Tag | Content |
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EnhancerAtlas ID | HS023-12116 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr19:2493810-2496530 |
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 | TGCTACGTGC ATTTACCTCC TGGTCTCTGT GTGCTCCTAA GTTGTGTATT TCTTTCAGAT 60 AGTACCAAGA GAAGTGAGGT TGCTGGGTCC CCGTAACCTT ATAGGGTAAA TACTATTATT 120 ACATCCACTT TGTTGATCGG GAGAATAGAC GCCGCCAGGC CTCCTGTCTC TCGCTTTCAC 180 ACAAAGGCAC ATACGGCAGA CACGGACCCC CATCACTCAT CCATCACTTT CCCATCACTC 240 ACCGCAGACC CTCCAGGACC CACGCAGAAA CCCAGGGCTC CCCCACGGTG CACGCAGCAC 300 CCAGGCTGCC CGCCCTCCAC CCAGGGCCGC GTCACGCCCG ACACCCCCGG AACAGACGCC 360 TATGAGGCCT GCAGCTCCAG ACGGGCTGCA GACACACAGC GATTTGTTCA TCTTTCCAGC 420 CACCCCGTCT GGTCCTGACA GTAATTAGCT CCCAGACTGG TGGGGAGACG GTGAACAGCC 480 TGAGAGTCAT CGCCCACGGC TCCACGCCCA CAGGCCACGG GCACCGGGAG AGAGGGTGAA 540 TGAGTGTGTG TGTGTGTGTG AGTGTGTGTG TCCGGAATCT GTACTCTCCA GCCAGGGCTC 600 CCCATCCTCC TGCAAAGGGC CAGCACCGTG CACGGGTACC CACGGCGCCT TCCAAGGGGA 660 ACGTGCACAG GCATACCCAC TGTTCATTCC ACGAAGGATC GTGCACACGC ATGCCTACCT 720 TTGCATTTCA CGCGGGATTG TGCACACGCA TGTCCACCGT GCCTTCCACG CGGGATCGTG 780 CACACGCATG TCCACGAACT CCTGCACACC TACACCCACC AGGCCTGCCC ATGCGATGCG 840 TCCCTGCAGA CCCACTGTGG ACGCCTGCTT GTCGGCGTCC TGCGCATCCC GCGTGAGTGG 900 AGTGTGCACT CGTGGAGGGG GCGACTGAGT GCGGGGCAAG CGCAAGCGCA AGCACACTGG 960 GCTCGCGGAG GGTGGAGAGA GGCCGTGCGC GTTCCCGGGG CTGGCGCGGA GGTGGGGTCA 1020 GCGGCGCGGG AGAACGCCCC GCCCCGCTAC CGCCAGCCCG GAAGACCCAC GGCGGCGGGC 1080 GCTGGCGTCA CGGGTTTCCA CTGGGGCCCC GGCGCCGGGG CCGGGATTCC CTGGCGCAGG 1140 AACGCCCGTG ACGGCGGCGC CTGCCTGCGT CGGCCACGCT GGGAGGTTTG AGCCTGGGGA 1200 TGACATCAGC CCCTGCGTTT CTGGAGCTGG CCCGGGCGGG ACGGGGACTT GGAGAAAGCA 1260 GTGACACCCA CTTTCGTTGA CTGCCAACCC GTGCAGAGCG CTTAGTGCGT GTCCGACCGT 1320 GAGCTGAGCG CTGTGATGCG GGTGCTGTTA ATGTCCCATT GCACAGATGG GGAAACTGAG 1380 GCCGGCGCAC TGCCCGCCCC GCCGGGCCCC CAGAGTGAGG GCCCGGGGCT GGGAGCAGCC 1440 TTTTCCCAGC GCCCTCTGCA GTGTAGAGTC CCACCAGCTT GTCTCCCGCT CTCTCCTGCA 1500 CAAGCCGGCT CAGAGAGGGT CTGCGGGTGT CCTGGCACCA CCCAGCAAGT TGGGTGCTGC 1560 AGCCAGCTCT GTCCATACAG TTGGTCTCTG CCCAGCTGCG GTGGCCAGGG GCGGTGCCTG 1620 AGCCAGGGCG CCCGGGCGGC CCGGTGGGGT GTGCCCAGCC GCTGCCTTCC TGCTGACGCC 1680 GGTGCCAAGG GATCTAAATA TAGCCTGGGA GGAGGCAAGG GCTATTTTTA ACGCGAGTGG 1740 CTTGGCCCCT CCCAGTTCCC GGGTCAGGAG CCCTTTGGTC CAGGATTTTG GGGAGGGGCA 1800 GGGGCGAGGG GGAGCCAGGG GCCCCACACC CGCCTGGGCC TGCCCCTCTG CCCACACCTG 1860 GCCCTGGAAG ACTCTAGGGG ACGAAGGGCC GTAGAGGGAG GGCAGGGTGG GGGGGCTGTC 1920 GCAGGTCACC TTTCTTAAAC GCCACCTCCT CTCTAGCTGC CGACCAGCCC TGGCCTTTTG 1980 TTGGGCCCAG AGACTGCTTT CTATTTTGGG AAGGTGTTGG AATAATTTCC TTGGCTATTT 2040 TTAGCCGGTT CGGGGATTCC TCCACTCAGG CTGGCCGCCC TGCCTCTCCT CCTCCTCCTC 2100 CTCCTCCTAG TCGTCTTCCT CCTCCCGGCA GACCCAAGGG CGGCCTCCTT CATGGAGGGC 2160 AGTCAGGGAC ACACAGTCCC TGAGCCAGAC CCAGAATGGG GAGACCCCTA TATTTCCTGG 2220 GTCGGGGAGG GAAGGGAGCT CTGAAGGGCG TTCCCACGTT CCAGGTGAGC AGGACTTTCA 2280 GACCTCTGGG AATCCATGAC GCCAGGTATC TGAATTCTGT CTCCAGGGCA GGGTGGGGCG 2340 ACCCAGCAGC CTCTGACCTT TCACCTCCTT TCAGGGTTGT CACAGGAAAG TGGCCTGCTG 2400 AGAACAGACC TTGACTCCCA CATCCCTAGG CTAGGGGCTC CCATGTTCCC AAGAGGAAGA 2460 TCAGTGTGAT GAGGGTAAAC TGAGGCACAG AGGGGACACT GGGATGGGAC ACATCTTGGG 2520 CTCATTCCCT GATGGTTTCA TTTCCTTCCA CATTCTACCT TTGTTTTTAA TTTTTTTTTT 2580 TGATTGTTTT GAGACAAGAC GGAGTCTCAC TCTGTCACCC AGGCTGGAAG AGTATGCAGT 2640 GGCACAATCT CGGCTCTCTG CAACCTCTGT CCTCTGGGTT CAAGCGATTC TCCAGCTTCA 2700 GCCCCCTGAG TAGCTGGGAT 2720
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