Tag | Content |
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EnhancerAtlas ID | HS023-25768 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr9:132198000-132201220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr9:132200821-132200833 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr9:132200825-132200837 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr9:132200829-132200841 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr9:132200833-132200845 | GTTTGTTTGTTT | + | 6.32 | KLF5 | MA0599.1 | chr9:132198754-132198764 | GGGGCGGGGC | - | 6.02 | Klf12 | MA0742.1 | chr9:132198032-132198047 | AAAGTGGGTGTGGTC | - | 6 | SP2 | MA0516.2 | chr9:132198288-132198305 | CTCACCCCCGCCCCCCT | + | 6.68 | ZEB1 | MA0103.3 | chr9:132200962-132200973 | CCCACCTGCCC | + | 6.14 | ZNF263 | MA0528.1 | chr9:132199563-132199584 | GGGGGAGGGAGGGAAAAAGTA | + | 6.14 | ZNF263 | MA0528.1 | chr9:132199061-132199082 | GCCCCCTCCTCTCCTTCCTCT | - | 6.67 | ZNF263 | MA0528.1 | chr9:132199069-132199090 | CTCTCCTTCCTCTCATCCCCC | - | 6.86 | ZNF263 | MA0528.1 | chr9:132200201-132200222 | GAAGGAGGACAAGGAAGGAGG | + | 7.32 |
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| Number of super-enhancer constituents: 14 | ID | Coordinate | Tissue/cell |
SE_03826 | chr9:132198602-132200840 | Brain_Angular_Gyrus | SE_05879 | chr9:132197530-132201368 | Brain_Hippocampus_Middle | SE_08629 | chr9:132198292-132201334 | Brain_Inferior_Temporal_Lobe | SE_25152 | chr9:132199093-132200668 | Colon_Crypt_3 | SE_26594 | chr9:132199119-132200724 | Esophagus | SE_33461 | chr9:132197505-132200840 | H2171 | SE_34236 | chr9:132200005-132200774 | HCT-116 | SE_46624 | chr9:132198288-132198847 | Ovary | SE_46624 | chr9:132198848-132200736 | Ovary | SE_53365 | chr9:132198838-132200495 | Spleen | SE_55039 | chr9:132198719-132200499 | Stomach_Smooth_Muscle | SE_56735 | chr9:132199701-132200481 | VACO_400 | SE_61500 | chr9:132144538-132260190 | Toledo | SE_65248 | chr9:132197946-132201145 | Pancreatic_islets |
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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: 2 | ID | Chromosome | Start | End |
GH09I129435 | chr9 | 132198059 | 132200616 | GH09I129438 | chr9 | 132200680 | 132201079 |
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Enhancer Sequence | CCCTCTCTGA GCCTCACTTT TTTCTCACCT GTAAAGTGGG TGTGGTCACA GTGAGGACTC 60 CTCGAGGCCT GCATGTCCAG AGCAGAACCG AGCCAGGCAA ACAGAACCAG CGTCATCGTT 120 ATCCCTGTGA CTTTCTGCAA ACTCCAGCCT GCCCTGCCTG TCTCCTGCAG GCGGCTACCT 180 CTGGGCAGGT GCAGGTTTCA GGGTGCATAT GGAGGGGAAG TGATGGTGGG GGTACCCCGT 240 GTTTGCAGAG CTGGCGGGAG ACCACGGCAT TCCTATGGCC CATGTCCCCT CACCCCCGCC 300 CCCCTGCCCC AGCGCTGCTG AACCTCGACG TGTGTGTCTG AAGGTCTCCA TCCGTGCCTC 360 TCCAGACGTT GCCCACCTTC CCCTTTGCTG GGCAGTTTGT GTAACGCGGC CAGCAGGCAC 420 CGCGAGGCCT TGCTTCCTCA CCTCTCGCCC GCTGTCGGAG CTCCATGAGT TGAGCTTGAC 480 TGTCCGGGGA GTGGAGCCAC CTCTAGCAGG TACTTGGGTG TACCTGTTAT CACCCATCTG 540 TCAGCTGCCG CTAGACAGCA GAGGGAGCCC AGCATGGGGG AGAGAGGGGA CACTCAGAGG 600 GTTGTCTGAG CAGAGGTGGT TCTTTCAGAA TCAGAGGAAG GTTGTTGGGT CCTACTCCTT 660 