Tag | Content |
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EnhancerAtlas ID | HS188-06138 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr19:2494300-2496470 |
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 | CGCCCACGGC TCCACGCCCA CAGGCCACGG GCACCGGGAG AGAGGGTGAA TGAGTGTGTG 60 TGTGTGTGTG AGTGTGTGTG TCCGGAATCT GTACTCTCCA GCCAGGGCTC CCCATCCTCC 120 TGCAAAGGGC CAGCACCGTG CACGGGTACC CACGGCGCCT TCCAAGGGGA ACGTGCACAG 180 GCATACCCAC TGTTCATTCC ACGAAGGATC GTGCACACGC ATGCCTACCT TTGCATTTCA 240 CGCGGGATTG TGCACACGCA TGTCCACCGT GCCTTCCACG CGGGATCGTG CACACGCATG 300 TCCACGAACT CCTGCACACC TACACCCACC AGGCCTGCCC ATGCGATGCG TCCCTGCAGA 360 CCCACTGTGG ACGCCTGCTT GTCGGCGTCC TGCGCATCCC GCGTGAGTGG AGTGTGCACT 420 CGTGGAGGGG GCGACTGAGT GCGGGGCAAG CGCAAGCGCA AGCACACTGG GCTCGCGGAG 480 GGTGGAGAGA GGCCGTGCGC GTTCCCGGGG CTGGCGCGGA GGTGGGGTCA GCGGCGCGGG 540 AGAACGCCCC GCCCCGCTAC CGCCAGCCCG GAAGACCCAC GGCGGCGGGC GCTGGCGTCA 600 CGGGTTTCCA CTGGGGCCCC GGCGCCGGGG CCGGGATTCC CTGGCGCAGG AACGCCCGTG 660 ACGGCGGCGC CTGCCTGCGT CGGCCACGCT GGGAGGTTTG AGCCTGGGGA TGACATCAGC 720 CCCTGCGTTT CTGGAGCTGG CCCGGGCGGG ACGGGGACTT GGAGAAAGCA GTGACACCCA 780 CTTTCGTTGA CTGCCAACCC GTGCAGAGCG CTTAGTGCGT GTCCGACCGT GAGCTGAGCG 840 CTGTGATGCG GGTGCTGTTA ATGTCCCATT GCACAGATGG GGAAACTGAG GCCGGCGCAC 900 TGCCCGCCCC GCCGGGCCCC CAGAGTGAGG GCCCGGGGCT GGGAGCAGCC TTTTCCCAGC 960 GCCCTCTGCA GTGTAGAGTC CCACCAGCTT GTCTCCCGCT CTCTCCTGCA CAAGCCGGCT 1020 CAGAGAGGGT CTGCGGGTGT CCTGGCACCA CCCAGCAAGT TGGGTGCTGC AGCCAGCTCT 1080 GTCCATACAG TTGGTCTCTG CCCAGCTGCG GTGGCCAGGG GCGGTGCCTG AGCCAGGGCG 1140 CCCGGGCGGC CCGGTGGGGT GTGCCCAGCC GCTGCCTTCC TGCTGACGCC GGTGCCAAGG 1200 GATCTAAATA TAGCCTGGGA GGAGGCAAGG GCTATTTTTA ACGCGAGTGG CTTGGCCCCT 1260 CCCAGTTCCC GGGTCAGGAG CCCTTTGGTC CAGGATTTTG GGGAGGGGCA GGGGCGAGGG 1320 GGAGCCAGGG GCCCCACACC CGCCTGGGCC TGCCCCTCTG CCCACACCTG GCCCTGGAAG 1380 ACTCTAGGGG ACGAAGGGCC GTAGAGGGAG GGCAGGGTGG GGGGGCTGTC GCAGGTCACC 1440 TTTCTTAAAC GCCACCTCCT CTCTAGCTGC CGACCAGCCC TGGCCTTTTG TTGGGCCCAG 1500 AGACTGCTTT CTATTTTGGG AAGGTGTTGG AATAATTTCC TTGGCTATTT TTAGCCGGTT 1560 CGGGGATTCC TCCACTCAGG CTGGCCGCCC TGCCTCTCCT CCTCCTCCTC CTCCTCCTAG 1620 TCGTCTTCCT CCTCCCGGCA GACCCAAGGG CGGCCTCCTT CATGGAGGGC AGTCAGGGAC 1680 ACACAGTCCC TGAGCCAGAC CCAGAATGGG GAGACCCCTA TATTTCCTGG GTCGGGGAGG 1740 GAAGGGAGCT CTGAAGGGCG TTCCCACGTT CCAGGTGAGC AGGACTTTCA GACCTCTGGG 1800 AATCCATGAC GCCAGGTATC TGAATTCTGT CTCCAGGGCA GGGTGGGGCG ACCCAGCAGC 1860 CTCTGACCTT TCACCTCCTT TCAGGGTTGT CACAGGAAAG TGGCCTGCTG AGAACAGACC 1920 TTGACTCCCA CATCCCTAGG CTAGGGGCTC CCATGTTCCC AAGAGGAAGA TCAGTGTGAT 1980 GAGGGTAAAC TGAGGCACAG AGGGGACACT GGGATGGGAC ACATCTTGGG CTCATTCCCT 2040 GATGGTTTCA TTTCCTTCCA CATTCTACCT TTGTTTTTAA TTTTTTTTTT TGATTGTTTT 2100 GAGACAAGAC GGAGTCTCAC TCTGTCACCC AGGCTGGAAG AGTATGCAGT GGCACAATCT 2160 CGGCTCTCTG 2170
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