Tag | Content |
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EnhancerAtlas ID | HS034-14952 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr19:18228210-18229790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EGR1 | MA0162.3 | chr19:18228781-18228795 | CCCGCCCCCGCACT | + | 6.21 | EGR3 | MA0732.1 | chr19:18228780-18228795 | CCCCGCCCCCGCACT | + | 6.83 | EGR4 | MA0733.1 | chr19:18228780-18228796 | CCCCGCCCCCGCACTC | + | 6.16 | KLF14 | MA0740.1 | chr19:18228423-18228437 | GGGTGGGCGTGGTA | - | 6.08 | KLF16 | MA0741.1 | chr19:18228599-18228610 | GCCCCGCCCCC | + | 6.02 | KLF16 | MA0741.1 | chr19:18228764-18228775 | GCCCCGCCCCC | + | 6.02 | KLF16 | MA0741.1 | chr19:18228779-18228790 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr19:18228599-18228609 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr19:18228764-18228774 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr19:18228779-18228789 | GCCCCGCCCC | + | 6.02 | SP1 | MA0079.4 | chr19:18228761-18228776 | CAGGCCCCGCCCCCA | + | 6.56 | SP3 | MA0746.2 | chr19:18228424-18228437 | GGTGGGCGTGGTA | - | 6.37 | SP4 | MA0685.1 | chr19:18228761-18228778 | CAGGCCCCGCCCCCAAC | + | 6.57 | SP8 | MA0747.1 | chr19:18228424-18228436 | GGTGGGCGTGGT | - | 6.32 | Zfx | MA0146.2 | chr19:18228761-18228775 | CAGGCCCCGCCCCC | - | 6.19 |
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| Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
SE_03607 | chr19:18228860-18229540 | Brain_Angular_Gyrus | SE_03607 | chr19:18229563-18230152 | Brain_Angular_Gyrus | SE_04405 | chr19:18227552-18228448 | Brain_Anterior_Caudate | SE_04405 | chr19:18228707-18231550 | Brain_Anterior_Caudate | SE_05422 | chr19:18228732-18231107 | Brain_Cingulate_Gyrus | SE_06334 | chr19:18227733-18231497 | Brain_Hippocampus_Middle | SE_07235 | chr19:18227822-18231343 | Brain_Hippocampus_Middle_150 | SE_08343 | chr19:18228675-18231084 | Brain_Inferior_Temporal_Lobe | SE_10753 | chr19:18227967-18228613 | CD19_Primary | SE_10753 | chr19:18228829-18231042 | CD19_Primary | SE_19731 | chr19:18227880-18228741 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19731 | chr19:18228750-18231627 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22919 | chr19:18227678-18228683 | CD8_primiary | SE_22919 | chr19:18228828-18231785 | CD8_primiary | SE_60731 | chr19:18199190-18231325 | DHL6 | SE_62682 | chr19:18196873-18231497 | 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 |
GH19I018117 | chr19 | 18228011 | 18232079 |
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Enhancer Sequence | GCTGATGGCC TTTCCCGCCA CACACAGACA GAGCATGTCA GACGCCCCGA CTCAATTTGC 60 CAAACACACC CTCTATGCCA GTCCGGTGCT GGGAGCTGCT GGGACCCTAA GGAGCCCCCA 120 GCCTGGGGAA GACATAGCCG GACAGACAGG AAAGCGGGTT TTTCAGAGGA GAGGACGCAG 180 TTTTGCCAGG CTAGATTCCA AGCAGTGGGG CCAGGGTGGG CGTGGTAGCA TGAGCCGGCC 240 AGGACGCTGG GGTGGGTCTT GGGTGCCGCA CTGAGAAGGG GTCAGTGCTC TGGGAGAGAG 300 GAAAAAGATG GAGGGAGCGA TTAGATTTAC ATTTTAGCAG AAAGGAGCCA AAATGCCTGC 360 CCCTAGCTCG AGGTTAAGGT GCTGCCAACG CCCCGCCCCC GCCGCCCGCG GTCGTAGCAA 420 CGCCCGGCCT CAGCCGCCCG CGGCCCTAGC AACGCTCCGC CTCTCCGCCC GCGGCCATGG 480 CAGCGCCCCG CCCACTCGCC GGCACGCGGG TCCGCCGGCC TCGCTTCCGC GTCGCTCGCT 540 CCGCCTCCCG ACAGGCCCCG CCCCCAACGG CCCCGCCCCC GCACTCGCCT GGGCGGAGTT 600 CCAGTCGCGC TCGGGGGCGC GCGCTTCCTT CTCGCCGCCC CCCCATCCCC GCAGCCCCGT 660 GCGCCCCCCT CCCTGTCCGG CTCCGCGGGG CTCCTGGGGC CGATCCCACC GCCGAGGCCT 720 CCCTTCCCGG CCTCGGGCGG CTGCGGCGGC ACAAAGGGAA GCAGCATGTC CGACCCCAGC 780 TACTGGACGG CGGTGGCGGC TCCCGGCCAT CGGAGCCGCC TGGCAAAAGG CGCGCTGCTG 840 CAGCGCTCCA AGAGGTAGGG GGCACGGCGC CGGCGAAGGC TCGGCGGCCA GCCGAGCAAA 900 CAGGAGTTGC CAGAAGTGTG TCCTGGCCGC GTGGCGCGGA CCACGGCGAG CGTCTGTCTG 960 TGGCAGCAGT GGGAAGGGGG GAGGACGCCT GTGGATCGAG GTGTCCCCTG GGGTCCCTGG 1020 CACCCTCCTT TCGCCCCTCG TTCCCTGGAC TGGGGTGTCT GTCCGCCAGC GTCGCAGCTG 1080 GGGTGGTGAC AGACAGGAGT GAGTTGAGAT TGAGCTAGGA TTTGAACCCG GGTGTCCAGG 1140 GCTGGGCAGA ACCAGGGAGG AACTTCTTGG AAAAACTGAG GCTGATCTGC CGCTGGGGGT 1200 CCATTCAGCA GAAATGTTGG CTCAGAAGCA AATATTTACT GCACGAGGCT GGCATTTGGG 1260 TGGGGTGTCA GGAGTCCAGA TAGTTGGGGT TAACCCCCGC CAAAGCCTCA CCGCTCTTGG 1320 AGTCTCAGTT TCCCCTTTTG AAAAGCAGAG AGGATAAGTG AGGGCTGTGG ATTCTACCAG 1380 ACCTGGGTTC AAATTTCGAC TCAGCCACTA CCAGGCTGTG TGACCTCAAG TAGCTCCTTA 1440 ACCTCTCTGT GCTTGGGTTT CTCATTGGTG CTGGACTGGG GCAAAGTCTG GGCGGTGGGA 1500 CCAGCTACCG AAAGACCTTG AATGCTGAGT CCAGGGCTTA AACTTACCTC CAAGATCGTG 1560 GGGAGCATTG GAGGGGGAAT 1580
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