Tag | Content |
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EnhancerAtlas ID | HS105-40059 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:38692640-38694500 |
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) |
IRF1 | MA0050.2 | chr19:38693232-38693253 | AAAGAAAAAAAGAAAGGAAAG | - | 6.28 | MAX | MA0058.3 | chr19:38694194-38694204 | AGCACGTGGT | - | 6.02 | MYCN | MA0104.4 | chr19:38694299-38694311 | GGCCACGTGGTC | + | 6.52 | MYCN | MA0104.4 | chr19:38694299-38694311 | GGCCACGTGGTC | - | 6.52 | Nr2f6(var.2) | MA0728.1 | chr19:38693011-38693026 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65256 | chr19:38692879-38695341 | Pancreatic_islets |
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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 |
GH19I038202 | chr19 | 38692880 | 38695341 |
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Enhancer Sequence | AGGTTTCCCT GGGAACACCC GGGTTCATAC CAGCGGCAGG CCTGTGCAGT GGAAGAGGCT 60 TACCCAGAGA GAGGCAGCCA TGTGGGTCAC CCCCACCACT CTCCGGGCGG AAGCTGATAT 120 AGCAGCTACT CCCCCCTCCT AACAGACTTG GAAGTCATTA CACTGCACCT GTCTGTGCAC 180 TGGGGATCCA CAGTGACCAA GACAGACTCT GCCCAGTCCC AACAGATCTC CCAGTCCAGC 240 AGAGACGACA CTTGAATCAA TACACACACA GTTGTTTCGC TTCCAACTTT GAACACTGCT 300 AAGCAGGCCG GGCGCGGTGG CTCACGCCTG TAAACCCAGC ACTTTGGGAG GCCAAGGTGG 360 GTGGATCACT TGAGGTCAGG AGTTCAAGAC CAGCCTGACC AACATGGTGA AACCCCATCT 420 CTACTAAAAA TACAAAAATT AGCCGGGCGT GGTGGTGCGT GCCTGTAATC CCAGCTACTC 480 GAGAGGCTGT GGCAGGAGAA TTGCTTGAAC CCGGGAGGCG AAGCTTGCAG TGAGCCAAGA 540 TCGAGCCACT GCACTCCAGC CTGGGCCACA GAGGGAGACT CCATCTCAAA AAAAAGAAAA 600 AAAGAAAGGA AAGCTGCTAG GCAGTGTCTC CCAATCCCCC AGCCCTGTGC CTCTCGTCAG 660 CCCCGTCGCT GCCAATCTCC CGCCTGTCTG CTCCTTCGTC TCCTCCTCTG CAGATTCCTA 720 AACCTCACAG ACTTCTGCCT CACGCTCACC CTTCCCAGCC TCCCTGCCAG GTGCCGTGCT 780 GGGCTGTCTG AGGACCTAGT GGCAACTGAG GCCAGGCCTG GCCCTCAGGA AGCTTCACGG 840 GGGAAGGAAG AGGACGGGGA CAGATCTCTC ACATTTGTCA TCTCACGCGT GGCTTCTCAC 900 ATTCAGCGCA GCATATTTGA CTGCACTCAC TTGGCAGAAA ACAAAATTAA AAAGAGGCAG 960 AGAGAATGTA AATGGCACAT TCTGCCTGTA CATGGATTTA AATAGTGCAT TTCACACTCG 1020 TCTGCACACC TCACGGTTCA GGGTTCTATA TACAACCATC CGTGCACTGT ACTTCATGGG 1080 CAGTGGGAGC AATTTTTGAG GGTAATTTTG ACTTCTTGCT TTTCACACTC TGGCTTCAGA 1140 ACTCAACCTC CACCACGAAC GTAGGCCCCA CTGTAATTAC AAGAAATCAG CAGTTCCAGA 1200 TGGTGCTGCT GGGCTGAGGG GCAGGAGCAG CATGGGCTGT GGGAAGCAGC GGGACCTGTG 1260 GCCCCTGGGC GGCGCTCCTG GAGTCCATTT GCCCCCATCT CCCTCTGCAG CTGCAGATCC 1320 CCAAGACTCA GCAGCAAGGT TGTAGGAAAG GGTGGGCGAG GCAGGAGGGC CAGCCCCCGA 1380 CCGCCACCGC CTCTGTGCCT GTGCACGCAC GGCATCCAGT GGAGCCTCCT TCAGCCCCAA 1440 CTCCAAGCAG GAAAGGGCTG CGCGTTCTCT GCAGCGGCCA GGCAGGCCCA GGGCTGGGAG 1500 GATCTGCAGA GGGGCAGCTA CTGGCCATGG GCCCCTGATT CAAATCCTAG CACCAGCACG 1560 TGGTAGCCAT GCAGCACCTC CAAAGGCCAC AGTGGGCAGA GGAGCTCTGT GAGATGAGCC 1620 GGGCAGTCTG GGGCTTGTTG CGGGGTGGCT CTCAGTGACG GCCACGTGGT CAGCATCACT 1680 GCCAGGACCA TTGTTGGTCC TGCCCACAAG GGCAGGTCCT TTTGACCATC TGTCCATTCT 1740 CGTGCTTCCT GTGCCTGGAC CCGCCAGGTG CTCAGCAGGT GTCTGTAGAG TGGGCTCTTT 1800 GTATCCTGGA GGTACGAAGA AGGGGTCCTC CCTGAAGTCA CATGCACGGC CCAGCCTCAG 1860
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