Tag | Content |
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EnhancerAtlas ID | HS127-14817 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr19:2494470-2496590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr19:2494845-2494855 | GCCCCGCCCC | + | 6.02 | MEF2A | MA0052.3 | chr19:2495843-2495855 | GCTATTTTTAGC | - | 6.44 | MEF2B | MA0660.1 | chr19:2495843-2495855 | GCTATTTTTAGC | - | 6.92 | MEF2C | MA0497.1 | chr19:2495842-2495857 | GGCTATTTTTAGCCG | - | 6.18 | NR2C2 | MA0504.1 | chr19:2496163-2496178 | TGACCTTTCACCTCC | - | 6.86 | Nr2f6 | MA0677.1 | chr19:2496163-2496177 | TGACCTTTCACCTC | - | 6.6 | Rxra | MA0512.2 | chr19:2496163-2496177 | TGACCTTTCACCTC | - | 6.8 | Sox3 | MA0514.1 | chr19:2496367-2496377 | CCTTTGTTTT | + | 6.02 | ZNF263 | MA0528.1 | chr19:2495893-2495914 | CTCTCCTCCTCCTCCTCCTCC | - | 10.75 | ZNF263 | MA0528.1 | chr19:2495896-2495917 | TCCTCCTCCTCCTCCTCCTCC | - | 12.34 | ZNF263 | MA0528.1 | chr19:2495887-2495908 | CCCTGCCTCTCCTCCTCCTCC | - | 6.26 | ZNF263 | MA0528.1 | chr19:2495703-2495724 | GAGGGAGGGCAGGGTGGGGGG | + | 6.31 | ZNF263 | MA0528.1 | chr19:2495884-2495905 | CCGCCCTGCCTCTCCTCCTCC | - | 6.52 | ZNF263 | MA0528.1 | chr19:2495890-2495911 | TGCCTCTCCTCCTCCTCCTCC | - | 8.02 | Zfx | MA0146.2 | chr19:2495638-2495652 | CCCGCCTGGGCCTG | + | 6.37 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_24383 | chr19:2494354-2496521 | Colon_Crypt_2 | SE_25170 | chr19:2493927-2496709 | Colon_Crypt_3 | SE_27369 | chr19:2493818-2496400 | Esophagus | SE_31940 | chr19:2493882-2496463 | Gastric | SE_37152 | chr19:2490278-2499382 | HSMMtube | SE_41828 | chr19:2494229-2496540 | LNCaP | SE_43297 | chr19:2493861-2496458 | Lung | SE_44558 | chr19:2493529-2496658 | NHDF-Ad | SE_48020 | chr19:2494513-2496167 | Pancreas | SE_50943 | chr19:2493885-2496560 | Sigmoid_Colon | SE_54295 | chr19:2494465-2496352 | Spleen | SE_65706 | chr19:2493855-2496674 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 2494705 | 2495117 | chr19 | 2495780 | 2495940 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I002490 | chr19 | 2490659 | 2497696 |
