Tag | Content |
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EnhancerAtlas ID | HS157-05696 |
Organism | Homo sapiens |
Tissue/cell | PANC-1 |
Coordinate | chr17:989840-992180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF14 | MA0740.1 | chr17:990825-990839 | AAGGGGGCGGGGCC | - | 6.15 | KLF16 | MA0741.1 | chr17:990827-990838 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr17:990828-990838 | GGGGCGGGGC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr17:989959-989974 | TGAACTCCTGACCTC | - | 6.22 | Nr2f6(var.2) | MA0728.1 | chr17:992047-992062 | TGAACTCCTGACCTC | - | 6.22 | RREB1 | MA0073.1 | chr17:990546-990566 | GGGTGGGGGTAGGGGTGGGG | - | 6.27 | SP4 | MA0685.1 | chr17:990778-990795 | AAAGAGGGCGGGGCCTG | - | 6.24 | SP4 | MA0685.1 | chr17:990824-990841 | AAAGGGGGCGGGGCCGG | - | 6.54 | Stat4 | MA0518.1 | chr17:990958-990972 | CTTCCAGGAAAAGG | + | 6.67 | ZNF263 | MA0528.1 | chr17:990285-990306 | GAGGGAGGAGGGAGGGGAGAC | + | 6.79 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_01841 | chr17:990015-991936 | Aorta | SE_23220 | chr17:990087-991720 | Colon_Crypt_1 | SE_23794 | chr17:990282-991706 | Colon_Crypt_2 | SE_24832 | chr17:990194-991785 | Colon_Crypt_3 | SE_26634 | chr17:989867-991898 | Esophagus | SE_28034 | chr17:989906-991951 | Fetal_Intestine | SE_29195 | chr17:990014-992004 | Fetal_Intestine_Large | SE_31579 | chr17:989866-992999 | Gastric | SE_40640 | chr17:989922-991977 | Left_Ventricle | SE_42080 | chr17:990188-991700 | LNCaP | SE_42145 | chr17:989917-991877 | Lung | SE_49097 | chr17:990322-991723 | Right_Atrium | SE_49495 | chr17:990311-991745 | Right_Ventricle | SE_50313 | chr17:990063-991915 | Sigmoid_Colon | SE_52631 | chr17:990132-991707 | Small_Intestine | SE_54272 | chr17:990363-991768 | Spleen | SE_65254 | chr17:989820-995951 | 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 |
chr17 | 990609 | 991624 | chr17 | 990720 | 991732 |
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| Number: 2 | ID | Chromosome | Start | End |
GH17I001086 | chr17 | 990011 | 992101 | GH17I001088 | chr17 | 992161 | 993042 |
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Enhancer Sequence | AGTGATTCTC CTGCCTCAGC CTCCTGACTA ACTGGGACTA CAGGCACGCA CCACCACACC 60 CGGCTAGTTT TTGTATTTTT AGTAGAGACA GGGTTTCGTC ATATTGGTCA GGCTGGTCTT 120 GAACTCCTGA CCTCAGGTGA TCCACCCGCC TCCGCCTCCC AAAGTGCTGG GATTACGGGC 180 GTGAGCCACC ACGCCTGGCT TAGACACATT TTTAAAGTAC ATGCAGCTGG GAGCTGTGGT 240 ACACACACCT ATAGCCCTCG CTACTTGGGA GACTGAGGTG