Tag | Content |
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EnhancerAtlas ID | HS092-13767 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:124488060-124489380 |
Target genes | Number: 18 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr12:124489234-124489246 | TCTATTTATAGC | - | 6.62 | MEF2B | MA0660.1 | chr12:124489234-124489246 | TCTATTTATAGC | - | 6.52 | ZNF263 | MA0528.1 | chr12:124488787-124488808 | GGTGGAGGGAGGGCATAAGGA | + | 6.22 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I124003 | chr12 | 124488521 | 124488690 |
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Enhancer Sequence | CAGCCTCTGG AGTAGCTGGG ATTACAGGTG CGTGCCACCA TGCCCAGCTA ATTTTTGTAT 60 TTTTAGTAGA GACGGGGTTT CACCATGTTG GTCAGGCTGG TCTCGAACAC CTGATGTCAT 120 GATCCACCTG CCTTGGCCTC CCAAAGTGAC GGGATTACAA GCGTGAGCCA ATGCGCCCAG 180 CCTGCTTCTA TTTTCTTAAT CAGAAACAGG CTCTTGGCAG GTTATCAGCC ACGAGTGAGG 240 GAGTCAGAGG GAAGATGGGA GATTTGAAGA GAAAGGAGAA TGATGAAGTA GCAATTTAAA 300 GTATTGGGAA AATGTGTGTA CTGAAGACTT TTGGAGGAAT TTAGGGGCAC TCCAGTGCCC 360 ATTTGAGATG TGTGGTCGTG AGTTAAATAA ACCTGGCATT ATTCAGCCAC TTGGGTGCGT 420 GTATGGATAG ATGGAGAGTT GGGTTTGAAT AAGGTGCGGT GTCACTGAGA GTAGGTGGGG 480 CCAGAGAGTT CTGGTGAGCG CAGAGAGAAG CTGTGGACAA CAGACAGGGA ACAAAGGGTC 540 AGGCCACTGG GTGCAAGCCT ACTGCATGAA GTTCCTGGAG CCAGTTAACT GGAAGGGGAG 600 GGAGCACCCG GTGTCCAAGA ATGGGTTGCT TAACACAGAT TTGGGAGGGA GCACAGTTTC 660 TGGGGGTGAT AGAGCTAGAG TGTGGCCATG GAAACAGTGA TGATGACAGA AGAGAGAGGT 720 GAACCTGGGT GGAGGGAGGG CATAAGGAAC CCAAGCCAGC ATGGAAGCCA GGAAGTAAAG 780 ACAAACAGGG CCACATTAGT AGGACAAAGA TTGAAAGAGG ACTGGAGGTC CTGAGGGAGC 840 AAAGAAAAGG TTCCATAGGA TTAACAGAGC AGAAAGCTGG AACAGGATGT TTTGGTTAAA 900 GGCTAGAGTT TCACTCAAGA TGGACAGATT GCTTACAGAC TTCTGGACTT GCATAGGTTG 960 GTGTTGTCAG TGGAGGCGGA GGCAATGTTT ATTTAGCTTT GTAATTTAGA ACACTGTTGT 1020 ATTCTTTCTT ACGGCTTTAG ATTGTCATAC AGGGATTTTC TAAGCCAGGG GTCCCCAACC 1080 TGTGGGCCAC AGATGGGTAC CAGTCCATGG CCTGTTAGGA ACCAAGGCCA CACAGCATGA 1140 GGTGAGTGGT GGGAAGAAAG CCAGTGAAGC TTCATCTATT TATAGCTGCT CCCCATTGCT 1200 TGCATTACCT CCTGAGCTCC ACCTCCTTTC AGATCAGCGG CGGCATTAGA TTCTCGTAGG 1260 GGCGTGAACC CTGTTGTAAA CTGTACACGC AAGGGATCTA GGTTGCACGC TCCTTATGCG 1320
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