Tag | Content |
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EnhancerAtlas ID | HS184-31861 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr9:139000990-139003460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr9:139003051-139003064 | TTCCAGAACCTTC | + | 6.3 | KLF5 | MA0599.1 | chr9:139001284-139001294 | GCCCCGCCCC | + | 6.02 | MAFF | MA0495.3 | chr9:139002714-139002729 | TTCCTGACTCAGCAC | - | 6.03 | MAFF | MA0495.3 | chr9:139002046-139002061 | ACGCTGAATCAGCAC | + | 6.25 | MAFF | MA0495.3 | chr9:139002046-139002061 | ACGCTGAATCAGCAC | - | 6.3 | MAFG | MA0659.1 | chr9:139002043-139002064 | AAAACGCTGAATCAGCACTCA | + | 6.63 | MAFG | MA0659.1 | chr9:139002043-139002064 | AAAACGCTGAATCAGCACTCA | - | 6.87 | MAFK | MA0496.2 | chr9:139002712-139002731 | ACTTCCTGACTCAGCACTC | - | 6.25 | MYC | MA0147.3 | chr9:139002412-139002424 | CAGCACGTGGCC | - | 6.37 | TP53 | MA0106.3 | chr9:139001670-139001688 | GGCATGCCCGGGCACGCT | + | 6.05 | TP53 | MA0106.3 | chr9:139001670-139001688 | GGCATGCCCGGGCACGCT | - | 6.83 | ZEB1 | MA0103.3 | chr9:139001291-139001302 | CCCACCTGCCC | + | 6.14 |
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| Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
SE_06335 | chr9:138999308-139004425 | Brain_Hippocampus_Middle | SE_24880 | chr9:138998517-139002637 | Colon_Crypt_3 | SE_27238 | chr9:138998249-139002839 | Esophagus | SE_34358 | chr9:138998996-139003846 | HCT-116 | SE_41290 | chr9:138999650-139002647 | Left_Ventricle | SE_42022 | chr9:139001070-139002421 | LNCaP | SE_42851 | chr9:138998999-139002813 | Lung | SE_47727 | chr9:139000981-139001614 | Pancreas | SE_48413 | chr9:139000434-139002369 | Psoas_Muscle | SE_49310 | chr9:139000245-139002578 | Right_Atrium | SE_50914 | chr9:138998248-139002848 | Sigmoid_Colon | SE_63238 | chr9:138991973-139023521 | GLC16 | SE_65568 | chr9:138998988-139004881 | Pancreatic_islets | SE_67042 | chr9:138998256-139002692 | H2171 | SE_69162 | chr9:139000391-139003532 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 139001832 | 139002080 | chr9 | 139002200 | 139002512 |
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Enhancer Sequence | TCACAGGGCG GGGACACCGA GGTTCTCCCA TAAATTAACC AAGCCCCTTT ACGAAGCCCC 60 TTCCCAAATA GAGCCGGCGC CCTCCTCCCC TGGGCCCGGG TCACCGCTGG GTCAGCGCCT 120 ACCGGCTCCC CAGGCCTGCC CCATGCCCTC AGCTAGAGGC AAACCCAAGC TCATGGGCGC 180 AGCGAAGCTG GCAGGAGGGG CCCTGGGGGC TGTGGCTCAC CCCTGCATGG CCCTCCTGCT 240 GCCCTGAGAG CCCCTTGGCT CCGGCTGTCC CCATTAGTCG GGTAGGACTC TTGGGCCCCG 300 CCCCACCTGC CCCTTCCAGT CTCCGCCCAG GTCAGGACGG CAGGTGGCCC