Tag | Content |
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EnhancerAtlas ID | HS007-03324 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr11:112619310-112620530 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr11:112619852-112619867 | TGACCTTTCACCCTT | - | 6.48 | Nr2f6 | MA0677.1 | chr11:112619852-112619866 | TGACCTTTCACCCT | - | 6.38 | PLAG1 | MA0163.1 | chr11:112619860-112619874 | CACCCTTGGCCCCC | - | 6.46 | Rxra | MA0512.2 | chr11:112619852-112619866 | TGACCTTTCACCCT | - | 6.63 | ZNF263 | MA0528.1 | chr11:112619897-112619918 | AGAGGAGGGAGCAAGGGAAGG | + | 6.28 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_03529 | chr11:112619145-112619670 | Brain_Angular_Gyrus | SE_03529 | chr11:112619775-112620286 | Brain_Angular_Gyrus | SE_05265 | chr11:112618618-112620285 | Brain_Cingulate_Gyrus | SE_06321 | chr11:112618870-112620411 | Brain_Hippocampus_Middle | SE_08094 | chr11:112618470-112620523 | Brain_Inferior_Temporal_Lobe |
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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 |
GH11I112747 | chr11 | 112618471 | 112620523 |
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Enhancer Sequence | GCTTCAGGGT CTGTCCTCCA GGATCTCTTG TCCACAGTTT CAATGTCAGA AGCTAAATCA 60 CAGAGAACAG AAATCATGAT GAGCTGAGCT TCTGAGGCAA AGTTGGGGAG CTGCTTCAAA 120 CCCTGGCTGT CAATTCAGGG GCTGGGGGGA GAGAATCTGA ATTACACAGG CAAAGTGAGT 180 GTGGGAGGGT CTTGAATCCA GAAAAGCTGC AAACCAGGAG TAACCAGGCA GGTGGGCAGA 240 GGGTGGCTTG CATTCTGGAG CTGTCGGCTG CTGCCTGCAG CAATCTTTGG AGCAGTCCCA 300 GCATGGGCGA GTGTGGGCTG TGCAGGGACA AACAGGCAGA GGAGAGTGGC AGGGCTGTGC 360 ATGGCCCCCT CACTGCTGCT GAGACCTGCT TTCTGCCAGG GAACTCCTCG GGTGGTTGCA 420 GGGGGCAGGC TGGCTAGAAA CACTTTGGGA GCAGATGTCT CGGGGAAAGG CAGCATTTCT 480 CAAAGTTGGT TGGACGTCTG CCAGCCTGCC TCCTGGCCCA TGTCACAGCC CCCTAGGCTC 540 TGTGACCTTT CACCCTTGGC CCCCAGTTCC CCTGCATGAG GCCAGGGAGA GGAGGGAGCA 600 AGGGAAGGGG TCAGAGCTAT GAATCTTTCC AGCTGGCTAG GAGGGATTAT CACCGCATAA 660 TAAATCCAGG GCCAGGCGTG TTTATGAGGC TCTCGGAAGC TGCAGGAACA ATATCATTTA 720 GAAAACATTG ATGCTCACGA GGCGAAGGCA ATCCCACCCC CTTCCCTTAT TTATGAGGCA 780 TGTTGGGTAA TTAAGTGAGA GCTGGGAAGG GAGGTGGTTG GGAGAAGATC ACCCCTAAAT 840 AATCCTGCCT GGTGAAGCCA CCATCTGGGC TGTTGTGCAG CAAGGATGGC CCCCATATGG 900 TTGGATAGTT TATGAGCAGA GCAGTGATCC AGGGGCTAAG GAAGAAATAC TTAAGAAATA 960 TAAGTAGACT CACACAGATG TGGTCTGAGC TCCAGGAGGA CAGAGACCAC AACTTATTCA 1020 TTGTTATAAC CCTGGAACCC ATCACAGTGT CTGGCATATG GTACTTGCTT AATGTACATT 1080 GTTGAATAAA TTCATTCATC CATGCATTGG AGAACAATTT GACGGGTGTC TATATGTGCC 1140 AGATTCTGCA CTTGATACAC ACTGCTTTGT AACAATGAAC AAGACAGACA CAGCTTCTGC 1200 CTTCATGCAG CTTATGATTT 1220
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