Tag | Content |
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EnhancerAtlas ID | HS145-11396 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr19:2493690-2496250 |
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 | 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 | CGAGTGCGTT CCTCTTGACT GCTGAACTTT CATTCTATGA ACCGACCTCC GTTGACCTGT 60 TCCCCTCTGA ATGGAGGGGT ATTTGAGCTC TTCCCAGGTT TTGGTGATGA GGAACAAAGC 120 TGCTACGTGC ATTTACCTCC TGGTCTCTGT GTGCTCCTAA GTTGTGTATT TCTTTCAGAT 180 AGTACCAAGA GAAGTGAGGT TGCTGGGTCC CCGTAACCTT ATAGGGTAAA TACTATTATT 240 ACATCCACTT TGTTGATCGG GAGAATAGAC GCCGCCAGGC CTCCTGTCTC TCGCTTTCAC 300 ACAAAGGCAC ATACGGCAGA CACGGACCCC CATCACTCAT CCATCACTTT CCCATCACTC 360 ACCGCAGACC CTCCAGGACC CACGCAGAAA CCCAGGGCTC CCCCACGGTG CACGCAGCAC 420 CCAGGCTGCC CGCCCTCCAC CCAGGGCCGC GTCACGCCCG ACACCCCCGG AACAGACGCC 480 TATGAGGCCT GCAGCTCCAG ACGGGCTGCA GACACACAGC GATTTGTTCA TCTTTCCAGC 540 CACCCCGTCT GGTCCTGACA GTAATTAGCT CCCAGACTGG TGGGGAGACG GTGAACAGCC 600 TGAGAGTCAT CGCCCACGGC TCCACGCCCA CAGGCCACGG GCACCGGGAG AGAGGGTGAA 660 TGAGTGTGTG TGTGTGTGTG AGTGTGTGTG TCCGGAATCT GTACTCTCCA GCCAGGGCTC 720 CCCATCCTCC TGCAAAGGGC CAGCACCGTG CACGGGTACC CACGGCGCCT TCCAAGGGGA 780 ACGTGCACAG GCATACCCAC TGTTCATTCC ACGAAGGATC GTGCACACGC ATGCCTACCT 840 TTGCATTTCA CGCGGGATTG TGCACACGCA TGTCCACCGT GCCTTCCACG CGGGATCGTG 900 CACACGCATG TCCACGAACT CCTGCACACC TACACCCACC AGGCCTGCCC ATGCGATGCG 960 TCCCTGCAGA CCCACTGTGG ACGCCTGCTT GTCGGCGTCC TGCGCATCCC GCGTGAGTGG 1020 AGTGTGCACT CGTGGAGGGG GCGACTGAGT GCGGGGCAAG CGCAAGCGCA AGCACACTGG 1080 GCTCGCGGAG GGTGGAGAGA GGCCGTGCGC GTTCCCGGGG CTGGCGCGGA GGTGGGGTCA 1140 GCGGCGCGGG AGAACGCCCC GCCCCGCTAC CGCCAGCCCG GAAGACCCAC GGCGGCGGGC 1200 GCTGGCGTCA CGGGTTTCCA CTGGGGCCCC GGCGCCGGGG CCGGGATTCC CTGGCGCAGG 1260 AACGCCCGTG ACGGCGGCGC CTGCCTGCGT CGGCCACGCT GGGAGGTTTG AGCCTGGGGA 1320 TGACATCAGC CCCTGCGTTT CTGGAGCTGG CCCGGGCGGG ACGGGGACTT GGAGAAAGCA 1380 GTGACACCCA CTTTCGTTGA CTGCCAACCC GTGCAGAGCG CTTAGTGCGT GTCCGACCGT 1440 GAGCTGAGCG CTGTGATGCG GGTGCTGTTA ATGTCCCATT GCACAGATGG GGAAACTGAG 1500 GCCGGCGCAC TGCCCGCCCC GCCGGGCCCC CAGAGTGAGG GCCCGGGGCT GGGAGCAGCC 1560 TTTTCCCAGC GCCCTCTGCA GTGTAGAGTC CCACCAGCTT GTCTCCCGCT CTCTCCTGCA 1620 CAAGCCGGCT CAGAGAGGGT CTGCGGGTGT CCTGGCACCA CCCAGCAAGT TGGGTGCTGC 1680 AGCCAGCTCT GTCCATACAG TTGGTCTCTG CCCAGCTGCG GTGGCCAGGG GCGGTGCCTG 1740 AGCCAGGGCG CCCGGGCGGC CCGGTGGGGT GTGCCCAGCC GCTGCCTTCC TGCTGACGCC 1800 GGTGCCAAGG GATCTAAATA TAGCCTGGGA GGAGGCAAGG GCTATTTTTA ACGCGAGTGG 1860 CTTGGCCCCT CCCAGTTCCC GGGTCAGGAG CCCTTTGGTC CAGGATTTTG GGGAGGGGCA 1920 GGGGCGAGGG GGAGCCAGGG GCCCCACACC CGCCTGGGCC TGCCCCTCTG CCCACACCTG 1980 GCCCTGGAAG ACTCTAGGGG ACGAAGGGCC GTAGAGGGAG GGCAGGGTGG GGGGGCTGTC 2040 GCAGGTCACC TTTCTTAAAC GCCACCTCCT CTCTAGCTGC CGACCAGCCC TGGCCTTTTG 2100 TTGGGCCCAG AGACTGCTTT CTATTTTGGG AAGGTGTTGG AATAATTTCC TTGGCTATTT 2160 TTAGCCGGTT CGGGGATTCC TCCACTCAGG CTGGCCGCCC TGCCTCTCCT CCTCCTCCTC 2220 CTCCTCCTAG TCGTCTTCCT CCTCCCGGCA GACCCAAGGG CGGCCTCCTT CATGGAGGGC 2280 AGTCAGGGAC ACACAGTCCC TGAGCCAGAC CCAGAATGGG GAGACCCCTA TATTTCCTGG 2340 GTCGGGGAGG GAAGGGAGCT CTGAAGGGCG TTCCCACGTT CCAGGTGAGC AGGACTTTCA 2400 GACCTCTGGG AATCCATGAC GCCAGGTATC TGAATTCTGT CTCCAGGGCA GGGTGGGGCG 2460 ACCCAGCAGC CTCTGACCTT TCACCTCCTT TCAGGGTTGT CACAGGAAAG TGGCCTGCTG 2520 AGAACAGACC TTGACTCCCA CATCCCTAGG CTAGGGGCTC 2560
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