Tag | Content |
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EnhancerAtlas ID | HS129-03786 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:229431660-229433110 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr1:229432639-229432654 | GGGCCAAAAATAGTA | + | 6.27 |
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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 |
GH01I229295 | chr1 | 229431613 | 229433439 |
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Enhancer Sequence | ATGCCAGCTC CCCCTGGTGA AGGAGGGTGC TCAGTGCCCT GCAGCCCAAA GGCTGGTCTT 60 GGCGAGGTGC CCTCCGTGCA GTGTGTGCTT TGTGTGTCCA GGGACGGTGG TGTGGCTGGC 120 ATCCAGGAAG CCCCTTAGCC CTTCCATCTG GGGTCTCAGA GGTCTTTGAA CGAGCCCCTA 180 CCACTGCTTT CCCCTGCAGA GAAATGTGTT TGTAAGGTTT TAGGTGGATA AAGCAATCCA 240 TGCTATTACA TTACATTTCT TGACATGATG CTTGGACACT TTCCTTAAGG TTCACAAAGC 300 TTTATGTATG GAAAGTTATT AGAAGTGAGT TGAGAGAGGG TGAGGACACA GACTCTGGGC 360 TGAGATTGCT GGGTTCAAAT CCCAGTTGCA GTCACTAGCT GATTGACCCT CTCAGGCCAG 420 GTGCTTCAGC TGCCTGGGCC TTAGTTTCCT TGTCTGTAAG ATGGAGATAG TAATAATCAC 480 ATGATCCTCA GGAGGTTATT GGGAGGTTTA AATTAGTTAA TGTGAAGCAG TTAGTAGCTG 540 TTTGTGACAT ATGGCAATTT AACTGAAATA AAAAATTCTG TTCCTCGATT GCACTGGCCA 600 CATTTCAGGT CCTCAGTAGC TACATGTGGC TGGTGACTAC CATATCAGGA CAGATTATAG 660 AACATTCCTA TCCATGAGGA AATCACATTC AGCAGTGCTG ATCTCAGTAG CACTGTCTTA 720 GAAATGTGTC ATCTAAATGG CATCATCTGG GGGCCCTTTC TGGGTAGGAA CCTGTCCAGT 780 GAGAGGATGT CACTCAGCAG CCGCTTCCCT CTTCCAATCT GTGTCCCGGG AGCCAGGCGT 840 TCTGAGAGGA GGAAGGCAGT TTCTGGCCCA GCCCTTCCTG CACTTGCCCA GGCAGTGAAA 900 GGCTCAGCCT GCTAAAGTGT GAAGTCATCA ATCAGGCTAG CAAAGTGCCA TGAGAAGAAC 960 TCAATCCTTA GACACATGAG GGCCAAAAAT AGTAAGTCTG AGAGTTGGTC CTGGAGTCAG 1020 ACAGAGCTGG TCAAGTCCTG ACTTTGCCAC TGGCTGCTGT ATGACCTAGG GCAACGTAAT 1080 TAATCTCTCT GGGCCTTGGA TTTCTCAGAG AAAAGGGGAA TAATGGCAGT CTGTGTCATG 1140 GAATCTTTAT AAAGAATCAA TGTGATAAAG TCCTGTAAAA CAAAGTGCTG GCACATTGCA 1200 AGGATTCATT AAGTGGCAGC AATTAGCTAT GAAATCTTGC CTACCAGAGT CTAGTGCCTT 1260 GCGCATGCTA AGAGCTCAAT AGATATTTGT CAATTGAATG AAGGAACATC TCTTTCCTTT 1320 TGCCCCATGA CTGGGCAAAC GAAAAATAAC AAAATATCTC ACTTGCTGTC TCATTTTACC 1380 AGAAACAAAA TGGAACAAAC TGTGGGTATG GTATATACTT GGTGCATTCA CGTTGTCTGA 1440 GTTATCTTAA 1450
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