756 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12092118 | TGGTGCATCCGGTGG[C/T]CTGCTTTTGACCCCC | 75725 |
rs586639629 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12048873 | ATCCTAGCACTGGAG[G/T]GGCAGACACTGGCAG | 75725 |
rs586691141 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975506 | CGGGTGTGTTGGGGT[A/G]CCCTGGACTGGCTGA | 75725 |
rs586723173 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12029282 | GAAACCTATAATCTT[G/T]CTAACAGTGTGGTTT | 75725 |
rs586735220 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032652 | TTTCCCCTCCAAAAA[A/C]CCCCTATTCCATCCA | 75725 |
rs586737079 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12083784 | GCAGTCTCTGGACGG[C/T]CATTCCTTCAGTCTC | 75725 |
rs586741211 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062290 | GGGTTTCCAGCCATG[C/T]ACTGACGCGTTGCTG | 75725 |
rs586756288 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971984 | ATGAATTTGCACATT[G/T]CCCTTTCTATCTCCA | 75725 |
rs586761311 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11978788 | GCTCTGGGGGGTCTG[A/G]TTGGTTGATATTGTT | 75725 |
rs586761985 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11959623 | TTACTTGAGCAAAGA[C/G]AGGACGCTAAACCTG | 75725 |
rs586807611 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12028995 | AGCCTTTGGATTACA[C/G]GTGAAAGTACATTTG | 75725 |
rs586840671 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12034509 | TGTAAGAAGAGCTCT[A/G]ATCAATAGAACAGCT | 75725 |
rs586845719 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975509 | GTGTGTTGGGGTGCC[C/T]TGGACTGGCTGAGGT | 75725 |
rs586845883 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12087095 | CTTGTTATATTCCCT[A/G]ATTTATCTTGTTTGT | 75725 |
rs586851627 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12064263 | GCCAATTTTTAAACC[A/G]TCAAAGAAACTCTTG | 75725 |
rs586853750 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11981738 | GAGACATAACAACAG[A/G]TCCTGAAGAAATCCA | 75725 |
rs586860425 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12006103 | GTTGTAGTTGTTGTT[A/G]TTGTTGTTTTGTTCT | 75725 |
rs586861385 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12078791 | TACCAGCACCTACAT[G/T]GGGATTGAGAACCAT | 75725 |
rs586869227 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11940191 | TAGTTCATATTGTTC[C/T]ACCTATAGGGTTGCA | 75725 |
rs586894881 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12060865 | ATCATTGAAAACTGT[A/G]CATTGTATCAACTCT | 75725 |
rs586924912 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11994076 | CATATCAGCTGATAT[A/G]TGCTGCATGATTGTT | 75725 |
rs586925289 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971799 | TGTAGATTCATTTCT[A/G]GGTCTTCAATTCTAT | 75725 |
rs586937043 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11918563 | TTTAAACCTCTGTAC[G/T]TAATAAAATACCACC | 75725 |
rs586939509 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12074683 | TGCCTTTTGTATGGA[A/G]TGAAATAAGAATCTC | 75725 |
rs586953451 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12095266 | TGTTTCTGCTGTCTC[A/G]TACTGCGGTTGTGGA | 75725 |
rs586964244 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12062166 | AACTGAGGATGACAA[A/G]ACAGGAAGTATGGCA | 75725 |
rs587019964 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12094583 | AGAAATGGCTGAGAT[A/G]GCTGTACAGCACTGT | 75725 |
rs587088297 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971017 | ATTTTCTGGTAGTAT[G/T]ATGTCCAATTTTCTG | 75725 |
rs587101734 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11995489 | CAAGTTCTAGTCTCC[C/T]GTTCCCTTTCTCCTC | 75725 |
rs587109999 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11909843 | AAGTAAGTAGATATA[C/T]AGAAATGCCATGATT | 75725 |
rs587111293 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975902 | ACAAGATGGCTCTCT[C/T]ACCTGCTCTGGTGGT | 75725 |
rs587115358 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12088361 | TAATTTTTTTTAATT[C/T]AAGTATGGCTGTGTG | 75725 |
rs587118343 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11956961 | TCCAATTTTCTGAGG[A/C]ACCACCAGACTGATT | 75725 |
