Tag | Content |
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EnhancerAtlas ID | HS091-13968 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:94420830-94423110 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr14:94422174-94422189 | AGGTCACGTTGCCCT | + | 6.99 | EWSR1-FLI1 | MA0149.1 | chr14:94421930-94421948 | GGAAGGGAGGAGGGCTGG | + | 6.04 | EWSR1-FLI1 | MA0149.1 | chr14:94421422-94421440 | CCTTCCTTCATTCATTCA | - | 6.56 | EWSR1-FLI1 | MA0149.1 | chr14:94421406-94421424 | CATTCATTGCTTCCTTCC | - | 7.14 | EWSR1-FLI1 | MA0149.1 | chr14:94421418-94421436 | CCTTCCTTCCTTCATTCA | - | 7.69 | EWSR1-FLI1 | MA0149.1 | chr14:94421414-94421432 | GCTTCCTTCCTTCCTTCA | - | 8.2 | EWSR1-FLI1 | MA0149.1 | chr14:94421410-94421428 | CATTGCTTCCTTCCTTCC | - | 8.73 | NR2C2 | MA0504.1 | chr14:94423005-94423020 | TGCCCTCTGCCCTCC | - | 6.45 | PLAG1 | MA0163.1 | chr14:94422951-94422965 | GGGGCCCCAGGGGG | + | 6.65 | RARA(var.2) | MA0730.1 | chr14:94420859-94420876 | AGGTCAGGCCAAGGCCA | + | 6.05 | Sox3 | MA0514.1 | chr14:94422636-94422646 | AAAACAAAGG | - | 6.02 |
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| Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
SE_16780 | chr14:94420893-94423754 | CD4_Naive_Primary_8pool | SE_19718 | chr14:94420438-94423655 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_26176 | chr14:94420751-94422722 | Duodenum_Smooth_Muscle | SE_27221 | chr14:94421547-94427161 | Esophagus | SE_40684 | chr14:94416759-94427307 | Left_Ventricle | SE_42615 | chr14:94419842-94427096 | Lung | SE_48057 | chr14:94415356-94427244 | Psoas_Muscle | SE_48827 | chr14:94419625-94421185 | Right_Atrium | SE_48827 | chr14:94421399-94426425 | Right_Atrium | SE_49510 | chr14:94421403-94422495 | Right_Ventricle | SE_50919 | chr14:94419796-94427101 | Sigmoid_Colon | SE_51124 | chr14:94421388-94433866 | Skeletal_Muscle | SE_52728 | chr14:94419707-94427187 | Small_Intestine | SE_54605 | chr14:94419515-94427015 | Stomach_Smooth_Muscle | SE_58336 | chr14:94405869-94468889 | Ly1 | SE_58879 | chr14:94405876-94468971 | Ly3 | SE_59615 | chr14:94417819-94449507 | Ly4 | SE_60397 | chr14:94402665-94450746 | DHL6 | SE_62757 | chr14:94419629-94446114 | Tonsil |
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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: 1 | ID | Chromosome | Start | End |
GH14I093953 | chr14 | 94419761 | 94432931 |
