Tag | Content |
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EnhancerAtlas ID | HS176-08219 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr11:116297990-116300310 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr11:116298457-116298468 | TCAAGGTCATT | + | 6.32 | Esrra | MA0592.2 | chr11:116298456-116298467 | CTCAAGGTCAT | + | 6.02 | Esrrg | MA0643.1 | chr11:116298457-116298467 | TCAAGGTCAT | + | 6.02 | Gata4 | MA0482.1 | chr11:116299290-116299301 | GGGAGATAAGA | - | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_63251 | chr11:116282793-116299761 | GLC16 |
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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 |
GH11I116426 | chr11 | 116297369 | 116300113 |
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Enhancer Sequence | TGGGAGAATC ACTTGAGCCT GGGAGGCGGA GGTTGCAGTG AGCCAAGATC ATGCCACTGT 60 ACTCCAGTCT GGGTGACAGA GTGAGACTCT GTCTCAAAAA AATAAAATAA ATAAAAAATA 120 AAAATAAAAT GGCCAGCTCA GAAATCATCT CCTCCAGCTT TAAAAATCTG AAATGTTCCT 180 GAATTAAGCT GAGCTTACAG TGCTGTAAAT GGTCTTTGGT GGTGTTGGCA TTACAAGGAA 240 GAATGACAGC AGAGTGATAT GAACTAAGTG GAGGGATCAG GGCATGGCCT CTGAAGGAGA 300 AAGATCTCAC CTTGAGCTAA TGTGAGGGCC CAGGGATCTA GAATCCTATC TAAACCCCAG 360 GCCTAACTAT CCCTCAATTC TACAATGTCA TAGCTTGGGA GCCTAAAAGC TGGACAGAGT 420 CGTCTCCTCT GAAATGGCCT AGCCCCTGTC CTTTCAGAGA GAGCTTCTCA AGGTCATTGC 480 AAAACCAGGC TCTCAAGGCC CCTCCCTACA GCCTCGGCTT TCCTCTCTAG GAGCAAAGTC 540 CCACCAAGAC CTGAACTCTA GCTGCAAGAA TTCAAGACGT GTTCAATTCA CTTCCAGGTT 600 CTCCTCCCAC CCACCACCAG CCCTCTATCC CCCAGAGCTA GGCAGCAGCT GCTGTTAGGA 660 GATCCTATCC AGCCCTGGCT TGACATTTCA ACAGCCCGAG ACCCAGAGAT AAAAGTTGTC 720 ACTGAACAAA GTTCATCCCC CTCTCCCGCT CCCTTCCTGG AGCCTCGATA GGCATCAGAA 780 TGGGCACTGA GATGGTCTCT CTTGCTTTCT ACTGCTGCTG CCGCTGCTGC AATTCCTGCT 840 TTTTATTTAG AGGGGTGGGG GGAGATTTCA CAACTGATGA TTACGAAGAA GCGGTTTATC 900 ACCTGTGCTT TTATGATTGT AGCGACTAAG GGGAAAAAGA TGTCTTTTCA GATAAGCATT 960 TGAAGGACGG GGAGAAAGAT TTTCAAAGCT CCCTTTGTTC TCCTGGAGGG CCACGCCATT 1020 GAGTTCTGGC AGGCAGCCCG GGAGAAAGGA GGATTTTAAA AACACAATCT GAGCTGGCTT 1080 CCAAACCCCT GCTCACCATC CCTGTCATCA ATTAGGGATG TTACTTAACA AGGGGTTTGG 1140 GCCATTGTCT CATCCAGCCT GCTTTCCCTA ATTGGATGCA GAGTGGTGAT GAATTATTTG 1200 GAAAAGGGCT CCACACTGCA GAGGTCATTG CTTTGGCCCC CTGACACTCA AGGCCAGCTC 1260 AGGCTGGGCT GGTGTGGGCC TCTGGGGCAT GTTGCTGGCA GGGAGATAAG AGAAGGACCT 1320 TTCTGAGGCC CCTCAGTGCA GGCGGAGAGC ACAGACCCAG AACCCAGAGA AGGGCAGGCT 1380 GCCAGTCCAT GCGGGGAACT GAAGGTGAGT GGCCAGGGAG AAGATGGGGG CCGCTCCTGT 1440 GGCCTCTGCC ACCCCCAGCC CCCACTCCAG TTTCTGAAGA TGGAGCTCGG TGAGCACAGA 1500 GAGCTTTAAG GCCTCAGTCC ACAAAGGGAC GGGTCTGAAT TCGTTAGGTC AAACTGCCAT 1560 AGACTCATAA ATATTGTGCC CAGAATCCCC CAGACCCTGA GTTACGGACT GAGTCCACCA 1620 AAGGTTAAGA AATGGCCATC ATCCTCAGCA AAGGAAAATG CATCCTCCAC AGCTTCCAAT 1680 GGAGAGAACT CTAGGTGAAA GAGAAGCTGG ATCCCATGGC ACACTGGGTT GCCCTTACCT 1740 TTGGAAATGA CTGAGGCCCA GAGTTCAGGA TGCTCCCCCA CTTTACCCTG CTGTCCCAAG 1800 TGTGGGACCA TTTTCTTTCT TCCTCACAGT GTAACTGAGA TCAAACTGCA ATGTTTCAAT 1860 AAAACCTTAC TAAATGCCCA GAAGAAACAA AAGAGAAAAC AGAGTAATAC AAAATCAGAT 1920 CATCATCAGG TTTAAGACCT ACAGTTGGCT CACGTTCAAC TTGGAGCCCT CATAAGTTGC 1980 CTCCCCACCA GGGTGGATCC CCAGCTTGCC TCCCTTGCCA GAGGCAAGCT TTCCCCAGCT 2040 CATCCAGGAT GCTGGAAGTT CATATCCAAG CAAGAGAGAT GGAGTTACCC TCCAACCTAC 2100 CTAAGACCTG CCTTCTAACT CCTGAGTTCT GTCTAGAACC TACCTCTTGG CTGTATAATT 2160 AAGGTAGGGA GGCCGGGCGC AGTGGCTCAC GTCTGCAATC CAGCACTTTG GAAGGCTGAG 2220 GCGGGCAGAT CACTTGAGGT CGGGCGTTCG AGACCAGCCT GGCCAACATG GTGAAACCCC 2280 ATCTTTACTA AAAATACAAA AATTAGCCAG GCGTGGTGGT 2320
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