GGAGGATCAC TTGAGCCCGA 300 GTTCAAGTCC AGCCTGGACA ACATAGCAAG ACCTTTTTTT TTTTTTAAAG TACAGGCCAA 360 CCCAAAATAG ATACAGATAT GTAGTAAACA CACAAACTGC AGTCTGGAAG GCTATCCACC 420 AAATTCATGC CAGTAGCTGC TTCAAGAGGG AGGAGGGAGG GGAGACTCCA CCTTCATGTG 480 TGACGCTGTA TTTTCTTCAT TAGAAGGTTC TGCTGTTATT CTTTGGAGTT TCTGGTTTAA 540 ATGTTTTTCA ATACAGCAGC AAGGGGGATA CAGCTGCTGC CTGGCTTCCT CAGGGGCCTC 600 TGCTTCCCAC CAAGGTGCTG GGGGAAGTGG GCTGCTGTGG ACCCCCACCC CGGACCACTC 660 TGCTTTCTGC AGGATCCTCA TGCTCCCCAA GGACCCAGAG AGGCTGGGGT GGGGGTAGGG 720 GTGGGGGCAG GCTGGCCGCA GCATCGGCTG AGCCTGGAGC CTCCCAGTAC AGAGGCAGAG 780 CCCTTTGAGG AAGCTGGTGG GGCAGGGGAG CGGGGGGCAT CTGGAAAAGC CAGAGGGGAG 840 CGCGAGTGGG GACGCCCGGC GTGACGCCAA GGCCAGAGGC ATTCAGGTCT CAGCTGCAGA 900 AGGGCAGGAC TTTAAAAGGG GGCAGGGCCG GACTTTTAAA AGAGGGCGGG GCCTGAGTTT 960 TAAAGGGGGT GGGGCCTGAC CTTAAAAGGG GGCGGGGCCG GACGGGAGGG AGTTTATTTC 1020 CTTTTCCAGG GAGTACTGAG GCCCGGCCCA TCAATGCCCA CGCTACACGA GGCATACTAG 1080 ACAGTCGCTG CCTAAGCCAA AGTCAGATCA CCGATATTCT TCCAGGAAAA GGCTCCTCTT 1140 GCCCCCTTTC CCACAAGAAG GAGAAAGCCT GGAGGCCCGG GTTGGCACAC CACCCTCCCA 1200 GGAGCCAGGG GCAGGAGCCA GCCGTGCGGA GGCCTGCGTC CAGGGTCACG GTAATCTCAG 1260 GGACTGCCGC TGCCACAGTC ACCCCAGGCG GTAGGGCCCG AGGCCTGGCT TGGCAGGTTC 1320 ATTAACTGGG AAGTGCAGGT TGCCTGGAAA CAGCAGCCTG GCACTGGAGT GATCTCATAA 1380 AACAAACAGC AGAGACGCTA ATTCCCTTCT CTCAGTAACG AATAATCAAA TACCCAGAGT 1440 CTTCGGCTGA AAATAAACCA CCTCCGGATG CCAGACCTGA CCCGGCTCCC CCCGGGCCCT 1500 CCCAAATCTG CAGCCCCAGG GGCCTCAGGC ATCGGTTCAC GATGCTGGGG AGGGAAAGTG 1560 GTGGGTAGCA GATTCACGGC CAGGCCTGTG GAGCCAAGAC CAGAACCGGG GACAGCCAGG 1620 TCCAAGTGAC AAAGATAAAC TGTGACAGCG TTTCCAGCAA CCCTAGGTTT GCTCTCCTCT 1680 ACCCTCCTGA GGGATGAGGA GAGGATGCCC CCCAGGCCAC TCAGCTCAGG TGAGCAGGCA 1740 GTGATGACAG GTGTTCACCA TCCCTGAACC GGAGGGAGCA GGGGGGGGTA TGCTAGAACC 1800 AGAGTGTGGC ATTCCCTTGG AAGGATACCT TCCAGGGTGC CTCTTCCCAA TTTAATAATA 1860 ATAATAATAA TAATAATAAT AATAATAATA ATAATGGCAC TGATGATAAT GACCAGTTAT 1920 TGAGTACTTA TTAATTTATG ATGTTCCAGG CCCTGTTCCA AGCACTTTTT CTTTTACTTT 1980 ATTGTATTCT ATTTCTTTTT TTGAGACAGA GTCTTGCTCT TGTCGCCCAG GCTGGAGTGG 2040 AGTGGCACGA TCTCGGCTCA CTACAACCTC TGCCTCCCGA GTTCAAGCGA TTCTCCCACC 2100 TCAGCCTCCC GAGTAGTAGC TGGGATCACA GGTGCGTGTT ATCATGCCCG GCTAATTTTT 2160 GTATTTTTAG TAGAAACGGG GTTTCACCAT GTTGGCCAAG CTGGTCTTGA ACTCCTGACC 2220 TCAGGTGATC CGCCCACCTT GGCCTCCCAA AGTGTTGCTG GGATTATAAG CGTGAGCCAC 2280 TGTGCCCAGC CATTTTTTTT TTTTTTTTTT TTTGAGACAG AGTCTCAGTC TGTCATCCAG 2340
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