CCCCCCAAAC CCCTCAGAGC GAGGATCCTG ACCGTCCCTC TTTCTAGCTG CGTGACCCTG 720 GTTGAGTGGG CTCCTCACAG GTGAGGTTCA AGGAGGGGCG GGGCGTCTTG CCTGGAGGTC 780 TCCCAGATGG GGAATCCAAG CCCTAAAAAG GCATAATAAC TCGGAGCTGT GTTTCCACCC 840 CGACCCCGCC CCCCGCTCCC CGCAGAGTAC TGAGCCGGAA AGGAAGGAGG GAGACTGAGG 900 CAGCTCGGAG TCACTGTAGT GGGTGTGAGG AGTGCACTGA GCCCTGTGGG GAGGAACGAG 960 GGAGGACACA GCTGGCGGGT GCCTCAGAGC CGCCCCCCAC GCTAGGCTGC CTTCAGGCAG 1020 CCCCTGCAAA CTGTGAACCC AGAAAAGCCT CTCTCTTCCT GGCCCCCTCC TCTCCTTCCT 1080 CTCATCCCCC CAACTTTGCA GCCTTCCCTG GCTTCCTCCT TTCATTGGAG AACAGGCAGA 1140 CGCTCACCAG GGCCGGGTGT TCACGTGTGT GCATATGTGC CAGTGTGCAC ACGTATGCGT 1200 GCTCCCATAA CATGCATGTT TTTCTGAGGG TGTGTGCACG CGTGCGTGTG TGCATCGTGC 1260 GGTGTGCGTT AGGTGCACAC GTGCATGCGT GTGCCTTATG TTGTGCGTGT GAGTGTGTGT 1320 GTGTGTGCGC GCGCGCGCGT GCCTGACCGC GGCGTGCGTG CCGGCGGGAG GAGGGGGCGC 1380 CGAGGCCGGG CAGGGGATTT AAAGCTGCTT TCGCGGCTGC CGGCGTGAGC GCTCGTGATA 1440 AACAGCCCGG AGCCGAGCCG CCGCGCAGCC GGGCGGGAGG CTGCGTATCA GAGCTCCTGG 1500 CAGGCTCGCA AAAAGCTGTC CCCGGCCCGC CGCCGCTCTA TCAGCCCACG GAGGGAGGGC 1560 GGCGGGGGAG GGAGGGAAAA AGTATTTGCT TCAGCCCTTA ATCACGGAAT TTGAAATCCC 1620 AGCGAGTCGG TGCCATTTAT TTTCAGAGGC TGTCAAGGCT GGTTTCAGCA TTTAAAAGAA 1680 AGGAGGATAA AACGCATTTG CATTTCTCCC CCACTCTCGC TGCGCGCTCG CCGGCGCTCC 1740 CCCTCGTTCC CTGCGCAGCT CGCGGGTCGG GCGTTGGCGG GGAGGGGGAG GCCAGAGGCT 1800 TTTCAAGGCG CTGGGGGCTC CGGCCGGCCC GGTGGGGGCC TCCCCCCGCC AGAGTCAGGG 1860 GTGTCGGGCG ATTCCGGGGT GGGGGCCCGA GTCTGGTCCA GCGGGGCTCT GGGTGGCAGA 1920 GGGGGGAAGG TTAAGCGGGG CTGCTGGCTT GGGGAATTTG GGGCCGTCCG CGGGGCTCTC 1980 CTCGGGCTCC AAGCTTTCAC CCCAGAAAAC AGCCCTGAAC CCCAAATTTG CTCCAGCCCC 2040 AGGGGGCCCT ACCTGCCCTT CCTGGCTTCC CCAGTGGAAA TCTAAGGTAC TGGAGGCTTC 2100 CAGGGGAGCC AGGGCACCCC TAGGACAACC CCCTCTCTCT GCAGATGGGG AAACTGAGGC 2160 CTGGAAACAG AGAACGGTGG GACCAAGGTC ACATGATGGC GGAAGGAGGA CAAGGAAGGA 2220 GGCTGACTGC GTATCCAGCA CGTGTTCCGT GCCAAGCCTG TGCAGGGGCC AAGGACCGGG 2280 GTCTCTGGAC AGCGCCGGTT GCTGGGTCCC ACGCTGGGCG ACAGGGCCTT TGCAATCAGG 2340 CCGACAGGGT TTGAACCCTT GCCGCGGCAC TTTCCAGATG GCCTTGGCCA CTGTCCCCTC 2400 TCTGACCTTC AGATGGAGCC CATGGCACCT CCGGAGGGGG TGTGTGCTTC CAGGACCAAA 2460 TCCACTTGTG CGTGGTTAGG CACGAGGTGG GGGGAGGCGG CTCAGCCACC GGGACCTGTC 2520 CTGCCTCCAC CCTCTGTGCA ACCCCTTTCC TTGCCTTTTG TCTCTGTTGC TTTTGGGGGG 2580 TGATTAGCCG CTAGCTCAGC GGCTAGAGGA TTCTCTCCCG GAAAAGGCTC CGGAGTTGAG 2640 GCCCAGACCC CCAGGGCAAG ACGGAATCTG CTCCCCAGGG CACTAACTGA GACTCGGTTC 2700 CCTCACTGGT AAAATGAGAA AACTCACTTA TGGTCAGGGG TCCCCGAGTT AATGCCAGTG 2760 AATTCCTTGG CAGAGCATCA AGCACTTGGA GAAGCCCCCA CCCCCGGTCA TTGTGATGAT 2820 GGTTTGTTTG TTTGTTTGTT TGTTTTGAGA CGGAGTCTCG CTCTGTCGCC CAGGCTGGAG 2880 TGCAGTGGCG CGATCTCGGC TCACTGCAAG CTCTGCCTCC CGGGTTCACG CCATTCAGGT 2940 GATGATGTTT TTTATTTATG TGCCCACCTG CCCCACTCCG TAGGGCCCCT CGAGGCCAGG 3000 ACTGCACCGT TCATCTCGGA ATTCGCTTGT TCCTAACTTA GGGGAGTGGC GCCGAGACAC 3060 CGTGTAGCGC CCATGCCAAG GAGGAAGCGA GACAGCAGGA GCGGAGGAAA GAACCCCGGG 3120 CTGTGTTGAG GAAGCCTCCT ACTTTTGCCT GAAGTGAGGT TGTTGTTGTT GTTGTTGTTG 3180 TTTTTTCCAC GTGCCTTATT CATCCACGTA ACCTCAGCCT 3220
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