Tag | Content |
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EnhancerAtlas ID | HS047-32353 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr8:22079470-22081730 |
Target genes | Number: 10 | 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) |
HSF1 | MA0486.2 | chr8:22079546-22079559 | GAACATTCCAGAA | - | 6.59 | ZNF263 | MA0528.1 | chr8:22081674-22081695 | GGAGCAGGAAGGGCTGGGAGG | + | 6.66 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27590 | chr8:22080710-22082529 | Esophagus | SE_29206 | chr8:22074822-22080416 | Fetal_Intestine_Large | SE_35070 | chr8:22079727-22082418 | HeLa |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 22079511 | 22079655 | chr8 | 22079899 | 22080739 |
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| Number: 2 | ID | Chromosome | Start | End |
GH08I022222 | chr8 | 22079736 | 22079835 | GH08I022223 | chr8 | 22081356 | 22082717 |
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Enhancer Sequence | GCTGCGTGTG GTCGAGGAGG GAGGAAGCCA GCCCAGCTCC CAGCCCTCCC CCAGCCGCCT 60 CCACTAGTCG CAAATAGAAC ATTCCAGAAT GCAAGAGCAG GGAGGGCCCT GGAGAGGGAT 120 TCAACCAGCC CACTCCTTCT CAGAGAAGAG ATATGAAGCT GTCACTCCCC AGCTTGAAAC 180 CCTTTGATGG GGTGTGTGTG AAAAACACGG CGGCTCATGA TCTGATCTCT GTGGTCTCCT 240 TGCCACTCCC CACCTCCTGC CACCCCATCC ACTTACCCAC CCCCTGCACA CACAGTCTCC 300 TGCCTCCGTG ACCCCTATGC AGGACTCTTC CCTCTGCTGC ACTGACTGCC CTCTCCACCT 360 TCCTCCGTCT GGCTTGGCAA ACTTCTAATT AGCCTTCAAG CTTCAGTCAA GCGTCTGCTC 420 CCCTCTAAAA CCTCCCAGGA ACAGCAGACA CCTGCACTTG ACAAATTTTT GGCTTCCTAC 480 TATGTGCAGG ACACCCAATC TTCTCACTAT GTTGCCCAGG CTGGACTTGA ACTCCTGGCC 540 TCAAGTGATC CTCCTGCTTC AGCCTCCCAA AGTGCTAGGA TTGCAGGTGT GAGCCACTTC 600 ACCTGGCCAG GACACTGAAC TGTGCTCAAC AATTACACGT ACTTTTTACA TGAAATCTTT 660 CCATACTGTC TCTCTGACTG GATTCTGAGG TTCTCAAAAG AGTGAACTGT GCCTTTATCT 720 TTACATCCTG GCACCAAGTA AGGTGCCTGG CACCCATGAG TGCTCTCTAT CTCTCCCACT 780 CTCGCTGATA AAGGAGCCCA AACTGGGCCA CTGACTTGCT TTCCAGGCTG GAGTGCAGTG 840 GTGCAATCAC AGCTCACTGC AAGCTCGAAC TCCTGGGCTC AAGCAATCCA CACCCGGCTA 900 ATTCTTTAAA TTTTTTGCAG AGGCTGGGGT CTCACTATGT TGCTCAGGCT AGTCTTGAAC 960 TCTTGGGGTC AAGAGATCCC ATCTCGGCCT CCCAACGTGG TAGGATTACA GGCTTGAGCC 1020 ACCAAGCAGG CCTTGCTTCT TTAATACAAA CCCCAAAGAC TCCCAAGGTC CTCACTGCCC 1080 TGAGGTTAAA ACTGCCCTGA CTGTAAGGAT AAAGACAGAC AGAGGCCGGG CGTGGTGGCT 1140 CATGCCTGTA ATCCCAGGAC CTTGGGAGGC CGAGGTGGGC GGATCACCTG AGGTCAGGAG 1200 TTTGAGACCA GCCTGGCCAA CATGGTGAAA CCCCACTTCA TTAAAAATAC AAAAATTAGC 1260 CGGGCATGGT GGCGCATACC TGTGGTCCCA GCTACTCAAG AGGCTGAGGC AGGAGAATCA 1320 TTTTAACCCA GAAGGCAGAG GTTGTAGTGA GCAGAGATCG CGCCCCTGCA CTCCAGCCTG 1380 GGTGACAGAG AAGACGCCAT CTCAAAAAAA AAAAAAAAAA AAAAGGCAGA GCAGCTGCTT 1440 GCCCTGGCTG AGCCTCAGAA GGATGCGGCC TTGGAGCACT TGCCAGCAGG CCCGGGGATG 1500 GTGGGTACTC CTGGTCCTGC CTCACATTGC CTGGTCCTGG CTGTCCTCAG TAACAAGTGA 1560 CTCCCTGGCT CGAATGAACA AGTGCTTCCC TCTGGGCCTC AGGCTCCTCT TCTGTAGGCT 1620 GAGGGTGTTG GATCAGATCA CCAATTTTCA AACACTTTTG GACTGCAGCA ACTCTCTTTT 1680 TATCCCCAAA AGAAATTATA CGTGGAAGGG TCACAGGCAA ATAAAATTGA GGCTACTCTG 1740 ACTGGAGGTC AGGTGTGGGG CCCACCAAGC CTCAACCTCT GGTCCCCCCA ACCCCATGGC 1800 AGCATTCTAA GGGGTTCACT GACATGTCTC CCTGGAGGGA GCACCCAGTT TGAAAACCGA 1860 CGAGCTGGGT GCTTCCTCGA ACCCTTTGTG ATCAGAACAC TCATTTTGTG CACTCCCTGC 1920 CACCTTCCCT TTGGCCCCAG GGCCTGAATC GGAGAGACCT GTGGTGGTAG ACCCCTGTGA 1980 AAGGAACTGT CCCAGAGTGG GAGCAAACCC AGACCTCATT CTCCCAGGCT CATTAGTACA 2040 ACACTCTTGC AGAAGGCCCT GTCCCCAGAG CCCTTGATCT TCCCTGAGCC CAATCCCCAA 2100 AGTAGCAGTC TCTTCAGAGC CAGCCTGGTG ACGTCAGGAC ATGTCAACCC TAGAGGAGGG 2160 ACTGGCAGCC ACGAGGGTGG GGGTGACCTC AGACAGCCAG GACAGGAGCA GGAAGGGCTG 2220 GGAGGGAGGA GAGGCCCGGC GGGTCCAGCC GGGAGCCCGC 2260
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