Tag | Content |
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EnhancerAtlas ID | HS091-08804 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:117095470-117096640 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN | MA0488.1 | chr11:117096181-117096194 | TGGATGATGTCAT | + | 6.74 | JUND(var.2) | MA0492.1 | chr11:117096180-117096195 | GTGGATGATGTCATG | + | 6.18 | NR2C2 | MA0504.1 | chr11:117095552-117095567 | TGCCCTTTGACCTGC | - | 6.51 | Nr2f6(var.2) | MA0728.1 | chr11:117095996-117096011 | TGAACTCCTGACCTC | - | 6.22 | Nr2f6 | MA0677.1 | chr11:117095552-117095566 | TGCCCTTTGACCTG | - | 6.2 | Rxra | MA0512.2 | chr11:117095552-117095566 | TGCCCTTTGACCTG | - | 6.03 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_01609 | chr11:117093689-117095609 | Aorta |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I117223 | chr11 | 117094478 | 117096462 |
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Enhancer Sequence | GCTGTTGAGA AATAAATACC TAGAGGGGAC AGCCAGAGCC AGGCTGCGGC TACCCACCCA 60 GCGCCTCCCA GTCTCAGCTG GCTGCCCTTT GACCTGCAGC TCTTAACTCC TCCCAAGGGT 120 TCCACTTAAA GGCTTCCGTG ATTAAAAGGC ACAGGGTTCA AAGGTCCATC CCCTCTCCAA 180 AGTGGAAAAC AGAAGTGTGC TAAGGCTCTT CTTTTCCTTG TGAATGTCCC CATAGCCCAT 240 AGTGGCAGAG AGGGACAGAG GTCACTCATC TCCTGATCTA GGGATCAGAG ACATGTAGAC 300 CTTTTTTTTT TTTTTTTTTT CTCCTGAAAC GGCGTCTTCC TCTGTTGCCC AGGCTGAAGT 360 GCAATGGCGC GATTTTGGCT CACTGCCACC TCCACCTCCC AGGTTCAAGC GATTCTCCTG 420 CCTCAGCCTC TGGAGTAGCT GGGATTACAG GTGCCCACCA CCAAGCCTGG CTAATTTTTG 480 TATTTTTAGT AGAGATGGGG TTTCACCATG TTGGTCAGGC AGGTCTTGAA CTCCTGACCT 540 CAAGCAATCC ACATGCCTCA GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGCA 600 CCTGGCCCAA CTCGTAGGGT AGAAGGCAGA GCGCCCATGA ACTTCTGTGG AAGCTCTTGG 660 TTCTCAGGTT GAGGAGTTCT CTATTCTGTC TCTATCGGGA AGTGTACCCT GTGGATGATG 720 TCATGGATTT AAGGGAGGTA TGTCGGGGGA GGAACAGGTG CCATCAATGC CATGTGGGCC 780 CCCAACCCCA TTTCCTTCTT GTCCAGTCCA GCACAGCCAT GCCCTGAAGG TGCAGTGCAT 840 TGGCGTGGGG TGGGGGATTG GTGTTGGGCA TTCAGCTGGC CTGTGGATGG AGAAGAAAGC 900 CCGCTTTCTT GCAGAGGCCT TAGGAGTTTA GAAAACAAAT AAATGTGCAC AGGCCAGGGC 960 TTCTCATGTG GCAATCTGAT TACGGGGGTG ACGGGGGCTT AAGGTTGAGT GCCCAGTGGC 1020 TGGGAATCTA GAGAAATGAA GGCAATGGAC TTATTAGCTG AACCCAATGA GGAGACCCCT 1080 GCTCCGGCCT AAGTCAGCCC ACTGGTTGGG ATTTTGTTGG CGGATTTGTC CCAGGTGCTC 1140 CAGGCTCTTG CCCTCTCATC TGCAGCTCTG 1170
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