Tag | Content |
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EnhancerAtlas ID | HS085-01487 |
Organism | Homo sapiens |
Tissue/cell | Heart |
Coordinate | chr19:2493800-2496470 |
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 | GGAACAAAGC TGCTACGTGC ATTTACCTCC TGGTCTCTGT GTGCTCCTAA GTTGTGTATT 60 TCTTTCAGAT AGTACCAAGA GAAGTGAGGT TGCTGGGTCC CCGTAACCTT ATAGGGTAAA 120 TACTATTATT ACATCCACTT TGTTGATCGG GAGAATAGAC GCCGCCAGGC CTCCTGTCTC 180 TCGCTTTCAC ACAAAGGCAC ATACGGCAGA CACGGACCCC CATCACTCAT CCATCACTTT 240 CCCATCACTC ACCGCAGACC CTCCAGGACC CACGCAGAAA CCCAGGGCTC CCCCACGGTG 300 CACGCAGCAC CCAGGCTGCC CGCCCTCCAC CCAGGGCCGC GTCACGCCCG ACACCCCCGG 360 AACAGACGCC TATGAGGCCT GCAGCTCCAG ACGGGCTGCA GACACACAGC GATTTGTTCA 420 TCTTTCCAGC CACCCCGTCT GGTCCTGACA GTAATTAGCT CCCAGACTGG TGGGGAGACG 480 GTGAACAGCC TGAGAGTCAT CGCCCACGGC TCCACGCCCA CAGGCCACGG GCACCGGGAG 540 AGAGGGTGAA TGAGTGTGTG TGTGTGTGTG AGTGTGTGTG TCCGGAATCT GTACTCTCCA 600 GCCAGGGCTC CCCATCCTCC TGCAAAGGGC CAGCACCGTG CACGGGTACC CACGGCGCCT 660 TCCAAGGGGA ACGTGCACAG GCATACCCAC TGTTCATTCC ACGAAGGATC GTGCACACGC 720 ATGCCTACCT TTGCATTTCA CGCGGGATTG TGCACACGCA TGTCCACCGT GCCTTCCACG 780 CGGGATCGTG CACACGCATG TCCACGAACT CCTGCACACC TACACCCACC AGGCCTGCCC 840 ATGCGATGCG TCCCTGCAGA CCCACTGTGG ACGCCTGCTT GTCGGCGTCC TGCGCATCCC 900 GCGTGAGTGG AGTGTGCACT CGTGGAGGGG GCGACTGAGT GCGGGGCAAG CGCAAGCGCA 960 AGCACACTGG GCTCGCGGAG GGTGGAGAGA GGCCGTGCGC GTTCCCGGGG CTGGCGCGGA 1020 GGTGGGGTCA GCGGCGCGGG AGAACGCCCC GCCCCGCTAC CGCCAGCCCG GAAGACCCAC 1080 GGCGGCGGGC GCTGGCGTCA CGGGTTTCCA CTGGGGCCCC GGCGCCGGGG CCGGGATTCC 1140 CTGGCGCAGG AACGCCCGTG ACGGCGGCGC CTGCCTGCGT CGGCCACGCT GGGAGGTTTG 1200 AGCCTGGGGA TGACATCAGC CCCTGCGTTT CTGGAGCTGG CCCGGGCGGG ACGGGGACTT 1260 GGAGAAAGCA GTGACACCCA CTTTCGTTGA CTGCCAACCC GTGCAGAGCG CTTAGTGCGT 1320 GTCCGACCGT GAGCTGAGCG CTGTGATGCG GGTGCTGTTA ATGTCCCATT GCACAGATGG 1380 GGAAACTGAG GCCGGCGCAC TGCCCGCCCC GCCGGGCCCC CAGAGTGAGG GCCCGGGGCT 1440 GGGAGCAGCC TTTTCCCAGC GCCCTCTGCA GTGTAGAGTC CCACCAGCTT GTCTCCCGCT 1500 CTCTCCTGCA CAAGCCGGCT CAGAGAGGGT CTGCGGGTGT CCTGGCACCA CCCAGCAAGT 1560 TGGGTGCTGC AGCCAGCTCT GTCCATACAG TTGGTCTCTG CCCAGCTGCG GTGGCCAGGG 1620 GCGGTGCCTG AGCCAGGGCG CCCGGGCGGC CCGGTGGGGT GTGCCCAGCC GCTGCCTTCC 1680 TGCTGACGCC GGTGCCAAGG GATCTAAATA TAGCCTGGGA GGAGGCAAGG GCTATTTTTA 1740 ACGCGAGTGG CTTGGCCCCT CCCAGTTCCC GGGTCAGGAG CCCTTTGGTC CAGGATTTTG 1800 GGGAGGGGCA GGGGCGAGGG GGAGCCAGGG GCCCCACACC CGCCTGGGCC TGCCCCTCTG 1860 CCCACACCTG GCCCTGGAAG ACTCTAGGGG ACGAAGGGCC GTAGAGGGAG GGCAGGGTGG 1920 GGGGGCTGTC GCAGGTCACC TTTCTTAAAC GCCACCTCCT CTCTAGCTGC CGACCAGCCC 1980 TGGCCTTTTG TTGGGCCCAG AGACTGCTTT CTATTTTGGG AAGGTGTTGG AATAATTTCC 2040 TTGGCTATTT TTAGCCGGTT CGGGGATTCC TCCACTCAGG CTGGCCGCCC TGCCTCTCCT 2100 CCTCCTCCTC CTCCTCCTAG TCGTCTTCCT CCTCCCGGCA GACCCAAGGG CGGCCTCCTT 2160 CATGGAGGGC AGTCAGGGAC ACACAGTCCC TGAGCCAGAC CCAGAATGGG GAGACCCCTA 2220 TATTTCCTGG GTCGGGGAGG GAAGGGAGCT CTGAAGGGCG TTCCCACGTT CCAGGTGAGC 2280 AGGACTTTCA GACCTCTGGG AATCCATGAC GCCAGGTATC TGAATTCTGT CTCCAGGGCA 2340 GGGTGGGGCG ACCCAGCAGC CTCTGACCTT TCACCTCCTT TCAGGGTTGT CACAGGAAAG 2400 TGGCCTGCTG AGAACAGACC TTGACTCCCA CATCCCTAGG CTAGGGGCTC CCATGTTCCC 2460 AAGAGGAAGA TCAGTGTGAT GAGGGTAAAC TGAGGCACAG AGGGGACACT GGGATGGGAC 2520 ACATCTTGGG CTCATTCCCT GATGGTTTCA TTTCCTTCCA CATTCTACCT TTGTTTTTAA 2580 TTTTTTTTTT TGATTGTTTT GAGACAAGAC GGAGTCTCAC TCTGTCACCC AGGCTGGAAG 2640 AGTATGCAGT GGCACAATCT CGGCTCTCTG 2670
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