Tag | Content |
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EnhancerAtlas ID | HS091-11124 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:121771800-121773080 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr12:121772590-121772602 | ACTAAAAATAGC | + | 6.18 | MEF2B | MA0660.1 | chr12:121772590-121772602 | ACTAAAAATAGC | + | 6.62 | MEF2C | MA0497.1 | chr12:121772588-121772603 | ATACTAAAAATAGCT | + | 6.66 | ZEB1 | MA0103.3 | chr12:121772273-121772284 | GGGCAGGTGGG | - | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09417 | chr12:121771206-121772594 | CD14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH12I121333 | chr12 | 121771207 | 121772594 | GH12I121334 | chr12 | 121772661 | 121772830 |
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Enhancer Sequence | TGGCCCAGTG GCTCATGCTT GTAATCCCAG CACTTTGGAA GGCCAAGGTG GGAGGATTGC 60 TGGAAGCCAG GAGTTTGAAA CCAGCCTGGG TAACAAAGCA AGATCCTACC TCTACAAAAA 120 ATAATTTTTA AAAAAATTAG CTGGGCATTG TGGTGCATGC CTGTAGTCAC AGCTAGGAGG 180 CTGAGATGGA CTGCTTGCTT GAGCCCATGA GTTTGAGGTT ACAGTTAGCT ATGATCATAC 240 TACTGCACTC CAGCCTGGGT GACTGAGTGA GACCTTGTCT CTTAAAAACA AAAACAAAAA 300 CCTGACAACC AGAGATAAAA AGAATTCCCT AGGTGCTGCC TGACACAGAG AAAGGGATAG 360 ATGTCTCCAT TATTGAACTG TGAACACTAT GCTCCCATTA ATACACGCTA TAGTCTGTAT 420 AGAAGGATGC CTGTAGCAAA GACCACACTT CTCTCAACTG GTAAAAAGCC ACAGGGCAGG 480 TGGGGGGGTG AAGGGATCTT TGAATTAGTA ATTTCCCACC TTTCACCATT ATTTACATTA 540 TTTCATTATT TCCAAGATAG CCTCCATGTT TTGAAAGTTG TTTTATCTAC TTAATTCTAT 600 TTACTAAAAC ATAATTGATC GATTTTCCTA TTTCTATTCA TTAAAAACAG AGGCACACTG 660 AGGCAACAGT ATAAACCAGT GTCACCTGAC TGAGCAGCCT GAATTCTACC TGAAAGCAAA 720 CCTGACTTTC AGTAAGCCTA TGTAGTCTTT CATCCAGTAA AGGTACAACT GCCTTCTGGC 780 TTTTTGAAAT ACTAAAAATA GCTTCTGCAT CCCCATTTTT ACCTCCAAAA AATCCTTTAG 840 GGACTCTCTG GCCTAATGAC CTAATTTCTT TTTCACTGAA CGGCCTGTTG TTCTTAGAAG 900 TAATGAAAGA GGCTAGGCAC TAAGACGGCA ATGTTACATA GTGACACTAG GGGGCAGACT 960 ATTTAGGCAG AAGGTTTTCA TAAACTGTTC CAGTGCCAAT AAGGTTCCCT CTATGGAAGT 1020 TACTGACTAG TCCAGGTTGA TGAGCTGCTT TCCTATCTTC TTTTTAAAAA ATACATTTTT 1080 TAAAAATGCA TCACAATTAA CATTTGAGAA TTCATTTCTT CCATTTCTTT TCCCTTTTCT 1140 TTTCTCCCAA AATAGCAAAT CTTTATTTAT TTTTTCTTTT TTTTTGAGAC GGAGTTTCAC 1200 TCTTGTTGCC CAGGCTGGAG TGCAATGGCG TGCTCTCGGC TCACTGCAAC CTCCACCTCC 1260 CGGGTTCAAG CGATTCTCCT 1280
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