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Enhancer Sequence | ACGTGCACAG GCATACCCAC TGTTCATTCC ACGAAGGATC GTGCACACGC ATGCCTACCT 60 TTGCATTTCA CGCGGGATTG TGCACACGCA TGTCCACCGT GCCTTCCACG CGGGATCGTG 120 CACACGCATG TCCACGAACT CCTGCACACC TACACCCACC AGGCCTGCCC ATGCGATGCG 180 TCCCTGCAGA CCCACTGTGG ACGCCTGCTT GTCGGCGTCC TGCGCATCCC GCGTGAGTGG 240 AGTGTGCACT CGTGGAGGGG GCGACTGAGT GCGGGGCAAG CGCAAGCGCA AGCACACTGG 300 GCTCGCGGAG GGTGGAGAGA GGCCGTGCGC GTTCCCGGGG CTGGCGCGGA GGTGGGGTCA 360 GCGGCGCGGG AGAACGCCCC GCCCCGCTAC CGCCAGCCCG GAAGACCCAC GGCGGCGGGC 420 GCTGGCGTCA CGGGTTTCCA CTGGGGCCCC GGCGCCGGGG CCGGGATTCC CTGGCGCAGG 480 AACGCCCGTG ACGGCGGCGC CTGCCTGCGT CGGCCACGCT GGGAGGTTTG AGCCTGGGGA 540 TGACATCAGC CCCTGCGTTT CTGGAGCTGG CCCGGGCGGG ACGGGGACTT GGAGAAAGCA 600 GTGACACCCA CTTTCGTTGA CTGCCAACCC GTGCAGAGCG CTTAGTGCGT GTCCGACCGT 660 GAGCTGAGCG CTGTGATGCG GGTGCTGTTA ATGTCCCATT GCACAGATGG GGAAACTGAG 720 GCCGGCGCAC TGCCCGCCCC GCCGGGCCCC CAGAGTGAGG GCCCGGGGCT GGGAGCAGCC 780 TTTTCCCAGC GCCCTCTGCA GTGTAGAGTC CCACCAGCTT GTCTCCCGCT CTCTCCTGCA 840 CAAGCCGGCT CAGAGAGGGT CTGCGGGTGT CCTGGCACCA CCCAGCAAGT TGGGTGCTGC 900 AGCCAGCTCT GTCCATACAG TTGGTCTCTG CCCAGCTGCG GTGGCCAGGG GCGGTGCCTG 960 AGCCAGGGCG CCCGGGCGGC CCGGTGGGGT GTGCCCAGCC GCTGCCTTCC TGCTGACGCC 1020 GGTGCCAAGG GATCTAAATA TAGCCTGGGA GGAGGCAAGG GCTATTTTTA ACGCGAGTGG 1080 CTTGGCCCCT CCCAGTTCCC GGGTCAGGAG CCCTTTGGTC CAGGATTTTG GGGAGGGGCA 1140 GGGGCGAGGG GGAGCCAGGG GCCCCACACC CGCCTGGGCC TGCCCCTCTG CCCACACCTG 1200 GCCCTGGAAG ACTCTAGGGG ACGAAGGGCC GTAGAGGGAG GGCAGGGTGG GGGGGCTGTC 1260 GCAGGTCACC TTTCTTAAAC GCCACCTCCT CTCTAGCTGC CGACCAGCCC TGGCCTTTTG 1320 TTGGGCCCAG AGACTGCTTT CTATTTTGGG AAGGTGTTGG AATAATTTCC TTGGCTATTT 1380 TTAGCCGGTT CGGGGATTCC TCCACTCAGG CTGGCCGCCC TGCCTCTCCT CCTCCTCCTC 1440 CTCCTCCTAG TCGTCTTCCT CCTCCCGGCA GACCCAAGGG CGGCCTCCTT CATGGAGGGC 1500 AGTCAGGGAC ACACAGTCCC TGAGCCAGAC CCAGAATGGG GAGACCCCTA TATTTCCTGG 1560 GTCGGGGAGG GAAGGGAGCT CTGAAGGGCG TTCCCACGTT CCAGGTGAGC AGGACTTTCA 1620 GACCTCTGGG AATCCATGAC GCCAGGTATC TGAATTCTGT CTCCAGGGCA GGGTGGGGCG 1680 ACCCAGCAGC CTCTGACCTT TCACCTCCTT TCAGGGTTGT CACAGGAAAG TGGCCTGCTG 1740 AGAACAGACC TTGACTCCCA CATCCCTAGG CTAGGGGCTC CCATGTTCCC AAGAGGAAGA 1800 TCAGTGTGAT GAGGGTAAAC TGAGGCACAG AGGGGACACT GGGATGGGAC ACATCTTGGG 1860 CTCATTCCCT GATGGTTTCA TTTCCTTCCA CATTCTACCT TTGTTTTTAA TTTTTTTTTT 1920 TGATTGTTTT GAGACAAGAC GGAGTCTCAC TCTGTCACCC AGGCTGGAAG AGTATGCAGT 1980 GGCACAATCT CGGCTCTCTG CAACCTCTGT CCTCTGGGTT CAAGCGATTC TCCAGCTTCA 2040 GCCCCCTGAG TAGCTGGGAT TACAGGTGCA CGCCACCATG CCCAGCTAAG TTTTGTATTT 2100 TTAGTAGAGA CGGGGTTTCA 2120
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