Tag | Content |
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EnhancerAtlas ID | HS161-06204 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr16:88365510-88368500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr16:88365815-88365829 | GGAAAATGACTCAT | + | 6.76 | NFE2L1 | MA0089.2 | chr16:88366879-88366894 | CTTGCTGAGTCACGG | - | 6.39 | NFE2L1 | MA0089.2 | chr16:88366925-88366940 | CTTGCTGAGTCACGG | - | 6.39 | NFE2L1 | MA0089.2 | chr16:88366971-88366986 | CTTGCTGAGTCACGG | - | 6.39 | NFE2L1 | MA0089.2 | chr16:88367017-88367032 | CTTGCTGAGTCACGG | - | 6.39 | NFE2L1 | MA0089.2 | chr16:88367063-88367078 | CTTGCTGAGTCACGG | - | 6.39 | NFE2L1 | MA0089.2 | chr16:88367109-88367124 | CTTGCTGAGTCACGG | - | 6.39 | NFE2L1 | MA0089.2 | chr16:88367155-88367170 | CTTGCTGAGTCATGG | - | 6.93 | Nfe2l2 | MA0150.2 | chr16:88366881-88366896 | TGCTGAGTCACGGAA | - | 6.12 | Nfe2l2 | MA0150.2 | chr16:88366927-88366942 | TGCTGAGTCACGGAA | - | 6.12 | Nfe2l2 | MA0150.2 | chr16:88366973-88366988 | TGCTGAGTCACGGAA | - | 6.12 | Nfe2l2 | MA0150.2 | chr16:88367019-88367034 | TGCTGAGTCACGGAA | - | 6.12 | Nfe2l2 | MA0150.2 | chr16:88367065-88367080 | TGCTGAGTCACGGAA | - | 6.12 | Nfe2l2 | MA0150.2 | chr16:88367111-88367126 | TGCTGAGTCACGGAA | - | 6.12 | Nfe2l2 | MA0150.2 | chr16:88367157-88367172 | TGCTGAGTCATGGAA | - | 6.59 | Nr2f6(var.2) | MA0728.1 | chr16:88368190-88368205 | AGGTTCAAAAGGTCA | + | 6.54 | PLAG1 | MA0163.1 | chr16:88367174-88367188 | GGGGCCCACGGGTG | + | 6.72 | RARA | MA0729.1 | chr16:88368190-88368208 | AGGTTCAAAAGGTCAAAC | + | 6.16 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_37096 | chr16:88363014-88367885 | HSMMtube | SE_37096 | chr16:88367971-88369937 | HSMMtube | SE_40317 | chr16:88364946-88368976 | K562 | SE_52151 | chr16:88363221-88368143 | Skeletal_Muscle_Myoblast | SE_63934 | chr16:88363127-88369465 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I088329 | chr16 | 88363452 | 88369472 |
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Enhancer Sequence | AGCTCAGGAT GCAGGCTTTA GGAGTAGCCC CCTCCTCATT CACAGGAATA TGAAGGCCTG 60 GCATGGCAGT GACTTGCCCA AGGCCACTGT GCCAAGAGCA GAGCTGGGTT TGACCCTCTG 120 TCTCCGCATG GCCCTTGGCA GCCCCCGAGT CCCCTTTGGC AGATAGCTTT CCTCACAGCC 180 CTGAGGACAG GCATGATGGG ACAGGGAGTC TCTCTCCACC CCCTCCTTGG TGTTTAGTTG 240 ACATCAGTAA AGCCACCGAA GGAATCTTTC AGAAATAAAC AAAGTTGCAT TTTTTGACAG 300 AGGATGGAAA ATGACTCATA GGAAATCAGC ATTCCAAGTG CACTACCCCA TTAGGTATTA 360 AGCGGGTCGG GTTTCGGCAC AGCGTCCAAG AATGCTGTGG CTTATTGCAG GAGGATGACA 420 CCGTCTGTGT GGGGAGCTGG CGCGGGTGCC TGAGGCCTGG AAGCACCCGT GGGAACCCAT 480 GATGTGCCGT CACCGCGTGC CCTGCCCCCT CTGTGCCGGC TCTCCTGGCA GTGCTGAGCA 540 CCGCCACGCT TGGGCACAGC CTTGCCGCTG GCCCTGGCCT TGAGCAAGGT CCTTGCAGCA 600 TCACTGGATG CTGGGTTCTA ATTTGGCTCT GAATCTGACT TGCAGGTTTG GGCCATTCCA 660 GAAGAATAAA