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Enhancer Sequence | TGTGAGAGGA AGGAGTGGGT CAGTCCTCAA GGTCAGGCCA AGGCCAGGCC AGGGGGCCTC 60 TCTCTCAGGA GTGCTGGCAG TGGAGTCACT CGGTCCTCGT CCCTGCTGGT TCCAGGATGA 120 GCACTCAGCC CCCTGCAGCC CAGTGGCTGC AAGAGGACTG GGGGATCCCT CCATCTCTGT 180 GGCTTTCCAT GGCTGCCGGG AATGTTATAC CAAAACCAAT TCTACCAAGA GGATTCAGGC 240 ACACAATGCC AGCCTCCTAG AGGGTGGCTA ACCACCCACA TGTGAGGCAC TTGTGATAAT 300 TAAATGCTTT CCCTGAGTAT AGCACTCTAG CATTTACCAG GCACGCCCAT CTCGGGGGCC 360 CCCTCTTAAC CCTGAGCATA TCTCTGGGGT CTTCCAACTC CTCTCCTTGC CCTGTCGCTT 420 ATTCCTACTC CCAGTACATC CAGCTGCAGA AAAAAAATAT ATACTGGAAG GATTAATAAA 480 TTTGAAGCCT TCACAGTTTA AAACTTCTGA ATGTCAAAAA GATTTGAGGG CTAAAGTGAA 540 GCCGTTCCTT GCTTGGCTTG TTAAAGTCCC TTTGTTCATT CATTGCTTCC TTCCTTCCTT 600 CATTCATTCA CTGAGCTCCC TACCTCATCC TTGGAGAGTC CGTGAGAACC ACGATGTCTA 660 TGCCTCTCAG ATCCACTTTT GGGGAGGCTT CTGCATCAAT AGTCCCATTT CCCAGATGGA 720 GAAGGTGAGG CTGGAGGCAG GCCTCATTCC CAGGACACCC ACGCCATGTT GGGCTAGGAT 780 GGGCTCTGGG CGGTCTCTGC CACCAGCCCC TGCACTCTCC CAGCCACTTC CTCCAGCGTG 840 AGCAGCACTT CCTCCTGACT CTCAGACTCT GTGGTTATTA ATGGTGTCAG AGCACAGATG 900 CCGGTGAAGC AACAGACCCA GCAAGGACGA TGGGAAACTG ATCAGATAAG TCCTGAGGTC 960 CCCATCAGCA CCGTCACTGC CACCTTGACG AGTTCCACTT AGGAACAGCC AGAGCAGCCC 1020 CTGTCAGCAT CAGGAAAAGC CCAGTGGGGG TATGTGCCCC CCTTTTCCTG GAGTGTCTCC 1080 AAAGGGACCC CAGCTGAAGT GGAAGGGAGG AGGGCTGGCT TTTCTCGTGG CCTTGGCGAG 1140 CAGGGCGTGG TGCAGTGTCG TGAGAACACT TTCAGGACCT GCCGCCCAGC TTGGGTCTCT 1200 CCAGCTGTGA TGCAAGGACC CTGGAGCCCT CAGCCCACAT ATTCACAGCT TCTCCATGAC 1260 CTCAGGCAAA GTCCCCGCCC TATGAGTGGG GGAGGGTTCT GGGGGTGTCA GGCCATCAGA 1320 GTAGTAAGCT GGACGGGACC CTAGAGGTCA CGTTGCCCTC TCCAGCCGTG TCCTGCAGAG 1380 AAGGGAGACT CAGAGGGGAC AGCGACTCTC AGGCAGTCAT GCAGGAGGTG GCAGTAGCTG 1440 AGACCAGCTC TGGGTCTCCC TTTTCCAGAT TGTCAACCAC TCCACACACC CACCACACCA 1500 AGGAAGTGGA GGGCGACAGG ATTTGAAAAA GGCTGGGAAG GAGAAAGAAA ATATTGGCCA 1560 ATTGCCTCCT CCCTTCTCTA CAACGTAACT GAGTGAGGAA ATGCAGTTCC AGTGATAGGG 1620 TCCCTCTTTT GCTTTTGGCT GCTTCCGGGG TCACTATTCC AGGGGTACAG AGAGGGGAGG 1680 GAGGCAGAAT TATTTTCTAA GGAGCGCATT AGCCCTGCCC CCTGGTGCCA GGCAAACAGA 1740 GCCCCTGCAG CTTAGATTAT TTCTGGATTT TAGCACCTGG CACTTCACAA ATAAGGGCAA 1800 ATAAACAAAA CAAAGGCTGT GGGTGTGGGC ATTTTGGATG TACCCACAGC GATGGCATGG 1860 GGGAAAGTGA GACTGGGACA AACAGAAGGG TGCAGCCAAC TCATCAAGTT CAACTCCAAG 1920 CTCTCCTGGG CCTCTGGGGT TCTAAGGCCA TCTCCCCAAT TTCCCTCGTG CTGGGTCCCC 1980 AGTTTCAGAG CCCCATGGGG CTCCTCCAGC ACTCAGGTCC CATGCTGGGG GCATCTGAGG 2040 GGGGGATCAC CAGCATGCCT GGCTGGAAGT TCCTTGAGGA CTGAAGTCTG TGGCCACCAA 2100 GCCCATCTCA GCAGGAGCAG TGGGGCCCCA GGGGGGCACC CCTAGAAGGA GCGTGCCTGG 2160 CAGGTGCCTC CATAGTGCCC TCTGCCCTCC TGGGGGCTGT GGGCCTGCTT CCCACCCTCC 2220 CTGCCATCCC AGTTAGCGGA GTGAACTTGG ATGGTCCTGG GGCCAGACAG GAGTCACTTA 2280
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