Tag | Content |
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EnhancerAtlas ID | HS182-21385 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr8:145243680-145245640 |
Target genes | Number: 12 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr8:145244635-145244646 | TCTTCCCGCCC | - | 6.14 | HNF4G | MA0484.1 | chr8:145244180-145244195 | TGGACTTTGCCCTGA | - | 6.17 | Hnf4a | MA0114.3 | chr8:145244178-145244194 | TCTGGACTTTGCCCTG | - | 6.38 | KLF14 | MA0740.1 | chr8:145244707-145244721 | GGGTGGGCGTGGCA | - | 6.47 | SP3 | MA0746.2 | chr8:145244708-145244721 | GGTGGGCGTGGCA | - | 7.12 | SP8 | MA0747.1 | chr8:145244708-145244720 | GGTGGGCGTGGC | - | 6.62 |
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Enhancer Sequence | TATAAGTGAG GAAACTGAGG CACAAAGAGG CTGAATAACT CGTCCCAGGC CATACACCTG 60 GGGAGTGGGA GAGCCAGGAC TAGGCCAGCC TGCACCTCTG AGCTGCCTTT TAAAGCAGAT 120 GTGGGAAGAA CTGCTAGGAA ATCAGAAGGG GAGACTACAG CTCAGAAAAA TGGGGCAAGA 180 AAAGGCCAGA ACCACACAGC CAGCCAACAT ACACACAGAA AGGTGATTAG CCCACTATCT 240 GCAAAGCGGT GTTATCTCAC ATTAAGCAGT TTGGAGAAAA TTAAAAGTAA TTGTTTGAAA 300 ATACCAAGTT TAGATTGTGC TTTGGAGCAG GGCCTGTAGC AGCGAGCTAT TGGGATTGGC 360 ACTTGGCAGC CACTCTGGAG AGAGTGGGCC CATCAGAAGA ACTCAAGATT GGGGCAGCTG 420 AGGTGGTCCC AGCAGCACCC CCTTGGTCTT GTGCCTTGTG CAGCCCCTCC CCGTGCGGTG 480 GGTGCATCCT TTCAGGGCTC TGGACTTTGC CCTGAAGCTC ATGGTCCCTT TGTGTTTCCT 540 CCTCCAGTTT CTGCGTCTCC GCCTGGTCCT CAGCAGGGCT GTGTGAAAGG TGCTGGCCTC 600 AGTTTATCTC CCTGTGCCCC CATGTTCCCC CTTCACCCGG GGCCCAGCCC CACTGACCAC 660 TTGCACATCA CCTGAGTTCG GCCCATGTCC TGGGCTCCAG GCCCTACAGC CAGTGTTTTC 720 TGACTCTCCA CCCAGATGTC CATACCACTC GAAGCCTGGG TGGCCACCTG CCCAGCCTCT 780 GCCCGCTCCC AGCTCTGCCC GCTCCCAGCT CTGCCCTCAG GGTCAGCCCA AGGCCACCGC 840 TGAGTCACAT CCACAGTCAC TGGCACACTG TCAGGAGCCG CCCACCCGTG GGAGGGCCTC 900 ATGCTGACCC TGGCATCCTG GTGCCCCTCC GCCCTGCCAT TGTTCTCCCT GTGGCTCTTC 960 CCGCCCACAC TGTGCCCAGC ACGGCAGCCT TGGGCAGAAT GTGTGGCACA AGTCTGTCTG 1020 TGAGGATGGG TGGGCGTGGC ACTGCTCCTC TTGTCTCTGT GGCAGACTGG AGTGGGCAGG 1080 AACTTGTGGG CAGAGGGCAT TTTGGGGAGG AGGTTGGTAC TTGCACCAGT TTTCTTTGGT 1140 GACAAGCACC AAGTGCAAAT TAGGTGGCTT CAAACAACAG AAATGTATTT TCTCACAGTT 1200 TTGGAGACTG GAAGTCCAAG CTCAAGATGT TGGCAGGATT GGTTCCTTCT TGGGAGCCCA 1260 GAGACAGAAT TCATTTCAGG CTCCCCAGCT TCTGGTGGGG CCATGGATTC TGGGTGTCCT 1320 TGGCCTGAGG CTGCCTCGCC CCAGTCTGTG CCTCCATGTC ACATGGCCAT CTTCCTCCTG 1380 CCTCTGCATC TCTTCTTATA AGGATGTTGT CATGTTGGAG TTACAGCCCA CCCTACTTTG 1440 CTATGACCCC ATTTTAACAG TCACATCTGG CCAGGCGCGG TGGCTGATGC CTGTAATCTC 1500 AGCACTTTGG GAGGCCAAGG TGGGCAGATC ACTTGAGGTC AGCAGTTTGA AACCAGCCTG 1560 GCCAACATGG TGAAACCCTG TCTCTTCTAA AAATTAGCCA AGTATGATGG TACACCCCTG 1620 TAGTTCCAGC TAGTCAGGAG GCTAAGGCAG GAGAATTGCT TGAACCTGGG AGGCAAAGGT 1680 TGTAATGAGC TGAGATCAAG CCACTGCATT CCAGCCTGGG TGACACAGCA AGACTGTGTC 1740 ACAACACACC AGCCTGAGTG ACAGACCGAG CAAGACTCTG TCTCAAAAAA AGTCACATCT 1800 GCAAAAACCC TATTTCCAAT AAGGCCATGA ATTTGGAGGG ACACTTTTCA TCCTGTGTAG 1860 TCCTGGAGTT GTGTGCTTGG CTGGTGTTCT AGGGAGGGCA TCTTGCAGGC CGTGGGATTT 1920 CTGGAAGGGG CAGGAGGCAG ACATAGGTGC TGAGGATCGT 1960
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