rs587120342 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11971850 | TCACTGTACCAGTAC[C/T]GTGCAGTGTTTATCA | 75725 |
rs587129561 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12035780 | TCACTCTGTAGACCA[A/G]GCTGGCCTCGAACTC | 75725 |
rs587152349 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11982143 | TTCTCTTATGAATAT[C/T]GATGCAAAAATCCTC | 75725 |
rs587158621 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11959758 | ACGTAGTACAGATAA[C/T]TTTAAAATATATCTT | 75725 |
rs587189898 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12057138 | GTATCCATATGTAGG[C/T]AACCTGAATCCCATA | 75725 |
rs587221655 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972561 | TTAGTCAGATTGCTT[C/T]GAGTTTCTCTCCATT | 75725 |
rs587223614 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11981607 | AACTATTCAAAGAAT[G/T]AACCAAACGAGGAGT | 75725 |
rs587229766 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11957940 | TTTATATCCAGCTAC[G/T]TCACCGAAGCTGTTT | 75725 |
rs587235236 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11985470 | AATTAACTCTGCTTC[C/T]AGGAGACAACTGAGG | 75725 |
rs587282893 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984532 | CTATAGACTGCCATA[C/T]CTGGGGATCCATCCC | 75725 |
rs587284767 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12049912 | TACTTTATTCATTTG[A/G]CCTCTGGGATTTTAT | 75725 |
rs587286562 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12020204 | GAACAAAAGCAACTT[A/G]AACAGGAAAGATTTT | 75725 |
rs587287786 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11973904 | GTCAATTTTGGAGGA[G/T]GTACCATGTGGCGCT | 75725 |
rs587296510 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11941115 | CTGAAAGTGTGTATA[A/G]AGCTGATAATTACTT | 75725 |
rs587298263 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970530 | TAGTCTCTGGATAGT[A/C]CATCCTTTCCTCTTA | 75725 |
rs587315524 | snp | C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032293 | TGTGTGTGTGTGTGT[C/G]TGTGTCTGTGTGTGT | 75725 |
rs587321501 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11975880 | TGGTCTCCAAGGGAC[A/T]CAGGACACAAGATGG | 75725 |
rs587337518 | snp | A/C | | | intron-variant | Phf14 | GRCm38.p3 | 6:11956876 | GGAGCATGTGTCCTT[A/C]TTACATGTTGGAGCA | 75725 |
rs587463873 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12055348 | AGAGGGACATGGGGA[A/G]GGAGAGATGGAGGGA | 75725 |
rs587464153 | snp | A/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984996 | ATGTAATTGAGGAAA[A/G]TATGTAATAAAAAAT | 75725 |
rs587474747 | snp | G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11938685 | CAGAGGGAAAAGCCA[G/T]GGCTCATCACAGAAG | 75725 |
rs587479257 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11970942 | GAACATAGTGGAGCA[C/T]GTGTTCTTATTACCA | 75725 |
rs587487871 | snp | A/G | | | intron-variant, utr-variant-3-prime | Phf14 | GRCm38.p3 | 6:12010096 | GTACCCCCGGAGCTC[A/G]TGTCTAGCTGCATAT | 75725 |
rs587489727 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12065122 | ACACACACACACACA[C/T]ACACACAAAACTTCA | 75725 |
rs587491045 | snp | C/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12097983 | CTCCCCCTCCCCCTC[C/T]CCCTCCCCCTCTCCC | 75725 |
rs587503557 | snp | A/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11972895 | TATTTTTGCACCGAT[A/T]TTCATAAGAGAAATT | 75725 |
rs864265227 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12019310 | CATACATACATACAT[A/G/T]CATACATACATACAT | 75725 |
rs864269439 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:12054798 | TGTTGTTATTTGGGG[A/G/T]TTTTTGTTTGGTTGA | 75725 |
rs864278346 | snp | A/G/T | | | intron-variant | Phf14 | GRCm38.p3 | 6:11984918 | GCCAAAAAAAAAAAA[A/G/T]GGGAATGGGTGGGTA | 75725 |
rs864280691 | snp | G/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | Phf14 | GRCm38.p3 | 6:11926052 | CGCAGGGCGGCCGGT[G/T]CGGGCCTAGCGCCCC | 75725 |
rs864302787 | snp | A/C/G | | | intron-variant | Phf14 | GRCm38.p3 | 6:12032233 | TCTGTGTGTGTGTGT[A/C/G]TGTGTGTCTGTGTGT | 75725 |
rs864318130 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Phf14 | GRCm38.p3 | 6:12013404 | TGTTCTTTTTGGTTT[G/T]TTTTTTTTTTTTTTA | 75725 |