Tag | Content |
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EnhancerAtlas ID | HS101-20795 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr19:2494260-2496450 |
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 | CCCAGACTGG TGGGGAGACG GTGAACAGCC TGAGAGTCAT CGCCCACGGC TCCACGCCCA 60 CAGGCCACGG GCACCGGGAG AGAGGGTGAA TGAGTGTGTG TGTGTGTGTG AGTGTGTGTG 120 TCCGGAATCT GTACTCTCCA GCCAGGGCTC CCCATCCTCC TGCAAAGGGC CAGCACCGTG 180 CACGGGTACC CACGGCGCCT TCCAAGGGGA ACGTGCACAG GCATACCCAC TGTTCATTCC 240 ACGAAGGATC GTGCACACGC ATGCCTACCT TTGCATTTCA CGCGGGATTG TGCACACGCA 300 TGTCCACCGT GCCTTCCACG CGGGATCGTG CACACGCATG TCCACGAACT CCTGCACACC 360 TACACCCACC AGGCCTGCCC ATGCGATGCG TCCCTGCAGA CCCACTGTGG ACGCCTGCTT 420 GTCGGCGTCC TGCGCATCCC GCGTGAGTGG AGTGTGCACT CGTGGAGGGG GCGACTGAGT 480 GCGGGGCAAG CGCAAGCGCA AGCACACTGG GCTCGCGGAG GGTGGAGAGA GGCCGTGCGC 540 GTTCCCGGGG CTGGCGCGGA GGTGGGGTCA GCGGCGCGGG AGAACGCCCC GCCCCGCTAC 600 CGCCAGCCCG GAAGACCCAC GGCGGCGGGC GCTGGCGTCA CGGGTTTCCA CTGGGGCCCC 660 GGCGCCGGGG CCGGGATTCC CTGGCGCAGG AACGCCCGTG ACGGCGGCGC CTGCCTGCGT 720 CGGCCACGCT GGGAGGTTTG AGCCTGGGGA TGACATCAGC CCCTGCGTTT CTGGAGCTGG 780 CCCGGGCGGG ACGGGGACTT GGAGAAAGCA GTGACACCCA CTTTCGTTGA CTGCCAACCC 840 GTGCAGAGCG CTTAGTGCGT GTCCGACCGT GAGCTGAGCG CTGTGATGCG GGTGCTGTTA 900 ATGTCCCATT GCACAGATGG GGAAACTGAG GCCGGCGCAC TGCCCGCCCC GCCGGGCCCC 960 CAGAGTGAGG GCCCGGGGCT GGGAGCAGCC TTTTCCCAGC GCCCTCTGCA GTGTAGAGTC 1020 CCACCAGCTT GTCTCCCGCT CTCTCCTGCA CAAGCCGGCT CAGAGAGGGT CTGCGGGTGT 1080 CCTGGCACCA CCCAGCAAGT TGGGTGCTGC AGCCAGCTCT GTCCATACAG TTGGTCTCTG 1140 CCCAGCTGCG GTGGCCAGGG GCGGTGCCTG AGCCAGGGCG CCCGGGCGGC CCGGTGGGGT 1200 GTGCCCAGCC GCTGCCTTCC TGCTGACGCC GGTGCCAAGG GATCTAAATA TAGCCTGGGA 1260 GGAGGCAAGG GCTATTTTTA ACGCGAGTGG CTTGGCCCCT CCCAGTTCCC GGGTCAGGAG 1320 CCCTTTGGTC CAGGATTTTG GGGAGGGGCA GGGGCGAGGG GGAGCCAGGG GCCCCACACC 1380 CGCCTGGGCC TGCCCCTCTG CCCACACCTG GCCCTGGAAG ACTCTAGGGG ACGAAGGGCC 1440 GTAGAGGGAG GGCAGGGTGG GGGGGCTGTC GCAGGTCACC TTTCTTAAAC GCCACCTCCT 1500 CTCTAGCTGC CGACCAGCCC TGGCCTTTTG TTGGGCCCAG AGACTGCTTT CTATTTTGGG 1560 AAGGTGTTGG AATAATTTCC TTGGCTATTT TTAGCCGGTT CGGGGATTCC TCCACTCAGG 1620 CTGGCCGCCC TGCCTCTCCT CCTCCTCCTC CTCCTCCTAG TCGTCTTCCT CCTCCCGGCA 1680 GACCCAAGGG CGGCCTCCTT CATGGAGGGC AGTCAGGGAC ACACAGTCCC TGAGCCAGAC 1740 CCAGAATGGG GAGACCCCTA TATTTCCTGG GTCGGGGAGG GAAGGGAGCT CTGAAGGGCG 1800 TTCCCACGTT CCAGGTGAGC AGGACTTTCA GACCTCTGGG AATCCATGAC GCCAGGTATC 1860 TGAATTCTGT CTCCAGGGCA GGGTGGGGCG ACCCAGCAGC CTCTGACCTT TCACCTCCTT 1920 TCAGGGTTGT CACAGGAAAG TGGCCTGCTG AGAACAGACC TTGACTCCCA CATCCCTAGG 1980 CTAGGGGCTC CCATGTTCCC AAGAGGAAGA TCAGTGTGAT GAGGGTAAAC TGAGGCACAG 2040 AGGGGACACT GGGATGGGAC ACATCTTGGG CTCATTCCCT GATGGTTTCA TTTCCTTCCA 2100 CATTCTACCT TTGTTTTTAA TTTTTTTTTT TGATTGTTTT GAGACAAGAC GGAGTCTCAC 2160 TCTGTCACCC AGGCTGGAAG AGTATGCAGT 2190
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