CAGCAGGGCT 360 GGCCTGAGAT GGAGGAACGC GGCCCCGACC CGGGCTATGG GGAGACTCTG GATGTGGCGG 420 TGGATCCGCT GACGGGGCTT TGGGATGTGA TTATTTCCTG GGGGCTGACG GTAGCCCAGG 480 AGCACCAAGA CCCAGCTCTG CCTTCCGCCT CCCACGGGGC CTCTCCTCTG CAGGAGGCCA 540 TACAAGGACT GCACGGAAGG GGAGCGGCCC CGCAGGGAGG GGGCGCCTGG CAGCCCGCCC 600 GCCGCAGCAG CCTGCAACCC CGCCCCCAGG CGCAGTGCGC GCCACAGCAG CCCTGCCAGA 660 GCCCGTGTGA CACAGCTGCC GGCATGCCCG GGCACGCTGC CCAGCTGGGC TGGGGGAGGG 720 GCGCCGGGCC AGGAGCCGCT GAATCAGCTG CACCCGGACG GCCCCGCCTG GGCAAGGATG 780 CTGGTGCGGC GGGGCGCTCT CTCTTTTGGG AACCGTCAGG AGGCGCGCCA GGCGGTGGGG 840 TGGGGGGTGT TTCTGGACTG CGGCCTCTGC AGCCTGCTGC ATGGGAAGTG CGGCTCACCG 900 GGGCTGGGTG CAGGGCAGCC CCCGCCTCCG AGGGCATGAG CGGAGGCCTG CAGGGAGGGC 960 CTGGGCAGAG AGGGGCCCTT TCCAAAGGAG ACCCATAAGG AAGAAGAGAA ACGCACTGGC 1020 CTCTGCAGAT CGAAGCACGT TTGTCTCCCC CAGAAAACGC TGAATCAGCA CTCACAGCAC 1080 TGCCAGGGCC CGCGCCCTCC TCCGATCGCA CGCTGGAGGG GACAGGCCCT TCCAAGATCA 1140 CGGAGCATCA ATATCACCAT CGACGCAGCG GCACCGGGGG AGTCATGCTC TGGTCTGGAG 1200 TGGGGGCCGC GCCTGGCCCT GCCGTCCTTC CTGCTGGGGG CTGTGTTTGG AGCCGGGCAC 1260 CTTCCCCCTC AGCCCCTGCT GTCCTGTCCT GCCCCCTGCG GAGGGGCGGG AGGTGGAGGA 1320 CATTCCTGTG TGTGTGCGTT TGGGGTGGTT TTGCCTGTGG AGGCTGCACA TGGGGGCTCT 1380 GACGGGGCAG CCTTCCGAGG CCACCCTGTG CTGGGGATGG GACAGCACGT GGCCCATCTT 1440 GACCGAGCAT CTTAGATCTT GAAATCCCCA GCACCACCCC CTTCCAGCCA CTGCCTGCCC 1500 TCTGCTGGCT CCTCAGCTTG GATTCCACTT TTCAGCAACA GAGACCCCCG GTCTGGTGCC 1560 CAAGCTGGTG TCCCCGTGTG GTGGACGACG GGGAAAGGGG GGCTCTGGGA GCCACTCGGC 1620 ACAATCCCCC TGGGCCAGGC ACAGACTGAA AATCAGACCC CACTAAGTCA ACAGCCCCGG 1680 GCTGGCTTTG GTGGCTTCCT CCACACCCCG CGCCCGGCTG TGACTTCCTG ACTCAGCACT 1740 CTGTTCAGCC TGAGATGGAG CCGCTCCCCA CCTCCAGGCC TCCCTCCCAC CCGTCTCCAC 1800 CCAGGGGCCG CCCTCCCCAG AGCCCCTCTG ATTCCTCCCT CCCCGGCCCG CCCAGCTCCC 1860 CCTCAGCTTC GCGCCTGCCT TGGGCTGGAC ACCTTCTCTG TGGTCCAGGC TCAGGGATTG 1920 GTCCAGGGCC GCCCACCCTC CCCCATCCCC CAGGCCGAAC ACTGACCTCT GGTGCCAGGC 1980 TCCTCACTGC CAAACCCATG ACTCCCAAAC CCACTGCTGT CACTGGGGGC CTCTCATCCA 2040 GCCAGCGCCG GGCAGCTCTG ATTCCAGAAC CTTCCCGGCA CGTTCCTGAC CTCCAGGCCA 2100 GTCTGCAGCT ACCTCCACTT CCCACCGTCC CCAGGAGCAG CCAGCGGCCC TCCCTGCCCA 2160 CACCTGTCCT TCCCAGCTCA CTCAGGTCCG GCCGCCACCC TGAGTCCCCG GGGCCACTTC 2220 CCTCCTTCGC AGGCAACCGA GGCCACTTGC AGTGGGAGGG GAACCGCTGT ATGGACCAGC 2280 CGCCTCGTAA GGATGGATCC TGTCTCCTAA CCGGCTCCCA ACTCCCTCCG AAGCGGCTGC 2340 GCGCTGCCTG AGATCTCTGC AGGAAGCCGC AGCGGCCACA TGCTTAGGTT CTGTCTCAAC 2400 ACCTTCCCAG TCCTCGACTC CTCACCACTG CTGGAAGCTT CTGGAAGCCT CCAGGCCTGC 2460 AGGTCACTCC 2470
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