Tag | Content |
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EnhancerAtlas ID | HS176-37985 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr7:99160120-99161480 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr7:99160950-99160962 | TTTATTTTTAGA | - | 6.07 | Nr2f6(var.2) | MA0728.1 | chr7:99161159-99161174 | CGAACTCTTGACCTC | - | 6.24 | STAT1 | MA0137.3 | chr7:99160533-99160544 | TTTCTAGGAAA | + | 6.14 | Znf423 | MA0116.1 | chr7:99160441-99160456 | AGACCCCAGGGTGGC | + | 6.21 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27485 | chr7:99155363-99161884 | Esophagus |
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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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Enhancer Sequence | AGGACTTCCT TATTATTCGG TTTATCTATT TGAATTTCTT TACTTTCTTG TTTCTTCCTA 60 AGTATAAGGT CTCTGAGAAG GTCTGTAGAG TGTGGCTTAG ATTCCAGGAC TTAGAACCTC 120 TGAATCCTTA TCTTTCACAT CGTCTTCTCC GGGAGGGGTA ATTAACGTTT GTTTGGGGGT 180 GCCAAGAAGA GACATTCTCC TCCTTATCCC CAGTTCATGT TTATGGCCAT TGTGGGGCAT 240 CTTTTCCCTT TTAGCAAAGG GAAACTTTCT TGTGCTTTGC TTGATTTCTC ACCGTTCTTT 300 TCTTTTCCAT TTTTGTAGGA GAGACCCCAG GGTGGCCTCC CAACCTCCAA CCAGACACTT 360 TCCTCTTTGT TATCTCAGTG TCCCTGTATT AGAGAATTGA AGAATTTCCC ATTTTTCTAG 420 GAAAAAGAAA TGCCGTTTAT TTAAAAAGAC AGGCTAAATT CCTTCTTGTT GAGTAGTCCC 480 TCACCCCTTA AGATCCCCAG ATGTATCTCC AAGCAGGCAG AACTTGAGAT GTCATTTGAA 540 GGCATGACTC ACTGTGAGTA CATTTCAGTG AGTCACCCAG AATGGTAATC CCACGTAACC 600 ACACCCAGGG CAGCAGAAAT CTCAGATGTT TACCCCATGC TGAGGTGGGG TCAATGCTTA 660 ACTCATGTCT CTCCCTTGTC ATTTTGAAAG GTACAGTGGG AAGCTGGGAT TAGCCAAGCT 720 GTAGTGCTGC TGGGAAGCAT CAGTGGGGTT TGTCGGCAGC TCCCTTGGTG TGAGCATTGT 780 TCCTTTTTCT TTAGTTTATT TTTTATATTA TATTATATTT TTTATTTTAT TTTATTTTTA 840 GATGGAGTTT CACTCTTGTT GCCCAGGCTG GAGTGCAGTG GTGCAATCTC AACTCACTAC 900 AACCTCTGCC TTCCAGGTTC AAGCGATTCT CCTGCCTCAG CCTCCCAAGT AGCTGGGATT 960 ACAGGCATGG GCCACCACGC CCGCCTAATT TTGTATTTTT AGTAGAGACG GGGTTTCACC 1020 ATGCTGGTCA GGCTGATCTC GAACTCTTGA CCTCAAGTGA TCCACCTTCC TTGGCCTCCC 1080 AAAGTGCTGG AATTACAGGC ATGAGCCACC GCACCCAGCC TCCTTTTTCT TTAGTTTCTT 1140 GCTTGCTTCT GCACTCTTCT TTTTGTGTGT GTAAATACTG AATCATGCAT TTTCTTTTCT 1200 TTTTTTTTTT TCCGTTGGCT TTGTCTATGC TGGTGGCATC CAGGGCATTG CTTTGTCTCC 1260 CTGATTATGC TCAGGATTCA AGGTCTTCTT ATTTGTGGGG AGGCAGGCTG CCCACTGGGA 1320 CGGTTTTTAG TGTGTTTTCC ATTCCTGGCT CTTTAATCTT 1360
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