Tag | Content |
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EnhancerAtlas ID | HS105-13851 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:45067400-45068690 |
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) |
TFAP2A | MA0003.3 | chr11:45067769-45067780 | AGCCTCAGGCA | + | 6.32 | ZNF263 | MA0528.1 | chr11:45068427-45068448 | TGTCCTGCCTCCTCCTCCTCC | - | 6.68 | ZNF263 | MA0528.1 | chr11:45068430-45068451 | CCTGCCTCCTCCTCCTCCTCC | - | 6.82 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_33426 | chr11:45060876-45080805 | H2171 | SE_66866 | chr11:45060876-45080805 | H2171 |
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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 |
GH11I045045 | chr11 | 45066690 | 45069025 |
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Enhancer Sequence | AAGTGTTCAG CCAGCCACAC ACAGTGAGTT CCTGCCCACT GAATAACTTC CCTCCTCCAC 60 TCCTGTCCAC TCTGCTCCCT GGTGGCTTGT TGGCAGCAGG GAACTGATTA AAACCAATCA 120 GCCAATTTAC CCTGGAGAAT CCGGGATGTG GTGCTCCAGG TCGCAGCTGG CATGGGCTGA 180 GACTGCAGGT GAAGGCATAG GTGTCTGTGC TGCCTCCACG AGCCAGTGGG GGTGGACGGA 240 GATCCACGGG GTGCGTGAGT CACAGGATAT TGCTCAAGAT GACAACAGAC AAAAAACAGA 300 CTAAAGCCCA GGAGACGACC AAGTGATTAC TTTTTAAATC AAGAACTCTT TACAGATTTC 360 TGCTAGGCCA GCCTCAGGCA ACAGGGGTCA AAGAAGAGTC TAGCTGGGAA TTGTAAAAGG 420 AAACAGGAAA CTTGTTTCCT GCCGATTGGC AGGAAGTGTG AGCAGGAGTG GTTTATATTT 480 GGAAAGAGAA AGGTAAGGAG GGGGACCTAG GGAGTCTCTG TGGTCTGAAA ATGCTGTTGA 540 CGTGGACAGT CCACCTTGCT GAGCTCAGCG TTGCCCCGAT CTCCTGGGAG TGAGGACGGG 600 CGCGGTTCCG ATGCTTCACA GCGTGAATCT GCATCTTTTA TTCACCTTCT CTAAGCCTCA 660 GTTTCCTCAT CTGCACAATG AAGAGAAGGA AGCCCACCCC CCACCCCCAG GAGATGTGAA 720 ATGTCAATAG ACCAGTGTAT GAAGTGCCCT GCACATAGCC GGTGCTTAGC AAATGGTAGC 780 TTATGATATT ATTGTCATCA AAGTCTCCGG GTGCTGTGAA AGATAGGAAG GTCAGAAAAT 840 ACTTTTCTGA GCTCGTGACA AACTGGGCCT TGGACGAGCA GGCAAGGTGA GAAGGAAGCG 900 CCAGGCAGAG GGAACAGCCT GACCAAAGGC TCAGAGGTGG GACGGGGGGG AGCTTATTTG 960 GGCCACACAA CTGGCAGGTC CTGATTCTCA CCCCACTCCC AACTATGACT TTGGGAGGCT 1020 GTCTGTCTGT CCTGCCTCCT CCTCCTCCTC CCAATGGCTA TCTCGGTGGG AGTCCTAGGG 1080 AGCAGGGTGA GGGCACTGGG GGAAGGAGAG GCAGGTTTTG GCGGCTCGGG CAGGTGGCAG 1140 TGGCAAGGGC CAGAGAGAAC AGGCTGTGGT CTAGTTAATC AGCCCGGACA CATCTGATTA 1200 CCAAGAGGGG ACGAGGACAG TCCCAAGGAG GGGCAGGACA TCCTACATCT CTCCATCTAG 1260 GGTTGCTAGA TTTAGCAAAA ACAACAGACA 1290
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