Tag | Content |
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EnhancerAtlas ID | HS136-04120 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr12:289100-290480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYCN | MA0104.4 | chr12:289809-289821 | GGCCACGTGGGC | + | 6.27 | MYCN | MA0104.4 | chr12:289809-289821 | GGCCACGTGGGC | - | 6.27 | ZIC1 | MA0696.1 | chr12:289287-289301 | GACCACCTGCTGAG | + | 6.13 | ZIC3 | MA0697.1 | chr12:289287-289302 | GACCACCTGCTGAGC | + | 6.09 | ZIC4 | MA0751.1 | chr12:289287-289302 | GACCACCTGCTGAGC | + | 6.12 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65535 | chr12:281259-289389 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 289711 | 289811 | chr12 | 289742 | 289883 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I000180 | chr12 | 289304 | 290156 |
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Enhancer Sequence | GGATGGAGAG CTACAGTCCG TGCATCTCCC TCCATAATGA CCCTTTGTAG ATGGGAGAAT 60 GTCAGACTCA TCAGTCATAG ACTTAGAATG CTCCCAGTAA GGGGTCCCAG GATGTACTGG 120 TTTCTGGCTG AGAGCAGTGA CCCAGAGCTA GTGCTGGAAA TCAGGGTGAA CTGAACCGTA 180 AGTTTGAGAC CACCTGCTGA GCACTGTTTC AGGTGCTGGG GGCTATGCAG TGAAGGGGAC 240 AGGGAAAGTT CACACTGGGG GGTGTCATCA ACAAGAAATG GAGCAGCTGC CTTCACACAG 300 AGGATGGTGA CCCCGCTGGG GTGATGGGGA GAGCCTGTTT TAGGGTGAAC ATTCAAGGAA 360 GGCCTCTCCA AGGAGGAGAA TTCAACAAGG TCAAGGTCTG GTCTGAGGGC AGGTGAACAG 420 TTCGGAGACC ATCACTTCAA GTCAAATGAC CACATATTTA TGAGGCAGAA ACCAAGACAG 480 TTTGTCAAAA AACTGTTTCC TGATATATGT GTTTACTTAC ATGAAAAAAT CTTATGAATT 540 AAGTGTAAAC ATGAATTCAA AACATCTTTA CTGAGGAAAG CAAAATTGGT CTTCTAGCAA 600 ATCCAGGGCA GACGGTCACC AGTCACAGGC CAGGAGAGGA AGTGCTTGAG AGTGAGCAGT 660 CAGGCGCTCT GGACAGGCAA GGATGGGGCC GGGGGTGGGG CAGAGCTTAG GCCACGTGGG 720 CAGCCACCAC CACAGGAAGA CCAGGCCACC GAAGTAGACC GCAGAAAGCA CAAACCAGCA 780 ACAGTGAAGT CAGGCTACCC TGAGCCGAGG CAGCTGCTGC CCAGAGCAAG CACGTGCTTG 840 TGTGACCCTG CATAGGGATG GGGAGCAGCC CACTCCAGGT CAAGGCAGCC TGCTGTCCAC 900 CTCCTCCTCT GTCACCTCAA ACCAAGAGGG CTCAGGTTTG CCATTTTCAA ATTTTTCCTG 960 TATTTATGTT TCAAAGAAGG GGCCTTGGTC TGTCGCCCAG GCTGGAGTGC ACTGGTACGA 1020 TCACAGCTTA CTGCAGCCTG CAACTCCTGG GCTGAAAGGA CCCTGCCGCC TCAGCCTCCC 1080 AAGTAGCCCA GACTACAGGT GCATGTCGCC ACGCCCTGCT GATTTTTAAA TTACTATTAT 1140 TATTTTTGTA GAGATGAGGG TCTCTCTCCA GCCTGGCCAA CATGGTGAAA CCCCGTCTCT 1200 ACTAAAAATG CAAAAATTAG CCAGGCATGG TGGCGTGAGC CCATAATCAC AGCTACTTGG 1260 GAGGCTGAGG CATGAGAATC GCTTGAACTT GGGGGGCGGA GGTTGCAGTG ACCCGGAATC 1320 ATGCCACTGC ACTGCAGCCT GGGCGACAGA GCGAGACTCT GTCTCAAAAT AAATAAATAA 1380
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