CCTTTCTGTG TGCACCTCTG GCAGGCAGCC ACCTGGCATA GGCCATGTGA 720 GGCAGGGAGA GGGAAGGCAC CATGAAAATC AACAAAGCAA GTCCTCCCCT AAGGGACTCC 780 AGAACCCGTG GGTTGAGATG GGCAGGATGG GGGAGGGGGG GCTGCTGGGA ACAGGGTGAG 840 GGCCCCCAGC ACCACTGCTC AGGCCGGCTC TCACAGCCTG CAAACCCTTC CCACAAGACT 900 CCACACAAGC AGCCTCTGCA GCCAGCCTCC TCACCGTTTC ACAGACGAGA AGACCAAGGC 960 CCCGGGTTGC CCCTTGAGTC TGGGCACTGG AGACCCAGTC ATGCTGCTTT CCAGCCCATG 1020 ACCTTCCCAC CCCCCTGTCA GAGCCACCGA GCTGTGTCCC CAGGAGCCAC GTCCCTGCCC 1080 AGCCTCTGTG GCACCCAGAG GTGCACTCTG GCACCAGGAC ACACCCCGTG GGTCCTTGTG 1140 CTGCTGCTCA TTGGTGATTT GGCGGTAAAC CTTAGAGGGA GGAGGCCTGC TGGGATCATG 1200 TGCCCACTGC CCATGCTGTG GCCTCTGTGG GCAAAGCGAG TGTCCCCACA TCCACCGTCC 1260 ATCCGTGAGT CCCCTGCTTG ATGCTTCCTG AGAGCCTCCA CCCACCCAGA GGGAAACCAG 1320 GTGTGGTCTC CAAGCCGGTG GGTACGGCCA GGGGAGAGAA GGCTCCGGAC TTGCTGAGTC 1380 ACGGAAGAGG GGCCCATGGG TGGAGAAGGC TCGGACTTGC TGAGTCACGG AAGAGGGGCC 1440 CATGGGTGGA GAAGGCTCGG ACTTGCTGAG TCACGGAAGA GGGGCCCATG GGTGGAGAAG 1500 GCTCGGACTT GCTGAGTCAC GGAAGAGGGG CCCATGGGTG GAGAAGGCTC GGACTTGCTG 1560 AGTCACGGAA GAGGGGCCCA TGGGTGGAGA AGGCTCGGAC TTGCTGAGTC ACGGAAGAGG 1620 GGCCCATGGG TGGAGAAGGC TCGGACTTGC TGAGTCATGG AAGAGGGGCC CACGGGTGAC 1680 TGAGCGACAG TTACAACTTG GAGACATTTC CTTCCAGCAA AGATGCAAAG GTGGGGCATG 1740 AAGGCAGGAG CACGGAAGTC TTTGCATGTG TGGCCGGGGC TGCCTGCCCA GGGAAGGCAT 1800 TTTCATTCTT CCCACGGATG CGGGCCCGCG AGGTGGGGCT GGTAGTAAAG ATCCCGAGGA 1860 GAATAAAAAC ACACCAAGAA CCGGAGCACT TCACACACTT GAGCAAGGGA GAGTGACGGC 1920 TGCGTGGCAG GGGGTGGGGG GGACGTGGGG GCAGTTGCAG TGTGTGTGTG TGTGTTTGTG 1980 TGTCTGTGTG TGTGTTTTTG TGCATCTGTG TGTGTCTGTG TGTGTCTACA TGTGTATGTG 2040 TTTGTGTGTC TGCATGTGTG TCTGTGTGCA TCTGTGTGTA TCTGTGTGTG TCTGTGTCTA 2100 TGTGTTTGTG TGTGTGTGTC TGTGTGTGCA TGTGTGTCTC TGTGTGTCTG TGTCTGTGTG 2160 TGTCTGTGTG TGTGTGTCTA TGTGCATGTG TATGTCTGTG TCTGTGTGTC TGTGTCTGTG 2220 TGTGTGCCCA AGGGAGGCAG GCGTGAAGCT AAGGAAGTCT TGCTCTGTGT TACAAATGTC 2280 ACTCCCTTTC CTAAGAGACC AAAGAGTTAA GAAATTTTTC AGGTTTGTTG AGATGCTGGA 2340 CTAAGCTGGA CTAAGCCTCC TGTGAATGCC CCCTTTGAAA AAAATTCTGG GGATGGATGG 2400 TAAAAAACAA CAACAACAAT CTTACCTGAA ACGCTCGGGA CCAGAAGTGT TTTGGTTTTG 2460 ATTTTTGTCA CATTTGGGAA TGTTTGCCTT ACGCTGACCA GTTGAGCATC CCTGACCCAG 2520 CATCTGAAAT CAGACATGCT CCAGGGAGCA TTTCCCAAGA GCATCATGTC AGAGCTCAAA 2580 CAATTTTGGG TTCTGGGGCA TTTTGGGTTA GGGATACTCA ACCTGTATGA CCCAGGGTGT 2640 GCACACATCA CAGAGCCGGG AGTGATTCAT CTGTCCCAGA AGGTTCAAAA GGTCAAACTG 2700 TGACCAATTC ATGTCCACCT GGAGCCGATG ACTGTGGCCT TATTTCATAT AAGGGTGTCG 2760 GCAGATATGA TTGCACTAAA GATCTCAAGA TGAGGTTGTC CTGGACCAGG GTGGGGCCTA 2820 AATCCTATGA AAGCGTCATA AGGAAAAGGG AGCCTGAGAT GGGAAGATGC CGACGGGAGG 2880 ACACACATGT GATGGATACA GATGAGGGAG CCGTGTGGGA AGATGCCGAC GGGAGGACAC 2940 ATGTGACAGA GACGGACGTG GGAGCCGTGA AGGAAGATGC CGACGGAACG 2990
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